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rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11492.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12040"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12010"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12072"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12198"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12260" xmlns="http://purl.org/rss/1.0/"><title>5-year oncologic outcomes of Endoscopic Extraperitoneal Radical Prostatectomy (EERPE) for prostate cancer: Results from a medium-volume United Kingdom centre</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12260</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">5-year oncologic outcomes of Endoscopic Extraperitoneal Radical Prostatectomy (EERPE) for prostate cancer: Results from a medium-volume United Kingdom centre</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">McNeill AS, Good DW, Stewart GD, Stolzenburg JU</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:34.127022-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12260</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12260</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12260</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12260-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To determine the 5-year oncologic outcome of Endoscopic Extraperitoneal Radical Prostatectomy (EERPE) from a medium volume centre thereby providing much needed data on the oncologic outcomes from the United Kingdom.</p></div></div>
<div class="section" id="bju12260-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>From January 2006 to January 2012, 575 patients underwent EERPE for localized prostate cancer by a single surgeon who had completed a modular training programme.
Follow-up was standard as per local hospital policy and data collected in our prospective database. A retrospective review on patient demographics, PSA, pathological T stages, Gleason scores, margin status and biochemical recurrence data was performed. Biochemical recurrence was defined by a PSA level &gt;0.2ng/ml.</p></div></div>
<div class="section" id="bju12260-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Mean patient age was 62-years (range = 40.3 - 76.5), mean follow-up was 30 months (range =12 – 72). Median operative time 135min (IQR= 120-170), median blood loss 200mls (IQR=100-250mls).
135/575 (23.5%) had positive surgical margins (PSM). PSM rate for pT2 disease was 66/406 (16.3%) and for pT3 disease 68/168 (40.5%). Overall BCR-free survival at 5-years was 81.5%. Multivariate Cox analysis showed that positive surgical margin, Gleason score, D'Amico risk category and pT stage were independent predictors of biochemical recurrence-free survival.</p></div></div>
<div class="section" id="bju12260-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>This assessment of oncologic results of EERPE, which includes the surgical learning curve, demonstrates that the adoption of EERPE after mentored fellowship training translates into mid-term oncologic outcomes in line with retropubic/transperitoneal laparoscopic approaches and with large volume centres worldwide which have pioneered LRP.
This study shows that EERPE in a medium volume 2<sup>nd</sup> generation laparoscopic centre produces results with good 5-year oncologic outcome, comparable to other major series, for patients in the United Kingdom.</p></div></div>
]]></content:encoded><description>


Objective
To determine the 5-year oncologic outcome of Endoscopic Extraperitoneal Radical Prostatectomy (EERPE) from a medium volume centre thereby providing much needed data on the oncologic outcomes from the United Kingdom.


Patients and Methods
From January 2006 to January 2012, 575 patients underwent EERPE for localized prostate cancer by a single surgeon who had completed a modular training programme.
Follow-up was standard as per local hospital policy and data collected in our prospective database. A retrospective review on patient demographics, PSA, pathological T stages, Gleason scores, margin status and biochemical recurrence data was performed. Biochemical recurrence was defined by a PSA level &gt;0.2ng/ml.


Results
Mean patient age was 62-years (range = 40.3 - 76.5), mean follow-up was 30 months (range =12 – 72). Median operative time 135min (IQR= 120-170), median blood loss 200mls (IQR=100-250mls).
135/575 (23.5%) had positive surgical margins (PSM). PSM rate for pT2 disease was 66/406 (16.3%) and for pT3 disease 68/168 (40.5%). Overall BCR-free survival at 5-years was 81.5%. Multivariate Cox analysis showed that positive surgical margin, Gleason score, D'Amico risk category and pT stage were independent predictors of biochemical recurrence-free survival.


Conclusion
This assessment of oncologic results of EERPE, which includes the surgical learning curve, demonstrates that the adoption of EERPE after mentored fellowship training translates into mid-term oncologic outcomes in line with retropubic/transperitoneal laparoscopic approaches and with large volume centres worldwide which have pioneered LRP.
This study shows that EERPE in a medium volume 2nd generation laparoscopic centre produces results with good 5-year oncologic outcome, comparable to other major series, for patients in the United Kingdom.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12259" xmlns="http://purl.org/rss/1.0/"><title>Histology core specific evaluation of the ESUR standardized scoring system of multiparametric MRI of the prostate</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12259</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histology core specific evaluation of the ESUR standardized scoring system of multiparametric MRI of the prostate</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Timur H. Kuru, Matthias C. Roethke, Philip Rieker, Wilfried Roth, Michael Fenchel, Markus Hohenfellner, Heinz-Peter Schlemmer, Boris A. Hadaschik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:32.876423-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12259</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12259</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12259</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12259-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To evaluate the Prostate Imaging Reporting and Data System (PIRADS) in multiparametric MRI (mp-MRI) based on single cores and single core histology.
To calculate positive and negative predictive values of different modalities of mp-MRI.</p></div></div>
<div class="section" id="bju12259-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>We performed MRI-targeted TRUS-guided perineal prostate biopsies on 50 patients (mean age 66, mean PSA 9.9 ng/ml) with suspicion for prostate cancer. The biopsy trajectories of every core taken were documented in three dimensions in a 3D-prostate model.
Every core was evaluated separately for prostate cancer and the performed biopsy trajectories were projected on mp-MRI images.
PIRADS scores of 1177 cores were then assessed by a histology-blinded uro-radiologists in T2w, DCE, DWI and spectroscopy.</p></div></div>
<div class="section" id="bju12259-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The PIRADS score was significantly higher in cores positive for cancer as compared to negative cores.
There was significant correlation between the PIRADS score and histopathology in every modality.
ROC analysis showed excellent specificity for T2 (90% peripheral zone / 97% transition zone) and DWI (98%/97%) images regardless of the prostate region observed. These numbers decreased for DCE (80%/93%) and MRS (76%/83%).
All modalities demonstrate NPVs of 99% if a threshold of 2 (for T2, DCE, and MRS) or 3 (for DWI) is used. However PPVs were low.</p></div></div>
<div class="section" id="bju12259-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Our results show that PIRADS scoring is feasible for clinical routine and allows standardized reporting.
PIRADS can be used as a decision support system for targeting of suspicious lesions.
mp-MRI has a high negative predictive value for prostate cancer and, thus, might be a valuable tool in the initial diagnostic work-up.</p></div></div>
]]></content:encoded><description>


Objectives
To evaluate the Prostate Imaging Reporting and Data System (PIRADS) in multiparametric MRI (mp-MRI) based on single cores and single core histology.
To calculate positive and negative predictive values of different modalities of mp-MRI.


Patients and Methods
We performed MRI-targeted TRUS-guided perineal prostate biopsies on 50 patients (mean age 66, mean PSA 9.9 ng/ml) with suspicion for prostate cancer. The biopsy trajectories of every core taken were documented in three dimensions in a 3D-prostate model.
Every core was evaluated separately for prostate cancer and the performed biopsy trajectories were projected on mp-MRI images.
PIRADS scores of 1177 cores were then assessed by a histology-blinded uro-radiologists in T2w, DCE, DWI and spectroscopy.


Results
The PIRADS score was significantly higher in cores positive for cancer as compared to negative cores.
There was significant correlation between the PIRADS score and histopathology in every modality.
ROC analysis showed excellent specificity for T2 (90% peripheral zone / 97% transition zone) and DWI (98%/97%) images regardless of the prostate region observed. These numbers decreased for DCE (80%/93%) and MRS (76%/83%).
All modalities demonstrate NPVs of 99% if a threshold of 2 (for T2, DCE, and MRS) or 3 (for DWI) is used. However PPVs were low.


Conclusion
Our results show that PIRADS scoring is feasible for clinical routine and allows standardized reporting.
PIRADS can be used as a decision support system for targeting of suspicious lesions.
mp-MRI has a high negative predictive value for prostate cancer and, thus, might be a valuable tool in the initial diagnostic work-up.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12258" xmlns="http://purl.org/rss/1.0/"><title>Prospective evaluation of urinary incontinence, voiding symptoms and quality of life after open and robot-assisted radical prostatectomy.</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12258</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Prospective evaluation of urinary incontinence, voiding symptoms and quality of life after open and robot-assisted radical prostatectomy.</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Inge Geraerts, Hendrik Van Poppel, Nele Devoogdt, Ben Van Cleynenbreugel, Steven Joniau, Marijke Van Kampen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:14.516373-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12258</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12258</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12258</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Since many years radical prostatectomy (RP) is the preferred therapeutic option for patients with localized or locally advanced prostate cancer [1]. Open radical prostatectomy (ORP) has been the most commonly used surgical technique for decades. Recently, robot-assisted radical prostatectomy (RARP) has become an equal alternative [2]. Despite the large number of radical prostatectomies performed, urinary incontinence (UI) remains a common postoperative sequel [3-6].
Several studies compared UI after ORP and RARP. Different studies found that patients achieved continence much earlier after RARP than after ORP [7-9], other studies could not confirm this [10-12]. The international prostate symptom score (IPSS) for evaluation of voiding symptoms was used in several studies [13-15]. IPSS scores ameliorated after surgery in all studies.</p></div>
]]></content:encoded><description>
Since many years radical prostatectomy (RP) is the preferred therapeutic option for patients with localized or locally advanced prostate cancer [1]. Open radical prostatectomy (ORP) has been the most commonly used surgical technique for decades. Recently, robot-assisted radical prostatectomy (RARP) has become an equal alternative [2]. Despite the large number of radical prostatectomies performed, urinary incontinence (UI) remains a common postoperative sequel [3-6].
Several studies compared UI after ORP and RARP. Different studies found that patients achieved continence much earlier after RARP than after ORP [7-9], other studies could not confirm this [10-12]. The international prostate symptom score (IPSS) for evaluation of voiding symptoms was used in several studies [13-15]. IPSS scores ameliorated after surgery in all studies.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12257" xmlns="http://purl.org/rss/1.0/"><title>Laparoscopic And Robotic Continent Urinary Diversions (Mitrofanoff And Yang-Monti Conduits) In A Consecutive Series Of 15 Adults Patients: Saint Augustin Technique</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12257</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Laparoscopic And Robotic Continent Urinary Diversions (Mitrofanoff And Yang-Monti Conduits) In A Consecutive Series Of 15 Adults Patients: Saint Augustin Technique</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Denis Rey, Elie Helou, Marco Oderda, Jacopo Robbiani, Laurent Lopez, Pierre-Thierry Piechaud</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:13.143766-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12257</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12257</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12257</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract (250 words)</h3>
<div class="section" id="bju12257-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To present a series of 15 laparoscopic and robotic Mitrofanoff and Yang-Monti vesicostomies in an adult population, in order to assess the feasibility and safety of these minimally invasive approaches.</p></div></div>
<div class="section" id="bju12257-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><p>From 2009 to 2012, fifteen patients underwent laparoscopic (N=11) or robotic (N=4) construction of vesicostomy by a single surgeon (DR): Mitrofanoff appendicovesicostomy (N=11) or double Yang-Monti ileal conduit (N=4). Fourteen patients underwent concomitant augmentation enterocystoplasty.
Indications for surgery included neurogenic bladder (N=11) and urethral dysfunction (N=4).
The patients were evaluated postoperatively by means of a cystography. Quality of life (QoL) was evaluated by means of an internally developed questionnaire.</p></div></div>
<div class="section" id="bju12257-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>All surgeries were successfully completed with no conversions. Operative time was always less than 5 hours. Mean blood loss was 150 cc. Mean follow-up was 22 months.
Early postoperative complications included: deep retro-vesical abscess (N=2) and upper urinary tract infections (N=4). One patient had perioperative cardiac failure.
Late postoperative complications included: stomal stenosis (N=2), persistent low-pressure bladder incontinence (N=1), recurrent infections (N=1). Surgical excision of the conduit was necessary in one patient.
Postoperatively, patients demonstrated complete bladder emptying and no leak on follow-up cystography. According to our QoL questionnaire, 87% of our patients (N=13) do not regret the surgery.</p></div></div>
<div class="section" id="bju12257-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>While a longer follow-up is needed to assess the durability of our results, this series demonstrates that the laparoscopic and robotic approaches for the construction of continent urinary diversions are feasible and safe in an adult population.</p></div></div>
]]></content:encoded><description>


Objective
To present a series of 15 laparoscopic and robotic Mitrofanoff and Yang-Monti vesicostomies in an adult population, in order to assess the feasibility and safety of these minimally invasive approaches.


Patients and methods
From 2009 to 2012, fifteen patients underwent laparoscopic (N=11) or robotic (N=4) construction of vesicostomy by a single surgeon (DR): Mitrofanoff appendicovesicostomy (N=11) or double Yang-Monti ileal conduit (N=4). Fourteen patients underwent concomitant augmentation enterocystoplasty.
Indications for surgery included neurogenic bladder (N=11) and urethral dysfunction (N=4).
The patients were evaluated postoperatively by means of a cystography. Quality of life (QoL) was evaluated by means of an internally developed questionnaire.


Results
All surgeries were successfully completed with no conversions. Operative time was always less than 5 hours. Mean blood loss was 150 cc. Mean follow-up was 22 months.
Early postoperative complications included: deep retro-vesical abscess (N=2) and upper urinary tract infections (N=4). One patient had perioperative cardiac failure.
Late postoperative complications included: stomal stenosis (N=2), persistent low-pressure bladder incontinence (N=1), recurrent infections (N=1). Surgical excision of the conduit was necessary in one patient.
Postoperatively, patients demonstrated complete bladder emptying and no leak on follow-up cystography. According to our QoL questionnaire, 87% of our patients (N=13) do not regret the surgery.


Conclusions
While a longer follow-up is needed to assess the durability of our results, this series demonstrates that the laparoscopic and robotic approaches for the construction of continent urinary diversions are feasible and safe in an adult population.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12256" xmlns="http://purl.org/rss/1.0/"><title>Increased apoptosis and suburothelial inflammation in patients with ketamine-related cystitis – comparison with non-ulcer interstitial cystitis and controls</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12256</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Increased apoptosis and suburothelial inflammation in patients with ketamine-related cystitis – comparison with non-ulcer interstitial cystitis and controls</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cheng-Ling Lee, Yuan-Hong Jiang, Hann-Chorng Kuo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:11.024876-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12256</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12256</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12256</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12256-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To investigate suburothelial inflammation and urothelial dysfunction that occurs with ketamine-related cystitis (KC) and interstitial cystitis/bladder pain syndrome (IC/BPS).</p></div></div>
<div class="section" id="bju12256-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients And Methods</h4><div class="para"><p>Bladder tissues from 16 patients with KC, 17 with IC/BPS, and 10 controls were analysed.
Immunofluorescence (IF) staining of the junction protein E-cadherin, tryptase (to assess mast cell activation) and TUNEL (to assess urothelial apoptosis ) were performed.
The fluorescence intensity of E-cadherin was measured by Image J method. The percentages of activated mast cells and apoptotic cells were calculated as positive cells per area unit (4 μm2).</p></div></div>
<div class="section" id="bju12256-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean age was 25.0 ± 3.8, 41.3 ± 13.7, and 50.5 ± 9.6 years in KC, IC/BPS and controls patients, respectively (p &lt; 0.05).
The distributions of E-cadherin in KC (10.1 ± 11.2) and IC/BPS (25.1 ± 16.3) tissues were significantly reduced compared to controls (42.4 ± 16.7) (both p &lt; 0.05).
The number of activated mast cell measured by tryptase signals in KC (6.5 ± 3.7) and IC/BPS (4.6 ± 3.0) were significantly increased compared to controls (1.3 ± 1.12) (both p &lt; 0.05).
TUNEL staining revealed a significant increase of apoptotic cells in KC (4.4 ± 2.5) and IC/BPS (2.4 ± 1.7) tissues compared to control tissues (0.1 ± 0.3) (both p &lt; 0.05).
KC tissues had significantly decreased expression of E-cadherin (p = 0.024) and significantly increased numbers of apoptotic cells (p = 0.02) than in IC/BPS tissues.
Increased numbers of apoptotic cells and decreased expression of E-cadherin significantly correlated with maximal bladder capacity in the overall patient samples (p &lt; 0.05).</p></div></div>
<div class="section" id="bju12256-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>KC and IC/BPS tissues both showed defective junction protein, increased suburothelial inflammation and increased urothelial cell apoptosis. Decreased expression of E-cadherin and increased apoptosis were more severe in KC than in IC/BPS bladder tissues. These findings were associated with the clinical symptoms of KC and IC/BPS.</p></div></div>
]]></content:encoded><description>


Objectives
To investigate suburothelial inflammation and urothelial dysfunction that occurs with ketamine-related cystitis (KC) and interstitial cystitis/bladder pain syndrome (IC/BPS).


Patients And Methods
Bladder tissues from 16 patients with KC, 17 with IC/BPS, and 10 controls were analysed.
Immunofluorescence (IF) staining of the junction protein E-cadherin, tryptase (to assess mast cell activation) and TUNEL (to assess urothelial apoptosis ) were performed.
The fluorescence intensity of E-cadherin was measured by Image J method. The percentages of activated mast cells and apoptotic cells were calculated as positive cells per area unit (4 μm2).


Results
The mean age was 25.0 ± 3.8, 41.3 ± 13.7, and 50.5 ± 9.6 years in KC, IC/BPS and controls patients, respectively (p &lt; 0.05).
The distributions of E-cadherin in KC (10.1 ± 11.2) and IC/BPS (25.1 ± 16.3) tissues were significantly reduced compared to controls (42.4 ± 16.7) (both p &lt; 0.05).
The number of activated mast cell measured by tryptase signals in KC (6.5 ± 3.7) and IC/BPS (4.6 ± 3.0) were significantly increased compared to controls (1.3 ± 1.12) (both p &lt; 0.05).
TUNEL staining revealed a significant increase of apoptotic cells in KC (4.4 ± 2.5) and IC/BPS (2.4 ± 1.7) tissues compared to control tissues (0.1 ± 0.3) (both p &lt; 0.05).
KC tissues had significantly decreased expression of E-cadherin (p = 0.024) and significantly increased numbers of apoptotic cells (p = 0.02) than in IC/BPS tissues.
Increased numbers of apoptotic cells and decreased expression of E-cadherin significantly correlated with maximal bladder capacity in the overall patient samples (p &lt; 0.05).


Conclusions
KC and IC/BPS tissues both showed defective junction protein, increased suburothelial inflammation and increased urothelial cell apoptosis. Decreased expression of E-cadherin and increased apoptosis were more severe in KC than in IC/BPS bladder tissues. These findings were associated with the clinical symptoms of KC and IC/BPS.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12255" xmlns="http://purl.org/rss/1.0/"><title>Comparison of Perioperative Outcomes of Robot-assisted Partial Nephrectomy versus Laparoscopic Partial Nephrectomy: a Meta-analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12255</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of Perioperative Outcomes of Robot-assisted Partial Nephrectomy versus Laparoscopic Partial Nephrectomy: a Meta-analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xiaohua Zhang, Zhoujun Shen, Shan Zhong, Zhaowei Zhu, Xianjin Wang, Tianyuan Xu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:49:00.292092-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12255</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12255</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12255</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12255-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To conduct a meta-analysis of the literature on the perioperative outcomes of robot-assisted partial nephrectomy (RAPN) compared with laparoscopic partial nephrectomy (LPN).</p></div></div>
<div class="section" id="bju12255-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><p>An electronic database search of MEDLINE, EMBASE, google scholar, and the Cochrane library was performed up to January 8, 2013.
All studies comparing RAPN with LPN were included. The outcome measures were the demographic parameters and the perioperative results, including operative time, warm ischemia time, blood loss, length of hospital stay, conversion rates, positive margin, and complications.
A meta-analysis of the results was conducted.</p></div></div>
<div class="section" id="bju12255-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A total of 766 patients were included, 425 patients in the RAPN group and 341 patients in the LPN group. There was no significant difference between the two groups in any of the demographic parameters (age: p=0.89; sex: p=0.31; malignant pathology: p=0.54; tumor size: p=0.99; or tumor laterality: p=0.06).
There was no difference between the two groups regarding operative times (p=0.75), estimated blood loss (p=0.75), conversion rates (p=0.52), positive margins (p= 0.61), complications (p=0.27), or length of hospital stay (p=0.27), except that the RAPN group had significantly shorter warm ischemia time than the LPN group (p =0.01; WMD: -3.65; 95% CI, -6.46 to -0.83).</p></div></div>
<div class="section" id="bju12255-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>This meta-analysis shows that RAPN provides equivalent perioperative outcomes to those of LPN with the advantage of a significantly shorter warm ischemia time.</p></div></div>
]]></content:encoded><description>


Objective
To conduct a meta-analysis of the literature on the perioperative outcomes of robot-assisted partial nephrectomy (RAPN) compared with laparoscopic partial nephrectomy (LPN).


Materials and Methods
An electronic database search of MEDLINE, EMBASE, google scholar, and the Cochrane library was performed up to January 8, 2013.
All studies comparing RAPN with LPN were included. The outcome measures were the demographic parameters and the perioperative results, including operative time, warm ischemia time, blood loss, length of hospital stay, conversion rates, positive margin, and complications.
A meta-analysis of the results was conducted.


Results
A total of 766 patients were included, 425 patients in the RAPN group and 341 patients in the LPN group. There was no significant difference between the two groups in any of the demographic parameters (age: p=0.89; sex: p=0.31; malignant pathology: p=0.54; tumor size: p=0.99; or tumor laterality: p=0.06).
There was no difference between the two groups regarding operative times (p=0.75), estimated blood loss (p=0.75), conversion rates (p=0.52), positive margins (p= 0.61), complications (p=0.27), or length of hospital stay (p=0.27), except that the RAPN group had significantly shorter warm ischemia time than the LPN group (p =0.01; WMD: -3.65; 95% CI, -6.46 to -0.83).


Conclusions
This meta-analysis shows that RAPN provides equivalent perioperative outcomes to those of LPN with the advantage of a significantly shorter warm ischemia time.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12254" xmlns="http://purl.org/rss/1.0/"><title>Outcomes after recto-anastomosis fistula repair in patients who underwent radical prostatectomy for prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12254</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Outcomes after recto-anastomosis fistula repair in patients who underwent radical prostatectomy for prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniel Pfalzgraf, Hendrik Isbarn, Philip Reiss, Wolf-Hartmut Meyer-Moldenhaue, Margit Fisch, Roland Dahlem</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:54.51999-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12254</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12254</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12254</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12254-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess fistula recurrence rate and quality of life after repair as well as the impact on continence and erection in patients with recto-anastomotic fistula after radical prostatectomy.
Even in the more recent publications the number of cases for recto-urinary fistulas after radical prostatectomy is relatively small. Success rates at fistula closure are good; however data regarding functional outcome and quality of life is more restricted.</p></div></div>
<div class="section" id="bju12254-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Retrospective study of patients treated for recto-urethral fistulas after radical prostatectomy between 1993 and 2008.
All 17 patients were assessed for fistula recurrence in 2007 and received a standardized non-validated questionnaire to assess quality of life in 2011; furthermore, a patient's chart review was performed.</p></div><div class="para"><p>Surgical technique: fistula closure was abdominal in ten patients, perineal in 5 and combined abdominal and perineal in two, some with tissue interposition.</p></div></div>
<div class="section" id="bju12254-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In 2007, follow-up was available for 14 patients, 1 was deceased, 2 lost to follow-up. Mean follow-up was 73.3 months, mean patient age 63 years.
In 2 patients, rectal injury during the initial surgery was reported; another 3 had undergone adjuvant radiation therapy (18%).
In 2011, another 2 patients were deceased; mean follow-up was 99.5 months (range, 44-184).
A strong improvement in Qol as compared to before surgery was found in 58% of patients, a slight improvement in 8%, no change in quality of life in 25%. 67% are very satisfied with the surgery, 33% are satisfied.</p></div></div>
<div class="section" id="bju12254-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Perineal or abdominal fistula repair yields excellent success rates and high patient satisfaction. However, urinary incontinence can be found in a number of patients postoperatively, requiring further treatment.</p></div></div>
]]></content:encoded><description>


Objectives
To assess fistula recurrence rate and quality of life after repair as well as the impact on continence and erection in patients with recto-anastomotic fistula after radical prostatectomy.
Even in the more recent publications the number of cases for recto-urinary fistulas after radical prostatectomy is relatively small. Success rates at fistula closure are good; however data regarding functional outcome and quality of life is more restricted.


Patients and Methods
Retrospective study of patients treated for recto-urethral fistulas after radical prostatectomy between 1993 and 2008.
All 17 patients were assessed for fistula recurrence in 2007 and received a standardized non-validated questionnaire to assess quality of life in 2011; furthermore, a patient's chart review was performed.
Surgical technique: fistula closure was abdominal in ten patients, perineal in 5 and combined abdominal and perineal in two, some with tissue interposition.


Results
In 2007, follow-up was available for 14 patients, 1 was deceased, 2 lost to follow-up. Mean follow-up was 73.3 months, mean patient age 63 years.
In 2 patients, rectal injury during the initial surgery was reported; another 3 had undergone adjuvant radiation therapy (18%).
In 2011, another 2 patients were deceased; mean follow-up was 99.5 months (range, 44-184).
A strong improvement in Qol as compared to before surgery was found in 58% of patients, a slight improvement in 8%, no change in quality of life in 25%. 67% are very satisfied with the surgery, 33% are satisfied.


Conclusions
Perineal or abdominal fistula repair yields excellent success rates and high patient satisfaction. However, urinary incontinence can be found in a number of patients postoperatively, requiring further treatment.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12253" xmlns="http://purl.org/rss/1.0/"><title>Nightly vs. on-demand sildenafil for penile rehabilitation after minimally-invasive nerve-sparing radical prostatectomy: Results of a randomized double-blind trial with placebo</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12253</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Nightly vs. on-demand sildenafil for penile rehabilitation after minimally-invasive nerve-sparing radical prostatectomy: Results of a randomized double-blind trial with placebo</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C.P. Pavlovich, A.W. Levinson, L.-M. Su, L.Z. Mettee, Z. Feng, T. J. Bivalacqua, B.J. Trock</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:40.96239-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12253</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12253</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12253</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12253-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To clarify the role of phosphodiesterase-5 inhibitors (PDE5i) in post-prostatectomy penile rehabilitation (PPPR)
To compare nightly and on-demand use of PDE5i after nerve-sparing minimally-invasive radical prostatectomy (RP)</p></div></div>
<div class="section" id="bju12253-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Single-institution, double-blind, randomized controlled trial of nightly versus on-demand 50mg sildenafil citrate after nerve-sparing minimally-invasive RP
100 pre-operatively potent men (age &lt; 65, IIEF-EF scores ≥ 26) who underwent nerve-sparing surgery
Randomized to either nightly sildenafil and on-demand placebo (nightly sildenafil group), or on-demand sildenafil and nightly placebo (on-demand sildenafil group; maximum on-demand dose 6 tablets/month) for 12 months, followed by a 1-month washout period
Validated measures of erectile function (IIEF-EF and EPIC) were compared between treatment groups over the entire 13-month time course using multivariable mixed linear regression models</p></div></div>
<div class="section" id="bju12253-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Treatment groups well-matched pre-operatively (mean age 54.3 vs. 54.6, baseline IIEF-EF 29.4 vs. 29.3, for nightly compared to on-demand sildenafil groups respectively)
No significant differences were found in erectile function between treatments (nightly sildenafil vs. on-demand sildenafil) at any single post-prostatectomy timepoint, after adjusting for potential confounding factors 
When evaluated over all timepoints simultaneously, no statistically significant effects of treatment group (nightly sildenafil vs. on-demand sildenafil) were found on recovery of potency assessed by absolute IIEF-EF values (p=0.765), percentage of men returning to an IIEF-EF &gt; 21 (p=0.830), or IIEF-EF recovery to a percentage of baseline value (p=0.778)
When evaluated over all timepoints simultaneously, no significant effects of treatment group were found on secondary endpoints such as assessments of potency (including EPIC item 59, response erections "firm enough for intercourse"), attempted intercourse frequency, or confidence</p></div></div>
<div class="section" id="bju12253-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Erectile recovery up to one year post-prostatectomy does not differ between previously potent men who use sildenafil nightly compared to on-demand
This trial does not support chronic nightly sildenafil as being any better than on-demand sildenafil for use in penile rehabilitation after nerve-sparing minimally-invasive RP</p></div></div>
]]></content:encoded><description>


Objectives
To clarify the role of phosphodiesterase-5 inhibitors (PDE5i) in post-prostatectomy penile rehabilitation (PPPR)
To compare nightly and on-demand use of PDE5i after nerve-sparing minimally-invasive radical prostatectomy (RP)


Patients and Methods
Single-institution, double-blind, randomized controlled trial of nightly versus on-demand 50mg sildenafil citrate after nerve-sparing minimally-invasive RP
100 pre-operatively potent men (age &lt; 65, IIEF-EF scores ≥ 26) who underwent nerve-sparing surgery
Randomized to either nightly sildenafil and on-demand placebo (nightly sildenafil group), or on-demand sildenafil and nightly placebo (on-demand sildenafil group; maximum on-demand dose 6 tablets/month) for 12 months, followed by a 1-month washout period
Validated measures of erectile function (IIEF-EF and EPIC) were compared between treatment groups over the entire 13-month time course using multivariable mixed linear regression models


Results
Treatment groups well-matched pre-operatively (mean age 54.3 vs. 54.6, baseline IIEF-EF 29.4 vs. 29.3, for nightly compared to on-demand sildenafil groups respectively)
No significant differences were found in erectile function between treatments (nightly sildenafil vs. on-demand sildenafil) at any single post-prostatectomy timepoint, after adjusting for potential confounding factors 
When evaluated over all timepoints simultaneously, no statistically significant effects of treatment group (nightly sildenafil vs. on-demand sildenafil) were found on recovery of potency assessed by absolute IIEF-EF values (p=0.765), percentage of men returning to an IIEF-EF &gt; 21 (p=0.830), or IIEF-EF recovery to a percentage of baseline value (p=0.778)
When evaluated over all timepoints simultaneously, no significant effects of treatment group were found on secondary endpoints such as assessments of potency (including EPIC item 59, response erections "firm enough for intercourse"), attempted intercourse frequency, or confidence


Conclusion
Erectile recovery up to one year post-prostatectomy does not differ between previously potent men who use sildenafil nightly compared to on-demand
This trial does not support chronic nightly sildenafil as being any better than on-demand sildenafil for use in penile rehabilitation after nerve-sparing minimally-invasive RP

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12252" xmlns="http://purl.org/rss/1.0/"><title>Robotic Partial Nephrectomy versus Laparoscopic Guided Cryoablation for the Small Renal Mass: redefining the minimally invasive gold standard</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12252</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Robotic Partial Nephrectomy versus Laparoscopic Guided Cryoablation for the Small Renal Mass: redefining the minimally invasive gold standard</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amr Emara, Sashi Kommu, Richard Hindley, Neil Barber</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:29.207549-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12252</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12252</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12252</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12252-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective:</h4><div class="para"><p>• To identify differences between ablative and extirpative minimally invasive techniques represented by laparoscopic guided cryoablation (LC) and robotic partial nephrectomy (RPN) respectively in treating small renal tumours in different aspects including safety, peri-operative morbidity and early oncological outcomes.</p></div></div>
<div class="section" id="bju12252-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><p>• Between June 2008 and April 2012 we have treated 56 patients with LC (group 1) and more recently we have performed RPN using the Da Vinci robotic platform; from October 2010 to April 2012 (group 2) 47 patients were treated using this approach.</p></div><div class="para"><p>• Intra-operative, post-operative and oncological outcomes were collected prospectively, analysed and compared for both groups.</p></div></div>
<div class="section" id="bju12252-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>• Median age was 69 and 60 for group 1 and 2 respectively (P&lt;0.05), while no significant difference was identified in disease stage, there was a significant difference in tumour size, the larger tumours being treated in group 2.</p></div><div class="para"><p>• Mean operative time was 146 min and 159 min for group 1 and 2 (P = 0.0941), whilst mean blood loss in the 1st group was 47 ml in comparison to 94 ml in group 2 (P =0.2505). Median hospital stay was the same for both groups (1 night) and he average warm ischemia time was 23 min in the 2nd group.</p></div><div class="para"><p>• Marginal change in pre and 6 weeks post-operative renal function was recorded (the mean post-operative increase in serum creatinine was 5.4 mmol/l in Group 1 and 9.2 mmol/l for group 2).</p></div><div class="para"><p>• 2/47 (4.3%) patients of group 2 were converted to laparoscopic radical nephrectomy due to difficulty in controlling bleeding during hilar dissection. Only two cases (3.6%) had recurrence in the cryotherapy group, both were treated with re-cryoablation. 5.4% from group 1 and 4.3% from group 2 had Clavien grade I post-operative complication, only one patient was recorded as Clavien grade II from group 2, while 1.8% and 4.3% of patients had Clavien III-b in group 1 and 2 respectively.</p></div></div>
<div class="section" id="bju12252-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>• Our data confirms that LC is a successful, minimally invasive and safe treatment option for the management of small renal tumours, however, the apparent similar characteristics of RPN suggest that an increasing proportion of patients, whatever their age or medical co-morbidities, may be reasonably offered a robotic assisted extirpative procedure with the likely benefit of a lower risk of local recurrence and the need for retreatment.</p></div></div>
]]></content:encoded><description>


Objective:
• To identify differences between ablative and extirpative minimally invasive techniques represented by laparoscopic guided cryoablation (LC) and robotic partial nephrectomy (RPN) respectively in treating small renal tumours in different aspects including safety, peri-operative morbidity and early oncological outcomes.


Patients and methods
• Between June 2008 and April 2012 we have treated 56 patients with LC (group 1) and more recently we have performed RPN using the Da Vinci robotic platform; from October 2010 to April 2012 (group 2) 47 patients were treated using this approach.
• Intra-operative, post-operative and oncological outcomes were collected prospectively, analysed and compared for both groups.


Results
• Median age was 69 and 60 for group 1 and 2 respectively (P&lt;0.05), while no significant difference was identified in disease stage, there was a significant difference in tumour size, the larger tumours being treated in group 2.
• Mean operative time was 146 min and 159 min for group 1 and 2 (P = 0.0941), whilst mean blood loss in the 1st group was 47 ml in comparison to 94 ml in group 2 (P =0.2505). Median hospital stay was the same for both groups (1 night) and he average warm ischemia time was 23 min in the 2nd group.
• Marginal change in pre and 6 weeks post-operative renal function was recorded (the mean post-operative increase in serum creatinine was 5.4 mmol/l in Group 1 and 9.2 mmol/l for group 2).
• 2/47 (4.3%) patients of group 2 were converted to laparoscopic radical nephrectomy due to difficulty in controlling bleeding during hilar dissection. Only two cases (3.6%) had recurrence in the cryotherapy group, both were treated with re-cryoablation. 5.4% from group 1 and 4.3% from group 2 had Clavien grade I post-operative complication, only one patient was recorded as Clavien grade II from group 2, while 1.8% and 4.3% of patients had Clavien III-b in group 1 and 2 respectively.


Conclusion
• Our data confirms that LC is a successful, minimally invasive and safe treatment option for the management of small renal tumours, however, the apparent similar characteristics of RPN suggest that an increasing proportion of patients, whatever their age or medical co-morbidities, may be reasonably offered a robotic assisted extirpative procedure with the likely benefit of a lower risk of local recurrence and the need for retreatment.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12251" xmlns="http://purl.org/rss/1.0/"><title>Tadalafil Once Daily in the Treatment of Lower Urinary Tract Symptoms Suggestive of Benign Prostatic Hyperplasia in Men without Erectile Dysfunction</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12251</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tadalafil Once Daily in the Treatment of Lower Urinary Tract Symptoms Suggestive of Benign Prostatic Hyperplasia in Men without Erectile Dysfunction</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gerald Brock, Gregory Broderick, Claus G Roehrborn, Lei Xu, David Wong, Lars Viktrup</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:22.961644-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12251</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12251</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12251</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12251-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess safety and efficacy of tadalafil once daily on lower urinary tract symptoms suggestive of clinical benign prostatic hyperplasia (BPH-LUTS) in men without erectile dysfunction (ED).</p></div><div class="para"><p>To compare these with effects in men with ED.</p></div></div>
<div class="section" id="bju12251-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Following a 4-week washout period and 4-week placebo run-in period, 1,089 men without ED (n=338) and with ED (n=751) were randomly assigned to placebo or tadalafil 5 mg once daily for 12 weeks in 3 global clinical studies with similar designs.</p></div><div class="para"><p>In the pooled dataset, post-hoc analyses of covariance assessed BPH-LUTS impact/severity using the International Prostate Symptom Score (IPSS), BPH Impact Index (BII), and IPSS Quality of Life (IPSS-QoL).</p></div><div class="para"><p>Safety was assessed using treatment-emergent adverse events.</p></div><div class="para"><p>Treatment-by-ED-status interaction assessed efficacy differences between yes/no-ED subgroups.</p></div></div>
<div class="section" id="bju12251-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Men without ED were similar in BPH-LUTS severity/previous therapy to men with ED.</p></div><div class="para"><p>Tadalafil significantly reduced BPH-LUTS from baseline versus placebo in men without ED (IPSS –5.4 vs –3.3, <em>p</em>&lt;0.01; IPSS voiding subscore –3.5 vs –2.0, <em>p</em>&lt;0.01; IPSS storage subscore –1.9 vs –1.3, <em>p</em>&lt;0.05).</p></div><div class="para"><p>Tadalafil also significantly improved quality of life from baseline versus placebo in men without ED (IPSS-QoL –1.0 vs –0.7, BII –1.4 vs –1.0; both <em>p</em>&lt;0.05).</p></div><div class="para"><p>Between-ED-subgroup interactions were not statistically significant (all <em>p</em>&gt;0.68).</p></div><div class="para"><p>Tadalafil was safe and well tolerated.</p></div></div>
<div class="section" id="bju12251-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Tadalafil 5 mg once daily improved BPH-LUTS in men without ED with a similar magnitude as that observed in men with ED.</p></div><div class="para"><p>The adverse event profile in men without ED was consistent with that observed in men with ED.</p></div></div>
]]></content:encoded><description>


Objectives
To assess safety and efficacy of tadalafil once daily on lower urinary tract symptoms suggestive of clinical benign prostatic hyperplasia (BPH-LUTS) in men without erectile dysfunction (ED).
To compare these with effects in men with ED.


Patients and Methods
Following a 4-week washout period and 4-week placebo run-in period, 1,089 men without ED (n=338) and with ED (n=751) were randomly assigned to placebo or tadalafil 5 mg once daily for 12 weeks in 3 global clinical studies with similar designs.
In the pooled dataset, post-hoc analyses of covariance assessed BPH-LUTS impact/severity using the International Prostate Symptom Score (IPSS), BPH Impact Index (BII), and IPSS Quality of Life (IPSS-QoL).
Safety was assessed using treatment-emergent adverse events.
Treatment-by-ED-status interaction assessed efficacy differences between yes/no-ED subgroups.


Results
Men without ED were similar in BPH-LUTS severity/previous therapy to men with ED.
Tadalafil significantly reduced BPH-LUTS from baseline versus placebo in men without ED (IPSS –5.4 vs –3.3, p&lt;0.01; IPSS voiding subscore –3.5 vs –2.0, p&lt;0.01; IPSS storage subscore –1.9 vs –1.3, p&lt;0.05).
Tadalafil also significantly improved quality of life from baseline versus placebo in men without ED (IPSS-QoL –1.0 vs –0.7, BII –1.4 vs –1.0; both p&lt;0.05).
Between-ED-subgroup interactions were not statistically significant (all p&gt;0.68).
Tadalafil was safe and well tolerated.


Conclusion
Tadalafil 5 mg once daily improved BPH-LUTS in men without ED with a similar magnitude as that observed in men with ED.
The adverse event profile in men without ED was consistent with that observed in men with ED.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12250" xmlns="http://purl.org/rss/1.0/"><title>Outcome in Patients with Exclusive Carcinoma in Situ (CIS) Following Radical Cystectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12250</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Outcome in Patients with Exclusive Carcinoma in Situ (CIS) Following Radical Cystectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pascal Zehnder, Felix Moltzahn, Siamak Daneshmand, Marya Leahy, Jie Cai, Gus Miranda, Georg Bartsch, Anirban P. Mitra, Donald G. Skinner, Eila C. Skinner, Inderbir S. Gill</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:16.106093-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12250</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12250</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12250</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Patients with carcinoma in situ (CIS) of the urinary bladder are at risk of progression to invasive disease and death if left untreated [1, 2]. Attempts to control CIS with transurethral bladder resection (TURB) alone are unsuccessful in most cases, and therefore not considered an ideal therapeutic option. In contrast, intravesical instillation of the immunostimulant Bacillus Calmette-Guérin (BCG) has become the treatment of choice, as induction and maintenance therapy are associated with reduced recurrence and risk of progression [3]. Despite this, a considerable proportion of patients may primarily fail to respond while others recur during the course of conservative treatment. There is no clear consensus for further therapeutic management of patients with recurrent CIS of the urinary bladder. Radical cystectomy (RC) remains an important therapeutic strategy in this scenario [4]. Due to its infrequent occurrence, only few reports exist on the outcome of patients after RC for either clinical (cCIS) or pathological CIS (pCIS) only. However, all such studies are substantially limited by including patients with tumor stages ≥T1 before or after RC and consecutively results do not reflect the outcome of an exclusive CIS only series [5-8]. We therefore evaluated the outcome of patients after RC for cCIS (+/- cTa) with no previous history of ≥cT1 disease in TURB specimens and exclusively pTIS in the RC specimens.</p></div>
]]></content:encoded><description>
Patients with carcinoma in situ (CIS) of the urinary bladder are at risk of progression to invasive disease and death if left untreated [1, 2]. Attempts to control CIS with transurethral bladder resection (TURB) alone are unsuccessful in most cases, and therefore not considered an ideal therapeutic option. In contrast, intravesical instillation of the immunostimulant Bacillus Calmette-Guérin (BCG) has become the treatment of choice, as induction and maintenance therapy are associated with reduced recurrence and risk of progression [3]. Despite this, a considerable proportion of patients may primarily fail to respond while others recur during the course of conservative treatment. There is no clear consensus for further therapeutic management of patients with recurrent CIS of the urinary bladder. Radical cystectomy (RC) remains an important therapeutic strategy in this scenario [4]. Due to its infrequent occurrence, only few reports exist on the outcome of patients after RC for either clinical (cCIS) or pathological CIS (pCIS) only. However, all such studies are substantially limited by including patients with tumor stages ≥T1 before or after RC and consecutively results do not reflect the outcome of an exclusive CIS only series [5-8]. We therefore evaluated the outcome of patients after RC for cCIS (+/- cTa) with no previous history of ≥cT1 disease in TURB specimens and exclusively pTIS in the RC specimens.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12249" xmlns="http://purl.org/rss/1.0/"><title>Positive Surgical Margins After Minimally Invasive Radical Prostatectomy in pT2 and pT3a Population Could be Considered as Pathological Upstaging</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12249</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Positive Surgical Margins After Minimally Invasive Radical Prostatectomy in pT2 and pT3a Population Could be Considered as Pathological Upstaging</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adil Ouzzane, François Rozet, Rafael Sanchez Salas, Marc Galiano, Eric Barret, Dominique Prapotnich, Xavier Cathelineau</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:48:09.047459-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12249</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12249</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12249</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12249-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To assess the prognostic significance of positive surgical margins (PSM) after minimally invasive radical prostatectomy (MIRP) in interaction with other established prognosis factors.</p></div></div>
<div class="section" id="bju12249-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><p>After institutional review board approval, we retrospectively analyzed data prospectively collected from 1998 to 2010 for 4628 consecutive patients with clinically localised prostate cancer who underwent MIRP. Biochemical recurrence (BCR) was defined by prostate-specific antigen (PSA) greater than 0.2 ng/ml. The impact of PSM on BCR was evaluated using multivariable Cox proportional hazards regression. Estimates of BCR-free survival were generated with the Kaplan-Meier method and compared among groups with the log-rank test.</p></div></div>
<div class="section" id="bju12249-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The median follow-up was 55 mo. On multivariable analysis, PSM was independent prognostic factor for recurrence (adjusted hazard ratio: 2.14 for positive vs negative margins; 95% confidence interval [CI], 1.86-2.45; p &lt; 0.001). Other independent predictors for BCR were preoperative PSA, date of surgery, pT stage, Gleason score and lymph node involvement (all <em>p</em> &lt; 0.001). The 5-yr BCR-free probability was 80.6% (95% CI, 79-82.2) for negative margins vs 51% (95% CI, 47-55) for positive margins (log rank p &lt; 0.001). pT2 and pT3a positive margins patients had similar prognosis as pT3a and pT3b negative margins, respectively (log rank <em>p</em> ≥ 0.05).</p></div></div>
<div class="section" id="bju12249-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>PSM after MIRP is associated with 2.14-fold increased risk of BCR. In pT2 and pT3a population, PSM could be considered as a pathological upstaging.</p></div></div>
]]></content:encoded><description>


Objective
To assess the prognostic significance of positive surgical margins (PSM) after minimally invasive radical prostatectomy (MIRP) in interaction with other established prognosis factors.


Patients and methods
After institutional review board approval, we retrospectively analyzed data prospectively collected from 1998 to 2010 for 4628 consecutive patients with clinically localised prostate cancer who underwent MIRP. Biochemical recurrence (BCR) was defined by prostate-specific antigen (PSA) greater than 0.2 ng/ml. The impact of PSM on BCR was evaluated using multivariable Cox proportional hazards regression. Estimates of BCR-free survival were generated with the Kaplan-Meier method and compared among groups with the log-rank test.


Results
The median follow-up was 55 mo. On multivariable analysis, PSM was independent prognostic factor for recurrence (adjusted hazard ratio: 2.14 for positive vs negative margins; 95% confidence interval [CI], 1.86-2.45; p &lt; 0.001). Other independent predictors for BCR were preoperative PSA, date of surgery, pT stage, Gleason score and lymph node involvement (all p &lt; 0.001). The 5-yr BCR-free probability was 80.6% (95% CI, 79-82.2) for negative margins vs 51% (95% CI, 47-55) for positive margins (log rank p &lt; 0.001). pT2 and pT3a positive margins patients had similar prognosis as pT3a and pT3b negative margins, respectively (log rank p ≥ 0.05).


Conclusion
PSM after MIRP is associated with 2.14-fold increased risk of BCR. In pT2 and pT3a population, PSM could be considered as a pathological upstaging.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12248" xmlns="http://purl.org/rss/1.0/"><title>Percutaneous nephrolithotomy under total ultrasound guidance: A 5-year study of over 700 cases</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12248</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Percutaneous nephrolithotomy under total ultrasound guidance: A 5-year study of over 700 cases</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Song Yan, Fei Xiang, Song Yongsheng</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:47:57.99031-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12248</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12248</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12248</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12248-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective:</h4><div class="para"><p>To evaluate the safety and efficacy of solo ultrasound-guided percutaneous nephrolithotomy (PCNL).</p></div></div>
<div class="section" id="bju12248-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>From May 2007 to July 2012, 24-Fr-tract PCNL was applied in 705 cases (679 patients; 26 with bilateral stones).</p></div><div class="para"><p>Caliceal puncture and dilation were performed under solo ultrasound (US)-guidance in all cases.</p></div><div class="para"><p>The procedure was evaluated for access success, post-procedural hospitalization duration, complications (modified Clavien system), stone clearance, and the need for auxiliary maneuvers.</p></div></div>
<div class="section" id="bju12248-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean operative time was 66 ± 25 min, with a mean post-procedural hospitalization time of 3.98 ± 1.34 days.</p></div><div class="para"><p>The patients experienced a mean hemoglobin level decrease of 2.24 ± 2.02 g/d; the overall stone-free rate, 4 weeks after surgery, was 92.6% in patients with a single calculus, and 82.9% in patients with staghorn or multiple calculi.</p></div><div class="para"><p>Auxiliary treatments, including shock wave lithotripsy in 52, re-PCNL in 41, and ureteroscopy in 18 patients, were performed 1 week after the primary procedure in 111 (15.7%) cases, for residual stones over 4 mm in size.</p></div><div class="para"><p>The sensitivities of intraoperative US-guidance and flexible nephroscopy for detecting significant residual stones and clinically insignificant residual fragments were 95.3% and 89.1%, respectively.</p></div><div class="para"><p>There were 94 grade 1 (13.3%), 17 grade 2 (2.4%), and 2 grade 3 (0.3%) complications; however, grade 4 or 5 complications were not encountered.</p></div></div>
<div class="section" id="bju12248-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Total US-guided PCNL is safe and convenient.</p></div><div class="para"><p>It may be performed without any major complications and with the advantage of preventing radiation hazards and damage to adjacent organs.</p></div></div>
]]></content:encoded><description>


Objective:
To evaluate the safety and efficacy of solo ultrasound-guided percutaneous nephrolithotomy (PCNL).


Patients and Methods
From May 2007 to July 2012, 24-Fr-tract PCNL was applied in 705 cases (679 patients; 26 with bilateral stones).
Caliceal puncture and dilation were performed under solo ultrasound (US)-guidance in all cases.
The procedure was evaluated for access success, post-procedural hospitalization duration, complications (modified Clavien system), stone clearance, and the need for auxiliary maneuvers.


Results
The mean operative time was 66 ± 25 min, with a mean post-procedural hospitalization time of 3.98 ± 1.34 days.
The patients experienced a mean hemoglobin level decrease of 2.24 ± 2.02 g/d; the overall stone-free rate, 4 weeks after surgery, was 92.6% in patients with a single calculus, and 82.9% in patients with staghorn or multiple calculi.
Auxiliary treatments, including shock wave lithotripsy in 52, re-PCNL in 41, and ureteroscopy in 18 patients, were performed 1 week after the primary procedure in 111 (15.7%) cases, for residual stones over 4 mm in size.
The sensitivities of intraoperative US-guidance and flexible nephroscopy for detecting significant residual stones and clinically insignificant residual fragments were 95.3% and 89.1%, respectively.
There were 94 grade 1 (13.3%), 17 grade 2 (2.4%), and 2 grade 3 (0.3%) complications; however, grade 4 or 5 complications were not encountered.


Conclusion
Total US-guided PCNL is safe and convenient.
It may be performed without any major complications and with the advantage of preventing radiation hazards and damage to adjacent organs.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12247" xmlns="http://purl.org/rss/1.0/"><title>Relative effectiveness of robot-assisted and standard laparoscopic prostatectomy as alternatives to open radical prostatectomy for treatment of localised prostate cancer: A systematic review and mixed treatment comparison meta-analysis.</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12247</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Relative effectiveness of robot-assisted and standard laparoscopic prostatectomy as alternatives to open radical prostatectomy for treatment of localised prostate cancer: A systematic review and mixed treatment comparison meta-analysis.</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Clare Robertson, Andrew Close, Cynthia Fraser, Tara Gurung, Xueli Jia, Pawana Sharma, Luke Vale, Craig Ramsay, Robert Pickard</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:47:49.420638-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12247</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12247</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12247</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12247-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To compare the effectiveness of robot-assisted and standard laparoscopic prostatectomy.</p></div></div>
<div class="section" id="bju12247-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>A care pathway was described</p></div><div class="para"><p>Systematic literature review based on a search of Medline, Medline in Process, Embase, Biosis, Science Citation Index, Cochrane Controlled Trials Register, Current Controlled Trials, Clinical Trials, WHO International Clinical Trials Registry and NIH Reporter, the HTA databases, the Database of Abstracts of Reviews of Effects, and relevant conference abstracts up to 31<sup>st</sup> October 2010). Additionally, reference lists were scanned, an expert panel consulted, and websites of manufacturers, professional organisations, and regulatory bodies were checked.</p></div><div class="para"><p>We selected randomised controlled trials (RCT) and non-randomised comparative studies published after 1<sup>st</sup> January 1995 including men with localised prostate cancer undergoing robotic or laparoscopic prostatectomy compared against the other procedure or against open prostatectomy. Studies where at least 90% of included men had clinical tumour stages T1 to T2 and which reported at least one of our specified outcomes were eligible for inclusion.</p></div><div class="para"><p>A mixed treatment comparison meta-analysis was performed to generate comparative statistics on specified outcomes.</p></div></div>
<div class="section" id="bju12247-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>We included data from 19,064 men across one RCT and 57 non-randomised comparative reports.</p></div><div class="para"><p>Robotic prostatectomy had lower risk of major intra-operative harms such as organ injury [0.4 % robotic <em>versus</em> 2.9% laparoscopic, odds ratio (95% credible interval) 0.16 (0.03 to 0.76)], and lower rate of a surgical margin positive for cancer [17.6% robotic <em>versus</em> 23.6% laparoscopic, odds ratio (95% credible interval) 0.69 (0.51 to 0.96)]. There was no evidence of a difference in the proportion of men with urinary incontinence at 12 months [odds ratio (95% credible interval) 0.55 (0.09 to 2.84)]. There were insufficient data on sexual dysfunction.</p></div><div class="para"><p>Surgeon learning rates for the procedures did not differ although data were limited.</p></div></div>
<div class="section" id="bju12247-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Men undergoing robotic prostatectomy appear to have reduced surgical morbidity, and a lower risk of a positive surgical margin which may reduce rates of cancer recurrence and need for further treatment. Considerable uncertainty surrounds these results.</p></div><div class="para"><p>We found no evidence that men undergoing robotic prostatectomy are disadvantaged in terms of early outcomes.</p></div><div class="para"><p>We were unable to determine longer term relative effectiveness.</p></div></div>
]]></content:encoded><description>


Objectives
To compare the effectiveness of robot-assisted and standard laparoscopic prostatectomy.


Methods
A care pathway was described
Systematic literature review based on a search of Medline, Medline in Process, Embase, Biosis, Science Citation Index, Cochrane Controlled Trials Register, Current Controlled Trials, Clinical Trials, WHO International Clinical Trials Registry and NIH Reporter, the HTA databases, the Database of Abstracts of Reviews of Effects, and relevant conference abstracts up to 31st October 2010). Additionally, reference lists were scanned, an expert panel consulted, and websites of manufacturers, professional organisations, and regulatory bodies were checked.
We selected randomised controlled trials (RCT) and non-randomised comparative studies published after 1st January 1995 including men with localised prostate cancer undergoing robotic or laparoscopic prostatectomy compared against the other procedure or against open prostatectomy. Studies where at least 90% of included men had clinical tumour stages T1 to T2 and which reported at least one of our specified outcomes were eligible for inclusion.
A mixed treatment comparison meta-analysis was performed to generate comparative statistics on specified outcomes.


Results
We included data from 19,064 men across one RCT and 57 non-randomised comparative reports.
Robotic prostatectomy had lower risk of major intra-operative harms such as organ injury [0.4 % robotic versus 2.9% laparoscopic, odds ratio (95% credible interval) 0.16 (0.03 to 0.76)], and lower rate of a surgical margin positive for cancer [17.6% robotic versus 23.6% laparoscopic, odds ratio (95% credible interval) 0.69 (0.51 to 0.96)]. There was no evidence of a difference in the proportion of men with urinary incontinence at 12 months [odds ratio (95% credible interval) 0.55 (0.09 to 2.84)]. There were insufficient data on sexual dysfunction.
Surgeon learning rates for the procedures did not differ although data were limited.


Conclusions
Men undergoing robotic prostatectomy appear to have reduced surgical morbidity, and a lower risk of a positive surgical margin which may reduce rates of cancer recurrence and need for further treatment. Considerable uncertainty surrounds these results.
We found no evidence that men undergoing robotic prostatectomy are disadvantaged in terms of early outcomes.
We were unable to determine longer term relative effectiveness.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12246" xmlns="http://purl.org/rss/1.0/"><title>Time to recurrence is a significant predictor of cancer-specific survival after recurrence in patients with recurrent renal cell carcinoma – Results from a comprehensive multi-centre database (CORONA/SATURN-Project)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12246</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Time to recurrence is a significant predictor of cancer-specific survival after recurrence in patients with recurrent renal cell carcinoma – Results from a comprehensive multi-centre database (CORONA/SATURN-Project)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sabine D. Brookman-May, Matthias May, Shahrokh F. Shariat, Giacomo Novara, Richard Zigeuner, Luca Cindolo, Ottavio De Cobelli, Cosimo De Nunzio, Sascha Pahernik, Manfred P. Wirth, Nicola Longo, Alchiede Simonato, Sergio Serni, Salvatore Siracusano, Alessandro Volpe, Giuseppe Morgia, Roberto Bertini, Orietta Dalpiaz, Christian Stief, Vincenzo Ficarra, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:47:37.426315-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12246</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12246</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12246</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12246-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>What′s known about the subject? And what does the study add?</h4><div class="para"><p>20-40% of renal cell carcinoma (RCC) patients will develop recurrence after surgery with curative intention, which will develop within the first five years after primary surgery in most cases, but also later (up to 45 years) in the follow-up (FU) in approximately 6-10% of patients. Time and pattern of metastasis show strong individual variations, and knowledge about those patients who are at risk for recurrence at different time-points would allow for an individualized aftercare and potentially also for initiation of early salvage treatment. Furthermore, the prognostic influence of time to recurrence (TTR) on cancer-specific survival (CSS) after disease recurrence is currently controversially discussed.</p></div><div class="para"><p>In this study, we evaluated the prognostic impact of TTR on CSS after recurrence in RCC patients undergoing radical nephrectomy or nephron sparing surgery. Differences in clinical and histopathological criteria between patients with early and late recurrence were evaluated as well. The study shows that, besides age, gender, tumour histology, and pT stage, also TTR is a significant predictor of CSS after recurrence in RCC patients who undergo primary surgery with curative intention. The earlier in the postsurgical FU recurrent disease occurs, the more reduced is survival after recurrence. Vice versa, the prognosis of patients in case of recurrence is improved with every day a patient stays disease-free after surgery up to four years from surgery, but not beyond this time-period.</p></div><div class="para"><p>Advanced age, male gender, advanced tumour diameter and stage, lymphovascular invasion, Fuhrman grade 3-4, and pN+ stage are more frequent in patients with early recurrence, which might provide the possibility of risk adapted aftercare. These data might be useful for implementation as risk stratification tool in clinical trials to avoid bias, i.e., to allow for equal representation of early and late recurrence patients in treatment arms.</p></div></div>
<div class="section" id="bju12246-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To assess the prognostic impact of time to recurrence (TTR) on cancer-specific survival (CSS) after recurrence in renal cell carcinoma (RCC) patients undergoing radical nephrectomy or nephron sparing surgery.</p></div><div class="para"><p>To analyze differences in clinical and histopathological criteria between patients with early and late recurrence.</p></div></div>
<div class="section" id="bju12246-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Of 13,107 RCC patients from an international multicentre database, 1,712 patients developed recurrence in the follow-up (FU) (median 50.1 months; IQR 25-106).</p></div><div class="para"><p>1,402 patients had recurrence within five years (Group A) and 310 patients beyond this time-period (Group B).</p></div><div class="para"><p>Differences in clinical and histopathological parameters between patients with early and late recurrence were analyzed.</p></div><div class="para"><p>The influence of TTR and further parameters on CSS after recurrence was assessed by Cox regression analysis.</p></div></div>
<div class="section" id="bju12246-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Male gender, advanced age, tumour diameter and stage, Fuhrman grade 3-4, lymphovascular invasion (LVI), and pN+ stage were significantly more frequent in patients with early recurrence, who had a significantly reduced 3-year CSS of 30% compared to Group B (41%; p=0.001).</p></div><div class="para"><p>Age, gender, tumour histology, pT stage, and continuous TTR (HR: 0.99, p=0.006; monthly interval) independently predicted CSS.</p></div><div class="para"><p>By inclusion of dichotomized TTR in the multivariable model, a significant influence of this parameter on CSS was present until 48 months after surgery, but not beyond this time-period.</p></div></div>
<div class="section" id="bju12246-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Advanced age, male gender, larger tumour diameters, LVI, Fuhrman grade 3-4, pN+ stage, and advanced tumour stages are associated with early recurrence.</p></div><div class="para"><p>Up to four years from surgery, a shorter TTR independently predicts a reduced CSS after recurrence.</p></div></div>
]]></content:encoded><description>


What′s known about the subject? And what does the study add?
20-40% of renal cell carcinoma (RCC) patients will develop recurrence after surgery with curative intention, which will develop within the first five years after primary surgery in most cases, but also later (up to 45 years) in the follow-up (FU) in approximately 6-10% of patients. Time and pattern of metastasis show strong individual variations, and knowledge about those patients who are at risk for recurrence at different time-points would allow for an individualized aftercare and potentially also for initiation of early salvage treatment. Furthermore, the prognostic influence of time to recurrence (TTR) on cancer-specific survival (CSS) after disease recurrence is currently controversially discussed.
In this study, we evaluated the prognostic impact of TTR on CSS after recurrence in RCC patients undergoing radical nephrectomy or nephron sparing surgery. Differences in clinical and histopathological criteria between patients with early and late recurrence were evaluated as well. The study shows that, besides age, gender, tumour histology, and pT stage, also TTR is a significant predictor of CSS after recurrence in RCC patients who undergo primary surgery with curative intention. The earlier in the postsurgical FU recurrent disease occurs, the more reduced is survival after recurrence. Vice versa, the prognosis of patients in case of recurrence is improved with every day a patient stays disease-free after surgery up to four years from surgery, but not beyond this time-period.
Advanced age, male gender, advanced tumour diameter and stage, lymphovascular invasion, Fuhrman grade 3-4, and pN+ stage are more frequent in patients with early recurrence, which might provide the possibility of risk adapted aftercare. These data might be useful for implementation as risk stratification tool in clinical trials to avoid bias, i.e., to allow for equal representation of early and late recurrence patients in treatment arms.


Objective
To assess the prognostic impact of time to recurrence (TTR) on cancer-specific survival (CSS) after recurrence in renal cell carcinoma (RCC) patients undergoing radical nephrectomy or nephron sparing surgery.
To analyze differences in clinical and histopathological criteria between patients with early and late recurrence.


Patients and Methods
Of 13,107 RCC patients from an international multicentre database, 1,712 patients developed recurrence in the follow-up (FU) (median 50.1 months; IQR 25-106).
1,402 patients had recurrence within five years (Group A) and 310 patients beyond this time-period (Group B).
Differences in clinical and histopathological parameters between patients with early and late recurrence were analyzed.
The influence of TTR and further parameters on CSS after recurrence was assessed by Cox regression analysis.


Results
Male gender, advanced age, tumour diameter and stage, Fuhrman grade 3-4, lymphovascular invasion (LVI), and pN+ stage were significantly more frequent in patients with early recurrence, who had a significantly reduced 3-year CSS of 30% compared to Group B (41%; p=0.001).
Age, gender, tumour histology, pT stage, and continuous TTR (HR: 0.99, p=0.006; monthly interval) independently predicted CSS.
By inclusion of dichotomized TTR in the multivariable model, a significant influence of this parameter on CSS was present until 48 months after surgery, but not beyond this time-period.


Conclusion
Advanced age, male gender, larger tumour diameters, LVI, Fuhrman grade 3-4, pN+ stage, and advanced tumour stages are associated with early recurrence.
Up to four years from surgery, a shorter TTR independently predicts a reduced CSS after recurrence.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12245" xmlns="http://purl.org/rss/1.0/"><title>Incidence and Predictors of Understaging in Patients with Clinical T1 Urothelial Carcinoma Undergoing Radical Cystectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12245</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Incidence and Predictors of Understaging in Patients with Clinical T1 Urothelial Carcinoma Undergoing Radical Cystectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jacob T. Ark, Kirk A. Keegan, Daniel A. Barocas, Todd M. Morgan, Matthew J. Resnick, Chaochen You, Michael S. Cookson, David F. Penson, Rodney Davis, Peter E. Clark, Joseph A. Smith, Sam S. Chang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:47:23.495265-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12245</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12245</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12245</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12245-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To evaluate predictors of understaging in patients with presumed non-muscle invasive bladder cancer (NMIBC) identified on transurethral resection of bladder tumor (TURBT) who underwent radical cystectomy (RC) with attention to the role of a restaging TURBT.</p></div></div>
<div class="section" id="bju12245-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><p>We retrospectively evaluated 279 consecutive patients with clinically staged T1 (cT1) disease following TURBT who underwent RC at our institution from April 2000 to July 2011. 60 of these cT1 patients had undergone a restaging TURBT prior to RC. The primary outcome measure was pathological staging of T2 or greater disease at the time of RC.</p></div></div>
<div class="section" id="bju12245-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>134 (48.0%) patients were understaged. Of the 60 patients who remained cT1 after a restaging TURBT, 28 (46.7%) were understaged. Solitary tumor (OR 0.43, 95% CI 0.25-0.76, p = 0.004) and fewer prior TURBTs (OR 0.84, 95% CI 0.71 – 1.00, p = 0.05) were independent risk factors for understaging.</p></div></div>
<div class="section" id="bju12245-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Despite the overall improvement in staging accuracy linked to restaging TURBTs, the risk of clinical understaging remains high in restaged patients found to have persistent T1 urothelial carcinoma who undergo RC. Solitary tumor and fewer prior TURBTs are independent risk factors for being understaged. Incorporating these predictors into preoperative risk stratification may allow for augmented identification of those patients with clinical NMIBC who stand to benefit most from RC.</p></div></div>
]]></content:encoded><description>


Objective
To evaluate predictors of understaging in patients with presumed non-muscle invasive bladder cancer (NMIBC) identified on transurethral resection of bladder tumor (TURBT) who underwent radical cystectomy (RC) with attention to the role of a restaging TURBT.


Materials and Methods
We retrospectively evaluated 279 consecutive patients with clinically staged T1 (cT1) disease following TURBT who underwent RC at our institution from April 2000 to July 2011. 60 of these cT1 patients had undergone a restaging TURBT prior to RC. The primary outcome measure was pathological staging of T2 or greater disease at the time of RC.


Results
134 (48.0%) patients were understaged. Of the 60 patients who remained cT1 after a restaging TURBT, 28 (46.7%) were understaged. Solitary tumor (OR 0.43, 95% CI 0.25-0.76, p = 0.004) and fewer prior TURBTs (OR 0.84, 95% CI 0.71 – 1.00, p = 0.05) were independent risk factors for understaging.


Conclusions
Despite the overall improvement in staging accuracy linked to restaging TURBTs, the risk of clinical understaging remains high in restaged patients found to have persistent T1 urothelial carcinoma who undergo RC. Solitary tumor and fewer prior TURBTs are independent risk factors for being understaged. Incorporating these predictors into preoperative risk stratification may allow for augmented identification of those patients with clinical NMIBC who stand to benefit most from RC.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12244" xmlns="http://purl.org/rss/1.0/"><title>EFFECT OF HUMAN PAPILLOMAVIRUS AND CHLAMYDIA TRACHOMATIS COINFECTION ON SPERM PARAMETERS IN YOUNG HETEROSEXUAL MEN WITH CHRONIC PROSTATITIS-RELATED SYMPTOMS</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12244</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">EFFECT OF HUMAN PAPILLOMAVIRUS AND CHLAMYDIA TRACHOMATIS COINFECTION ON SPERM PARAMETERS IN YOUNG HETEROSEXUAL MEN WITH CHRONIC PROSTATITIS-RELATED SYMPTOMS</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tommaso Cai, Florian M.E. Wagenlehner, Nicola Mondaini, Carolina D′Elia, Francesca Meacci, Serena Migno, Gianni Malossini, Sandra Mazzoli, Riccardo Bartoletti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T06:47:18.581729-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12244</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12244</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12244</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12244-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To investigate the effect of Human Papillomavirus (HPV) and Chlamydia trachomatis (Ct) co-infection on sperm concentration, motility and morphology, in a large cohort of young heterosexual male patients with chronic prostatitis-related symptoms.</p></div></div>
<div class="section" id="bju12244-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Patients with chronic prostatitis-related symptoms, attending the same Sexually Transmitted Diseases (STD) Centre from January 2005 and December 2010, were consecutively enrolled in this cross-sectional study. All patients underwent clinical and instrumental examination, microbiological cultures for common bacteria, DNA extraction, mucosal and serum antibodies evaluation for Ct, specific tests for HPV and semen parameter analysis. The semen parameters analysed were: volume, pH, sperm concentration, motility and morphology. Subjects were subdivided in two groups: Group A – patients with singular Ct infection and Group B - patients with Ct and HPV co-infection. The main outcome measurement was the effect of Ct and HPV co-infection on semen parameters.</p></div></div>
<div class="section" id="bju12244-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>1,003 out of 3,050 screened patients were enrolled (32.9%). 716 (71.3%) patients were allocated to group A, and 287 (28.7%) to group B. Statistically significant differences were reported in terms of percent motile sperm (df=1001; t=11.85; p&lt;0.001) and percent of normal morphological forms (df=1001; t=7.18; p&lt;0.001), while no differences were reported between the two groups in terms of semen volume or pH. According to WHO cut-off normal parameters (WHO 2010), 364 (50.8%) men in group A and 192 (66.8%) men in group B were considered sub-fertile (OR=1.95; 95% CI 1.46-2.60; p&lt;0.0001). No correlation between HPV genotype, mucosal IgA type and semen parameters was found.</p></div></div>
<div class="section" id="bju12244-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>In a population of prostatitis-related symptoms due to Ct infection, co-infection with HPV has a significant role in decreasing male fertility parameters, in particular with regards to sperm motility and morphology.</p></div></div>
]]></content:encoded><description>


Objective
To investigate the effect of Human Papillomavirus (HPV) and Chlamydia trachomatis (Ct) co-infection on sperm concentration, motility and morphology, in a large cohort of young heterosexual male patients with chronic prostatitis-related symptoms.


Patients and Methods
Patients with chronic prostatitis-related symptoms, attending the same Sexually Transmitted Diseases (STD) Centre from January 2005 and December 2010, were consecutively enrolled in this cross-sectional study. All patients underwent clinical and instrumental examination, microbiological cultures for common bacteria, DNA extraction, mucosal and serum antibodies evaluation for Ct, specific tests for HPV and semen parameter analysis. The semen parameters analysed were: volume, pH, sperm concentration, motility and morphology. Subjects were subdivided in two groups: Group A – patients with singular Ct infection and Group B - patients with Ct and HPV co-infection. The main outcome measurement was the effect of Ct and HPV co-infection on semen parameters.


Results
1,003 out of 3,050 screened patients were enrolled (32.9%). 716 (71.3%) patients were allocated to group A, and 287 (28.7%) to group B. Statistically significant differences were reported in terms of percent motile sperm (df=1001; t=11.85; p&lt;0.001) and percent of normal morphological forms (df=1001; t=7.18; p&lt;0.001), while no differences were reported between the two groups in terms of semen volume or pH. According to WHO cut-off normal parameters (WHO 2010), 364 (50.8%) men in group A and 192 (66.8%) men in group B were considered sub-fertile (OR=1.95; 95% CI 1.46-2.60; p&lt;0.0001). No correlation between HPV genotype, mucosal IgA type and semen parameters was found.


Conclusions
In a population of prostatitis-related symptoms due to Ct infection, co-infection with HPV has a significant role in decreasing male fertility parameters, in particular with regards to sperm motility and morphology.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12237" xmlns="http://purl.org/rss/1.0/"><title>Patients with penile cancer and the risk of (pre)malignant cervical lesions in female partners: a retrospective cohort analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12237</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patients with penile cancer and the risk of (pre)malignant cervical lesions in female partners: a retrospective cohort analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bruijn RE, Heideman DAM, Kenter GG, Beurden M, Tinteren H, Horenblas S</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-21T05:17:23.689773-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12237</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12237</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12237</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12237-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To determine if female partners of patients with penile cancer had more cervical lesions and neoplasia than to be expected from population based data.</p></div></div>
<div class="section" id="bju12237-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>We included all consecutive patients with primary penile carcinoma in the period 2004-2010. ● Results of the Dutch cervical cancer screening were used to consider (pre)malignant cervical lesions in female partners of patients with penile cancer.</p></div></div>
<div class="section" id="bju12237-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In total, 206 women were included. ● Gyneacological information was avaliable in 195 women: Normal smears were seen in 129 partners, ten smears were abnormal (5.1%, 95%CI 2.5-9.2). ● PAP 2 was found in five, PAP 3a in two, PAP 3b in two women and PAP 4 in one woman. ● Colposcopy in two women with PAP 3b showed CIN 3 in both. ● This prevalence was not different from baseline results in the general Dutch population.</p></div></div>
<div class="section" id="bju12237-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Female partners of patients with penile cancer did not show more premalignant cervical lesions than in the general population.</p></div></div>
]]></content:encoded><description>


Objective
To determine if female partners of patients with penile cancer had more cervical lesions and neoplasia than to be expected from population based data.


Patients and Methods
We included all consecutive patients with primary penile carcinoma in the period 2004-2010. ● Results of the Dutch cervical cancer screening were used to consider (pre)malignant cervical lesions in female partners of patients with penile cancer.


Results
In total, 206 women were included. ● Gyneacological information was avaliable in 195 women: Normal smears were seen in 129 partners, ten smears were abnormal (5.1%, 95%CI 2.5-9.2). ● PAP 2 was found in five, PAP 3a in two, PAP 3b in two women and PAP 4 in one woman. ● Colposcopy in two women with PAP 3b showed CIN 3 in both. ● This prevalence was not different from baseline results in the general Dutch population.


Conclusion
Female partners of patients with penile cancer did not show more premalignant cervical lesions than in the general population.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12236" xmlns="http://purl.org/rss/1.0/"><title>Elasticity as a biomarker for prostate cancer: A systematic review</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12236</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Elasticity as a biomarker for prostate cancer: A systematic review</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Good DW, Stewart GD, Hammer S, Scanlan P, Shu W, Phipps S, Reuben R, McNeill AS</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-21T05:17:21.21502-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12236</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12236</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12236</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12236-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To systematically review the range of methods of assessment of elasticity in the prostate to investigate its use as a biomarker for prostate cancer.</p></div></div>
<div class="section" id="bju12236-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>A systematic review of the electronic database PubMed was performed up to December 2012.
All relevant studies assessing the use of elasticity as a biomarker for prostate cancer were included except those not studying human prostates or reporting a sensitivity, specificity or quantitative elasticity value.</p></div></div>
<div class="section" id="bju12236-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>There has been a lot of interest in the use of elasticity in the detection of prostate cancer and there have been many publications using a variety of methods of detection. The most common method of assessment is an imaging method, called sonoelastography. Further imaging methods include ultrasound, 3-D ultrasound and MR elastography. These modalities are reviewed for sensitivity and specificity.
The other method of assessment is the mechanical method. These use quantitative elasticity values to differentiate benign from malignant areas of the prostate. This method of assessment has shown that the elasticity changes for differing Gleason grades and T stages of disease within the prostate. Quantitative elasticity values offer the potential of using “cut-off” elasticity values under which the prostate is benign.</p></div></div>
<div class="section" id="bju12236-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Tissue elasticity has great potential as a diagnostic and prognostic biomarker for prostate cancer and can be assessed using a variety of methods. Currently transrectal sonoelastography has the most evidence supporting its use in clinical practice.</p></div></div>
]]></content:encoded><description>


Objective
To systematically review the range of methods of assessment of elasticity in the prostate to investigate its use as a biomarker for prostate cancer.


Methods
A systematic review of the electronic database PubMed was performed up to December 2012.
All relevant studies assessing the use of elasticity as a biomarker for prostate cancer were included except those not studying human prostates or reporting a sensitivity, specificity or quantitative elasticity value.


Results
There has been a lot of interest in the use of elasticity in the detection of prostate cancer and there have been many publications using a variety of methods of detection. The most common method of assessment is an imaging method, called sonoelastography. Further imaging methods include ultrasound, 3-D ultrasound and MR elastography. These modalities are reviewed for sensitivity and specificity.
The other method of assessment is the mechanical method. These use quantitative elasticity values to differentiate benign from malignant areas of the prostate. This method of assessment has shown that the elasticity changes for differing Gleason grades and T stages of disease within the prostate. Quantitative elasticity values offer the potential of using “cut-off” elasticity values under which the prostate is benign.


Conclusion
Tissue elasticity has great potential as a diagnostic and prognostic biomarker for prostate cancer and can be assessed using a variety of methods. Currently transrectal sonoelastography has the most evidence supporting its use in clinical practice.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12235" xmlns="http://purl.org/rss/1.0/"><title>Snapshot of Transurethral resection of bladder tumours in the United Kingdom Audit (STUKA)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12235</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Snapshot of Transurethral resection of bladder tumours in the United Kingdom Audit (STUKA)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christine Gan, Amit Patel, Sarah Fowler, James Catto, Derek Rosario, Timothy O′Brien</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-16T01:21:43.363479-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12235</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12235</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12235</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12235-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the quality of transurethral resection of bladder tumour (TURBT) in the UK.
To evaluate the utility of a novel ‘snapshot’ methodology in carrying out national audits.</p></div></div>
<div class="section" id="bju12235-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><p>Every consultant Urologist in the UK was asked to contribute details of their first patient with a new bladder cancer treated with TURBT after midnight of 31st January 2010.
Responses were received from 192 consultants.</p></div></div>
<div class="section" id="bju12235-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The median time from referral to first Urology appointment was 11 days
(range 0-161 days), and the median time from first appointment to TURBT was 27 days (range 1-588 days).
12 (6.3%) patients underwent photodynamic diagnosis (PDD) assisted TURBT and 119 patients (61%) received a dose of Mitomycin C after TURBT.
The rate of major complications was low, with 5 incidences (2.6%) of bladder perforation.
There was no record of muscle present in resected specimens in 40 cases
(20.8%) and resection was considered incomplete in 26 cases (13.5%). 31 patients (16.1%) underwent early re-resection with residual tumour or CIS detected in 17 cases, although no tumour was upstaged.
Of the 37 patients classified with intermediate risk non muscle invasive bladder cancer (NMIBC), there were 9 recurrences (24.3%) at 3 months, and 13 recurrences (35.1%) at 1 year. Newly presenting muscle invasive bladder cancer (MIBC) managed with currently available treatments has a high mortality rate of 33.3% at 1 year.</p></div></div>
<div class="section" id="bju12235-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The quality of TURBT in the UK is high.
Areas for improvement include the timeliness of diagnosis and treatment, and improved care of patients with intermediate risk NMIBC and MIBC.
The snapshot methodology is promising but widening participation is a priority.</p></div></div>
]]></content:encoded><description>


Objectives
To determine the quality of transurethral resection of bladder tumour (TURBT) in the UK.
To evaluate the utility of a novel ‘snapshot’ methodology in carrying out national audits.


Patients and methods
Every consultant Urologist in the UK was asked to contribute details of their first patient with a new bladder cancer treated with TURBT after midnight of 31st January 2010.
Responses were received from 192 consultants.


Results
The median time from referral to first Urology appointment was 11 days
(range 0-161 days), and the median time from first appointment to TURBT was 27 days (range 1-588 days).
12 (6.3%) patients underwent photodynamic diagnosis (PDD) assisted TURBT and 119 patients (61%) received a dose of Mitomycin C after TURBT.
The rate of major complications was low, with 5 incidences (2.6%) of bladder perforation.
There was no record of muscle present in resected specimens in 40 cases
(20.8%) and resection was considered incomplete in 26 cases (13.5%). 31 patients (16.1%) underwent early re-resection with residual tumour or CIS detected in 17 cases, although no tumour was upstaged.
Of the 37 patients classified with intermediate risk non muscle invasive bladder cancer (NMIBC), there were 9 recurrences (24.3%) at 3 months, and 13 recurrences (35.1%) at 1 year. Newly presenting muscle invasive bladder cancer (MIBC) managed with currently available treatments has a high mortality rate of 33.3% at 1 year.


Conclusion
The quality of TURBT in the UK is high.
Areas for improvement include the timeliness of diagnosis and treatment, and improved care of patients with intermediate risk NMIBC and MIBC.
The snapshot methodology is promising but widening participation is a priority.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12232" xmlns="http://purl.org/rss/1.0/"><title>Copy number aberrations by multi-color fluorescence in situ hybridization predict prognosis in non-muscle-invasive bladder cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12232</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Copy number aberrations by multi-color fluorescence in situ hybridization predict prognosis in non-muscle-invasive bladder cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hideyasu Matsuyama, Kenzo Ikemoto, Satoshi Eguchi, Atsunori Oga, Shigeto Kawauchi, Yoshiaki Yamamoto, Yoshihisa Kawai, Hiroaki Matsumoto, Takahiko Hara, Kazuhiro Nagao, Shigeru Sakano, Kohsuke Sasaki</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:56:57.602067-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12232</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12232</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12232</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12232-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To study if UroVysion kit, a multicolor fluorescence in situ hybridization (FISH) detecting the copy number of chromosomes 3, 7, 9p21, and 17, may predict patient outcome in NMIBC.</p></div></div>
<div class="section" id="bju12232-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Totally 118 bladder washing solutions were prospectively collected from patients who underwent TURBT (median age: 50.5, male/female: 91/27, tumor grade 1/2/3: 18/52/42, stage pTis/Ta/T1: 8/62/42) from 2007 to 2010, analyzed by UroVysion to detect the copy number of chromosomes 3, 7, 9p21, and 17. Variant fraction, sum of non-modal copy number fraction of each chromosome, and % deletion of 9p21, fraction of null or one copy number of 9p21 locus was defined abnormal when percentage of each fraction was 16%, and 12% or more, respectively. Maffezzini risk criteria were also analyzed in our cohorts.</p></div></div>
<div class="section" id="bju12232-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Recurrence and disease progression were found in 57 (48.3%), and 12 (10.1%) cases, respectively with a median follow-up of 35.7 months. Multivariate analysis demonstrated that % 9p21 loss (&gt;12%) were an independent prognostic factor for recurrence (p&lt;0.0001, OR: 3.24, 95% CI: 1.85-5.62). As for disease progression, tumor grade, positive urine cytology, concurrent CIS, and mean VF (&gt;16%) were significant prognostic factors in univariate analysis. In multivariate analysis, mean VF (&gt;16%) turned out to be a prognostic factor for disease progression (p=0.0476, OR: 6.07, 95% CI: 1.02-57.45).</p></div></div>
<div class="section" id="bju12232-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>A multicolor-FISH analysis using commercially available kit could be a powerful molecular marker not only for diagnosis, but also for predicting patient prognosis in patients with NMIBC.</p></div></div>
]]></content:encoded><description>


Objective
To study if UroVysion kit, a multicolor fluorescence in situ hybridization (FISH) detecting the copy number of chromosomes 3, 7, 9p21, and 17, may predict patient outcome in NMIBC.


Patients and Methods
Totally 118 bladder washing solutions were prospectively collected from patients who underwent TURBT (median age: 50.5, male/female: 91/27, tumor grade 1/2/3: 18/52/42, stage pTis/Ta/T1: 8/62/42) from 2007 to 2010, analyzed by UroVysion to detect the copy number of chromosomes 3, 7, 9p21, and 17. Variant fraction, sum of non-modal copy number fraction of each chromosome, and % deletion of 9p21, fraction of null or one copy number of 9p21 locus was defined abnormal when percentage of each fraction was 16%, and 12% or more, respectively. Maffezzini risk criteria were also analyzed in our cohorts.


Results
Recurrence and disease progression were found in 57 (48.3%), and 12 (10.1%) cases, respectively with a median follow-up of 35.7 months. Multivariate analysis demonstrated that % 9p21 loss (&gt;12%) were an independent prognostic factor for recurrence (p&lt;0.0001, OR: 3.24, 95% CI: 1.85-5.62). As for disease progression, tumor grade, positive urine cytology, concurrent CIS, and mean VF (&gt;16%) were significant prognostic factors in univariate analysis. In multivariate analysis, mean VF (&gt;16%) turned out to be a prognostic factor for disease progression (p=0.0476, OR: 6.07, 95% CI: 1.02-57.45).


Conclusions
A multicolor-FISH analysis using commercially available kit could be a powerful molecular marker not only for diagnosis, but also for predicting patient prognosis in patients with NMIBC.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12229" xmlns="http://purl.org/rss/1.0/"><title>Clinical and sonographic features predict testicular torsion in children: a prospective study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12229</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clinical and sonographic features predict testicular torsion in children: a prospective study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael Boettcher, Thomas Krebs, Robert Bergholz, Katharina Wenke, Daniel Aronson, Konrad Reinshagen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:56:53.216592-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12229</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12229</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12229</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12233" xmlns="http://purl.org/rss/1.0/"><title>Sperm nuclear DNA fragmentation rate is associated with differential protein expression and enriched functions in human seminal plasma</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12233</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sperm nuclear DNA fragmentation rate is associated with differential protein expression and enriched functions in human seminal plasma</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paula Intasqui, Mariana Camargo, Paula T. Del Giudice, Deborah M. Spaine, Valdemir M. Carvalho, Karina H. M. Cardozo, Daniel S. Zylbersztejn, Ricardo P. Bertolla</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:30:48.688072-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12233</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12233</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12233</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12233-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>OBJECTIVE</h4><div class="para"><p>To analyze the proteomic profile of seminal plasma in search for proteins and post-genomic pathways associated with sperm DNA fragmentation.</p></div></div>
<div class="section" id="bju12233-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>MATERIALS AND METHODS</h4><div class="para"><p>A cross-sectional study including 89 subjects from a human reproduction service was carried out.
All semen samples were assessed for sperm DNA fragmentation using the Comet assay. Results from 60 sperm were analyzed by the Komet 6.0.1 software. Olive Tail Moment variable was used to form the Low and High sperm DNA fragmentation groups.
Seminal plasma proteins from these groups were pooled and used for proteomics analysis (2D nanoUPLC-ESI-MS<sup>E</sup>).
Quantitative data were used for functional enrichment studies.</p></div></div>
<div class="section" id="bju12233-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>RESULTS</h4><div class="para"><p>Seventy-two proteins were identified or quantified in seminal plasma. Of these, nine were differentially expressed in the Low group and twenty-one in the High group. Forty-two proteins were conserved between these groups.
Functional enrichment analysis indicates that sperm DNA fragmentation is related to functions such as lipoprotein particle remodeling and regulation, fatty acid binding and immune response. Proteins found exclusively in the Low group may be involved in correcting spermatogenesis and/or improving sperm function. Proteins in the High group were associated with increased innate immune response, sperm motility and/or maturation and inhibition of mitochondrial apoptosis.</p></div></div>
<div class="section" id="bju12233-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>CONCLUSION</h4><div class="para"><p>Protein expression and post-genomic pathways of seminal plasma differ according to the rate of sperm DNA integrity.</p></div></div>
]]></content:encoded><description>


OBJECTIVE
To analyze the proteomic profile of seminal plasma in search for proteins and post-genomic pathways associated with sperm DNA fragmentation.


MATERIALS AND METHODS
A cross-sectional study including 89 subjects from a human reproduction service was carried out.
All semen samples were assessed for sperm DNA fragmentation using the Comet assay. Results from 60 sperm were analyzed by the Komet 6.0.1 software. Olive Tail Moment variable was used to form the Low and High sperm DNA fragmentation groups.
Seminal plasma proteins from these groups were pooled and used for proteomics analysis (2D nanoUPLC-ESI-MSE).
Quantitative data were used for functional enrichment studies.


RESULTS
Seventy-two proteins were identified or quantified in seminal plasma. Of these, nine were differentially expressed in the Low group and twenty-one in the High group. Forty-two proteins were conserved between these groups.
Functional enrichment analysis indicates that sperm DNA fragmentation is related to functions such as lipoprotein particle remodeling and regulation, fatty acid binding and immune response. Proteins found exclusively in the Low group may be involved in correcting spermatogenesis and/or improving sperm function. Proteins in the High group were associated with increased innate immune response, sperm motility and/or maturation and inhibition of mitochondrial apoptosis.


CONCLUSION
Protein expression and post-genomic pathways of seminal plasma differ according to the rate of sperm DNA integrity.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12231" xmlns="http://purl.org/rss/1.0/"><title>Common prescription medication use and erectile dysfunction. Results from the Boston Area Community Health (BACH) Survey</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12231</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Common prescription medication use and erectile dysfunction. Results from the Boston Area Community Health (BACH) Survey</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Varant Kupelian, Susan A. Hall, John B. McKinlay</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:30:41.919386-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12231</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12231</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12231</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12231-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To investigate the association of ED with commonly used medications including antihypertensive, psychoactive medications, and pain and anti-inflammatory medications.</p></div></div>
<div class="section" id="bju12231-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects and Methods</h4><div class="para"><p>The Boston Area Community Health (BACH) Survey used a multistage stratified design to recruit a random sample of 2,301 men age 30-79. ED was assessed using the 5-item International Index of Erectile Function (IIEF-5).
Prescription medication use, captured using a combination of drug inventory and self-report with a prompt by indication, included in this analysis were antihypertensive agents (AHT), psychoactive medications, and pain and anti-inflammatory medications.
Logistic regression was used to estimate odds ratios of the association of medication use and ED and adjust for potential confounders including age, comorbid conditions, and sociodemographic and lifestyle factors.</p></div></div>
<div class="section" id="bju12231-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Multivariable analyses show benzodiazepines (adjusted OR=2.34, 95%CI: 1.03, 5.31) and tricyclic antidepressants (adjusted OR=3.35, 95%CI:1.09, 10.27) were associated with ED, while no association was observed for SSNRI/SNRIs and atypical antipsychotics.
AHT use, whether in monotherapy or in conjunction with other AHTs, and pain or anti-inflammatory medications were not associated with ED after accounting for confounding factors.</p></div></div>
<div class="section" id="bju12231-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Results of the BACH study suggest adverse effects of some psychoactive medications (benzodiazepines and tricyclic antidepressants).
No evidence of an association of AHT or pain and anti-inflammatory medication with ED was observed.</p></div></div>
]]></content:encoded><description>


Objectives
To investigate the association of ED with commonly used medications including antihypertensive, psychoactive medications, and pain and anti-inflammatory medications.


Subjects and Methods
The Boston Area Community Health (BACH) Survey used a multistage stratified design to recruit a random sample of 2,301 men age 30-79. ED was assessed using the 5-item International Index of Erectile Function (IIEF-5).
Prescription medication use, captured using a combination of drug inventory and self-report with a prompt by indication, included in this analysis were antihypertensive agents (AHT), psychoactive medications, and pain and anti-inflammatory medications.
Logistic regression was used to estimate odds ratios of the association of medication use and ED and adjust for potential confounders including age, comorbid conditions, and sociodemographic and lifestyle factors.


Results
Multivariable analyses show benzodiazepines (adjusted OR=2.34, 95%CI: 1.03, 5.31) and tricyclic antidepressants (adjusted OR=3.35, 95%CI:1.09, 10.27) were associated with ED, while no association was observed for SSNRI/SNRIs and atypical antipsychotics.
AHT use, whether in monotherapy or in conjunction with other AHTs, and pain or anti-inflammatory medications were not associated with ED after accounting for confounding factors.


Conclusions
Results of the BACH study suggest adverse effects of some psychoactive medications (benzodiazepines and tricyclic antidepressants).
No evidence of an association of AHT or pain and anti-inflammatory medication with ED was observed.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12230" xmlns="http://purl.org/rss/1.0/"><title>Genetic polymorphisms in the matrix metalloproteinases, tissue inhibitors of metalloproteinases and bladder cancer susceptibility</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12230</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic polymorphisms in the matrix metalloproteinases, tissue inhibitors of metalloproteinases and bladder cancer susceptibility</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Edyta Wieczorek, Edyta Reszka, Zbigniew Jablonowski, Ewa Jablonska, Magdalena Beata Krol, Adam Grzegorczyk, Jolanta Gromadzinska, Marek Sosnowski, Wojciech Wasowicz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:30:39.017042-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12230</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12230</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12230</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12230-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To elucidate genetic polymorphisms in the <em>MMP1</em> (rs1799750)<em>, MMP2</em> (rs243865)<em>, MMP9</em> (rs3918242)<em>, MMP12</em> (rs2276109) and <em>TIMP1</em> (rs2070584)<em>, TIMP3</em> (rs9619311) genes responsible for susceptibility to bladder cancer (BC).</p></div></div>
<div class="section" id="bju12230-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><p>We enrolled 241 BC patients and 199 controls.
Genomic DNA samples were extracted from peripheral blood and polymorphisms were analysed by the High Resolution Melting analysis and by the Real-Time polymerase chain reaction using TaqMan fluorescent probes.</p></div></div>
<div class="section" id="bju12230-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Out of the six evaluated polymorphisms of <em>MMPs</em> and <em>TIMPs</em>, only one was found to be associated with BC risk.
Significant difference was noted for <em>MMP1</em> (rs1799750) <em>2G/1G+1G/1G</em> genotype (OR, 0.62; 95% CI, 0.39-0.98; <em>P</em>=0.042).
Additionally, joint effect of this genotype on BC risk among ever smokes (OR, 0.51; 95% CI, 0.28-0.89; <em>P</em>=0.019), but not in never smokers was observed.
The combined genotype <em>MMP2</em> -1306<em>C/T</em> (rs243865) allele <em>T</em> with <em>MMP9</em> -1562<em>C/T</em> (rs3918242) allele <em>T</em> was found to increase BC risk (OR, 2.00; 95% CI, 1.10-3.62; <em>P</em>=0.022).</p></div></div>
<div class="section" id="bju12230-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Our results suggest that genetic variations in five polymorphisms of <em>MMPs</em> and <em>TIMPs</em> are not associated with a high risk of BC.
Only <em>MMP1</em> polymorphism may be related to the risk of BC, notably in ever-smokers.
Our study suggests that the effects of polymorphisms of <em>MMPs</em> and <em>TIMPs</em> on BC risk deserve further investigation.</p></div></div>
]]></content:encoded><description>

Objectives
To elucidate genetic polymorphisms in the MMP1 (rs1799750), MMP2 (rs243865), MMP9 (rs3918242), MMP12 (rs2276109) and TIMP1 (rs2070584), TIMP3 (rs9619311) genes responsible for susceptibility to bladder cancer (BC).


Patients and methods
We enrolled 241 BC patients and 199 controls.
Genomic DNA samples were extracted from peripheral blood and polymorphisms were analysed by the High Resolution Melting analysis and by the Real-Time polymerase chain reaction using TaqMan fluorescent probes.


Results
Out of the six evaluated polymorphisms of MMPs and TIMPs, only one was found to be associated with BC risk.
Significant difference was noted for MMP1 (rs1799750) 2G/1G+1G/1G genotype (OR, 0.62; 95% CI, 0.39-0.98; P=0.042).
Additionally, joint effect of this genotype on BC risk among ever smokes (OR, 0.51; 95% CI, 0.28-0.89; P=0.019), but not in never smokers was observed.
The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs3918242) allele T was found to increase BC risk (OR, 2.00; 95% CI, 1.10-3.62; P=0.022).


Conclusions
Our results suggest that genetic variations in five polymorphisms of MMPs and TIMPs are not associated with a high risk of BC.
Only MMP1 polymorphism may be related to the risk of BC, notably in ever-smokers.
Our study suggests that the effects of polymorphisms of MMPs and TIMPs on BC risk deserve further investigation.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12228" xmlns="http://purl.org/rss/1.0/"><title>Penile Rehabilitation after Radical Prostatectomy: What the Evidence Really Says</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12228</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Penile Rehabilitation after Radical Prostatectomy: What the Evidence Really Says</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mikkel Fode, Dana A. Ohl, David Ralph, Jens Sønksen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:30:37.562269-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12228</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12228</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12228</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Key messages</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The pathophysiology of post prostatectomy ED is believed to include neuropraxia, which leads to temporarily reduced oxygenation and subsequent structural changes in penile tissue. This results in veno-occlusive dysfunction. Therefore, penile rehabilitation programs focus on tissue oxygenation.
Animal studies support the use of PDE5I after cavernous nerve damage but results from human studies are contradictory. The largest study to date found no long term effect of neither daily nor on-demand PDE5I administration after RP compared to placebo.
The effects of Prostaglandin and VED are questionable and high quality studies are lacking.
Better documentation for current penile rehabilitation and/or better rehabilitation protocols are needed.
One must be careful to not repeat the statement that penile rehabilitation improves erectile function after RP so many times that it becomes a truth even without the proper scientific backing.</p></div>
]]></content:encoded><description>

The pathophysiology of post prostatectomy ED is believed to include neuropraxia, which leads to temporarily reduced oxygenation and subsequent structural changes in penile tissue. This results in veno-occlusive dysfunction. Therefore, penile rehabilitation programs focus on tissue oxygenation.
Animal studies support the use of PDE5I after cavernous nerve damage but results from human studies are contradictory. The largest study to date found no long term effect of neither daily nor on-demand PDE5I administration after RP compared to placebo.
The effects of Prostaglandin and VED are questionable and high quality studies are lacking.
Better documentation for current penile rehabilitation and/or better rehabilitation protocols are needed.
One must be careful to not repeat the statement that penile rehabilitation improves erectile function after RP so many times that it becomes a truth even without the proper scientific backing.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12227" xmlns="http://purl.org/rss/1.0/"><title>BILATERAL FOCAL ABLATION OF PROSTATE TISSUE USING LOW ENERGY DIRECT CURRENT (LEDC): A PRECLINICAL CANINE STUDY</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12227</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">BILATERAL FOCAL ABLATION OF PROSTATE TISSUE USING LOW ENERGY DIRECT CURRENT (LEDC): A PRECLINICAL CANINE STUDY</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matvey Tsivian, Thomas J Polascik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T22:30:22.848346-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12227</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12227</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12227</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12227-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To evaluate side effects, erectile function and capability to preserve adjacent tissues of bilateral focal prostate ablation using low energy direct current (LEDC) in a canine model.</p></div></div>
<div class="section" id="bju12227-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><p>Twelve male Beagle dogs underwent bilateral focal prostate ablation using the NanoKnife™ LEDC system.
Three 19G monopolar electrodes were transperineally placed on each side of the prostate under transrectal ultrasonographic (TRUS) guidance using a triangular probe array.
Intra- and postoperative side effects were recorded. Erectile function was evaluated at baseline and 4-5 and 26-27 days postoperatively.
The animals were terminated at 7(n=6) and 30 days (n=6) for gross and microscopic evaluation of the prostate and adjacent organs.</p></div></div>
<div class="section" id="bju12227-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Median prostate volume on TRUS was 12.1mL (range 8.9-17.2). The electrodes were placed at a median distances of 0.55-0.66cm from the capsule, urethra and rectum.
All procedures were completed successfully and recovery was uneventful. There were no episodes of urinary retention.
All animals were able to achieve erections postoperatively.
Pathological analyses revealed inflammatory changes in the ablation zone at 7 days and replacement by fibrosis at 30 days. On microscopic examination no histological injury to the capsule, urethra, rectal wall or nervous structures was identified.</p></div></div>
<div class="section" id="bju12227-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>In this study, bilateral focal prostate ablation using LEDC was safe and had a favorable side-effects profile limited to transient minor events.
LEDC ablation effectively spared adjacent structures as well as physiological functions in all animals.</p></div></div>
]]></content:encoded><description>


Objectives
To evaluate side effects, erectile function and capability to preserve adjacent tissues of bilateral focal prostate ablation using low energy direct current (LEDC) in a canine model.


Materials and Methods
Twelve male Beagle dogs underwent bilateral focal prostate ablation using the NanoKnife™ LEDC system.
Three 19G monopolar electrodes were transperineally placed on each side of the prostate under transrectal ultrasonographic (TRUS) guidance using a triangular probe array.
Intra- and postoperative side effects were recorded. Erectile function was evaluated at baseline and 4-5 and 26-27 days postoperatively.
The animals were terminated at 7(n=6) and 30 days (n=6) for gross and microscopic evaluation of the prostate and adjacent organs.


Results
Median prostate volume on TRUS was 12.1mL (range 8.9-17.2). The electrodes were placed at a median distances of 0.55-0.66cm from the capsule, urethra and rectum.
All procedures were completed successfully and recovery was uneventful. There were no episodes of urinary retention.
All animals were able to achieve erections postoperatively.
Pathological analyses revealed inflammatory changes in the ablation zone at 7 days and replacement by fibrosis at 30 days. On microscopic examination no histological injury to the capsule, urethra, rectal wall or nervous structures was identified.


Conclusions
In this study, bilateral focal prostate ablation using LEDC was safe and had a favorable side-effects profile limited to transient minor events.
LEDC ablation effectively spared adjacent structures as well as physiological functions in all animals.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12225" xmlns="http://purl.org/rss/1.0/"><title>Single-port transvesical laparoscopic radical prostatectomy for organ-confined prostate cancer: technique and outcomes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12225</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Single-port transvesical laparoscopic radical prostatectomy for organ-confined prostate cancer: technique and outcomes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xin Gao, Jun Pang, Jie Si-tu, Yun Luo, Hao Zhang, Liao-yuan Li, Yan Zhang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:21.48273-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12225</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12225</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12225</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Laparoscopic radical prostatectomy (LRP) has become a standard approach in the treatment of organ-confined prostate cancer. However, postoperative incontinence and loss of sexual function have significant adverse effects on quality of life. Although some modifications, including preservation of the bladder neck [1], sparing neurovascular bundles and apical modified dissection [2], have been implemented to improve the outcomes of postoperative continence and sexual function, achieving the rapid recovery of continence and sexual function remains a huge challenge.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Recently, Wilt et al reported that radical prostatectomy did not significantly reduce all-cause or prostate cancer mortality compared with observation among men with localized prostate cancer (PSA &lt;10 ng/mL, low risk) detected early through PSA testing over at least 12 years of follow-up [3]. However, in men with low risk organ-confined prostate cancer who present significant obstructive symptoms, radical prostatectomy should be recommended rather than transurethral resection of the prostate (TURP) to resolve the obstruction as well as control the prostate cancer. Therefore, regaining a high quality of life after radical prostatectomy has the priority besides cancer control.</p></div>
]]></content:encoded><description>
Laparoscopic radical prostatectomy (LRP) has become a standard approach in the treatment of organ-confined prostate cancer. However, postoperative incontinence and loss of sexual function have significant adverse effects on quality of life. Although some modifications, including preservation of the bladder neck [1], sparing neurovascular bundles and apical modified dissection [2], have been implemented to improve the outcomes of postoperative continence and sexual function, achieving the rapid recovery of continence and sexual function remains a huge challenge.
Recently, Wilt et al reported that radical prostatectomy did not significantly reduce all-cause or prostate cancer mortality compared with observation among men with localized prostate cancer (PSA &lt;10 ng/mL, low risk) detected early through PSA testing over at least 12 years of follow-up [3]. However, in men with low risk organ-confined prostate cancer who present significant obstructive symptoms, radical prostatectomy should be recommended rather than transurethral resection of the prostate (TURP) to resolve the obstruction as well as control the prostate cancer. Therefore, regaining a high quality of life after radical prostatectomy has the priority besides cancer control.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12224" xmlns="http://purl.org/rss/1.0/"><title>Need to void and attentional process interrelationships.</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12224</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Need to void and attentional process interrelationships.</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Jousse, D. Verollet, A Guinet-Lacoste, F. Le Breton, L Auclair, S Sheikh Ismael, G. Amarenco</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:14.02337-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12224</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12224</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12224</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The need to void is a bladder sensation which occurs many times a day in healthy people. This sensation is a key component in the continence micturition cycle. It can be altered in many bladder dysfunctions, such as an overactive or neurogenic bladder.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Usually, healthy people can postpone their desire to void, depending on the social situation in which the need occurs. Many individuals have the ability to defer voiding, despite a strong urge, if the circumstances dictate the need to wait. Conversely, a strong desire to void can also prevent people from concentrating or paying attention during activities such as holding a conversation or sitting for an examination.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Over the last ten years, many imaging studies have taken an interest in the cerebral integration of the sensation of the urge to void. In 2001, using a Positron Emissions Tomography (PET) study, Athwal et al. [1] showed that an increase in cerebral activity of the periaqueductal grey (PAG), midbrain stem, and cingulate cortex frontal lobe was associated with an increase in bladder volume, and that increased brain activity relating to decreased urge to void was seen in a different portion of the cingulate cortex, in the premotor cortex and in the hypothalamus. Some of these results were confirmed by Kuhtz –Buschbeck et al. [2].</p></div>
]]></content:encoded><description>
The need to void is a bladder sensation which occurs many times a day in healthy people. This sensation is a key component in the continence micturition cycle. It can be altered in many bladder dysfunctions, such as an overactive or neurogenic bladder.
Usually, healthy people can postpone their desire to void, depending on the social situation in which the need occurs. Many individuals have the ability to defer voiding, despite a strong urge, if the circumstances dictate the need to wait. Conversely, a strong desire to void can also prevent people from concentrating or paying attention during activities such as holding a conversation or sitting for an examination.
Over the last ten years, many imaging studies have taken an interest in the cerebral integration of the sensation of the urge to void. In 2001, using a Positron Emissions Tomography (PET) study, Athwal et al. [1] showed that an increase in cerebral activity of the periaqueductal grey (PAG), midbrain stem, and cingulate cortex frontal lobe was associated with an increase in bladder volume, and that increased brain activity relating to decreased urge to void was seen in a different portion of the cingulate cortex, in the premotor cortex and in the hypothalamus. Some of these results were confirmed by Kuhtz –Buschbeck et al. [2].
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12223" xmlns="http://purl.org/rss/1.0/"><title>IMAGE-DIRECTED, TISSUE-PRESERVING FOCAL THERAPY OF PROSTATE CANCER: A FEASIBILITY STUDY OF A NOVEL DEFORMABLE MR-US REGISTRATION SYSTEM</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12223</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">IMAGE-DIRECTED, TISSUE-PRESERVING FOCAL THERAPY OF PROSTATE CANCER: A FEASIBILITY STUDY OF A NOVEL DEFORMABLE MR-US REGISTRATION SYSTEM</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L Dickinson, Y Hu, HU Ahmed, C Allen, AP Kirkham, M Emberton, D Barratt</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:10.508382-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12223</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12223</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12223</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12223-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p><em>What is already known about the subject:</em> Imaging is now playing an increasingly important role in the detection and localisation of prostate cancer. Multi-parametric (mp) MRI in particular has shown promise as an accurate method for determining the focality of tumours, and has potential to inform the conduct of novel minimally-invasive, tissue-preserving (‘focal’) treatments, such that high precision may be achieved when treating a therapeutic target. However, reliably utilising this information has been technically challenging, as most minimally-invasive technologies are delivered using an ultrasound guidance platform. As a consequence, current forms of focal therapy within trials have typically used relatively large regions, such as a lobe or quadrant, as the therapeutic target. This often results in large discrepancies between the tumour and target volumes, potentially leading to under-treatment at the margins.</p></div></div>
<div class="section" id="bju12223-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To evaluate the feasibility in using a computer-assisted, deformable image registration software to enable three-dimensional, mpMRI-derived information on tumour location and extent to inform the planning and conduct of focal high-intensity focused ultrasound (HIFU) therapy.</p></div></div>
<div class="section" id="bju12223-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects/ Patients</h4><div class="para"><p>A nested pilot study of 26 consecutive men with a visible discrete focus on mpMRI, correlating with positive histology on transperineal template mapping biopsy, who underwent focal HIFU (Sonablate 500®) within a prospective, ethics committee approved multi-centre trial (‘INDEX’).</p></div></div>
<div class="section" id="bju12223-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Non-rigid image registration software developed in our institution was used to transfer data on the location and limits of the index lesion as defined by mpMRI.</p></div><div class="para"><p>Manual contouring of the prostate capsule and histologically-confirmed MR-visible lesion was performed pre-operatively by a urologist and uro-radiologist.</p></div><div class="para"><p>A deformable patient-specific computer model, which captures the location of the target lesion, was automatically generated for each patient and registered to a 3D TRUS volume using a small number (10-20) of manually-defined capsule points.</p></div><div class="para"><p>During the focal HIFU, the urologist could add additional sonications following image-registration if it was felt that the original treatment plan did not cover the lesion sufficiently with a margin</p></div></div>
<div class="section" id="bju12223-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Prostate capsule and lesion contouring was achieved in under 5 minutes pre-operatively. The mean time taken to register images was 6 minutes (range 3 – 16).</p></div><div class="para"><p>Additional treatment sonications were added in 13 of 26 cases leading to a mean additional treatment time of 45 secs (range 9 - 90).</p></div></div>
<div class="section" id="bju12223-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Non-rigid MR-US registration is feasible, efficient and can locate lesions on ultrasound.</p></div><div class="para"><p>The process has potential for improved accuracy of focal treatments, and improved diagnostic sampling strategies for prostate cancer.</p></div><div class="para"><p>Further work on whether deformable MR-US registration impacts on efficacy is required.</p></div></div>
]]></content:encoded><description>


What is already known about the subject: Imaging is now playing an increasingly important role in the detection and localisation of prostate cancer. Multi-parametric (mp) MRI in particular has shown promise as an accurate method for determining the focality of tumours, and has potential to inform the conduct of novel minimally-invasive, tissue-preserving (‘focal’) treatments, such that high precision may be achieved when treating a therapeutic target. However, reliably utilising this information has been technically challenging, as most minimally-invasive technologies are delivered using an ultrasound guidance platform. As a consequence, current forms of focal therapy within trials have typically used relatively large regions, such as a lobe or quadrant, as the therapeutic target. This often results in large discrepancies between the tumour and target volumes, potentially leading to under-treatment at the margins.


Objective
To evaluate the feasibility in using a computer-assisted, deformable image registration software to enable three-dimensional, mpMRI-derived information on tumour location and extent to inform the planning and conduct of focal high-intensity focused ultrasound (HIFU) therapy.


Subjects/ Patients
A nested pilot study of 26 consecutive men with a visible discrete focus on mpMRI, correlating with positive histology on transperineal template mapping biopsy, who underwent focal HIFU (Sonablate 500®) within a prospective, ethics committee approved multi-centre trial (‘INDEX’).


Methods
Non-rigid image registration software developed in our institution was used to transfer data on the location and limits of the index lesion as defined by mpMRI.
Manual contouring of the prostate capsule and histologically-confirmed MR-visible lesion was performed pre-operatively by a urologist and uro-radiologist.
A deformable patient-specific computer model, which captures the location of the target lesion, was automatically generated for each patient and registered to a 3D TRUS volume using a small number (10-20) of manually-defined capsule points.
During the focal HIFU, the urologist could add additional sonications following image-registration if it was felt that the original treatment plan did not cover the lesion sufficiently with a margin


Results
Prostate capsule and lesion contouring was achieved in under 5 minutes pre-operatively. The mean time taken to register images was 6 minutes (range 3 – 16).
Additional treatment sonications were added in 13 of 26 cases leading to a mean additional treatment time of 45 secs (range 9 - 90).


Conclusion
Non-rigid MR-US registration is feasible, efficient and can locate lesions on ultrasound.
The process has potential for improved accuracy of focal treatments, and improved diagnostic sampling strategies for prostate cancer.
Further work on whether deformable MR-US registration impacts on efficacy is required.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12222" xmlns="http://purl.org/rss/1.0/"><title>Predictive factors of postoperative complications after robotic assisted laparoscopic partial nephrectomy: a retrospective multicenter study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12222</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Predictive factors of postoperative complications after robotic assisted laparoscopic partial nephrectomy: a retrospective multicenter study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Mathieu, G. Verhoest, S. Droupy, A. Taille, F. Bruyere, N. Doumerc, P. Rischmann, C. Vaessen, M. Roupret, K. Bensalah</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:07.958631-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12222</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12222</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12222</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12222-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To analyze predictive factors of postoperative complications after robotic assisted laparoscopic partial nephrectomy (RALPN).</p></div></div>
<div class="section" id="bju12222-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and methods</h4><div class="para"><p>Data from 240 patients who underwent RALPN between 2009 and 2011 at 6 French centres were retrospectively reviewed. Clinical (age, BMI, ASA and Charlson score, anticoagulant treatment), tumoral (size, R.E.N.A.L Nephrometry score) and operative (surgeon experience, blood loss, opening of the collecting system, operative time) parameters were considered. Postoperative complications were classified according to the Clavien system. Univariate and multivariate regression models were used to assess the impact of these variables on the occurrence of global and major complications.</p></div></div>
<div class="section" id="bju12222-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Median age was 61 years (26-83). Tumours were of low complexity in 62% of cases. Median operative time, blood loss and warm ischemia time were 161 min (45-425), 100 ml (0-2500) and 20 min (0-59), respectively. Postoperative complications occurred in 79 (33%) patients. Complications were ≥ grade 3 in 25 (10%) patients and were mostly hemorrhagic. In multivariate analysis, surgeon's experience (HR 2.14 [1.07 - 4.27], p = 0.03) and blood loss (HR: 1.002 [1.001 - 1.003], p = 0.0002) were independent predictors of overall complications. When considering major complications, opening of the collecting system was the only factor that was significant (OR: 2.99 [1.2-7.26], p =0.02). Nephrometry RENAL score was not associated with post-operative complications.</p></div></div>
<div class="section" id="bju12222-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In our experience, RALPN is associated with a 30% risk of postoperative complications. Surgeon's experience, blood loss and opening of the collecting system were the three predictors of postoperative complications.</p></div></div>
]]></content:encoded><description>


Objective
To analyze predictive factors of postoperative complications after robotic assisted laparoscopic partial nephrectomy (RALPN).


Materials and methods
Data from 240 patients who underwent RALPN between 2009 and 2011 at 6 French centres were retrospectively reviewed. Clinical (age, BMI, ASA and Charlson score, anticoagulant treatment), tumoral (size, R.E.N.A.L Nephrometry score) and operative (surgeon experience, blood loss, opening of the collecting system, operative time) parameters were considered. Postoperative complications were classified according to the Clavien system. Univariate and multivariate regression models were used to assess the impact of these variables on the occurrence of global and major complications.


Results
Median age was 61 years (26-83). Tumours were of low complexity in 62% of cases. Median operative time, blood loss and warm ischemia time were 161 min (45-425), 100 ml (0-2500) and 20 min (0-59), respectively. Postoperative complications occurred in 79 (33%) patients. Complications were ≥ grade 3 in 25 (10%) patients and were mostly hemorrhagic. In multivariate analysis, surgeon's experience (HR 2.14 [1.07 - 4.27], p = 0.03) and blood loss (HR: 1.002 [1.001 - 1.003], p = 0.0002) were independent predictors of overall complications. When considering major complications, opening of the collecting system was the only factor that was significant (OR: 2.99 [1.2-7.26], p =0.02). Nephrometry RENAL score was not associated with post-operative complications.


Conclusion
In our experience, RALPN is associated with a 30% risk of postoperative complications. Surgeon's experience, blood loss and opening of the collecting system were the three predictors of postoperative complications.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12221" xmlns="http://purl.org/rss/1.0/"><title>Patterns of Management and Surveillance Imaging for Stage I Testicular Cancer amongst Medical Oncologists in Australia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12221</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patterns of Management and Surveillance Imaging for Stage I Testicular Cancer amongst Medical Oncologists in Australia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P Grimison, B Houghton, M Chatfield, GC Toner, ID Davis, J Martin, E Hovey, M R Stockler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:07.454526-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12221</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12221</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12221</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12221-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To determine patterns of management and surveillance imaging for stage I testicular cancer amongst Australian medical oncologists in Australia during 2010.</p></div></div>
<div class="section" id="bju12221-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects and methods</h4><div class="para"><p>The survey comprised 14 questions about management strategy and surveillance imaging for all patients with stage I testicular cancer treated over the previous 12 months.</p></div></div>
<div class="section" id="bju12221-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>52 medical oncologists documented the management for an estimated 470 patients.</p></div><div class="para"><p>For seminoma, management was surveillance in 33%, radiotherapy in 5%, and adjuvant carboplatin in 62%.</p></div><div class="para"><p>For non-seminoma, management was surveillance in 73%, adjuvant chemotherapy in 23%, and retro-peritoneal lymph node dissection in 4%.</p></div><div class="para"><p>Frequency of surveillance imaging was highly variable, and ≥ 10 CT scans were used by 38% of clinicians for seminoma and 46% of clinicians for non-seminoma.</p></div></div>
<div class="section" id="bju12221-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>We found considerable variation in management. The infrequent use of surveillance and frequent use of carboplatin for seminoma differs from international guidelines.</p></div><div class="para"><p>Radiation exposure from CT imaging should be reduced through standardised follow-up protocols, and possibly by alternate imaging modalities if validated in appropriate studies.</p></div></div>
]]></content:encoded><description>


Objective
To determine patterns of management and surveillance imaging for stage I testicular cancer amongst Australian medical oncologists in Australia during 2010.


Subjects and methods
The survey comprised 14 questions about management strategy and surveillance imaging for all patients with stage I testicular cancer treated over the previous 12 months.


Results
52 medical oncologists documented the management for an estimated 470 patients.
For seminoma, management was surveillance in 33%, radiotherapy in 5%, and adjuvant carboplatin in 62%.
For non-seminoma, management was surveillance in 73%, adjuvant chemotherapy in 23%, and retro-peritoneal lymph node dissection in 4%.
Frequency of surveillance imaging was highly variable, and ≥ 10 CT scans were used by 38% of clinicians for seminoma and 46% of clinicians for non-seminoma.


Conclusion
We found considerable variation in management. The infrequent use of surveillance and frequent use of carboplatin for seminoma differs from international guidelines.
Radiation exposure from CT imaging should be reduced through standardised follow-up protocols, and possibly by alternate imaging modalities if validated in appropriate studies.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12220" xmlns="http://purl.org/rss/1.0/"><title>A Comparison of Prostate Cancer Diagnosis in Patients Receiving Unrelated Urologic and Non-Urologic Cancer Care</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12220</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Comparison of Prostate Cancer Diagnosis in Patients Receiving Unrelated Urologic and Non-Urologic Cancer Care</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anthony T. Corcoran, Marc C. Smaldone, Brian L. Egleston, Jay Simhan, Serge Ginzburg, Todd M. Morgan, John Walton, David YT Chen, Rosalia Viterbo, Richard E. Greenberg, Robert G. Uzzo, Alexander Kutikov</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:19:04.848182-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12220</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12220</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12220</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12220-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To evaluate prostate cancer diagnosis rates and survival outcomes in patients receiving unrelated (non-prostate) urologic care as compared to patients receiving non-urologic care.</p></div></div>
<div class="section" id="bju12220-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><p>We conducted a population based study using the Surveillance Epidemiology and End Results (SEER) database to identify men who underwent surgical treatment of RCC (18,188) and CRC (45,093) from 1992 to 2008. Using SEER*stat software to estimate standardized incidence ratios (SIRs), we investigated rates of prostate cancer diagnosis in RCC and CRC patients. Adjusting for patient age, race, and year of diagnosis on multivariate analysis, Cox and Fine &amp; Gray proportional hazards regressions were used to evaluate overall and disease specific survival endpoints.</p></div></div>
<div class="section" id="bju12220-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Expected incidence of prostate cancer was higher in both RCC and CRC patients (SIR=1.36[1.27–1.46] vs. 1.06[1.02-1.11]). Adjusted prostate cancer SIRs were 30% higher (p&lt;0.001) in patients with RCC. Overall (HR=1.13, p&lt;0.001) and primary cancer (sHR=1.17, p&lt;0.001) adjusted mortalities were higher in patients with RCC with no significant difference in prostate cancer-specific mortality (sHR=0.827, p=0.391).</p></div></div>
<div class="section" id="bju12220-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Rates of prostate cancer diagnosis were higher in patients with RCC (a cohort with unrelated urologic cancer care) vs. CRC. Despite higher overall mortality in RCC patients, prostate cancer specific survival was similar in both groups. Opportunities may exist to better target prostate cancer screening in patients who receive non-prostate related urologic care. Furthermore, urologists should not feel obligated to perform PSA-screening for all patients receiving non-prostate related urologic care.</p></div></div>
]]></content:encoded><description>


Objective
To evaluate prostate cancer diagnosis rates and survival outcomes in patients receiving unrelated (non-prostate) urologic care as compared to patients receiving non-urologic care.


Materials and Methods
We conducted a population based study using the Surveillance Epidemiology and End Results (SEER) database to identify men who underwent surgical treatment of RCC (18,188) and CRC (45,093) from 1992 to 2008. Using SEER*stat software to estimate standardized incidence ratios (SIRs), we investigated rates of prostate cancer diagnosis in RCC and CRC patients. Adjusting for patient age, race, and year of diagnosis on multivariate analysis, Cox and Fine &amp; Gray proportional hazards regressions were used to evaluate overall and disease specific survival endpoints.


Results
Expected incidence of prostate cancer was higher in both RCC and CRC patients (SIR=1.36[1.27–1.46] vs. 1.06[1.02-1.11]). Adjusted prostate cancer SIRs were 30% higher (p&lt;0.001) in patients with RCC. Overall (HR=1.13, p&lt;0.001) and primary cancer (sHR=1.17, p&lt;0.001) adjusted mortalities were higher in patients with RCC with no significant difference in prostate cancer-specific mortality (sHR=0.827, p=0.391).


Conclusion
Rates of prostate cancer diagnosis were higher in patients with RCC (a cohort with unrelated urologic cancer care) vs. CRC. Despite higher overall mortality in RCC patients, prostate cancer specific survival was similar in both groups. Opportunities may exist to better target prostate cancer screening in patients who receive non-prostate related urologic care. Furthermore, urologists should not feel obligated to perform PSA-screening for all patients receiving non-prostate related urologic care.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12219" xmlns="http://purl.org/rss/1.0/"><title>Impaired cardiopulmonary reserve in an elderly population is related to postoperative morbidity and hospital length of stay after radical cystectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12219</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impaired cardiopulmonary reserve in an elderly population is related to postoperative morbidity and hospital length of stay after radical cystectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Prentis JM, Trenell MI, Vasdev N, French R, Dines G, Thorpe A, Snowden CP</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:56.506431-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12219</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12219</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12219</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology
</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12219-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>Radical cystectomy and conduit formation is curative but is associated with significant postoperative morbidity and mortality.</p></div><div class="para"><p>Our aim was to determine the relationship of preoperatively measured cardiopulmonary function, to the development of postoperative complications and hospital length of stay in a cohort of patients undergoing radical cystectomy.</p></div></div>
<div class="section" id="bju12219-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Consecutive patients planned to have radical cystectomy underwent cardiopulmonary exercise testing (CPET) to a standardised protocol.</p></div><div class="para"><p>The results of the CPET were blinded from the clinicians involved in the care of the patients.</p></div><div class="para"><p>Patients were prospectively monitored for the primary outcome of postoperative complications, as defined by a validated classification (Clavien-Dindo).</p></div><div class="para"><p>Secondary outcome included hospital length of stay and mortality.</p></div></div>
<div class="section" id="bju12219-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>82 patients underwent CPET prior to radical cystectomy. 8 patients did not subsequently undergo radical surgery and a further 5 patients did not exercise sufficiently to allow for appropriate determination of the cardiopulmonary variables of interest.</p></div><div class="para"><p>There was a significant difference in hospital length of stay between those patients who had a major perioperative complication (Clavien score &gt;3) to those that did not (16 vs 30 p&lt;0.0001 HR 3.6 95% CI 2.1-6.3).</p></div><div class="para"><p>The anaerobic threshold remained as the only significant independent predictor variable for the presence or absence of major postoperative complications (OR 0.74; 95% CI 0.57-0.97. p=0.03).</p></div><div class="para"><p>When the optimal predictive value of anaerobic threshold of 12ml/min/kg was used as a fitness marker, there was a significant relationship between fitness and length of hospital stay (Median Hospital LOS: Unfit 22 vs fit 16 days HR 0.47 95% CI 0.28 - 0.80 p=0.006)</p></div></div>
<div class="section" id="bju12219-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Impaired preoperative cardiopulmonary reserve was related to major morbidity, prolonged hospital stay and increased use of critical care resource after radical cystectomy.</p></div><div class="para"><p>This has important health and economic implications for risk assessment, rationalization of postoperative resource and the potential for therapeutic preoperative intervention with exercise therapy.</p></div></div>
]]></content:encoded><description>


Objective
Radical cystectomy and conduit formation is curative but is associated with significant postoperative morbidity and mortality.
Our aim was to determine the relationship of preoperatively measured cardiopulmonary function, to the development of postoperative complications and hospital length of stay in a cohort of patients undergoing radical cystectomy.


Methods
Consecutive patients planned to have radical cystectomy underwent cardiopulmonary exercise testing (CPET) to a standardised protocol.
The results of the CPET were blinded from the clinicians involved in the care of the patients.
Patients were prospectively monitored for the primary outcome of postoperative complications, as defined by a validated classification (Clavien-Dindo).
Secondary outcome included hospital length of stay and mortality.


Results
82 patients underwent CPET prior to radical cystectomy. 8 patients did not subsequently undergo radical surgery and a further 5 patients did not exercise sufficiently to allow for appropriate determination of the cardiopulmonary variables of interest.
There was a significant difference in hospital length of stay between those patients who had a major perioperative complication (Clavien score &gt;3) to those that did not (16 vs 30 p&lt;0.0001 HR 3.6 95% CI 2.1-6.3).
The anaerobic threshold remained as the only significant independent predictor variable for the presence or absence of major postoperative complications (OR 0.74; 95% CI 0.57-0.97. p=0.03).
When the optimal predictive value of anaerobic threshold of 12ml/min/kg was used as a fitness marker, there was a significant relationship between fitness and length of hospital stay (Median Hospital LOS: Unfit 22 vs fit 16 days HR 0.47 95% CI 0.28 - 0.80 p=0.006)


Conclusion
Impaired preoperative cardiopulmonary reserve was related to major morbidity, prolonged hospital stay and increased use of critical care resource after radical cystectomy.
This has important health and economic implications for risk assessment, rationalization of postoperative resource and the potential for therapeutic preoperative intervention with exercise therapy.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12218" xmlns="http://purl.org/rss/1.0/"><title>Bone metastases in germ cell tumours: lessons learned from a large retrospective study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12218</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bone metastases in germ cell tumours: lessons learned from a large retrospective study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M Jamal-Hanjani, A Karpathakis, A Kwan, D Mazhar, W Ansell, J Shamash, P Harper, S Rudman, T Powles, S Chowdhury</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:52.430023-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12218</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12218</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12218</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3>
<div class="section" id="bju12218-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective:</h4><div class="para"><p>To determine the characteristics of patients with germ cell cancer and bone metastases.</p></div></div>
<div class="section" id="bju12218-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>The case records of patients with known germ cell tumours (GCTs) within the Anglian Germ Cell Cancer Group database between January 2005 to March 2011 were reviewed retrospectively.
Data were collected for histopathology, presence of bone metastases at diagnosis or relapse, site of bone metastases and imaging modality used to confirm bone metastases, treatment received, response to treatment and overall survival.
We present here the largest unselected cohort of bone metastases in germ cell tumour patients.</p></div></div>
<div class="section" id="bju12218-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A total of 2,550 cases of GCT were reviewed and bone involvement was noted in 19 cases.
The primary site was either testicular (13/19), mediastinal (1/19) or unknown (5/19). The majority of cases were of non-seminomatous GCT (11/19, 58%) and only 3 cases of seminomatous GCT (3/19, 16%) with 5 cases in which diagnosis was based on clinical history and significantly raised germ cell tumour markers (5/19, 26%). In all of these 5 cases beta human chorionic gonadotropin was raised and in 3/5 cases alpha-fetoprotein was raised in keeping with non-seminomatous GCT.
Bone metastases were found at diagnosis (0.51%, 13/2550) or at relapse (0.24%, 6/2550). The sites of bone metastases were the vertebrae (15/19, 79%), pelvis (3/19, 16%), ribs (3/19, 16%) and femur (2/19, 11%). Ten patients (53%) had solitary, and 9 patients (47%) had multiple, sites of bone metastases. In patients presenting with bone metastases at diagnosis compared to relapse, the mortality rate was 23% (3/13) and 50% respectively (3/6).
After receiving one line of chemotherapy, 9 patients (47%) remained in remission not requiring further treatment, 6 (32%) required further chemotherapy due to subsequent relapse, 3 (16%) died after first-line chemotherapy and one was lost to follow-up.
At the time of data collection and based on the last clinic follow-up, 6 patients (32%) had died with a median follow-up [interquartile range] of 11.5 months [4.3, 24.8] and 10 (53%) remained alive with a median follow-up of 26 months [13.5, 48]. Three patients were lost to follow-up. Of the known patients alive, 8 (42%) remained in remission and 2 (11%) had recurrent disease requiring further treatment.</p></div></div>
<div class="section" id="bju12218-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Although bone disease in germ cell cancer is rare, awareness of this condition is important and there is a need for prospective evaluation of patient characteristics, treatment approaches and survival outcome in this group of patients.</p></div></div>
]]></content:encoded><description>


Objective:
To determine the characteristics of patients with germ cell cancer and bone metastases.


Patients and Methods
The case records of patients with known germ cell tumours (GCTs) within the Anglian Germ Cell Cancer Group database between January 2005 to March 2011 were reviewed retrospectively.
Data were collected for histopathology, presence of bone metastases at diagnosis or relapse, site of bone metastases and imaging modality used to confirm bone metastases, treatment received, response to treatment and overall survival.
We present here the largest unselected cohort of bone metastases in germ cell tumour patients.


Results
A total of 2,550 cases of GCT were reviewed and bone involvement was noted in 19 cases.
The primary site was either testicular (13/19), mediastinal (1/19) or unknown (5/19). The majority of cases were of non-seminomatous GCT (11/19, 58%) and only 3 cases of seminomatous GCT (3/19, 16%) with 5 cases in which diagnosis was based on clinical history and significantly raised germ cell tumour markers (5/19, 26%). In all of these 5 cases beta human chorionic gonadotropin was raised and in 3/5 cases alpha-fetoprotein was raised in keeping with non-seminomatous GCT.
Bone metastases were found at diagnosis (0.51%, 13/2550) or at relapse (0.24%, 6/2550). The sites of bone metastases were the vertebrae (15/19, 79%), pelvis (3/19, 16%), ribs (3/19, 16%) and femur (2/19, 11%). Ten patients (53%) had solitary, and 9 patients (47%) had multiple, sites of bone metastases. In patients presenting with bone metastases at diagnosis compared to relapse, the mortality rate was 23% (3/13) and 50% respectively (3/6).
After receiving one line of chemotherapy, 9 patients (47%) remained in remission not requiring further treatment, 6 (32%) required further chemotherapy due to subsequent relapse, 3 (16%) died after first-line chemotherapy and one was lost to follow-up.
At the time of data collection and based on the last clinic follow-up, 6 patients (32%) had died with a median follow-up [interquartile range] of 11.5 months [4.3, 24.8] and 10 (53%) remained alive with a median follow-up of 26 months [13.5, 48]. Three patients were lost to follow-up. Of the known patients alive, 8 (42%) remained in remission and 2 (11%) had recurrent disease requiring further treatment.


Conclusion
Although bone disease in germ cell cancer is rare, awareness of this condition is important and there is a need for prospective evaluation of patient characteristics, treatment approaches and survival outcome in this group of patients.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12217" xmlns="http://purl.org/rss/1.0/"><title>Clinical Performance of Serum Isoform [-2]Propsa (P2psa) and its Derivatives, Namely %P2psa and Phi (Prostate Health Index), in Men With a Family History of Prostate Cancer. Results From a Multicentre European Study (Prometheus Project)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12217</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clinical Performance of Serum Isoform [-2]Propsa (P2psa) and its Derivatives, Namely %P2psa and Phi (Prostate Health Index), in Men With a Family History of Prostate Cancer. Results From a Multicentre European Study (Prometheus Project)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Massimo Lazzeri, Alexander Haese, Alberto Abrate, Alexandre Taille, Joan Palou Redorta, Thomas McNicholas, Giovanni Lughezzani, Giuliana Lista, Alessandro Larcher, Vittorio Bini, Andrea Cestari, Nicolòmaria Buffi, Markus Graefen, Olivier Bosset, Philippe Le Corvoisier, Alberto Breda, Pablo Torre, Linda Fowler, Jacques Roux, Giorgio Guazzoni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:45.670694-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12217</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12217</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12217</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12217-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To test the sensitivity, specificity and accuracy of serum p2PSA, %p2PSA and PHI, in men with a family history of prostate cancer (PCa) undergoing prostatic biopsy for suspected PCa.
To evaluate the potential reduction of unnecessary biopsies and the characteristics of potentially missed cases of PCa that would result from using serum p2PSA, %p2PSA and PHI.</p></div></div>
<div class="section" id="bju12217-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>The analysis consisted of a nested case-control study from the PRO-psa Multicentric European Study (PROMEtheusS) project.
All patients had a PCa affected first degree relative (father, brother, son).
Multivariable logistic regression models were complemented by predictive accuracy analysis and decision curve analysis.</p></div></div>
<div class="section" id="bju12217-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Of the 1026 patients enrolled in the PROMEtheuS cohort, 158 (15.4%) had a PCa affected first-degree relative. p2PSA, %p2PSA and PHI values were significantly higher (p&lt;0.0001), and %fPSA values significantly lower (p&lt;0.0001) in the 71 patients with PCa (44.9%) compared to patients without PCa.
Univariable accuracy analysis showed %p2PSA (AUC: 0.733) and PHI (AUC: 0.733) to be the most accurate predictors of PCa at biopsy, significantly outperforming tPSA (AUC: 0.549), fPSA (AUC: 0.489) and %fPSA (AUC: 0.600) (p≤0.001). For %p2PSA a cut-off of 1.66 showed the best balance between sensitivity and specificity (70.4 and 70.1%; 95%C.I: 58.4-80.7 and 59.4-79.5 respectively). A PHI cut-off of 40 showed the best balance between sensitivity and specificity (respectively 64.8 and 71.3%; 95%C.I 52.5-75.8 and 60.6-80.5).
At 90% sensitivity, the cut-off of %p2PSA and PHI were respectively 1.20 and 25.5 with a specificity of 37.9 and 25.5%. At a %p2PSA cut-off of 1.20 a total of 39 (24.8%) biopsies could have been avoided, but 2 cancers with a Gleason score of 7 would have been missed. At a PHI cut-off of 25.5 a total of 27 (17.2%) biopsies could have been avoided and 2 (3.8%) cancers with a Gleason score of 7 would have been missed.</p></div><div class="para"><p>In multivariable logistic regression models, %p2PSA and PHI achieved independent predictor status and significantly increased the accuracy of multivariable models including PSA and prostate volume by 8.7 and 10% respectively (p ≤0.001).
p2PSA, %p2PSA and PHI were directly correlated with Gleason Score (rho: 0.247, p=0.038; rho: 0.366, p=0.002; rho: 0.464, p&lt;0.001, respectively).</p></div></div>
<div class="section" id="bju12217-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>%p2PSA and PHI are more accurate than tPSA, fPSA and %fPSA in predicting PCa in men with a family history of PCa
Consideration of %p2PSA and PHI results in the avoidance of several unnecessary biopsies.
p2PSA, %p2PSA and PHI correlate with cancer aggressiveness.</p></div></div>
]]></content:encoded><description>


Objective
To test the sensitivity, specificity and accuracy of serum p2PSA, %p2PSA and PHI, in men with a family history of prostate cancer (PCa) undergoing prostatic biopsy for suspected PCa.
To evaluate the potential reduction of unnecessary biopsies and the characteristics of potentially missed cases of PCa that would result from using serum p2PSA, %p2PSA and PHI.


Patients and Methods
The analysis consisted of a nested case-control study from the PRO-psa Multicentric European Study (PROMEtheusS) project.
All patients had a PCa affected first degree relative (father, brother, son).
Multivariable logistic regression models were complemented by predictive accuracy analysis and decision curve analysis.


Results
Of the 1026 patients enrolled in the PROMEtheuS cohort, 158 (15.4%) had a PCa affected first-degree relative. p2PSA, %p2PSA and PHI values were significantly higher (p&lt;0.0001), and %fPSA values significantly lower (p&lt;0.0001) in the 71 patients with PCa (44.9%) compared to patients without PCa.
Univariable accuracy analysis showed %p2PSA (AUC: 0.733) and PHI (AUC: 0.733) to be the most accurate predictors of PCa at biopsy, significantly outperforming tPSA (AUC: 0.549), fPSA (AUC: 0.489) and %fPSA (AUC: 0.600) (p≤0.001). For %p2PSA a cut-off of 1.66 showed the best balance between sensitivity and specificity (70.4 and 70.1%; 95%C.I: 58.4-80.7 and 59.4-79.5 respectively). A PHI cut-off of 40 showed the best balance between sensitivity and specificity (respectively 64.8 and 71.3%; 95%C.I 52.5-75.8 and 60.6-80.5).
At 90% sensitivity, the cut-off of %p2PSA and PHI were respectively 1.20 and 25.5 with a specificity of 37.9 and 25.5%. At a %p2PSA cut-off of 1.20 a total of 39 (24.8%) biopsies could have been avoided, but 2 cancers with a Gleason score of 7 would have been missed. At a PHI cut-off of 25.5 a total of 27 (17.2%) biopsies could have been avoided and 2 (3.8%) cancers with a Gleason score of 7 would have been missed.
In multivariable logistic regression models, %p2PSA and PHI achieved independent predictor status and significantly increased the accuracy of multivariable models including PSA and prostate volume by 8.7 and 10% respectively (p ≤0.001).
p2PSA, %p2PSA and PHI were directly correlated with Gleason Score (rho: 0.247, p=0.038; rho: 0.366, p=0.002; rho: 0.464, p&lt;0.001, respectively).


Conclusion
%p2PSA and PHI are more accurate than tPSA, fPSA and %fPSA in predicting PCa in men with a family history of PCa
Consideration of %p2PSA and PHI results in the avoidance of several unnecessary biopsies.
p2PSA, %p2PSA and PHI correlate with cancer aggressiveness.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12216" xmlns="http://purl.org/rss/1.0/"><title>Outpatient Laser Ablation of Non-Muscle Invasive Bladder Cancer; is it Safe, Tolerable and Cost-Effective?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12216</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Outpatient Laser Ablation of Non-Muscle Invasive Bladder Cancer; is it Safe, Tolerable and Cost-Effective?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kathie A Wong, Grace Zisengwe, Thanos Athanasiou, Tim O′Brien, Kay Thomas</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:31.035441-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12216</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12216</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12216</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12216-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To evaluate the safety, tolerability and effectiveness of outpatient (office-based) local anaesthetic laser ablation (OLA) of Non-muscle Invasive Bladder Cancer (NMIBC) in an elderly population with and without photodynamic diagnosis (PDD).
To compare the cost-effectiveness of outpatient laser ablation of NMIBC with inpatient cystodiathermy (IC).</p></div></div>
<div class="section" id="bju12216-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Prospective cohort study of patients with NMIBC treated with outpatient local anaesthetic laser ablation (OLA) by one consultant surgeon between March 2008 - July 2011
A subgroup of patients had PDD prior to laser ablation.
Safety and effectiveness determined by complications (time 0, 3/7, 3/12), patient tolerability (visual analogue score) and recurrence rates
Long-term costs and cost effectiveness of OLA and IC of NMIBC were evaluated using Markov modelling</p></div></div>
<div class="section" id="bju12216-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>74 OLA procedures (44 white light, 30 PDD) on 54 patients. Mean age 77 (Range 52-95). Over 50% had &gt;3 co-morbidities. Previous tumour histology ranged from G1pTa to T3.
One patient had haematuria for one week which settled spontaneously and did not require hospital admission. There were no other complications.
The procedure was well tolerated with pain scores of 0-2/10.
Additional lesions seen in 21% of patients with PDD that were not seen with white light.
At three months, the percentage of patients who had recurrence for OLA with white light and OLA with PDD were 10.6% and 4.3% respectively. At one year, 65.1% and 46.9% of patients had recurrence.
Cost of OLA is much lower than IC (£538 vs £1474), even with the addition of PDD (£912 vs £1844).
Over the course of a patient's lifetime, OLA was more clinically effective than IC (0.147 QALY, SD 0.059 QALY) and less costly (£2576.42, SD £7293.07<b>)</b>At a Cost-Effectiveness Threshold (CET) of 30,000 £/QALY as set by NICE, there is an 82% probability that OLA is cost-effective</p></div></div>
<div class="section" id="bju12216-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>This first report on the safety and tolerability of outpatient laser ablation of NMIBC and the feasibility of PDD as an adjunct
The first study to demonstrate the long term cost-effectiveness of OLA of NMIBC
Results support the use of OLA for the treatment of NMIBC especially in the elderly</p></div></div>
]]></content:encoded><description>


Objective
To evaluate the safety, tolerability and effectiveness of outpatient (office-based) local anaesthetic laser ablation (OLA) of Non-muscle Invasive Bladder Cancer (NMIBC) in an elderly population with and without photodynamic diagnosis (PDD).
To compare the cost-effectiveness of outpatient laser ablation of NMIBC with inpatient cystodiathermy (IC).


Patients and Methods
Prospective cohort study of patients with NMIBC treated with outpatient local anaesthetic laser ablation (OLA) by one consultant surgeon between March 2008 - July 2011
A subgroup of patients had PDD prior to laser ablation.
Safety and effectiveness determined by complications (time 0, 3/7, 3/12), patient tolerability (visual analogue score) and recurrence rates
Long-term costs and cost effectiveness of OLA and IC of NMIBC were evaluated using Markov modelling


Results
74 OLA procedures (44 white light, 30 PDD) on 54 patients. Mean age 77 (Range 52-95). Over 50% had &gt;3 co-morbidities. Previous tumour histology ranged from G1pTa to T3.
One patient had haematuria for one week which settled spontaneously and did not require hospital admission. There were no other complications.
The procedure was well tolerated with pain scores of 0-2/10.
Additional lesions seen in 21% of patients with PDD that were not seen with white light.
At three months, the percentage of patients who had recurrence for OLA with white light and OLA with PDD were 10.6% and 4.3% respectively. At one year, 65.1% and 46.9% of patients had recurrence.
Cost of OLA is much lower than IC (£538 vs £1474), even with the addition of PDD (£912 vs £1844).
Over the course of a patient's lifetime, OLA was more clinically effective than IC (0.147 QALY, SD 0.059 QALY) and less costly (£2576.42, SD £7293.07)At a Cost-Effectiveness Threshold (CET) of 30,000 £/QALY as set by NICE, there is an 82% probability that OLA is cost-effective


Conclusions
This first report on the safety and tolerability of outpatient laser ablation of NMIBC and the feasibility of PDD as an adjunct
The first study to demonstrate the long term cost-effectiveness of OLA of NMIBC
Results support the use of OLA for the treatment of NMIBC especially in the elderly

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12215" xmlns="http://purl.org/rss/1.0/"><title>Unaltered Oncologic Outcomes of Radical Cystectomy with Extended Lymphadenectomy Over Three Decades</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12215</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Unaltered Oncologic Outcomes of Radical Cystectomy with Extended Lymphadenectomy Over Three Decades</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pascal Zehnder, Urs E. Studer, Eila C. Skinner, George N. Thalmann, Gus Miranda, Beat Roth, Jie Cai, Frédéric D. Birkhäuser, Anirban P. Mitra, Fiona C. Burkhard, Ryan P. Dorin, Siamak Daneshmand, Donald G Skinner, Inderbir S. Gill</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:16.750225-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12215</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12215</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12215</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12215-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives:</h4><div class="para"><p>To evaluate oncologic outcome trends over the last three decades in patients following radical cystectomy (RC) and extended pelvic lymph node dissection (LND)</p></div></div>
<div class="section" id="bju12215-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>Retrospective analysis of the University of Southern California (USC) cystectomy cohort of patients (n=1488) operated with intent to cure from 1980-2005 for biopsy proven muscle-invasive urothelial bladder cancer
To focus on outcomes of unexpected (cN0M0) node-positive patients, the USC subset was extended with unexpected node-positive patients from the University of Berne (UB) (combined subgroup n=521)
Patients were grouped and compared according to decade of surgery (1980-1989/1990-1999/≥2000)
Survival probabilities were calculated with Kaplan-Meier plots, Logrank tests compared outcomes according to decade of surgery, followed by multivariable verification</p></div></div>
<div class="section" id="bju12215-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Ten year recurrence-free survival was 78-80% in patients with organ confined, node-negative disease, 53-60% in patients with extravesical, yet node-negative disease and approximately 30% in node-positive patients
Although the number of patients receiving systemic chemotherapy increased, no survival improvement was noted in either the entire USC cohort, or in the combined node-positive USC-UB cohort
In contrast, patient age at surgery increased progressively, suggesting a relative survival benefit</p></div></div>
<div class="section" id="bju12215-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Radical surgery remains the mainstay of therapy for muscle-invasive bladder cancer
Yet, our study reveals predictable outcomes but no survival improvement in patients undergoing RC over the last three decades
Any future survival improvements are likely to result from more effective systemic treatments and/or earlier detection of the disease</p></div></div>
]]></content:encoded><description>


Objectives:
To evaluate oncologic outcome trends over the last three decades in patients following radical cystectomy (RC) and extended pelvic lymph node dissection (LND)


Patients and Methods
Retrospective analysis of the University of Southern California (USC) cystectomy cohort of patients (n=1488) operated with intent to cure from 1980-2005 for biopsy proven muscle-invasive urothelial bladder cancer
To focus on outcomes of unexpected (cN0M0) node-positive patients, the USC subset was extended with unexpected node-positive patients from the University of Berne (UB) (combined subgroup n=521)
Patients were grouped and compared according to decade of surgery (1980-1989/1990-1999/≥2000)
Survival probabilities were calculated with Kaplan-Meier plots, Logrank tests compared outcomes according to decade of surgery, followed by multivariable verification


Results
Ten year recurrence-free survival was 78-80% in patients with organ confined, node-negative disease, 53-60% in patients with extravesical, yet node-negative disease and approximately 30% in node-positive patients
Although the number of patients receiving systemic chemotherapy increased, no survival improvement was noted in either the entire USC cohort, or in the combined node-positive USC-UB cohort
In contrast, patient age at surgery increased progressively, suggesting a relative survival benefit


Conclusions
Radical surgery remains the mainstay of therapy for muscle-invasive bladder cancer
Yet, our study reveals predictable outcomes but no survival improvement in patients undergoing RC over the last three decades
Any future survival improvements are likely to result from more effective systemic treatments and/or earlier detection of the disease

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12214" xmlns="http://purl.org/rss/1.0/"><title>IN-HOSPITAL MORTALITY AND FAILURE TO RESCUE AFTER RADICAL CYSTECTOMY</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12214</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">IN-HOSPITAL MORTALITY AND FAILURE TO RESCUE AFTER RADICAL CYSTECTOMY</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vincent Q. Trinh, Quoc-Dien Trinh, Zhe Tian, Jim C. Hu, Shahrokh F. Shariat, Paul Perrotte, Pierre I Karakiewicz, Maxine Sun</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:14.615583-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12214</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12214</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12214</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12214-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To illustrate the underlying variability in perioperative mortality following RC by analyzing failure-to-rescue (FTR) rates, i.e. deaths after complications.</p></div></div>
<div class="section" id="bju12214-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><p>Patients undergoing RC for non-metastatic BCa were identified using the Nationwide Inpatient Sample, between 1999-2009, resulting in a weighted estimate of 79972 patients. FTR was assessed according to patient and hospital characteristics, as well as complication type. Generalized linear regression analyses were performed.</p></div></div>
<div class="section" id="bju12214-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Overall, 26740 patients had a complication, corresponding to a FTR rate of 5.5%. Septicemia (odds ratio [OR]: 13.41, P&lt;0.001), cardiac (OR: 3.97, P&lt;0.001), wound (OR: 2.12, P&lt;0.001), genitourinary (OR: 1.62, P=0.045) and hematological (OR: 1.78, P=0.008) complications were associated with FTR. Older age (OR: 1.05, P&lt;0.001), increasing comorbidities (OR: 1.33, P&lt;0.001), Medicare (OR: 1.52, P=0.016), and Medicaid insurance status (OR: 2.10, P=0.029) were associated with higher odds of FTR. Conversely, increasing hospital volume (OR: 0.992, P=0.014) reduced the odds of FTR.</p></div></div>
<div class="section" id="bju12214-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Whereas both patient and hospital characteristics are accountable for increased odds of FTR, the occurrence of septicemia and cardiac complications were the most strongly correlated with higher risk of in-hospital mortality when complication(s) occur.</p></div></div>
]]></content:encoded><description>


Objective
To illustrate the underlying variability in perioperative mortality following RC by analyzing failure-to-rescue (FTR) rates, i.e. deaths after complications.


Materials and Methods
Patients undergoing RC for non-metastatic BCa were identified using the Nationwide Inpatient Sample, between 1999-2009, resulting in a weighted estimate of 79972 patients. FTR was assessed according to patient and hospital characteristics, as well as complication type. Generalized linear regression analyses were performed.


Results
Overall, 26740 patients had a complication, corresponding to a FTR rate of 5.5%. Septicemia (odds ratio [OR]: 13.41, P&lt;0.001), cardiac (OR: 3.97, P&lt;0.001), wound (OR: 2.12, P&lt;0.001), genitourinary (OR: 1.62, P=0.045) and hematological (OR: 1.78, P=0.008) complications were associated with FTR. Older age (OR: 1.05, P&lt;0.001), increasing comorbidities (OR: 1.33, P&lt;0.001), Medicare (OR: 1.52, P=0.016), and Medicaid insurance status (OR: 2.10, P=0.029) were associated with higher odds of FTR. Conversely, increasing hospital volume (OR: 0.992, P=0.014) reduced the odds of FTR.


Conclusions
Whereas both patient and hospital characteristics are accountable for increased odds of FTR, the occurrence of septicemia and cardiac complications were the most strongly correlated with higher risk of in-hospital mortality when complication(s) occur.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12213" xmlns="http://purl.org/rss/1.0/"><title>Renal Function and Cardiovascular Outcomes after Living Donor Nephrectomy in the United Kingdom: Quality and Safety Revisited</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12213</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Renal Function and Cardiovascular Outcomes after Living Donor Nephrectomy in the United Kingdom: Quality and Safety Revisited</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nilay Patel, Phil Mason, Sally Rushton, Alex Hudson, Rutger Ploeg, Peter Friend, Sanjay Sinha, Mark Sullivan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:10.741771-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12213</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12213</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12213</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12213-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective:</h4><div class="para"><p>To determine renal function and cardiovascular outcomes following living donor nephrectomy (LDN).
Living donor kidney transplantation has become established as the treatment of choice for end stage renal failure. Benefits to the recipient have to be balanced against peri-operative and long term health risks to the donor.</p></div></div>
<div class="section" id="bju12213-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects/patients and methods</h4><div class="para"><p>The UK Transplant Registry (UKTR) was used to identify 4,586 living donors who had donated a kidney for transplantation in the UK between 2001 and 2008.</p></div></div>
<div class="section" id="bju12213-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean GFR fell from 103 ml/min/1.73 m<sup>2</sup> pre donation to 58 ml/min/1.73 m<sup>2</sup> one year post donation.
One year post donation 60% of donors had a GFR below 60 ml/min/1.73 m<sup>2</sup>.
A post donation GFR below 60 ml/min/1.73m<sup>2</sup> was associated with older age, females, lower pre donation GFR, white ethnicity, earlier donation period, nonrelated donor type and BMI &gt; 25.
Over a two year period following LDN we observed an overall mortality rate of 0.39%, cardiovascular death in a single patient (mortality rate of 0.02%) and a major cardio-vascular event rate of 0.44%.</p></div></div>
<div class="section" id="bju12213-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In this study we demonstrate that mild renal dysfunction is common following LDN, however due to the short duration of follow up we are unable to comment on whether this subsequently leads to an increased risk of developing of cardio-vascular disease.</p></div></div>
]]></content:encoded><description>


Objective:
To determine renal function and cardiovascular outcomes following living donor nephrectomy (LDN).
Living donor kidney transplantation has become established as the treatment of choice for end stage renal failure. Benefits to the recipient have to be balanced against peri-operative and long term health risks to the donor.


Subjects/patients and methods
The UK Transplant Registry (UKTR) was used to identify 4,586 living donors who had donated a kidney for transplantation in the UK between 2001 and 2008.


Results
The mean GFR fell from 103 ml/min/1.73 m2 pre donation to 58 ml/min/1.73 m2 one year post donation.
One year post donation 60% of donors had a GFR below 60 ml/min/1.73 m2.
A post donation GFR below 60 ml/min/1.73m2 was associated with older age, females, lower pre donation GFR, white ethnicity, earlier donation period, nonrelated donor type and BMI &gt; 25.
Over a two year period following LDN we observed an overall mortality rate of 0.39%, cardiovascular death in a single patient (mortality rate of 0.02%) and a major cardio-vascular event rate of 0.44%.


Conclusion
In this study we demonstrate that mild renal dysfunction is common following LDN, however due to the short duration of follow up we are unable to comment on whether this subsequently leads to an increased risk of developing of cardio-vascular disease.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12212" xmlns="http://purl.org/rss/1.0/"><title>Causes of Death in Men with Prostate Cancer: An Analysis of 50,000 Men from the Thames Cancer Registry</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12212</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Causes of Death in Men with Prostate Cancer: An Analysis of 50,000 Men from the Thames Cancer Registry</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Simon Chowdhury, David Robinson, Declan Cahill, Alejo Rodriguez-Vida, Lars Holmberg, Henrik Møller</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T05:18:05.014264-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12212</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12212</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12212</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="bju12212-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives:</h4><div class="para"><p>To investigate causes of death in a UK cohort of prostate cancer patients.</p></div></div>
<div class="section" id="bju12212-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><p>We examined causes of death in a UK cohort of 50,066 men with prostate cancer diagnosed between 1997 and 2006 reported to the Thames Cancer Registry (TCR) and followed up to the end of 2007.
The underlying cause of death was taken from the death certificate.
Uptake of PSA screening was low in the UK during the period studied.
We examined the relationship between cause of death and patient characteristics at diagnosis including age, cancer stage, and treatment (within six months of diagnosis).</p></div></div>
<div class="section" id="bju12212-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>20,181 deaths occurred during the period
49·8% recorded as being due to prostate cancer, 17·8% to cardiovascular disease, 11·6% to other cancers, and 20·7% to other causes.
Irrespective of age, cancer stage, or treatment within six months of diagnosis, prostate cancer was an important cause of death ranging
from 31·6% to 74·3% of all deaths in different subgroups.</p></div></div>
<div class="section" id="bju12212-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>For men with prostate cancer diagnosed in a setting where uptake of PSA screening is low, our findings challenge the belief that prostate cancer is not an important cause of death.</p></div></div>
]]></content:encoded><description>


Objectives:
To investigate causes of death in a UK cohort of prostate cancer patients.


Patients and Methods
We examined causes of death in a UK cohort of 50,066 men with prostate cancer diagnosed between 1997 and 2006 reported to the Thames Cancer Registry (TCR) and followed up to the end of 2007.
The underlying cause of death was taken from the death certificate.
Uptake of PSA screening was low in the UK during the period studied.
We examined the relationship between cause of death and patient characteristics at diagnosis including age, cancer stage, and treatment (within six months of diagnosis).


Results
20,181 deaths occurred during the period
49·8% recorded as being due to prostate cancer, 17·8% to cardiovascular disease, 11·6% to other cancers, and 20·7% to other causes.
Irrespective of age, cancer stage, or treatment within six months of diagnosis, prostate cancer was an important cause of death ranging
from 31·6% to 74·3% of all deaths in different subgroups.


Conclusion
For men with prostate cancer diagnosed in a setting where uptake of PSA screening is low, our findings challenge the belief that prostate cancer is not an important cause of death.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12085" xmlns="http://purl.org/rss/1.0/"><title>Midterm oncological outcomes of laparoscopic vs open radical prostatectomy (RP)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12085</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Midterm oncological outcomes of laparoscopic vs open radical prostatectomy (RP)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gregory J. Wirth, Sarah P. Psutka, Brian F. Chapin, Shulin Wu, Chin-Lee Wu, Douglas M. Dahl</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-19T04:02:56.308076-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12085</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12085</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12085</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12085-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12085-list-0001" class="bullet">
<li>To compare the midterm risks of biochemical recurrence (BCR) and salvage radiation therapy (SRT) after laparoscopic (LRP) and open retropubic radical prostatectomy (RRP). Strong evidence that these techniques are comparable to the ‘gold standard’ of open RRP is lacking, as most comparative studies are limited by short follow-up or rely on historical controls.</li>
</ul></div></div>
<div class="section" id="bju12085-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12085-list-0002" class="bullet">
<li>We studied 1000 consecutive patients concurrently treated by either LRP or RRP between 2001 and 2005.</li>
<li>LRPs were performed by a single surgeon and RRP by four surgeons.</li>
<li>Primary outcomes were BCR and SRT. Survival analysis included relevant clinical and pathological variables.</li>
</ul></div></div>
<div class="section" id="bju12085-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12085-list-0003" class="bullet">
<li>Of 844 included patients, 244 underwent LRP and 600 RRP.</li> <li>Clinical and pathological characteristics were similar in both groups. Most patients had Gleason 6 tumours (68%) and pT2 disease (86%). The median follow-up was 6.1 years and median time to recurrence 3.4 years.</li>
<li>Overall, BCR occurred in 14% of patients: 13.1% after LRP and 14.7% after RRP.</li>
<li>SRT was performed in 10.7% of patients both after LRP and RRP. In uni- and multivariate Cox regression models, surgical technique was not a significant predictor of BCR or SRT.</li>
</ul></div></div>
<div class="section" id="bju12085-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12085-list-0004" class="bullet">
<li>Our results suggest that in high-volume centres, LRP provides equivalent oncological control to RRP.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To compare the midterm risks of biochemical recurrence (BCR) and salvage radiation therapy (SRT) after laparoscopic (LRP) and open retropubic radical prostatectomy (RRP). Strong evidence that these techniques are comparable to the ‘gold standard’ of open RRP is lacking, as most comparative studies are limited by short follow-up or rely on historical controls.



Patients and Methods

We studied 1000 consecutive patients concurrently treated by either LRP or RRP between 2001 and 2005.
LRPs were performed by a single surgeon and RRP by four surgeons.
Primary outcomes were BCR and SRT. Survival analysis included relevant clinical and pathological variables.



Results

Of 844 included patients, 244 underwent LRP and 600 RRP. Clinical and pathological characteristics were similar in both groups. Most patients had Gleason 6 tumours (68%) and pT2 disease (86%). The median follow-up was 6.1 years and median time to recurrence 3.4 years.
Overall, BCR occurred in 14% of patients: 13.1% after LRP and 14.7% after RRP.
SRT was performed in 10.7% of patients both after LRP and RRP. In uni- and multivariate Cox regression models, surgical technique was not a significant predictor of BCR or SRT.



Conclusion

Our results suggest that in high-volume centres, LRP provides equivalent oncological control to RRP.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12038" xmlns="http://purl.org/rss/1.0/"><title>Proposal of a method to assess and report the extent of residual neurovascular tissue present in radical prostatectomy specimens</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12038</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Proposal of a method to assess and report the extent of residual neurovascular tissue present in radical prostatectomy specimens</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Oscar Schatloff, Darian Kameh, Camilo Giedelman, Srinivas Samavedi, Haidar Abdul-Muhsin, Rafael F. Coelho, Sung Gu Kang, Kenneth J. Palmer, Vipul R. Patel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-19T04:00:32.017578-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12038</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12038</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12038</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotic &amp; Laparoscopic</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12038-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12038-list-0001" class="bullet">
<li>To propose a method to assess and report the amount of neurovascular tissue present in radical prostatectomy (RP) specimens.</li>
</ul></div></div>
<div class="section" id="bju12038-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12038-list-0002" class="bullet">
<li>The data of 133 consecutive patients who underwent robot-assisted RP by a single surgeon (V.R.P.) were prospectively collected.</li>
<li>Degree of nerve sparing (NS) was graded intraoperatively by the surgeon independently at either side as complete, partial or none.</li>
<li>A pathologist who was ‘blinded’ to the surgeon's classification measured the following parameters at the posterolateral aspect of the apex, base and mid prostate at either side of the RP specimen: length, width and area of neural tissue, number of nerves per high-power field and number of total slides containing neural tissue.</li>
<li>Measurements were correlated to the surgeon's intraoperative perception.</li>
</ul></div></div>
<div class="section" id="bju12038-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12038-list-0003" class="bullet">
<li>All measurements correlated significantly with surgeon's intent of NS at all locations (<em>P</em> = 0.001).</li>
<li>Among them, the cross-sectional area had the highest correlation coefficient (–0.550 at apex, –0.604 at mid prostate and –0.606 at the base).</li>
</ul></div></div>
<div class="section" id="bju12038-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12038-list-0004" class="bullet">
<li>The cross-sectional area of nerve tissue showed the highest correlation with surgeon's intent of NS at all locations.</li>
<li>Having a standardised method of assessing and reporting residual nerve tissue allows the surgeon to objectively evaluate the quality of nerve preservation and to compare the progress of his NS technique over time.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To propose a method to assess and report the amount of neurovascular tissue present in radical prostatectomy (RP) specimens.



Patients and Methods

The data of 133 consecutive patients who underwent robot-assisted RP by a single surgeon (V.R.P.) were prospectively collected.
Degree of nerve sparing (NS) was graded intraoperatively by the surgeon independently at either side as complete, partial or none.
A pathologist who was ‘blinded’ to the surgeon's classification measured the following parameters at the posterolateral aspect of the apex, base and mid prostate at either side of the RP specimen: length, width and area of neural tissue, number of nerves per high-power field and number of total slides containing neural tissue.
Measurements were correlated to the surgeon's intraoperative perception.



Results

All measurements correlated significantly with surgeon's intent of NS at all locations (P = 0.001).
Among them, the cross-sectional area had the highest correlation coefficient (–0.550 at apex, –0.604 at mid prostate and –0.606 at the base).



Conclusions

The cross-sectional area of nerve tissue showed the highest correlation with surgeon's intent of NS at all locations.
Having a standardised method of assessing and reporting residual nerve tissue allows the surgeon to objectively evaluate the quality of nerve preservation and to compare the progress of his NS technique over time.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12122" xmlns="http://purl.org/rss/1.0/"><title>Percutaneous cryoablation of renal tumours: outcomes from 171 tumours in 147 patients</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12122</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Percutaneous cryoablation of renal tumours: outcomes from 171 tumours in 147 patients</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David J. Breen, Timothy J. Bryant, Ausami Abbas, Beth Shepherd, Neil McGill, Jane A. Anderson, Richard C. Lockyer, Matthew C. Hayes, Steve L. George</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T08:35:28.427357-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12122</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12122</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12122</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12122-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12122-list-0001" class="bullet">
<li>To evaluate the technical and oncological efficacy of an image-guided cryoablation programme for renal tumours.</li>
</ul></div></div>
<div class="section" id="bju12122-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12122-list-0002" class="bullet">
<li>A prospective analysis of technical and radiological outcomes was undertaken after treatment of 171 consecutive tumours in 147 patients.</li>
<li>Oncological efficacy in a subset of 125 tumours in 104 patients with &gt;6 months' radiological follow-up and a further subset of 62 patients with solitary, biopsy-proven renal carcinoma was also analysed.</li>
<li>Factors influencing technical success, as determined by imaging follow-up, and complication rates were statistically analysed using a statistics software package and logistic regression analyses.</li>
</ul></div></div>
<div class="section" id="bju12122-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12122-list-0003" class="bullet">
<li>No variables were found to predict subtotal treatment, although gender (<em>P</em> = 0.08), tumour size of &gt;4 cm (<em>P</em> = 0.09) and central location of tumour (<em>P</em> = 0.07) approached significance.</li>
<li>Upper pole location was the single variable that was found to predict complications (<em>P</em> = 0.006).</li>
<li>Among the 104 patients (125 tumours), radiologically assessed at ≥6 months and with a mean radiological follow-up of 20.1 months, we found a single case of unexpected late local recurrence.</li>
</ul></div></div>
<div class="section" id="bju12122-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12122-list-0004" class="bullet">
<li>Percutaneous image-guided cryoablation, at a mean of 20.1 months' follow-up, appears to provide a safe and effective treatment option with a low complication rate.</li>
<li>Anteriorly sited tumours should not be considered a contraindication for percutaneous image-guided cryoablation.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the technical and oncological efficacy of an image-guided cryoablation programme for renal tumours.



Patients and Methods

A prospective analysis of technical and radiological outcomes was undertaken after treatment of 171 consecutive tumours in 147 patients.
Oncological efficacy in a subset of 125 tumours in 104 patients with &gt;6 months' radiological follow-up and a further subset of 62 patients with solitary, biopsy-proven renal carcinoma was also analysed.
Factors influencing technical success, as determined by imaging follow-up, and complication rates were statistically analysed using a statistics software package and logistic regression analyses.



Results

No variables were found to predict subtotal treatment, although gender (P = 0.08), tumour size of &gt;4 cm (P = 0.09) and central location of tumour (P = 0.07) approached significance.
Upper pole location was the single variable that was found to predict complications (P = 0.006).
Among the 104 patients (125 tumours), radiologically assessed at ≥6 months and with a mean radiological follow-up of 20.1 months, we found a single case of unexpected late local recurrence.



Conclusion

Percutaneous image-guided cryoablation, at a mean of 20.1 months' follow-up, appears to provide a safe and effective treatment option with a low complication rate.
Anteriorly sited tumours should not be considered a contraindication for percutaneous image-guided cryoablation.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12118" xmlns="http://purl.org/rss/1.0/"><title>The role of chronic prostatic inflammation in the pathogenesis and progression of benign prostatic hyperplasia (BPH)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12118</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The role of chronic prostatic inflammation in the pathogenesis and progression of benign prostatic hyperplasia (BPH)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giorgio Gandaglia, Alberto Briganti, Paolo Gontero, Nicola Mondaini, Giacomo Novara, Andrea Salonia, Alessandro Sciarra, Francesco Montorsi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T06:30:53.345588-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12118</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12118</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12118</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12118-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><ul id="bju12118-list-0001" class="bullet">
<li>Several different stimuli may induce chronic prostatic inflammation, which in turn would lead to tissue damage and continuous wound healing, thus contributing to prostatic enlargement.</li>
<li>Patients with chronic inflammation and benign prostatic hyperplasia (BPH) have been shown to have larger prostate volumes, more severe lower urinary tract symptoms (LUTS) and a higher probability of acute urinary retention than their counterparts without inflammation.</li>
<li>Chronic inflammation could be a predictor of poor response to BPH medical treatment. Thus, the ability to identify patients with chronic inflammation would be crucial to prevent BPH progression and develop target therapies.</li>
<li>Although the histological examination of prostatic tissue remains the only available method to diagnose chronic inflammation, different parameters, such as prostatic calcifications, prostate volume, LUTS severity, storage and prostatitis-like symptoms, poor response to medical therapies and urinary biomarkers, have been shown to be correlated with chronic inflammation.</li>
<li>The identification of patients with BPH and chronic inflammation might be crucial in order to develop target therapies to prevent BPH progression. In this context, clinical, imaging and laboratory parameters might be used alone or in combination to identify patients that harbour chronic prostatic inflammation.</li>
</ul></div></div>
]]></content:encoded><description>
 
Several different stimuli may induce chronic prostatic inflammation, which in turn would lead to tissue damage and continuous wound healing, thus contributing to prostatic enlargement.
Patients with chronic inflammation and benign prostatic hyperplasia (BPH) have been shown to have larger prostate volumes, more severe lower urinary tract symptoms (LUTS) and a higher probability of acute urinary retention than their counterparts without inflammation.
Chronic inflammation could be a predictor of poor response to BPH medical treatment. Thus, the ability to identify patients with chronic inflammation would be crucial to prevent BPH progression and develop target therapies.
Although the histological examination of prostatic tissue remains the only available method to diagnose chronic inflammation, different parameters, such as prostatic calcifications, prostate volume, LUTS severity, storage and prostatitis-like symptoms, poor response to medical therapies and urinary biomarkers, have been shown to be correlated with chronic inflammation.
The identification of patients with BPH and chronic inflammation might be crucial in order to develop target therapies to prevent BPH progression. In this context, clinical, imaging and laboratory parameters might be used alone or in combination to identify patients that harbour chronic prostatic inflammation.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12116" xmlns="http://purl.org/rss/1.0/"><title>Impact of lymphovascular invasion on oncological outcomes in patients with upper tract urothelial carcinoma after radical nephroureterectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12116</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impact of lymphovascular invasion on oncological outcomes in patients with upper tract urothelial carcinoma after radical nephroureterectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sophie Hurel, Morgan Rouprêt, Adil Ouzzane, François Rozet, Evanguelos Xylinas, Marc Zerbib, Alexis Arvin Berod, Alain Ruffion, Emilie Adam, Olivier Cussenot, Alain Houlgatte, Véronique Phé, François-Xavier Nouhaud, Henri Bensadoun, Francky Delage, Julien Guillotreau, Laurent Guy, Gilles Karsenty, Alexandre De La Taille, Pierre Colin, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T06:30:45.66869-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12116</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12116</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12116</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12116-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12116-list-0001" class="bullet">
<li>To assess the impact of lymphovascular invasion (LVI) on upper urinary tract urothelial carcinomas (UTUCs) in a multicentre study on cancer-specific survival (CSS), recurrence-free survival and metastasis-free survival (MFS).</li>
<li>To show the negative impact of LVI for patients with pN0/x disease and to stratify these patients into risk groups for metastatic relapse.</li>
</ul></div></div>
<div class="section" id="bju12116-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12116-list-0002" class="bullet">
<li>A multicentre retrospective study was performed on patients who underwent radical nephroureterectomy between 1995 and 2010.</li>
<li>LVI status was evaluated as a prognostic factor for survival using univariate and multivariate Cox regression analysis.</li>
</ul></div></div>
<div class="section" id="bju12116-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12116-list-0003" class="bullet">
<li>Overall, 551 patients were included and were divided into two groups: those without LVI (LVI−), <em>n</em> = 388 and those with LVI (LVI+), <em>n</em> = 163.</li>
<li>LVI+ status was associated with high stage and grade UTUC and lymph node metastasis (<em>P</em> &lt; 0.001).</li> <li>The 5-year CSS and MFS rates were significantly worse in the LVI+ group than in LVI− group (52.2 vs 84.5%, <em>P</em> &lt; 0.001 and 43.8 vs 82.7%, <em>P</em> &lt; 0.001, respectively).</li>
<li>In multivariate analysis, LVI+ status was an independent prognostic factor for CSS and MFS (<em>P</em> = 0.04 and <em>P</em> &lt; 0.001). These findings were confirmed for the pN0/x patient subgroup (<em>n</em> = 504, <em>P</em> &lt; 0.001).</li>
<li>In the pN0/x patient subgroup, we described a prognostic tool for MFS based on independent factors that permitted us to stratify patients into groups of high, intermediate or low risk of metastasis relapse.</li>
</ul></div></div>
<div class="section" id="bju12116-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12116-list-0004" class="bullet">
<li>The presence of LVI was a strong predictor of a poor outcome for UTUC.</li>
<li>When a lymphadenectomy has not been achieved, the report of LVI status is crucial to identfiy those patients at higher risk for metastatic relapse.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To assess the impact of lymphovascular invasion (LVI) on upper urinary tract urothelial carcinomas (UTUCs) in a multicentre study on cancer-specific survival (CSS), recurrence-free survival and metastasis-free survival (MFS).
To show the negative impact of LVI for patients with pN0/x disease and to stratify these patients into risk groups for metastatic relapse.



Patients and Methods

A multicentre retrospective study was performed on patients who underwent radical nephroureterectomy between 1995 and 2010.
LVI status was evaluated as a prognostic factor for survival using univariate and multivariate Cox regression analysis.



Results

Overall, 551 patients were included and were divided into two groups: those without LVI (LVI−), n = 388 and those with LVI (LVI+), n = 163.
LVI+ status was associated with high stage and grade UTUC and lymph node metastasis (P &lt; 0.001). The 5-year CSS and MFS rates were significantly worse in the LVI+ group than in LVI− group (52.2 vs 84.5%, P &lt; 0.001 and 43.8 vs 82.7%, P &lt; 0.001, respectively).
In multivariate analysis, LVI+ status was an independent prognostic factor for CSS and MFS (P = 0.04 and P &lt; 0.001). These findings were confirmed for the pN0/x patient subgroup (n = 504, P &lt; 0.001).
In the pN0/x patient subgroup, we described a prognostic tool for MFS based on independent factors that permitted us to stratify patients into groups of high, intermediate or low risk of metastasis relapse.



Conclusions

The presence of LVI was a strong predictor of a poor outcome for UTUC.
When a lymphadenectomy has not been achieved, the report of LVI status is crucial to identfiy those patients at higher risk for metastatic relapse.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12110" xmlns="http://purl.org/rss/1.0/"><title>Role of Immunotherapy in Castration-Resistant Prostate Cancer (CRPC)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12110</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Role of Immunotherapy in Castration-Resistant Prostate Cancer (CRPC)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cristina Suárez, Rafael Morales-Barrera, Victor Ramos, Isaac Núñez, Claudia Valverde, Jacques Planas, Juan Morote, Xavier Maldonado, Joan Carles</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T06:30:42.168685-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12110</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12110</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12110</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12118-sec-0013" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><ul id="bju12110-list-0001" class="bullet">
<li>Initial therapy for metastatic prostate cancer consists of androgenic suppression. However, this is only a palliative treatment with an effective duration that usually lasts 12–24 months. Historically, castration-resistant prostate cancer (CRPC) had been considered a chemoresistant tumour.</li>
<li>In 2004, docetaxel received USA Food and Drug Administration approval as a first-line treatment for metastatic prostate cancer, after two independent phase III trials showed an increased survival benefit. Recently, five new drugs have shown increased survival in CRPC: sipuleucel-T (assymptomatic or minimally symptomatic), abiraterone acetate (before and after docetaxel), cabazitaxel (after docetaxel), MDV3100 (after docetaxel) and radium-223 (not suitable for docetaxel or after docetaxel).</li>
<li>The identification of antigens in normal prostate tissue or prostate cancer that are recognised by immune effectors cells has resulted in several new studies based on immunotherapy.</li>
<li>Prostate cancer disease provides a test system to determine the efficacy of vaccines for different reasons. This cancer is a tumour that grows relatively slowly. Recurrence is often diagnosed early (with many patients presenting only with biochemical progression), there is a biological marker that can predict prognosis and outcome (PSA doubling time), various specific antigens have been identified and characterised, and vaccines can be used with a good safety profile combined with anti-androgen therapy, chemotherapy, or radiotherapy.</li>
<li>Here we provide a review of the main important immune treatments in CRPC.</li>
</ul></div></div>
]]></content:encoded><description>
 
Initial therapy for metastatic prostate cancer consists of androgenic suppression. However, this is only a palliative treatment with an effective duration that usually lasts 12–24 months. Historically, castration-resistant prostate cancer (CRPC) had been considered a chemoresistant tumour.
In 2004, docetaxel received USA Food and Drug Administration approval as a first-line treatment for metastatic prostate cancer, after two independent phase III trials showed an increased survival benefit. Recently, five new drugs have shown increased survival in CRPC: sipuleucel-T (assymptomatic or minimally symptomatic), abiraterone acetate (before and after docetaxel), cabazitaxel (after docetaxel), MDV3100 (after docetaxel) and radium-223 (not suitable for docetaxel or after docetaxel).
The identification of antigens in normal prostate tissue or prostate cancer that are recognised by immune effectors cells has resulted in several new studies based on immunotherapy.
Prostate cancer disease provides a test system to determine the efficacy of vaccines for different reasons. This cancer is a tumour that grows relatively slowly. Recurrence is often diagnosed early (with many patients presenting only with biochemical progression), there is a biological marker that can predict prognosis and outcome (PSA doubling time), various specific antigens have been identified and characterised, and vaccines can be used with a good safety profile combined with anti-androgen therapy, chemotherapy, or radiotherapy.
Here we provide a review of the main important immune treatments in CRPC.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12108" xmlns="http://purl.org/rss/1.0/"><title>Is diameter-axial-polar scoring predictive of renal functional damage in patients undergoing partial nephrectomy? An evaluation using technetium Tc 99m (99Tcm) diethylene-triamine-penta-acetic acid (DTPA) glomerular filtration rate</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12108</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Is diameter-axial-polar scoring predictive of renal functional damage in patients undergoing partial nephrectomy? An evaluation using technetium Tc 99m (99Tcm) diethylene-triamine-penta-acetic acid (DTPA) glomerular filtration rate</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Linhui Wang, Mingmin Li, Wei Chen, Zhenjie Wu, Chen Cai, Chun Xiang, Jing Sheng, Bing Liu, Qing Yang, Yinghao Sun</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T06:30:37.700308-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12108</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12108</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12108</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12108-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12108-list-0001" class="bullet">
<li>To identify the effects of diameter-axial-polar (DAP) scoring and other clinical variables on renal functional outcomes after partial nephrectomy (PN).</li>
</ul></div></div>
<div class="section" id="bju12108-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Material and Methods</h4><div class="para"><ul id="bju12108-list-0002" class="bullet">
<li>A total of 59 patients with complete radiographic, clinical and follow-up information were included for analysis.</li>
<li>Technetium Tc 99m (<sup>99</sup>Tc<sup>m</sup>)-diethylene-triamine-penta-acetic acid (DTPA) renal scintigraphy was used to determine the glomerular filtration rate (GFR) of both kidneys and each kidney individually.</li>
<li>All cross-sectional images were reviewed by a single radiologist and a DAP score was assigned.</li>
</ul></div></div>
<div class="section" id="bju12108-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12108-list-0003" class="bullet">
<li>The median decline in total GFR after PN was 13% at a median follow-up of 12 months (from 86.8 to 76.2 mL/min per 1.73 m<sup>2</sup>, <em>P</em> &lt; 0.001).</li>
<li>The median GFR of the operated kidney showed a significant decrease peri-operatively (42.4 to 27.1 mL/min per 1.73 m<sup>2</sup>, <em>P</em> &lt; 0.001). The function of the contralateral kidney showed a significant increase (43.5 to 48.8 mL/min per 1.73 m<sup>2</sup>, <em>P</em> &lt; 0.001).</li>
<li>On multivariate analysis, preoperative total GFR, ischaemia time and DAP sum score were independent predictors of absolute functional decline of the affected kidney (all <em>P</em> &lt; 0.001), while only preoperative total GFR and DAP sum score were significantly associated with the total absolute GFR reduction (all <em>P</em> &lt; 0.001).</li>
</ul></div></div>
<div class="section" id="bju12108-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12108-list-0004" class="bullet">
<li>Preoperative renal function status and DAP score of renal tumours are the primary determinants of long-term functional outcomes after PN, but renal ischaemia damage to the operated kidney after PN is possibly masked by functional compensation of the contralateral healthy kidney if only overall renal function is assessed.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To identify the effects of diameter-axial-polar (DAP) scoring and other clinical variables on renal functional outcomes after partial nephrectomy (PN).



Material and Methods

A total of 59 patients with complete radiographic, clinical and follow-up information were included for analysis.
Technetium Tc 99m (99Tcm)-diethylene-triamine-penta-acetic acid (DTPA) renal scintigraphy was used to determine the glomerular filtration rate (GFR) of both kidneys and each kidney individually.
All cross-sectional images were reviewed by a single radiologist and a DAP score was assigned.



Results

The median decline in total GFR after PN was 13% at a median follow-up of 12 months (from 86.8 to 76.2 mL/min per 1.73 m2, P &lt; 0.001).
The median GFR of the operated kidney showed a significant decrease peri-operatively (42.4 to 27.1 mL/min per 1.73 m2, P &lt; 0.001). The function of the contralateral kidney showed a significant increase (43.5 to 48.8 mL/min per 1.73 m2, P &lt; 0.001).
On multivariate analysis, preoperative total GFR, ischaemia time and DAP sum score were independent predictors of absolute functional decline of the affected kidney (all P &lt; 0.001), while only preoperative total GFR and DAP sum score were significantly associated with the total absolute GFR reduction (all P &lt; 0.001).



Conclusion

Preoperative renal function status and DAP score of renal tumours are the primary determinants of long-term functional outcomes after PN, but renal ischaemia damage to the operated kidney after PN is possibly masked by functional compensation of the contralateral healthy kidney if only overall renal function is assessed.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12084" xmlns="http://purl.org/rss/1.0/"><title>An analysis of patients with T2 renal cell carcinoma (RCC) according to tumour size: a population-based analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12084</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An analysis of patients with T2 renal cell carcinoma (RCC) according to tumour size: a population-based analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marco Bianchi, Andreas Becker, Quoc-Dien Trinh, Firas Abdollah, Zhe Tian, Shahrokh F. Shariat, Francesco Montorsi, Paul Perrotte, Markus Graefen, Pierre I. Karakiewicz, Maxine Sun</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T06:30:32.236228-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12084</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12084</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12084</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12084-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12084-list-0001" class="bullet">
<li>To examine the discriminant properties of the most contemporary version of the Tumour-Node-Metastasis (TNM) staging for renal cell carcinoma (RCC) sub-classification of T2 lesions according to a threshold size of 10 cm. Other thresholds were also assessed.</li>
</ul></div></div>
<div class="section" id="bju12084-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12084-list-0002" class="bullet">
<li>Between 1988 and 2006, within the Surveillance, Epidemiology, and End Results database, patients with T2 N0–2 M0–1 RCC treated with a nephrectomy were abstracted.</li>
<li>Tumour size was evaluated according to several thresholds: ≥8, ≥9, ≥10, ≥11, and ≥12 cm. Kaplan–Meier and life tables for cancer-specific mortality (CSM) were computed.</li>
<li>Several Cox regression modes were fitted for prediction of CSM, using different thresholds.</li>
<li>The predictive accuracy of various thresholds was compared using the area under the curve and methods of calibration.</li>
</ul></div></div>
<div class="section" id="bju12084-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12084-list-0003" class="bullet">
<li>In all, 4963 patients were identified. Kaplan–Meier analyses showed statistically significant CSM-free survival differences between all examined thresholds.</li>
<li>In multivariable Cox-regression models, all tested tumour size thresholds emerged as independent predictors of CSM.</li>
<li>Of all thresholds, the values of 9 (0.55) and 11 cm (0.55) achieved the highest discrimination in univariable analysis, followed by 10 (0.539), 12 (0.539), and 8 cm (0.531).</li>
<li>When the thresholds were combined with all other variables, the 11 cm (0.688) achieved the highest discrimination.</li>
</ul></div></div>
<div class="section" id="bju12084-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12084-list-0004" class="bullet">
<li>The discriminant properties of all examined thresholds showed very similar discriminant properties, which brings into questioning whether a dichotomization of pT2 tumours is really necessary.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To examine the discriminant properties of the most contemporary version of the Tumour-Node-Metastasis (TNM) staging for renal cell carcinoma (RCC) sub-classification of T2 lesions according to a threshold size of 10 cm. Other thresholds were also assessed.



Patients and Methods

Between 1988 and 2006, within the Surveillance, Epidemiology, and End Results database, patients with T2 N0–2 M0–1 RCC treated with a nephrectomy were abstracted.
Tumour size was evaluated according to several thresholds: ≥8, ≥9, ≥10, ≥11, and ≥12 cm. Kaplan–Meier and life tables for cancer-specific mortality (CSM) were computed.
Several Cox regression modes were fitted for prediction of CSM, using different thresholds.
The predictive accuracy of various thresholds was compared using the area under the curve and methods of calibration.



Results

In all, 4963 patients were identified. Kaplan–Meier analyses showed statistically significant CSM-free survival differences between all examined thresholds.
In multivariable Cox-regression models, all tested tumour size thresholds emerged as independent predictors of CSM.
Of all thresholds, the values of 9 (0.55) and 11 cm (0.55) achieved the highest discrimination in univariable analysis, followed by 10 (0.539), 12 (0.539), and 8 cm (0.531).
When the thresholds were combined with all other variables, the 11 cm (0.688) achieved the highest discrimination.



Conclusion

The discriminant properties of all examined thresholds showed very similar discriminant properties, which brings into questioning whether a dichotomization of pT2 tumours is really necessary.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12052" xmlns="http://purl.org/rss/1.0/"><title>Bladder carcinoma in situ (CIS) in Australia: a rising incidence for an under-reported malignancy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12052</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bladder carcinoma in situ (CIS) in Australia: a rising incidence for an under-reported malignancy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Weranja K.B. Ranasinghe, John Attia, Christopher Oldmeadow, Nathan Lawrentschuk, Jane Robertson, Tamra Ranasinghe, Damien Bolton, Raj Persad</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-10T06:17:42.751236-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12052</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12052</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12052</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Supplement Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12052-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12052-list-0002" class="bullet">
<li>To investigate the incidence of carcinoma <em>in situ</em> (CIS) in Australia and examine implications for its diagnosis and management, as CIS of the urinary bladder is a non-reportable disease in Australia.</li>
</ul></div></div> <div class="section" id="bju12052-sec-1003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><ul id="bju12052-list-0003" class="bullet">
<li>Analysis of annual hospitalisation data using Australian Institute of Health and Welfare (AIHW) datasets showed an increase in CIS from 2001 onwards.</li>
<li>To determine whether the increase seen with AIHW data represented a true increase in the rates offices, patient level data was examined using the Centre for Health record linkage (CHeReL) datasets.</li>
</ul></div></div>
<div class="section" id="bju12052-sec-1004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12052-list-0004" class="bullet">
<li>CHeReL linked data of 13 790 males and 5902 females, calculated the average incidence of CIS to be 20.9 per 100 000 and 6.5 per 100 000 respectively in those aged &gt; 50 years, showing a rapid increase in the rates of CIS from 2001.</li>
<li>There was an 11% (<em>P</em> = 0.04) and 14% (<em>P</em> = 0.02) annual increase in incidence of CIS in men and women and these rates increased with age.</li>
</ul></div></div>
<div class="section" id="bju12052-sec-1005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12052-list-0005" class="bullet">
<li>National data (AIHW) substantially underestimate the incidence of CIS in the Australian population.</li>
<li>Patient level data suggest CIS rates are rapidly increasing in Australia despite high treatment rates.</li>
<li>Closer surveillance and awareness of these high rates warrants further study and we recommend that CIS be considered a reportable disease.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To investigate the incidence of carcinoma in situ (CIS) in Australia and examine implications for its diagnosis and management, as CIS of the urinary bladder is a non-reportable disease in Australia.

 
Methods

Analysis of annual hospitalisation data using Australian Institute of Health and Welfare (AIHW) datasets showed an increase in CIS from 2001 onwards.
To determine whether the increase seen with AIHW data represented a true increase in the rates offices, patient level data was examined using the Centre for Health record linkage (CHeReL) datasets.



Results

CHeReL linked data of 13 790 males and 5902 females, calculated the average incidence of CIS to be 20.9 per 100 000 and 6.5 per 100 000 respectively in those aged &gt; 50 years, showing a rapid increase in the rates of CIS from 2001.
There was an 11% (P = 0.04) and 14% (P = 0.02) annual increase in incidence of CIS in men and women and these rates increased with age.



Conclusions

National data (AIHW) substantially underestimate the incidence of CIS in the Australian population.
Patient level data suggest CIS rates are rapidly increasing in Australia despite high treatment rates.
Closer surveillance and awareness of these high rates warrants further study and we recommend that CIS be considered a reportable disease.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12051" xmlns="http://purl.org/rss/1.0/"><title>A cost-minimisation analysis comparing photoselective vaporisation (PVP) and transurethral resection of the prostate (TURP) for the management of symptomatic benign prostatic hyperplasia (BPH) in Queensland, Australia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12051</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A cost-minimisation analysis comparing photoselective vaporisation (PVP) and transurethral resection of the prostate (TURP) for the management of symptomatic benign prostatic hyperplasia (BPH) in Queensland, Australia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jennifer A. Whitty, Paul Crosland, Kaye Hewson, Rajan Narula, Timothy R. Nathan, Peter A. Campbell, Andrew Keller, Paul A. Scuffham</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-10T06:17:37.488011-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12051</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12051</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12051</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Supplement Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12051-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12051-list-0002" class="bullet">
<li>To compare the costs of photoselective vaporisation (PVP) and transurethral resection of the prostate (TURP) for management of symptomatic benign prostatic hyperplasia (BPH) from the perspective of a Queensland public hospital provider.</li>
</ul></div></div>
<div class="section" id="bju12051-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12051-list-0003" class="bullet">
<li>A decision-analytic model was used to compare the costs of PVP and TURP.</li>
<li>Cost inputs were sourced from an audit of patients undergoing PVP or TURP across three hospitals.</li>
<li>The probability of re-intervention was obtained from secondary literature sources.</li>
<li>Probabilistic and multi-way sensitivity analyses were used to account for uncertainty and test the impact of varying key assumptions.</li>
</ul></div></div>
<div class="section" id="bju12051-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12051-list-0004" class="bullet">
<li>In the base case analysis, which included equipment, training and re-intervention costs, PVP was AU$ 739 (95% credible interval [CrI] –12 187 to 14 516) more costly per patient than TURP.</li>
<li>The estimate was most sensitive to changes in procedural costs, fibre costs and the probability of re-intervention.</li>
<li>Sensitivity analyses based on data from the most favourable site or excluding equipment and training costs reduced the point estimate to favour PVP (incremental cost AU$ –684, 95% CrI –8319 to 5796 and AU$ –100, 95% CrI –13 026 to 13 678, respectively). However, CrIs were wide for all analyses.</li>
</ul></div></div>
<div class="section" id="bju12051-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12051-list-0005" class="bullet">
<li>In this cost minimisation analysis, there was no significant cost difference between PVP and TURP, after accounting for equipment, training and re-intervention costs.</li>
<li>However, PVP was associated with a shorter length of stay and lower procedural costs during audit, indicating PVP potentially provides comparatively good value for money once the technology is established.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To compare the costs of photoselective vaporisation (PVP) and transurethral resection of the prostate (TURP) for management of symptomatic benign prostatic hyperplasia (BPH) from the perspective of a Queensland public hospital provider.



Patients and Methods

A decision-analytic model was used to compare the costs of PVP and TURP.
Cost inputs were sourced from an audit of patients undergoing PVP or TURP across three hospitals.
The probability of re-intervention was obtained from secondary literature sources.
Probabilistic and multi-way sensitivity analyses were used to account for uncertainty and test the impact of varying key assumptions.



Results

In the base case analysis, which included equipment, training and re-intervention costs, PVP was AU$ 739 (95% credible interval [CrI] –12 187 to 14 516) more costly per patient than TURP.
The estimate was most sensitive to changes in procedural costs, fibre costs and the probability of re-intervention.
Sensitivity analyses based on data from the most favourable site or excluding equipment and training costs reduced the point estimate to favour PVP (incremental cost AU$ –684, 95% CrI –8319 to 5796 and AU$ –100, 95% CrI –13 026 to 13 678, respectively). However, CrIs were wide for all analyses.



Conclusions

In this cost minimisation analysis, there was no significant cost difference between PVP and TURP, after accounting for equipment, training and re-intervention costs.
However, PVP was associated with a shorter length of stay and lower procedural costs during audit, indicating PVP potentially provides comparatively good value for money once the technology is established.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11657.x" xmlns="http://purl.org/rss/1.0/"><title>Outcomes of transperineal template-guided prostate biopsy in 409 patients</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11657.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Outcomes of transperineal template-guided prostate biopsy in 409 patients</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">James L. Symons, Andrew Huo, Carlo L. Yuen, Anne-Maree Haynes, Jayne Matthews, Robert L. Sutherland, Phillip Brenner, Phillip D. Stricker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T07:04:15.899472-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11657.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11657.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11657.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11657-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11657-list-1001" class="bullet">
<li>With an aging population and routine use of PSA testing, there is an increase in men undergoing biopsy to assess for prostate cancer. The most common route for accessing the prostate is through the rectum, which potentially exposes the patient to otherwise innocuous Enterobacteriaceae. The rising incidence of extended-spectrum beta-lactamase has been linked to a rise in post-TRUS biopsy infection rates internationally.</li>
<li>The study describes an alternative route for biopsy of the prostate that is associated with a very low infection rate, whilst still maintaining a good tumour detection rate.</li>
</ul></div></div>
<div class="section" id="bju11657-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11657-list-0001" class="bullet">
<li>To present the template-guided transperineal prostate biopsy (TPB) outcomes for patients of two urologists from a single institution.</li>
</ul></div></div>
<div class="section" id="bju11657-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11657-list-0002" class="bullet">
<li>We conducted a prospective study of 409 consecutive men who underwent TPB between December 2006 and June 2008 in a tertiary referral centre using a standardized 14-region technique.</li>
<li>The procedure was performed as day surgery under general anaesthesia with fluoroquinolone antibiotic cover.</li>
<li>Follow-up took place within 2 weeks, during which time men were interviewed using a standardized template.</li>
<li>Results were compared with those of the Australian national prostate biopsy audits performed by the Urological Society of Australia and New Zealand (USANZ).</li>
</ul></div></div>
<div class="section" id="bju11657-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11657-list-0003" class="bullet">
<li>Indications for biopsy included elevated prostate-specific antigen (PSA) level (75%), with a median PSA level of 6.5 ng/mL, abnormal digital rectal examination (8%) and active surveillance (AS) re-staging (18%).</li>
<li>The mean patient age was 63 years and two-thirds of patients were undergoing their first biopsy.</li>
<li>A positive biopsy was found in 232 men, 74% of whom had a Gleason score of ≥7. The overall cancer detection rate was 56.7% (USANZ 2005 national audit = 56.5%). Stratified between those having their first TPB or a repeat procedure (after a previous negative biopsy), the detection rates were 64.4 and 35.6%, respectively. Significantly higher detection rates were found in prostates &lt;50 mL in volume than in larger prostates (65.2 vs 38.3%, respectively, <em>P</em> &lt; 0.001).</li>
<li>Haematuria was the most common side effect (51.7%). Others included dysuria (16.4%), acute urinary retention (4.2%) and fever (3.2%). One patient (0.2%) had septicaemia requiring i.v. antibiotics.</li>
<li>Repeat biopsy was not associated with increased complication rates.</li>
</ul></div></div>
<div class="section" id="bju11657-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11657-list-0004" class="bullet">
<li>TPB is a safe and efficacious technique, with a cancer detection rate of 56.7% in the present series, and a low incidence of major side effects. Stratified by prostate volume, the detection rate of TPB was higher in smaller glands.</li>
<li>Given the relatively low rate of serious complications, clinicians could consider increasing the number of TPB biopsy cores in larger prostates as a strategy to improve cancer detection within this group. Conversely, in patients on AS programmes, a staging TPB may be a superior approach for patients undergoing repeat biopsy so as to minimize their risk of serious infection.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

With an aging population and routine use of PSA testing, there is an increase in men undergoing biopsy to assess for prostate cancer. The most common route for accessing the prostate is through the rectum, which potentially exposes the patient to otherwise innocuous Enterobacteriaceae. The rising incidence of extended-spectrum beta-lactamase has been linked to a rise in post-TRUS biopsy infection rates internationally.
The study describes an alternative route for biopsy of the prostate that is associated with a very low infection rate, whilst still maintaining a good tumour detection rate.


 Objective

To present the template-guided transperineal prostate biopsy (TPB) outcomes for patients of two urologists from a single institution.



Patients and Methods

We conducted a prospective study of 409 consecutive men who underwent TPB between December 2006 and June 2008 in a tertiary referral centre using a standardized 14-region technique.
The procedure was performed as day surgery under general anaesthesia with fluoroquinolone antibiotic cover.
Follow-up took place within 2 weeks, during which time men were interviewed using a standardized template.
Results were compared with those of the Australian national prostate biopsy audits performed by the Urological Society of Australia and New Zealand (USANZ).



Results

Indications for biopsy included elevated prostate-specific antigen (PSA) level (75%), with a median PSA level of 6.5 ng/mL, abnormal digital rectal examination (8%) and active surveillance (AS) re-staging (18%).
The mean patient age was 63 years and two-thirds of patients were undergoing their first biopsy.
A positive biopsy was found in 232 men, 74% of whom had a Gleason score of ≥7. The overall cancer detection rate was 56.7% (USANZ 2005 national audit = 56.5%). Stratified between those having their first TPB or a repeat procedure (after a previous negative biopsy), the detection rates were 64.4 and 35.6%, respectively. Significantly higher detection rates were found in prostates &lt;50 mL in volume than in larger prostates (65.2 vs 38.3%, respectively, P &lt; 0.001).
Haematuria was the most common side effect (51.7%). Others included dysuria (16.4%), acute urinary retention (4.2%) and fever (3.2%). One patient (0.2%) had septicaemia requiring i.v. antibiotics.
Repeat biopsy was not associated with increased complication rates.



Conclusions

TPB is a safe and efficacious technique, with a cancer detection rate of 56.7% in the present series, and a low incidence of major side effects. Stratified by prostate volume, the detection rate of TPB was higher in smaller glands.
Given the relatively low rate of serious complications, clinicians could consider increasing the number of TPB biopsy cores in larger prostates as a strategy to improve cancer detection within this group. Conversely, in patients on AS programmes, a staging TPB may be a superior approach for patients undergoing repeat biopsy so as to minimize their risk of serious infection.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12060" xmlns="http://purl.org/rss/1.0/"><title>Assessing the use of haemostatic sealants in tubeless percutaneous renal access and their effect on renal drainage and histology: an experimental porcine study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12060</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Assessing the use of haemostatic sealants in tubeless percutaneous renal access and their effect on renal drainage and histology: an experimental porcine study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christos Rigopoulos, Iason Kyriazis, Panagiotis Kallidonis, Christina Kalogeropoulou, Dimitra Koumoundourou, Ioannis Georgiopoulos, Theodore Petsas, Dimitrios Karnabatidis, Costantinos Constantinides, Evangelos Liatsikos</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T06:57:36.47771-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12060</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12060</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12060</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12060-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12060-list-0001" class="bullet">
<li>To evaluate the mid-term effects of haemostatic sealant application during tubeless percutaneous nephrolithotomy (PCNL) on renal drainage and histology in an <em>in vivo</em> porcine study.</li>
</ul></div></div>
<div class="section" id="bju12060-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12060-list-0002" class="bullet">
<li>Bilateral percutaneous access was established in 28 porcine renal units. At the end of the procedure, a type 1 absorbable fish origin collagen powder, a human fibrinogen- and thrombin-coated sponge or a cross-linked gelatin granule/topical thrombin matrix were randomly placed on the nephrostomy tracts. Four nephrostomy accesses were left intact and served as controls. No percutaneous tube, ureteric stent or bladder catheter was left in place postoperatively.</li>
<li>Computed tomography urography on postoperative days 1, 15, 30 and 40 was used to access renal drainage.</li>
<li>On postoperative day 40, all animals were killed and both kidneys from each animal were harvested for histological evaluation.</li>
</ul></div></div>
<div class="section" id="bju12060-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12060-list-0003" class="bullet">
<li>Evidence of risk for drainage occlusion after sealant application was found.</li>
<li>The use of haemostatic sealants was associated with significant histological lesions in the renal parenchyma, regardless of which sealant was used.</li>
<li>No sealant was identified as superior to the others.</li>
<li>Nephrostomy tracts that were left without sealant application (control group) were associated with no morbidity and fewer histopathological changes.</li>
</ul></div></div>
<div class="section" id="bju12060-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12060-list-0004" class="bullet">
<li>Based on these experimental results, the safety of the application of haemostatic sealants in tubeless PCNL should be reassessed, focusing not only on the potential of such materials to occlude urinary drainage but also on their effect on renal histology.</li>
<li>Further investigation is considered necessary.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To evaluate the mid-term effects of haemostatic sealant application during tubeless percutaneous nephrolithotomy (PCNL) on renal drainage and histology in an in vivo porcine study.



Materials and Methods

Bilateral percutaneous access was established in 28 porcine renal units. At the end of the procedure, a type 1 absorbable fish origin collagen powder, a human fibrinogen- and thrombin-coated sponge or a cross-linked gelatin granule/topical thrombin matrix were randomly placed on the nephrostomy tracts. Four nephrostomy accesses were left intact and served as controls. No percutaneous tube, ureteric stent or bladder catheter was left in place postoperatively.
Computed tomography urography on postoperative days 1, 15, 30 and 40 was used to access renal drainage.
On postoperative day 40, all animals were killed and both kidneys from each animal were harvested for histological evaluation.



Results

Evidence of risk for drainage occlusion after sealant application was found.
The use of haemostatic sealants was associated with significant histological lesions in the renal parenchyma, regardless of which sealant was used.
No sealant was identified as superior to the others.
Nephrostomy tracts that were left without sealant application (control group) were associated with no morbidity and fewer histopathological changes.



Conclusions

Based on these experimental results, the safety of the application of haemostatic sealants in tubeless PCNL should be reassessed, focusing not only on the potential of such materials to occlude urinary drainage but also on their effect on renal histology.
Further investigation is considered necessary.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11724.x" xmlns="http://purl.org/rss/1.0/"><title>Feasibility and oncological outcomes of laparoscopic treatment for local relapse of renal cell carcinoma</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11724.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Feasibility and oncological outcomes of laparoscopic treatment for local relapse of renal cell carcinoma</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Albert El Hajj, Ruban Thanigasalam, Vincent Molinié, Walid Massoud, Mohamed Fourati, Frederic Girard, Bernard Escudier, Hervé Baumert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T06:57:33.262198-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11724.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11724.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11724.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11724-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11724-list-0001" class="bullet">
<li>Local relapse of renal cell carcinoma following radical nephrectomy is rare, and surgical removal provides the only opportunity for cure. Open surgery has been established as the usual approach for these tumours. It is, however, associated with significant morbidity.</li>
<li>Our study describes the largest series of laparoscopic treatment of local relapse of renal cell carcinoma with the longest follow-up. We show that the laparoscopic approach is feasible in expert centres. It provides faster recovery and fewer complications with satisfactory oncological outcomes in selected patients.</li>
</ul></div></div>
<div class="section" id="bju11724-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11724-list-0002" class="bullet">
<li>To assess the feasibility and oncological outcomes of laparoscopic treatment for local relapse of renal cell carcinoma.</li>
</ul></div></div>
<div class="section" id="bju11724-sec-0009" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11724-list-0003" class="bullet">
<li>Nine patients were treated by a pure laparoscopic approach for local recurrence of a renal tumour between 2005 and 2011 by a single surgeon (HB), following an initial open radical nephrectomy for the primary tumour.</li>
<li>Clinical and histopathological data were collected prospectively and analysed retrospectively.</li>
<li>Seven patients were treated by a transperitoneal approach and two patients had a retroperitoneal approach.</li>
</ul></div></div>
<div class="section" id="bju11724-sec-0010" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11724-list-0004" class="bullet">
<li>Relapse occurred within a mean time of 83 months (7–168) following nephrectomy. Recurrent tumour size varied from 2.5 to 4.5 cm. All surgeries were performed laparoscopically without need for conversion.</li>
<li>Mean operative duration was 144 min (40–240), mean estimated blood loss was 430 mL (50–1300) and mean hospital stay was 4.5 days (3–6). Three patients had Clavien grade I intraoperative complications. Late complications were noted in two patients (Clavien I and IIIb).</li>
<li>Pathology confirmed clear cell carcinoma in all patients with an absence of sarcomatoid features and negative surgical margins.</li>
<li>Three patients had neoadjuvant treatment and two patients had adjuvant treatment. In all, 67% of patients were disease free with a mean follow-up period of 3 years.</li>
</ul></div></div>
<div class="section" id="bju11724-sec-0011" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11724-list-0005" class="bullet">
<li>Surgical removal of isolated local recurrence remains the only possibility of cure in patients with renal cell carcinoma.</li>
<li>We demonstrated that the laparoscopic approach is a safe and feasible alternative treatment option for selected cases with low morbidity and satisfactory oncological outcomes.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Local relapse of renal cell carcinoma following radical nephrectomy is rare, and surgical removal provides the only opportunity for cure. Open surgery has been established as the usual approach for these tumours. It is, however, associated with significant morbidity.
Our study describes the largest series of laparoscopic treatment of local relapse of renal cell carcinoma with the longest follow-up. We show that the laparoscopic approach is feasible in expert centres. It provides faster recovery and fewer complications with satisfactory oncological outcomes in selected patients.


 Objective

To assess the feasibility and oncological outcomes of laparoscopic treatment for local relapse of renal cell carcinoma.



Patients and Methods

Nine patients were treated by a pure laparoscopic approach for local recurrence of a renal tumour between 2005 and 2011 by a single surgeon (HB), following an initial open radical nephrectomy for the primary tumour.
Clinical and histopathological data were collected prospectively and analysed retrospectively.
Seven patients were treated by a transperitoneal approach and two patients had a retroperitoneal approach.



Results

Relapse occurred within a mean time of 83 months (7–168) following nephrectomy. Recurrent tumour size varied from 2.5 to 4.5 cm. All surgeries were performed laparoscopically without need for conversion.
Mean operative duration was 144 min (40–240), mean estimated blood loss was 430 mL (50–1300) and mean hospital stay was 4.5 days (3–6). Three patients had Clavien grade I intraoperative complications. Late complications were noted in two patients (Clavien I and IIIb).
Pathology confirmed clear cell carcinoma in all patients with an absence of sarcomatoid features and negative surgical margins.
Three patients had neoadjuvant treatment and two patients had adjuvant treatment. In all, 67% of patients were disease free with a mean follow-up period of 3 years.



Conclusions

Surgical removal of isolated local recurrence remains the only possibility of cure in patients with renal cell carcinoma.
We demonstrated that the laparoscopic approach is a safe and feasible alternative treatment option for selected cases with low morbidity and satisfactory oncological outcomes.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11720.x" xmlns="http://purl.org/rss/1.0/"><title>Phase II study of everolimus in metastatic urothelial cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11720.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Phase II study of everolimus in metastatic urothelial cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matthew I. Milowsky, Gopa Iyer, Ashley M. Regazzi, Hikmat Al-Ahmadie, Scott R. Gerst, Irina Ostrovnaya, Lan L. Gellert, Rana Kaplan, Ilana R. Garcia-Grossman, Deepa Pendse, Arjun V. Balar, Anne Marie Flaherty, Alisa Trout, David B. Solit, Dean F. Bajorin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T06:57:30.001462-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11720.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11720.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11720.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11720-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11720-list-0001" class="bullet">
<li>No recent advances have been made in the treatment of patients with advanced bladder cancer and, to date, targeted therapies have not resulted in an improvement in outcome. The mammalian target of rapamycin pathway has been shown to be up-regulated in bladder cancer and represents a rational target for therapeutic intervention.</li>
<li>In the present phase II study of everolimus, one near-complete response, one partial response and several minor responses suggest that everolimus possesses biological activity in a subset of patients with bladder cancer. To maximize benefit from targeted agents such as everolimus, the preselection of patients based on molecular phenotype is required.</li>
</ul></div></div>
<div class="section" id="bju11720-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11720-list-0002" class="bullet">
<li>To assess the efficacy and tolerability of everolimus in advanced urothelial carcimoma (UC).</li>
</ul></div></div>
<div class="section" id="bju11720-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11720-list-0003" class="bullet">
<li>The present study comprised a single-arm, non-randomized study in which all patients received everolimus 10 mg orally once daily continuously (one cycle = 4 weeks).</li>
<li>In total, 45 patients with metastatic UC progressing after one to four cytotoxic agents were enrolled between February 2009 and November 2010 at the Memorial Sloan-Kettering Cancer Center.</li>
<li>The primary endpoints were 2-month progression-free survival (PFS) and the safety of everolimus, with the secondary endpoint being the response rate.</li>
<li>A Simon minimax two-stage design tested the null hypothesis that the true two month PFS rate was ≤50%, as opposed to the alternative hypothesis of ≥70%.</li>
</ul></div></div>
<div class="section" id="bju11720-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11720-list-0004" class="bullet">
<li>The most common grade 3/4 toxicities were fatigue, infection, anaemia, lymphopaenia, hyperglycaemia and hypophosphataemia.</li>
<li>There were two partial responses in nodal metastases, with one patient achieving a 94% decrease in target lesions and remaining on drug at 26 months.</li>
<li>An additional 12 patients exhibited minor tumour regression.</li>
<li>There were 23 of 45 (51%) patients who were progression-free at 2 months with a median (95% CI) PFS of 2.6 (1.8–3.5) months and a median (95% CI) overall survival of 8.3 (5.5–12.1) months.</li>
<li>No clear association was observed between mammalian target of rapamycin pathway marker expression and 2-month PFS.</li>
</ul></div></div>
<div class="section" id="bju11720-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11720-list-0005" class="bullet">
<li>Although everolimus did not meet its primary endpoint, one partial response, one near-complete response and twelve minor regressions were observed.</li>
<li>Everolimus possesses meaningful anti-tumour activity in a subset of patients with advanced UC.</li>
<li>Studies aiming to define the genetic basis of everolimus activity in individual responders are ongoing.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

No recent advances have been made in the treatment of patients with advanced bladder cancer and, to date, targeted therapies have not resulted in an improvement in outcome. The mammalian target of rapamycin pathway has been shown to be up-regulated in bladder cancer and represents a rational target for therapeutic intervention.
In the present phase II study of everolimus, one near-complete response, one partial response and several minor responses suggest that everolimus possesses biological activity in a subset of patients with bladder cancer. To maximize benefit from targeted agents such as everolimus, the preselection of patients based on molecular phenotype is required.


 Objective

To assess the efficacy and tolerability of everolimus in advanced urothelial carcimoma (UC).



Patients and Methods

The present study comprised a single-arm, non-randomized study in which all patients received everolimus 10 mg orally once daily continuously (one cycle = 4 weeks).
In total, 45 patients with metastatic UC progressing after one to four cytotoxic agents were enrolled between February 2009 and November 2010 at the Memorial Sloan-Kettering Cancer Center.
The primary endpoints were 2-month progression-free survival (PFS) and the safety of everolimus, with the secondary endpoint being the response rate.
A Simon minimax two-stage design tested the null hypothesis that the true two month PFS rate was ≤50%, as opposed to the alternative hypothesis of ≥70%.



Results

The most common grade 3/4 toxicities were fatigue, infection, anaemia, lymphopaenia, hyperglycaemia and hypophosphataemia.
There were two partial responses in nodal metastases, with one patient achieving a 94% decrease in target lesions and remaining on drug at 26 months.
An additional 12 patients exhibited minor tumour regression.
There were 23 of 45 (51%) patients who were progression-free at 2 months with a median (95% CI) PFS of 2.6 (1.8–3.5) months and a median (95% CI) overall survival of 8.3 (5.5–12.1) months.
No clear association was observed between mammalian target of rapamycin pathway marker expression and 2-month PFS.



Conclusions

Although everolimus did not meet its primary endpoint, one partial response, one near-complete response and twelve minor regressions were observed.
Everolimus possesses meaningful anti-tumour activity in a subset of patients with advanced UC.
Studies aiming to define the genetic basis of everolimus activity in individual responders are ongoing.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11663.x" xmlns="http://purl.org/rss/1.0/"><title>Favourable long-term outcomes with brachytherapy-based regimens in men ≤60 years with clinically localized prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11663.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Favourable long-term outcomes with brachytherapy-based regimens in men ≤60 years with clinically localized prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marisa A. Kollmeier, Anthony Fidaleo, Xin Pei, Gil'ad Cohen, Marco Zaider, Quincy Mo, Brett Cox, Yoshiya Yamada, Michael J. Zelefsky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T06:57:23.822735-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11663.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11663.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11663.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11663-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11663-list-0001" class="bullet">
<li>Brachytherapy (BT)-based treatment for clinically localized prostate cancer is a well-accepted treatment strategy; however, there is concern that long-term outcomes and morbidity may not be acceptable in young patients (≤60 years).</li>
<li>We report our long-term experience with BT in men aged ≤ 60 years with a minimum of 2 years of post-treatment follow-up. Our results show low treatment-related morbidity and excellent long-term outcomes with BT-based treatment and suggest that such treatment should be offered to this patient population.</li>
</ul></div></div>
<div class="section" id="bju11663-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11663-list-0002" class="bullet">
<li>To report long-term outcomes of men ≤60 years treated with brachytherapy (BT) for low- and intermediate-risk prostate cancer.</li>
</ul></div></div>
<div class="section" id="bju11663-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11663-list-0003" class="bullet">
<li>Of 1655 patients treated with BT for clinically localized prostate cancer between January 1998 and May 2008 at Memorial Sloan-Kettering Cancer Center, 236 patients with National Comprehensive Cancer Network low- (<em>n</em> = 178) or intermediate-risk (<em>n</em> = 58) prostate cancer were ≤60 years old with a 3-year minimum follow-up, and represent the subjects of this report.</li>
<li>Brachytherapy was given either as monotherapy (<em>n</em> = 169) or with external beam radiation therapy (EBRT; <em>n</em> = 67). Forty-four patients (19%) received neoadjuvant cytoreductive hormone therapy. The ‘nadir+2’ definition was used for prostate-specific antigen (PSA) recurrence.</li>
<li>Common Terminology Criteria for Acute Events (CTCAE) v 3.0 was used to grade genitourinary (GU) and gastrointestinal (GI) toxicity. Potency was defined as the ability to obtain an erection suitable for intercourse or an International Index of Erectile Function score ≥ 22.</li>
<li>The Kaplan–Meier method and Cox regression were used for statistical analysis. The median follow-up was 83 months.</li>
</ul></div></div>
<div class="section" id="bju11663-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11663-list-0004" class="bullet">
<li>The 8-year PSA relapse-free survival (RFS), cancer-specific and overall survival rates for the entire cohort were 96, 99 and 96%, respectively.</li>
<li>For patients with low-risk disease, the 8-year PSA RFS rate was 97% and for intermediate-risk patients it was 94% (<em>P</em> = 0.34).</li>
<li>There was no difference in PSA RFS between BT alone and combined therapy (<em>P</em> = 0.17). Late grade ≥ 2 GU and GI toxicity was 14 and 3%, respectively.</li>
<li>Of 150 patients potent before treatment, 76 (51%) were potent at last follow-up, with 50/76 (66%) using no medication.</li>
<li>There was no significant difference in post-treatment potency between BT alone and BT with EBRT (<em>P</em> = 0.74).</li>
</ul></div></div>
<div class="section" id="bju11663-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11663-list-0005" class="bullet">
<li>Brachytherapy provides patients aged ≤ 60 years with low- and intermediate-risk prostate cancer with excellent outcomes and has a low risk of significant long-term GU or GI morbidity.</li>
<li>Erectile function is preserved in &gt;50% of patients and the majority do not require erectile dysfunction medication.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Brachytherapy (BT)-based treatment for clinically localized prostate cancer is a well-accepted treatment strategy; however, there is concern that long-term outcomes and morbidity may not be acceptable in young patients (≤60 years).
We report our long-term experience with BT in men aged ≤ 60 years with a minimum of 2 years of post-treatment follow-up. Our results show low treatment-related morbidity and excellent long-term outcomes with BT-based treatment and suggest that such treatment should be offered to this patient population.


 Objective

To report long-term outcomes of men ≤60 years treated with brachytherapy (BT) for low- and intermediate-risk prostate cancer.



Patients and Methods

Of 1655 patients treated with BT for clinically localized prostate cancer between January 1998 and May 2008 at Memorial Sloan-Kettering Cancer Center, 236 patients with National Comprehensive Cancer Network low- (n = 178) or intermediate-risk (n = 58) prostate cancer were ≤60 years old with a 3-year minimum follow-up, and represent the subjects of this report.
Brachytherapy was given either as monotherapy (n = 169) or with external beam radiation therapy (EBRT; n = 67). Forty-four patients (19%) received neoadjuvant cytoreductive hormone therapy. The ‘nadir+2’ definition was used for prostate-specific antigen (PSA) recurrence.
Common Terminology Criteria for Acute Events (CTCAE) v 3.0 was used to grade genitourinary (GU) and gastrointestinal (GI) toxicity. Potency was defined as the ability to obtain an erection suitable for intercourse or an International Index of Erectile Function score ≥ 22.
The Kaplan–Meier method and Cox regression were used for statistical analysis. The median follow-up was 83 months.



Results

The 8-year PSA relapse-free survival (RFS), cancer-specific and overall survival rates for the entire cohort were 96, 99 and 96%, respectively.
For patients with low-risk disease, the 8-year PSA RFS rate was 97% and for intermediate-risk patients it was 94% (P = 0.34).
There was no difference in PSA RFS between BT alone and combined therapy (P = 0.17). Late grade ≥ 2 GU and GI toxicity was 14 and 3%, respectively.
Of 150 patients potent before treatment, 76 (51%) were potent at last follow-up, with 50/76 (66%) using no medication.
There was no significant difference in post-treatment potency between BT alone and BT with EBRT (P = 0.74).



Conclusions

Brachytherapy provides patients aged ≤ 60 years with low- and intermediate-risk prostate cancer with excellent outcomes and has a low risk of significant long-term GU or GI morbidity.
Erectile function is preserved in &gt;50% of patients and the majority do not require erectile dysfunction medication.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12112" xmlns="http://purl.org/rss/1.0/"><title>Improving risk stratification in patients with prostate cancer managed by active surveillance: a nomogram predicting the risk of biopsy progression</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12112</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Improving risk stratification in patients with prostate cancer managed by active surveillance: a nomogram predicting the risk of biopsy progression</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Viacheslav Iremashvili, Joshua Burdick-Will, Mark S. Soloway</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T05:33:26.390414-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12112</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12112</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12112</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12112-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12112-list-0001" class="bullet">
<li>To develop a clinical tool that integrates different risk factors and provides individual predictions of the risk of biopsy progression in patients with prostate cancer managed by active surveillance.</li>
</ul></div></div>
<div class="section" id="bju12112-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12112-list-0002" class="bullet">
<li>Our analysis included 205 patients on active surveillance, each of whom had had at least two surveillance biopsies.</li>
<li>We used the Cox proportional hazard regression model to analyse the association between different risk factors and progression-free survival over successive biopsies. This multivariate model was then used to develop a nomogram.</li>
<li>Discrimination and calibration of the nomogram were internally validated using 200 bootstrap resamplings.</li>
</ul></div></div>
<div class="section" id="bju12112-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12112-list-0003" class="bullet">
<li>The median follow-up of patients free of progression was 4.6 years. A total of 58 (28%) patients experienced progression.</li>
<li>Factors significantly associated with progression were: overall number of positive cores in the diagnostic and first surveillance biopsies, race and prostate-specific antigen density.</li>
<li>The bootstrapping concordance index of the nomogram including these variables was 81%.</li>
<li>The nomogram tended to underestimate the probability of progression but it identified fairly accurately the distinct groups of patients at low, intermediate and high risk of progression.</li>
</ul></div></div>
<div class="section" id="bju12112-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12112-list-0004" class="bullet">
<li>In the development cohort, the nomogram was able to separate patients with respect to their risk of biopsy progression.</li>
<li>Since accurate risk stratification is essential to optimize patient care, this tool, if external validation confirms its performance, may prove useful for both the counselling and management of patients with low-volume, Gleason 6 prostate cancer.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To develop a clinical tool that integrates different risk factors and provides individual predictions of the risk of biopsy progression in patients with prostate cancer managed by active surveillance.



Materials and Methods

Our analysis included 205 patients on active surveillance, each of whom had had at least two surveillance biopsies.
We used the Cox proportional hazard regression model to analyse the association between different risk factors and progression-free survival over successive biopsies. This multivariate model was then used to develop a nomogram.
Discrimination and calibration of the nomogram were internally validated using 200 bootstrap resamplings.



Results

The median follow-up of patients free of progression was 4.6 years. A total of 58 (28%) patients experienced progression.
Factors significantly associated with progression were: overall number of positive cores in the diagnostic and first surveillance biopsies, race and prostate-specific antigen density.
The bootstrapping concordance index of the nomogram including these variables was 81%.
The nomogram tended to underestimate the probability of progression but it identified fairly accurately the distinct groups of patients at low, intermediate and high risk of progression.



Conclusions

In the development cohort, the nomogram was able to separate patients with respect to their risk of biopsy progression.
Since accurate risk stratification is essential to optimize patient care, this tool, if external validation confirms its performance, may prove useful for both the counselling and management of patients with low-volume, Gleason 6 prostate cancer.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12079" xmlns="http://purl.org/rss/1.0/"><title>Patterns of care and outcomes of radiotherapy for lymph node positivity after radical prostatectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12079</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patterns of care and outcomes of radiotherapy for lymph node positivity after radical prostatectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joshua R. Kaplan, Keith J. Kowalczyk, Tudor Borza, Xiangmei Gu, Stuart R. Lipsitz, Paul L. Nguyen, David F. Friedlander, Quoc-Dien Trinh, Jim C. Hu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T05:33:17.007481-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12079</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12079</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12079</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12079-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12079-list-0001" class="bullet">
<li>To evaluate the use and outcomes of adjuvant radiation therapy (ART) for men with lymph node (LN)-positive disease after radical prostatectomy (RP) using a population-based approach.</li>
</ul></div></div>
<div class="section" id="bju12079-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12079-list-0002" class="bullet">
<li>Surveillance, Epidemiology, and End Results (SEER)-Medicare linked data from 1995 to 2007 was used to identify 577 men with LN metastases discovered during RP and absence of distant metastases, of which 177 underwent ART ≤1 year of RP.</li>
<li>Propensity score models were used to compare overall mortality and prostate cancer-specific mortality (PCSM) for men that did and those that did not receive ART.</li>
</ul></div></div>
<div class="section" id="bju12079-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12079-list-0003" class="bullet">
<li>Men in both groups received adjuvant androgen-deprivation therapy at similar rates after propensity weighting adjustments (33.6% vs 33.7%, P = 0.977).</li>
<li>ART was not associated with differences in overall (5.09 vs 3.77 events per 100 person-years, P = 0.153) or PCSM (2.89 vs 1.31, P = 0.090) relative to men who did not receive ART.</li>
</ul></div></div>
<div class="section" id="bju12079-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12079-list-0004" class="bullet">
<li>ART after RP in men with LN-positive prostate cancer was not associated with improved overall or disease-specific survival, in contrast to previous single-centre studies.</li>
<li>Prospective randomised studies are needed to assess the effectiveness of ART in this patient population.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the use and outcomes of adjuvant radiation therapy (ART) for men with lymph node (LN)-positive disease after radical prostatectomy (RP) using a population-based approach.



Patients and Methods

Surveillance, Epidemiology, and End Results (SEER)-Medicare linked data from 1995 to 2007 was used to identify 577 men with LN metastases discovered during RP and absence of distant metastases, of which 177 underwent ART ≤1 year of RP.
Propensity score models were used to compare overall mortality and prostate cancer-specific mortality (PCSM) for men that did and those that did not receive ART.



Results

Men in both groups received adjuvant androgen-deprivation therapy at similar rates after propensity weighting adjustments (33.6% vs 33.7%, P = 0.977).
ART was not associated with differences in overall (5.09 vs 3.77 events per 100 person-years, P = 0.153) or PCSM (2.89 vs 1.31, P = 0.090) relative to men who did not receive ART.



Conclusions

ART after RP in men with LN-positive prostate cancer was not associated with improved overall or disease-specific survival, in contrast to previous single-centre studies.
Prospective randomised studies are needed to assess the effectiveness of ART in this patient population.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11754.x" xmlns="http://purl.org/rss/1.0/"><title>Bacillus Calmette-Guérin immunotherapy for genitourinary cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11754.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bacillus Calmette-Guérin immunotherapy for genitourinary cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nilay M. Gandhi, Alvaro Morales, Donald L. Lamm</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-20T08:16:07.306375-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11754.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11754.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11754.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11754-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11754-list-5001" class="bullet">
<li>The administration of Bacillus Calmette-Guérin (BCG) immunotherapy has become the standard of care for high-grade non-muscle invasive bladder cancer (NMIBC) and carcinoma in-situ (CIS) in terms of prevention of recurrence and progression. While most agree on a 6 week induction cycle, various maintenance schedules (if any at all) have been implemented without a unifying consensus.</li>
<li>This review assesses the historical emergence of BCG immunotherapy, beginning with its discovery as a vaccinatin for tuberculosis to its effect on the host immune system and potential therapeutic benefits for various oncologic conditions. The data establishing BCG immunotherapy as the standard of care for high-grade NMIBC and CIS over other bladder instillation modalities is presented in addition to the effect maintenance BCG therapy has on sustaining the immuno-protective effect.</li>
</ul></div></div>
<div class="section" id="bju11754-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><ul id="bju11754-list-0001" class="bullet">
<li>Bacillus Calmette-Guérin (BCG) immunotherapy is currently the most effective treatment of non-muscle invasive bladder cancer and one of the most successful applications of immunotherapy to the treatment of cancer.</li>
<li>This review summarises the history and development of BCG as a modern cancer treatment, appraises current optimal application of BCG immunotherapy in bladder cancer, discusses promising new therapies closely related to BCG, and briefly explores the possibility that BCG or related treatments may have an application in other urological malignancies.</li>
<li>BCG is a nonspecific stimulant to the reticuloendothelial system and induces a local inflammatory response with the infiltration of granulocytes followed by macrophages and lymphocytes, particularly helper T cells.</li>
<li>The initial BCG controlled trial showed a statistically significant reduction in tumour recurrence and found the advantage increased with duration of follow-up. Similar results were reported in much higher risk patients in an independent concurrent study. Follow-up suggested that a single 6-week course of intravesical BCG provided long-term protection (up to 10 years) from tumour recurrence and even reduced disease progression.</li>
<li>While induction BCG (six weekly instillations) reduced recurrence, progression and mortality at 10 years, this advantage was lost by 15 years, and patients remained at high risk for progression without the use of maintenance BCG.</li>
<li>In a meta-analysis by the Cochrane group, induction BCG was found to be markedly superior to mitomycin C in high-risk patients but not in low-risk patients. Additionally, the National Comprehensive Cancer Network guidelines lists the use of intravesical BCG as preferred therapy, citing Category 1 data for high-grade Ta, all T1, and any Tis tumours.</li>
<li>Maintenance BCG therapy may be the most important advance in BCG treatment of bladder cancer since the initial introduction. The risk of tumour recurrence and disease progression is life-long in most patients, but the immune stimulation induced by BCG wanes with time.</li>
<li>Logarithmic dose reduction of BCG in patients with increasing side-effects will typically prevent escalation of toxicity.</li>
<li>Simple dose reduction, appropriate antibiotics, and understanding treatment contraindications have greatly increased the safety of BCG. The 3-week maintenance schedule for 3 years has been evaluated in randomised clinical trials and appears to be the current optimal treatment.</li>
<li>With the success achieved in bladder cancer and the relative safety and economy of BCG, consideration should be given to further research for its effectiveness in other genitourinary malignancies.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The administration of Bacillus Calmette-Guérin (BCG) immunotherapy has become the standard of care for high-grade non-muscle invasive bladder cancer (NMIBC) and carcinoma in-situ (CIS) in terms of prevention of recurrence and progression. While most agree on a 6 week induction cycle, various maintenance schedules (if any at all) have been implemented without a unifying consensus.
This review assesses the historical emergence of BCG immunotherapy, beginning with its discovery as a vaccinatin for tuberculosis to its effect on the host immune system and potential therapeutic benefits for various oncologic conditions. The data establishing BCG immunotherapy as the standard of care for high-grade NMIBC and CIS over other bladder instillation modalities is presented in addition to the effect maintenance BCG therapy has on sustaining the immuno-protective effect.


 
Bacillus Calmette-Guérin (BCG) immunotherapy is currently the most effective treatment of non-muscle invasive bladder cancer and one of the most successful applications of immunotherapy to the treatment of cancer.
This review summarises the history and development of BCG as a modern cancer treatment, appraises current optimal application of BCG immunotherapy in bladder cancer, discusses promising new therapies closely related to BCG, and briefly explores the possibility that BCG or related treatments may have an application in other urological malignancies.
BCG is a nonspecific stimulant to the reticuloendothelial system and induces a local inflammatory response with the infiltration of granulocytes followed by macrophages and lymphocytes, particularly helper T cells.
The initial BCG controlled trial showed a statistically significant reduction in tumour recurrence and found the advantage increased with duration of follow-up. Similar results were reported in much higher risk patients in an independent concurrent study. Follow-up suggested that a single 6-week course of intravesical BCG provided long-term protection (up to 10 years) from tumour recurrence and even reduced disease progression.
While induction BCG (six weekly instillations) reduced recurrence, progression and mortality at 10 years, this advantage was lost by 15 years, and patients remained at high risk for progression without the use of maintenance BCG.
In a meta-analysis by the Cochrane group, induction BCG was found to be markedly superior to mitomycin C in high-risk patients but not in low-risk patients. Additionally, the National Comprehensive Cancer Network guidelines lists the use of intravesical BCG as preferred therapy, citing Category 1 data for high-grade Ta, all T1, and any Tis tumours.
Maintenance BCG therapy may be the most important advance in BCG treatment of bladder cancer since the initial introduction. The risk of tumour recurrence and disease progression is life-long in most patients, but the immune stimulation induced by BCG wanes with time.
Logarithmic dose reduction of BCG in patients with increasing side-effects will typically prevent escalation of toxicity.
Simple dose reduction, appropriate antibiotics, and understanding treatment contraindications have greatly increased the safety of BCG. The 3-week maintenance schedule for 3 years has been evaluated in randomised clinical trials and appears to be the current optimal treatment.
With the success achieved in bladder cancer and the relative safety and economy of BCG, consideration should be given to further research for its effectiveness in other genitourinary malignancies.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12066" xmlns="http://purl.org/rss/1.0/"><title>Neutrophil gelatinase-associated lipocalin (NGAL) levels in response to unilateral renal ischaemia in a novel pilot two-kidney porcine model</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12066</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Neutrophil gelatinase-associated lipocalin (NGAL) levels in response to unilateral renal ischaemia in a novel pilot two-kidney porcine model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jonathan L. Silberstein, Preston C. Sprenkle, Daniel Su, Nicholas E. Power, Tatum V. Tarin, Paula Ezell, Daniel D. Sjoberg, Andrew Feifer, Martin Fleisher, Paul Russo, Karim A. Touijer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-19T05:48:10.042071-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12066</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12066</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12066</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12066-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12066-list-0001" class="bullet">
<li>To test a novel porcine two-kidney model for evaluating the effect of controlled acute kidney injury (AKI) related to induced unilateral ischaemia on both renal units (RUs)</li>
<li>To use neutrophil gelatinase-associated lipocalin (NGAL) and physiological serum and urinary markers to assess AKI and renal function.</li>
</ul></div></div>
<div class="section" id="bju12066-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><ul id="bju12066-list-0002" class="bullet">
<li>Twelve female Yorkshire pigs had bilateral cutaneous ureterostomies placed laparoscopically with identical duration of pneumoperitoneum for all cases.</li>
<li>An experimental group (<em>n</em> = 9) underwent induced unilateral renal ischaemia with left hilar clamping of timed duration (15, 30, 60 min) and a control group (<em>n</em> = 3) had no induced renal ischaemia.</li>
<li>Urine was collected and analysed from each RU to assess creatinine and NGAL concentration preoperatively and at multiple postoperative time points. Serum was collected and analysed daily for creatinine and NGAL levels.</li>
<li>Statistical comparisons were made using the rank-sum and sign-rank tests.</li>
</ul></div></div>
<div class="section" id="bju12066-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12066-list-0003" class="bullet">
<li>Three pigs were excluded because of intra-operative and postoperative complications.</li> <li>In the RUs that experienced renal ischaemia (<em>n</em> = 7),the median urine volume was lower (<em>P</em> = 0.04) at 6, 12, 24 and 48 h and the median NGAL concentration was higher (<em>P</em> = 0.04) at 12 and 48 h compared with the RUs of control pigs that experienced no renal ischaemia (<em>n</em> = 2).</li>
<li>When comparing the ischaemic (left) RU of the pigs in the experimental group with their contralateral non-ischaemic (right) RU, ischaemic RUs had a lower median cumulative urine volume at 6, 12, 24 and 48 h (<em>P</em> = 0.05) and a higher median NGAL concentration at 12, 24 and 48 h (<em>P</em> &lt; 0.05).</li> <li>At 48 h, no significant increase was found in serum NGAL in pigs in the experimental group compared with controls (<em>P</em> = 0.2).</li>
<li>Creatinine clearance (CC) was lower in ischaemic RUs compared with non-ischaemic RUs 1 day after surgery (<em>P</em> = 0.04) with decreasing CC as the duration of ischaemia increased.</li>
</ul></div></div>
<div class="section" id="bju12066-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12066-list-0004" class="bullet">
<li>We have developed a promising novel small-scale pilot surgical model that allowed the evaluation of bilateral RU function separately during and after unilateral renal ischaemia.</li>
<li>The induction of unilateral renal ischaemia corresponds with physiological changes in both the ischaemic and contralateral RU.</li>
<li>AKI as measured by increases in NGAL and decreased renal function as measured by decreases in CC, are specific to the RU exposed to ischaemia.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To test a novel porcine two-kidney model for evaluating the effect of controlled acute kidney injury (AKI) related to induced unilateral ischaemia on both renal units (RUs)
To use neutrophil gelatinase-associated lipocalin (NGAL) and physiological serum and urinary markers to assess AKI and renal function.



Methods

Twelve female Yorkshire pigs had bilateral cutaneous ureterostomies placed laparoscopically with identical duration of pneumoperitoneum for all cases.
An experimental group (n = 9) underwent induced unilateral renal ischaemia with left hilar clamping of timed duration (15, 30, 60 min) and a control group (n = 3) had no induced renal ischaemia.
Urine was collected and analysed from each RU to assess creatinine and NGAL concentration preoperatively and at multiple postoperative time points. Serum was collected and analysed daily for creatinine and NGAL levels.
Statistical comparisons were made using the rank-sum and sign-rank tests.



Results

Three pigs were excluded because of intra-operative and postoperative complications. In the RUs that experienced renal ischaemia (n = 7),the median urine volume was lower (P = 0.04) at 6, 12, 24 and 48 h and the median NGAL concentration was higher (P = 0.04) at 12 and 48 h compared with the RUs of control pigs that experienced no renal ischaemia (n = 2).
When comparing the ischaemic (left) RU of the pigs in the experimental group with their contralateral non-ischaemic (right) RU, ischaemic RUs had a lower median cumulative urine volume at 6, 12, 24 and 48 h (P = 0.05) and a higher median NGAL concentration at 12, 24 and 48 h (P &lt; 0.05). At 48 h, no significant increase was found in serum NGAL in pigs in the experimental group compared with controls (P = 0.2).
Creatinine clearance (CC) was lower in ischaemic RUs compared with non-ischaemic RUs 1 day after surgery (P = 0.04) with decreasing CC as the duration of ischaemia increased.



Conclusions

We have developed a promising novel small-scale pilot surgical model that allowed the evaluation of bilateral RU function separately during and after unilateral renal ischaemia.
The induction of unilateral renal ischaemia corresponds with physiological changes in both the ischaemic and contralateral RU.
AKI as measured by increases in NGAL and decreased renal function as measured by decreases in CC, are specific to the RU exposed to ischaemia.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12063" xmlns="http://purl.org/rss/1.0/"><title>Age-stratified outcomes of holmium laser enucleation of the prostate</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12063</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Age-stratified outcomes of holmium laser enucleation of the prostate</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chinedu O. Mmeje, Rafael Nunez-Nateras, Jonathan N. Warner, Mitchell R. Humphreys</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-19T05:32:12.178613-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12063</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12063</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12063</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12063-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12063-list-0001" class="bullet">
<li>To present the first age-stratified assessment of outcomes after holmium laser enucleation of the prostate (HoLEP) for the treatment of lower urinary tract symptoms resulting from prostate enlargement.</li>
</ul></div></div>
<div class="section" id="bju12063-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12063-list-0002" class="bullet">
<li>We retrospectively analysed and compared the morbidity, and the peri-operative and functional outcomes of patients aged 50–59, 60–69, 70–79 and ≥80 years. Complications at 30 days were stratified using the Clavien system.</li>
<li>Functional outcomes were assessed using the International Prostate Symptom Score (IPSS), maximum urinary flow rate (Q<sub>max</sub>), post-void residual urine volume (PVR) and urinary continence.</li>
</ul></div></div>
<div class="section" id="bju12063-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12063-list-0003" class="bullet">
<li>A total of 311 patients underwent HoLEP for obstructive voiding symptoms from August 2007 to June 2011, of whom 22 patients were aged 50–59 years, 91 were aged 60–69 years, 153 were aged 70–79 years, and 45 were aged ≥80 years.</li>
<li>The overall morbidity rates were similar among the age groups (20, 24.4, 21.6 and 22.1% for groups 1, 2, 3 and 4, respectively), as were the incidence of significant complications (Clavien grade ≥ III), change in serum haemoglobin level, and length of hospital stay.</li>
<li>Patients ≥80 years did have a longer catheterization time (3.4 days) than patients aged 50–59 years (1.68 days).</li>
<li>By 1 year there were no significant differences in urinary continence, IPSS, Q<sub>max</sub>, or PVR among the age groups.</li>
</ul></div></div>
<div class="section" id="bju12063-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12063-list-0004" class="bullet">
<li>Overall morbidity, hospital stay, and 1-year functional outcomes of HoLEP were similar among all age groups.</li>
<li>This study shows that HoLEP is a safe and effective treatment for benign prostatic hyperplasia regardless of age.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To present the first age-stratified assessment of outcomes after holmium laser enucleation of the prostate (HoLEP) for the treatment of lower urinary tract symptoms resulting from prostate enlargement.



Patients and Methods

We retrospectively analysed and compared the morbidity, and the peri-operative and functional outcomes of patients aged 50–59, 60–69, 70–79 and ≥80 years. Complications at 30 days were stratified using the Clavien system.
Functional outcomes were assessed using the International Prostate Symptom Score (IPSS), maximum urinary flow rate (Qmax), post-void residual urine volume (PVR) and urinary continence.



Results

A total of 311 patients underwent HoLEP for obstructive voiding symptoms from August 2007 to June 2011, of whom 22 patients were aged 50–59 years, 91 were aged 60–69 years, 153 were aged 70–79 years, and 45 were aged ≥80 years.
The overall morbidity rates were similar among the age groups (20, 24.4, 21.6 and 22.1% for groups 1, 2, 3 and 4, respectively), as were the incidence of significant complications (Clavien grade ≥ III), change in serum haemoglobin level, and length of hospital stay.
Patients ≥80 years did have a longer catheterization time (3.4 days) than patients aged 50–59 years (1.68 days).
By 1 year there were no significant differences in urinary continence, IPSS, Qmax, or PVR among the age groups.



Conclusions

Overall morbidity, hospital stay, and 1-year functional outcomes of HoLEP were similar among all age groups.
This study shows that HoLEP is a safe and effective treatment for benign prostatic hyperplasia regardless of age.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12068" xmlns="http://purl.org/rss/1.0/"><title>Regulatory T cells, interleukin (IL)-6, IL-8, Vascular endothelial growth factor (VEGF), CXCL10, CXCL11, epidermal growth factor (EGF) and hepatocyte growth factor (HGF) as surrogate markers of host immunity in patients with renal cell carcinoma</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12068</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Regulatory T cells, interleukin (IL)-6, IL-8, Vascular endothelial growth factor (VEGF), CXCL10, CXCL11, epidermal growth factor (EGF) and hepatocyte growth factor (HGF) as surrogate markers of host immunity in patients with renal cell carcinoma</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marianeve Polimeno, Maria Napolitano, Susan Costantini, Luigi Portella, Arianna Esposito, Francesca Capone, Eliana Guerriero, AnnaMaria Trotta, Serena Zanotta, Luigi Pucci, Nicola Longo, Sisto Perdonà, Sandro Pignata, Giuseppe Castello, Stefania Scala</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:45:26.019413-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12068</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12068</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12068</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12068-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12068-list-0001" class="bullet">
<li>To identify a phenotype that could be informative and prognostic in patients with renal cell carcinoma (RCC) peripheral blood was evaluated for TH1, TH2, regulatory T cells (Tregs), natural killer (NK) and NKT cells and for cytokines/chemokines.</li>
</ul></div></div>
<div class="section" id="bju12068-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12068-list-0002" class="bullet">
<li>Peripheral blood from 77 patients with RCC and 40 healthy controls was evaluated by flow cytometry using monoclonal antibodies against CD4, CD25, FoxP3, CD45RA, CD45RO, CD152, CD184, CD279, CD3, CD16, CD56, CD161, CD158a, CD4, CD26, CD30, CD183 and CD184.</li>
<li>A concomitant evaluation of 38 molecules was conducted in patients’ serum using a multiplex biometric ELISA-based immunoassay.</li>
</ul></div></div>
<div class="section" id="bju12068-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12068-list-0003" class="bullet">
<li>The number of NK cells CD3<sup>−</sup>/CD16<sup>+</sup>, CD3<sup>−</sup>/CD16<sup>+</sup>/CD161<sup>+</sup> (NK) and CD3<sup>−</sup>/CD16<sup>+</sup>/CD161<sup>+</sup>/CD158a<sup>+</sup> (NK- Kir 2+) was greater in the patients with RCC (<em>P</em> &lt; 0.05); and the number of Treg cells CD4<sup>+</sup>/CD25<sup>high</sup><sup>+</sup>/FOXP3<sup>+</sup> and the subset CD4<sup>+</sup>/CD25<sup>high</sup><sup>+</sup>/FOXP3<sup>+</sup>/CD45RA<sup>+</sup> (naïve) and CD45R0<sup>+</sup>(memory) cells, were greater in the patients with RCC (<em>P</em> &lt; 0.001).</li> <li>An increase in the following was observed in the serum of patients with RCC compared with healthy controls: interleukin (IL)-4, IL-6, IL-8, IL-10, G-CSF, CXCL10, CXCL11, hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF). According to Ingenuity Pathway Analysis (IPA), CXCL10, IL-6, IL-8, epidermal growth factor (EGF), HGF and VEGF were associated with a network that controls cellular movement, tissue development and cellular growth.</li>
<li>Kaplan–Meier analysis for disease-free survival showed that high numbers of CD4<sup>+</sup>/CD25<sup>high</sup><sup>+</sup>/FOXP3<sup>+</sup>/CD45RA<sup>+</sup> (Treg naïve) and low numbers of CD3<sup>−</sup>/CD16<sup>+</sup>/CD161<sup>+</sup>/CD158a<sup>+</sup> (NK-Kir+) cells predict short disease-free survival in patients with RCC.</li>
</ul></div></div>
<div class="section" id="bju12068-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12068-list-0004" class="bullet">
<li>Concomitant evaluation of Treg (CD4<sup>+</sup>/CD25<sup>high</sup><sup>+</sup>/FOXP3<sup>+</sup> and CD4<sup>+</sup>/CD25<sup>high</sup><sup>+</sup>/FOXP3<sup>+</sup>/CD45RA<sup>+</sup>) and of six soluble factors (IL-6, IL-8 ,VEGF, CXCL10, CXCL11, EGF, HGF) might be a surrogate marker of host immunity in patients with RCC.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To identify a phenotype that could be informative and prognostic in patients with renal cell carcinoma (RCC) peripheral blood was evaluated for TH1, TH2, regulatory T cells (Tregs), natural killer (NK) and NKT cells and for cytokines/chemokines.



Patients and Methods

Peripheral blood from 77 patients with RCC and 40 healthy controls was evaluated by flow cytometry using monoclonal antibodies against CD4, CD25, FoxP3, CD45RA, CD45RO, CD152, CD184, CD279, CD3, CD16, CD56, CD161, CD158a, CD4, CD26, CD30, CD183 and CD184.
A concomitant evaluation of 38 molecules was conducted in patients’ serum using a multiplex biometric ELISA-based immunoassay.



Results

The number of NK cells CD3−/CD16+, CD3−/CD16+/CD161+ (NK) and CD3−/CD16+/CD161+/CD158a+ (NK- Kir 2+) was greater in the patients with RCC (P &lt; 0.05); and the number of Treg cells CD4+/CD25high+/FOXP3+ and the subset CD4+/CD25high+/FOXP3+/CD45RA+ (naïve) and CD45R0+(memory) cells, were greater in the patients with RCC (P &lt; 0.001). An increase in the following was observed in the serum of patients with RCC compared with healthy controls: interleukin (IL)-4, IL-6, IL-8, IL-10, G-CSF, CXCL10, CXCL11, hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF). According to Ingenuity Pathway Analysis (IPA), CXCL10, IL-6, IL-8, epidermal growth factor (EGF), HGF and VEGF were associated with a network that controls cellular movement, tissue development and cellular growth.
Kaplan–Meier analysis for disease-free survival showed that high numbers of CD4+/CD25high+/FOXP3+/CD45RA+ (Treg naïve) and low numbers of CD3−/CD16+/CD161+/CD158a+ (NK-Kir+) cells predict short disease-free survival in patients with RCC.



Conclusion

Concomitant evaluation of Treg (CD4+/CD25high+/FOXP3+ and CD4+/CD25high+/FOXP3+/CD45RA+) and of six soluble factors (IL-6, IL-8 ,VEGF, CXCL10, CXCL11, EGF, HGF) might be a surrogate marker of host immunity in patients with RCC.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12067" xmlns="http://purl.org/rss/1.0/"><title>Validation of serum C-reactive protein (CRP) as an independent prognostic factor for disease-free survival in patients with localised renal cell carcinoma (RCC)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12067</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Validation of serum C-reactive protein (CRP) as an independent prognostic factor for disease-free survival in patients with localised renal cell carcinoma (RCC)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michela Martino, Tobias Klatte, Christoph Seemann, Matthias Waldert, Andrea Haitel, Georg Schatzl, Mesut Remzi, Peter Weibl</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:45:17.380042-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12067</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12067</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12067</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12067-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12067-list-0001" class="bullet">
<li>To validate high-sensitivity C-reactive protein (hs-CRP) serum levels as an independent marker for disease-free survival (DFS) in clinically localised clear cell renal cell carcinoma (ccRCC).</li>
</ul></div></div>
<div class="section" id="bju12067-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12067-list-0002" class="bullet">
<li>In all, 403 consecutive patients with clinically localised (T1–3N0M0) ccRCC treated by radical or partial nephrectomy were enrolled.</li>
<li>Preoperative serum levels of hs-CRP were evaluated as both a continuous and categorical variables.</li>
<li>Associations with clinical (age, gender) and pathological variables (T classification, grade, tumour necrosis) were assessed with the chi-square and Kruskal–Wallis tests.</li>
<li>Univariable and multivariable Cox proportional hazards models were fitted. The prognostic accuracy (PA) was assessed with Harrell's C-index.</li>
</ul></div></div>
<div class="section" id="bju12067-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12067-list-0003" class="bullet">
<li>The mean hs-CRP level was 1.32 mg/dL. The hs-CRP levels were associated with T classification (<em>P</em> = 0.05), high-grade disease (P &lt; 0.001) and tumour necrosis (<em>P</em> = 0.003).</li>
<li>After a median follow-up of 43 months, 41 patients (10.1%) had developed disease recurrence. With each unit increase in hs-CRP levels, the risk of recurrence increased by 10% (hazard ratio 1.10, <em>P</em> = 0.015).</li>
<li>The thresholds of 0.5 and 0.75 mg/dL showed the best discrimination for stratification of patients according to the probability of recurrence.</li>
<li>These categorically coded hs-CRP levels were identified as independent prognostic factors in multivariable analyses (<em>P</em> &lt; 0.001) and led to a significant increase in the PA of a multivariable base model containing the variables of the <em>‘Stage, Size, Grade and Necrosis’</em> (SSIGN) score.</li>
</ul></div></div>
<div class="section" id="bju12067-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12067-list-0004" class="bullet">
<li>This study validates preoperative serum hs-CRP levels as independent prognostic factor after surgery for localised ccRCC.</li>
<li>Hs-CRP may be included in standard prognostic modelling after surgery and may guide surveillance and inclusion in adjuvant clinical trials.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To validate high-sensitivity C-reactive protein (hs-CRP) serum levels as an independent marker for disease-free survival (DFS) in clinically localised clear cell renal cell carcinoma (ccRCC).



Patients and Methods

In all, 403 consecutive patients with clinically localised (T1–3N0M0) ccRCC treated by radical or partial nephrectomy were enrolled.
Preoperative serum levels of hs-CRP were evaluated as both a continuous and categorical variables.
Associations with clinical (age, gender) and pathological variables (T classification, grade, tumour necrosis) were assessed with the chi-square and Kruskal–Wallis tests.
Univariable and multivariable Cox proportional hazards models were fitted. The prognostic accuracy (PA) was assessed with Harrell's C-index.



Results

The mean hs-CRP level was 1.32 mg/dL. The hs-CRP levels were associated with T classification (P = 0.05), high-grade disease (P &lt; 0.001) and tumour necrosis (P = 0.003).
After a median follow-up of 43 months, 41 patients (10.1%) had developed disease recurrence. With each unit increase in hs-CRP levels, the risk of recurrence increased by 10% (hazard ratio 1.10, P = 0.015).
The thresholds of 0.5 and 0.75 mg/dL showed the best discrimination for stratification of patients according to the probability of recurrence.
These categorically coded hs-CRP levels were identified as independent prognostic factors in multivariable analyses (P &lt; 0.001) and led to a significant increase in the PA of a multivariable base model containing the variables of the ‘Stage, Size, Grade and Necrosis’ (SSIGN) score.



Conclusions

This study validates preoperative serum hs-CRP levels as independent prognostic factor after surgery for localised ccRCC.
Hs-CRP may be included in standard prognostic modelling after surgery and may guide surveillance and inclusion in adjuvant clinical trials.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12065" xmlns="http://purl.org/rss/1.0/"><title>Survival after radical prostatectomy for clinically localised prostate cancer: a population-based study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12065</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Survival after radical prostatectomy for clinically localised prostate cancer: a population-based study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martin Andreas Røder, Klaus Brasso, Ib Jarle Christensen, Jørgen Johansen, Niels Christian Langkilde, Helle Hvarness, Steen Carlsson, Henrik Jakobsen, Michael Borre, Peter Iversen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:45:07.727526-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12065</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12065</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12065</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12065-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12065-list-0001" class="bullet">
<li>To describe survival and cause of death in a nationwide cohort of Danish patients with prostate cancer undergoing radical prostatectomy (RP).</li>
<li>To describe risk factors associated with prostate cancer mortality.</li>
</ul></div></div>
<div class="section" id="bju12065-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12065-list-0002" class="bullet">
<li>Observational study of 6489 men with localised prostate cancer treated with RP at six different hospitals in Denmark between 1995 and 2011.</li>
<li>Survival was described using Kaplan–Meier estimates. Causes of death were obtained from the national registry and cross-checked with patient files.</li>
<li>Cumulative incidence of death, any cause and prostate cancer-specific, was described using Nelson–Aalen estimates.</li>
<li>Risk for prostate cancer death was analysed in a Cox multivariate regression model using the covariates: age, cT-category, PSA level and biopsy Gleason score.</li>
</ul></div></div>
<div class="section" id="bju12065-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12065-list-0003" class="bullet">
<li>The median follow-up was 4 years. During follow-up, 328 patients died, 109 (33.2%) from prostate cancer and 219 (66.8%) from other causes. Six patients (0.09%) died ≤30 days of RP.</li>
<li>In multivariate analysis, cT-category was a predictor of prostate cancer death (<em>P</em> &lt; 0.001). Compared with T1 disease, both cT2c (hazard ratio [HR] 2.2) and cT3 (HR 7.2) significantly increased the risk of prostate cancer death. For every doubling of PSA level the risk of prostate cancer death was increased by 34.8% (<em>P</em> &lt; 0.001). Biopsy Gleason score 4 + 3 and ≥8 were associated with an increased risk of prostate cancer death compared with biopsy Gleason score ≤ 6 of 2.3 and 2.7 (<em>P</em> = 0.003), respectively.</li>
<li>The cumulative hazard of all-cause and prostate cancer-specific mortality after 10 years was 15.4% (95% confide3nce interval [CI] 13.2–17.7) and 6.6% (95% CI 4.9–8.2) respectively.</li>
</ul></div></div>
<div class="section" id="bju12065-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12065-list-0004" class="bullet">
<li>We present the first survival analysis of a complete, nationwide cohort of men undergoing RP for localised prostate cancer.</li>
<li>The main limitation of the study was the relatively short follow-up.</li>
<li>Interestingly, our national results are comparable to high-volume, single institution, single surgeon series.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To describe survival and cause of death in a nationwide cohort of Danish patients with prostate cancer undergoing radical prostatectomy (RP).
To describe risk factors associated with prostate cancer mortality.



Patients and Methods

Observational study of 6489 men with localised prostate cancer treated with RP at six different hospitals in Denmark between 1995 and 2011.
Survival was described using Kaplan–Meier estimates. Causes of death were obtained from the national registry and cross-checked with patient files.
Cumulative incidence of death, any cause and prostate cancer-specific, was described using Nelson–Aalen estimates.
Risk for prostate cancer death was analysed in a Cox multivariate regression model using the covariates: age, cT-category, PSA level and biopsy Gleason score.



Results

The median follow-up was 4 years. During follow-up, 328 patients died, 109 (33.2%) from prostate cancer and 219 (66.8%) from other causes. Six patients (0.09%) died ≤30 days of RP.
In multivariate analysis, cT-category was a predictor of prostate cancer death (P &lt; 0.001). Compared with T1 disease, both cT2c (hazard ratio [HR] 2.2) and cT3 (HR 7.2) significantly increased the risk of prostate cancer death. For every doubling of PSA level the risk of prostate cancer death was increased by 34.8% (P &lt; 0.001). Biopsy Gleason score 4 + 3 and ≥8 were associated with an increased risk of prostate cancer death compared with biopsy Gleason score ≤ 6 of 2.3 and 2.7 (P = 0.003), respectively.
The cumulative hazard of all-cause and prostate cancer-specific mortality after 10 years was 15.4% (95% confide3nce interval [CI] 13.2–17.7) and 6.6% (95% CI 4.9–8.2) respectively.



Conclusions

We present the first survival analysis of a complete, nationwide cohort of men undergoing RP for localised prostate cancer.
The main limitation of the study was the relatively short follow-up.
Interestingly, our national results are comparable to high-volume, single institution, single surgeon series.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12034" xmlns="http://purl.org/rss/1.0/"><title>Seminal vesicle involvement at salvage radical prostatectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12034</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seminal vesicle involvement at salvage radical prostatectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joshua J. Meeks, Marc Walker, Melanie Bernstein, James A. Eastham</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:45:00.322438-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12034</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12034</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12034</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12034-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12034-list-0001" class="bullet">
<li>To describe the incidence and clinical outcomes of seminal vesicle invasion (SVI) at salvage radical prostatectomy (SRP) and to describe the accuracy of SV biopsy. As SRP is used after biochemical recurrence (BCR) of prostate cancer after radiotherapy (RT) to gain local oncological control. The SVs receive lower doses of radiation from external-beam RT (EBRT) to avoid rectal exposure and are not targeted with brachytherapy (BT) with low-risk prostate cancer.</li>
</ul></div></div>
<div class="section" id="bju12034-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12034-list-0002" class="bullet">
<li>SRP was performed on 206 men with BCR after RT at a tertiary care institution between 1998 and 2011. Post-RT biopsy and SRP specimens were reviewed by a genitourinary pathologist.</li>
</ul></div></div>
<div class="section" id="bju12034-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12034-list-0003" class="bullet">
<li>SVI was detected in 65 (32%) of 206 patients. No difference was found between EBRT alone (65% vs 63%) and BT (29% vs 31%) with or without EBRT in patients with SVI. Men with SVI had higher rates of cT3 disease (20% vs 8%) and Gleason score ≥ 8 at SRP (52% vs 21%).</li>
<li>BCR-free survival at 5 years was 18% and 56% in patients with and without SVI (hazard ratio 2.85, 95% confidence interval 1.87–4.36, <em>P</em> &lt; 0.001), yet the rate of local recurrence was low (11%).</li>
<li>Prostate cancer was identified in nine of 18 patients who underwent SV biopsy and was the only location of prostate cancer in two patients.</li>
</ul></div></div>
<div class="section" id="bju12034-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12034-list-0004" class="bullet">
<li>SVI is a prognostic indicator for BCR after SRP, but local recurrence in patients with SVI after SRP remains low.</li>
<li>We recommend SV biopsy to improve staging and cancer detection in men with BCR after radiotherapy.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To describe the incidence and clinical outcomes of seminal vesicle invasion (SVI) at salvage radical prostatectomy (SRP) and to describe the accuracy of SV biopsy. As SRP is used after biochemical recurrence (BCR) of prostate cancer after radiotherapy (RT) to gain local oncological control. The SVs receive lower doses of radiation from external-beam RT (EBRT) to avoid rectal exposure and are not targeted with brachytherapy (BT) with low-risk prostate cancer.



Patients and Methods

SRP was performed on 206 men with BCR after RT at a tertiary care institution between 1998 and 2011. Post-RT biopsy and SRP specimens were reviewed by a genitourinary pathologist.



Results

SVI was detected in 65 (32%) of 206 patients. No difference was found between EBRT alone (65% vs 63%) and BT (29% vs 31%) with or without EBRT in patients with SVI. Men with SVI had higher rates of cT3 disease (20% vs 8%) and Gleason score ≥ 8 at SRP (52% vs 21%).
BCR-free survival at 5 years was 18% and 56% in patients with and without SVI (hazard ratio 2.85, 95% confidence interval 1.87–4.36, P &lt; 0.001), yet the rate of local recurrence was low (11%).
Prostate cancer was identified in nine of 18 patients who underwent SV biopsy and was the only location of prostate cancer in two patients.



Conclusions

SVI is a prognostic indicator for BCR after SRP, but local recurrence in patients with SVI after SRP remains low.
We recommend SV biopsy to improve staging and cancer detection in men with BCR after radiotherapy.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12030" xmlns="http://purl.org/rss/1.0/"><title>Transurethral resection of the prostate in kidney transplant recipients: urological and renal functional outcomes at long-term follow-up</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12030</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Transurethral resection of the prostate in kidney transplant recipients: urological and renal functional outcomes at long-term follow-up</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alessandro Volpe, Michele Billia, Marco Quaglia, Matteo Vidali, Giansilvo Marchioro, Giovanni Ceratti, Filippo Sogni, Elisa De Lorenzis, Paolo De Angelis, Andrea Airoldi, Piero Stratta, Carlo Terrone</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:44:55.606791-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12030</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12030</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12030</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12030-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12030-list-0001" class="bullet">
<li>To assess prospectively the safety and efficacy of transurethral resection of the prostate (TURP) for the treatment of lower urinary tract symptoms attributable to benign prostatic hyperplasia (BPH) in patients who have undergone renal transplantation (RT).</li>
<li>To assess the impact of TURP on renal graft function.</li>
</ul></div></div>
<div class="section" id="bju12030-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12030-list-0002" class="bullet">
<li>Urological and renal functional outcomes of TURP performed in RT recipients for treatment of lower urinary tract obstruction attributable to BPH were prospectively assessed in a series of 32 consecutive patients with follow-up of ≥48 months.</li>
<li>Maximum urinary flow rate (Q<sub>max</sub>) at uroflowmetry, International Prostate Symptom Score (IPSS), post-void residual urine volume (PVR), haemoglobin and serum creatinine (sCr) levels were recorded before TURP and 1, 6, 24 and 48 months after the procedure. The trends in these variables after TURP were evaluated.</li>
<li>Early and delayed complications were assessed and graded according to the Clavien classification system.</li>
</ul></div></div>
<div class="section" id="bju12030-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12030-list-0003" class="bullet">
<li>TURP was performed at a mean of 6 months after RT.</li>
<li>No intraoperative complications occurred. Seven postoperative complications were observed (21.9%): two Clavien grade II and five Clavien grade IIIa.</li>
<li>Q<sub>max</sub>, IPSS and PVR improved significantly after surgery and the improvement was maintained until 48 months. No patient required a repeat TURP during follow-up.</li>
<li>SCr levels significantly decreased 1 and 6 months after TURP and did not significantly increase at long-term follow-up.</li>
</ul></div></div>
<div class="section" id="bju12030-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12030-list-0004" class="bullet">
<li>TURP for lower urinary tract obstruction attributable to BPH in RT recipients is safe and effective since it improves urinary flow, bladder emptying and related urinary symptoms.</li>
<li>TURP allows an early significant improvement of graft function that is maintained at a follow-up of 48 months.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To assess prospectively the safety and efficacy of transurethral resection of the prostate (TURP) for the treatment of lower urinary tract symptoms attributable to benign prostatic hyperplasia (BPH) in patients who have undergone renal transplantation (RT).
To assess the impact of TURP on renal graft function.



Patients and Methods

Urological and renal functional outcomes of TURP performed in RT recipients for treatment of lower urinary tract obstruction attributable to BPH were prospectively assessed in a series of 32 consecutive patients with follow-up of ≥48 months.
Maximum urinary flow rate (Qmax) at uroflowmetry, International Prostate Symptom Score (IPSS), post-void residual urine volume (PVR), haemoglobin and serum creatinine (sCr) levels were recorded before TURP and 1, 6, 24 and 48 months after the procedure. The trends in these variables after TURP were evaluated.
Early and delayed complications were assessed and graded according to the Clavien classification system.



Results

TURP was performed at a mean of 6 months after RT.
No intraoperative complications occurred. Seven postoperative complications were observed (21.9%): two Clavien grade II and five Clavien grade IIIa.
Qmax, IPSS and PVR improved significantly after surgery and the improvement was maintained until 48 months. No patient required a repeat TURP during follow-up.
SCr levels significantly decreased 1 and 6 months after TURP and did not significantly increase at long-term follow-up.



Conclusions

TURP for lower urinary tract obstruction attributable to BPH in RT recipients is safe and effective since it improves urinary flow, bladder emptying and related urinary symptoms.
TURP allows an early significant improvement of graft function that is maintained at a follow-up of 48 months.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11599.x" xmlns="http://purl.org/rss/1.0/"><title>Novel prototype sewing device, EndoSew®, for minimally invasive surgery: an extracorporeal ileal conduit construction pilot study in 10 patients</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11599.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Novel prototype sewing device, EndoSew®, for minimally invasive surgery: an extracorporeal ileal conduit construction pilot study in 10 patients</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Beat Roth, Frédéric D. Birkhäuser, George N. Thalmann, Pascal Zehnder</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T08:44:52.965214-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11599.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11599.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11599.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Step-by-Step</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11599-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11599-list-1001" class="bullet">
<li>The EndoSew<sup>®</sup> prototype was first tested in a porcine model several years ago. The investigators found it both simple to master and reliable, its greatest advantage being a 2.4-fold time saving compared with straight laparoscopic suturing. In addition to that publication, there is a single case report describing the performance of an open EndoSew<sup>®</sup> suture to close parts (16 cm) of an ileal neobladder. The time for suturing the 16 cm ileum was 25 min, which is in line with our experience. The knowledge on this subject is limited to these two publications.</li>
<li>We report on the first consecutive series of ileal conduits performed in humans using the novel prototype sewing device EndoSew<sup>®</sup>. The study shows that the beginning and the end of the suture process represent the critical procedural steps. It also shows that, overall, the prototype sewing machine has the potential to facilitate the intracorporeal suturing required in reconstructive urology for construction of urinary diversions.</li>
</ul></div></div>
<div class="section" id="bju11599-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11599-list-0001" class="bullet">
<li>To evaluate the feasibility and safety of the novel prototype sewing device EndoSew<sup>®</sup> in placing an extracorporeal resorbable running suture for ileal conduits.</li>
</ul></div></div>
<div class="section" id="bju11599-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11599-list-0002" class="bullet">
<li>We conducted a prospective single-centre pilot study of 10 consecutive patients undergoing ileal conduit, in whom the proximal end of the ileal conduit was closed extracorporeally using an EndoSew<sup>®</sup> running suture.</li>
<li>The primary endpoint was the safety of the device and the feasibility of the sewing procedure which was defined as a complete watertight running suture line accomplished by EndoSew<sup>®</sup> only<em>.</em> Watertightness was assessed using methylene blue intraoperatively and by loopography on postoperative days 7 and 14.</li>
<li>Secondary endpoints were the time requirements and complications ≤30 days after surgery.</li>
</ul></div></div>
<div class="section" id="bju11599-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11599-list-0003" class="bullet">
<li>A complete EndoSew<sup>®</sup> running suture was feasible in nine patients; the suture had to be abandoned in one patient because of mechanical failure.</li> <li>In three patients, two additional single freehand stitches were needed to anchor the thread and to seal tiny leaks. Consequently, all suture lines in 6/10 patients were watertight with EndoSew<sup>®</sup> suturing alone and in 10/10 patients after additional freehand stitches.</li>
<li>The median (range) sewing time was 5.5 (3–10) min and the median (range) suture length was 4.5 (2–5.5) cm.</li>
<li>There were no suture-related complications.</li>
</ul></div></div>
<div class="section" id="bju11599-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11599-list-0004" class="bullet">
<li>The EndoSew<sup>®</sup> procedure is both feasible and safe.</li>
<li>After additional freehand stitches in four patients all sutures were watertight.</li>
<li>With further technical refinements, EndoSew<sup>®</sup> has the potential to facilitate the intracorporeal construction of urinary diversions.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The EndoSew® prototype was first tested in a porcine model several years ago. The investigators found it both simple to master and reliable, its greatest advantage being a 2.4-fold time saving compared with straight laparoscopic suturing. In addition to that publication, there is a single case report describing the performance of an open EndoSew® suture to close parts (16 cm) of an ileal neobladder. The time for suturing the 16 cm ileum was 25 min, which is in line with our experience. The knowledge on this subject is limited to these two publications.
We report on the first consecutive series of ileal conduits performed in humans using the novel prototype sewing device EndoSew®. The study shows that the beginning and the end of the suture process represent the critical procedural steps. It also shows that, overall, the prototype sewing machine has the potential to facilitate the intracorporeal suturing required in reconstructive urology for construction of urinary diversions.


 Objective

To evaluate the feasibility and safety of the novel prototype sewing device EndoSew® in placing an extracorporeal resorbable running suture for ileal conduits.



Patients and Methods

We conducted a prospective single-centre pilot study of 10 consecutive patients undergoing ileal conduit, in whom the proximal end of the ileal conduit was closed extracorporeally using an EndoSew® running suture.
The primary endpoint was the safety of the device and the feasibility of the sewing procedure which was defined as a complete watertight running suture line accomplished by EndoSew® only. Watertightness was assessed using methylene blue intraoperatively and by loopography on postoperative days 7 and 14.
Secondary endpoints were the time requirements and complications ≤30 days after surgery.



Results

A complete EndoSew® running suture was feasible in nine patients; the suture had to be abandoned in one patient because of mechanical failure. In three patients, two additional single freehand stitches were needed to anchor the thread and to seal tiny leaks. Consequently, all suture lines in 6/10 patients were watertight with EndoSew® suturing alone and in 10/10 patients after additional freehand stitches.
The median (range) sewing time was 5.5 (3–10) min and the median (range) suture length was 4.5 (2–5.5) cm.
There were no suture-related complications.



Conclusions

The EndoSew® procedure is both feasible and safe.
After additional freehand stitches in four patients all sutures were watertight.
With further technical refinements, EndoSew® has the potential to facilitate the intracorporeal construction of urinary diversions.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11640.x" xmlns="http://purl.org/rss/1.0/"><title>Reporting positive surgical margins after radical prostatectomy: time for standardization</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11640.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reporting positive surgical margins after radical prostatectomy: time for standardization</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philip A. Fontenot, Ahmed M. Mansour</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-14T06:50:00.489135-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11640.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11640.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11640.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11640-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11640-list-1001" class="bullet">
<li>It is known that positive surgical margins (PSMs) after radical prostatectomy (RP) in patients with prostate cancer are a significant predictor of biochemical recurrence (BCR). Furthermore, no general consensus exists in the literature on how specific PSM-associated prognostic variables, namely, location, focality, length, uniformity of specimen and Gleason score at the margin, influence BCR or assist in clinical decision-making.</li>
<li>The study shows the inconsistencies in the reporting of PSMs and PSM-associated prognostic variables in the current literature and suggests the implementation of a novel scoring system, the F.U.S.E. score, which quantifies the anatomical and pathological variables associated with PSMs and represents a standardized methodology for reporting PSMs in the literature.</li>
</ul></div></div>
<div class="section" id="bju11640-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11640-list-0001" class="bullet">
<li>To assess the consistency of reporting on positive surgical margins (PSMs) and associated prognostic variables after radical prostatectomy (RP) in the current literature</li>
<li>To provide a standardized methodology for quantifying the characteristics and the prognostic impact of PSMs after RP.</li>
</ul></div></div>
<div class="section" id="bju11640-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11640-list-0002" class="bullet">
<li>We conducted a review of articles that assessed the prognostic value of characteristics of PSMs after RP. The articles were identified using a MEDLINE search.</li>
<li>The methodology and quality of the reporting of PSMs were analysed according to six criteria defined according to the guidelines of the College of American Pathologists and the International Society of Uropathologists.</li>
<li>Forty-four studies, involving ≥100 patients and published from January 2005 to the present, were reviewed.</li>
</ul></div></div>
<div class="section" id="bju11640-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11640-list-0003" class="bullet">
<li>Each of the 44 studies was assessed for their reporting of the six defined PSM criteria, as well as for the significance of PSM characteristics on biochemical recurrence (BCR).</li>
<li>The definition of a PSM was the only criterion that was consistently reported.</li>
<li>All studies were deficient in defining and reporting one or more of the PSM criteria. Major inconsistencies were observed in the reporting of PSM site and length, and the presence of intraprostatic incision.</li>
<li>The many conflicting reports gave little insight into the true significance of particular PSM-associated variables on BCR.</li>
</ul></div></div>
<div class="section" id="bju11640-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11640-list-0004" class="bullet">
<li>There is a lack of consistency in the reporting on and prognostic significance of PSMs and PSM-associated prognostic variables.</li>
<li>We hypothesize that these conflicting results are partly attributable to a lack of use of a standardized reporting methodology for PSMs. Implementation of a previously reported standardized scoring system for PSMs may help eliminate these inconsistencies in the future.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

It is known that positive surgical margins (PSMs) after radical prostatectomy (RP) in patients with prostate cancer are a significant predictor of biochemical recurrence (BCR). Furthermore, no general consensus exists in the literature on how specific PSM-associated prognostic variables, namely, location, focality, length, uniformity of specimen and Gleason score at the margin, influence BCR or assist in clinical decision-making.
The study shows the inconsistencies in the reporting of PSMs and PSM-associated prognostic variables in the current literature and suggests the implementation of a novel scoring system, the F.U.S.E. score, which quantifies the anatomical and pathological variables associated with PSMs and represents a standardized methodology for reporting PSMs in the literature.


 Objectives

To assess the consistency of reporting on positive surgical margins (PSMs) and associated prognostic variables after radical prostatectomy (RP) in the current literature
To provide a standardized methodology for quantifying the characteristics and the prognostic impact of PSMs after RP.



Patients and Methods

We conducted a review of articles that assessed the prognostic value of characteristics of PSMs after RP. The articles were identified using a MEDLINE search.
The methodology and quality of the reporting of PSMs were analysed according to six criteria defined according to the guidelines of the College of American Pathologists and the International Society of Uropathologists.
Forty-four studies, involving ≥100 patients and published from January 2005 to the present, were reviewed.



Results

Each of the 44 studies was assessed for their reporting of the six defined PSM criteria, as well as for the significance of PSM characteristics on biochemical recurrence (BCR).
The definition of a PSM was the only criterion that was consistently reported.
All studies were deficient in defining and reporting one or more of the PSM criteria. Major inconsistencies were observed in the reporting of PSM site and length, and the presence of intraprostatic incision.
The many conflicting reports gave little insight into the true significance of particular PSM-associated variables on BCR.



Conclusions

There is a lack of consistency in the reporting on and prognostic significance of PSMs and PSM-associated prognostic variables.
We hypothesize that these conflicting results are partly attributable to a lack of use of a standardized reporting methodology for PSMs. Implementation of a previously reported standardized scoring system for PSMs may help eliminate these inconsistencies in the future.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12062" xmlns="http://purl.org/rss/1.0/"><title>Complementary and alternative medicine (CAM) in prostate and bladder cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12062</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Complementary and alternative medicine (CAM) in prostate and bladder cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yiannis Philippou, Marios Hadjipavlou, Shahid Khan, Abhay Rane</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-13T06:32:49.441444-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12062</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12062</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12062</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12062-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>To provide an overview of the scientific and clinical studies underlying the most common vitamin and herbal preparations used in prostate and bladder cancer and evaluate the evidence behind them. A literature search was undertaken on PubMed using various keywords relating to the use of complementary and alternative medicine (CAM) in prostate and bladder cancer. Vitamin E and selenium supplementation can potentially have adverse effects by increasing the risk of prostate cancer. Initial clinical studies of pomegranate and green tea, investigating their chemotherapeutic properties in prostate and bladder cancer have yielded encouraging results. Curcumin, resveratrol, and silibinin have potential anticancer properties through multiple molecular targets; their clinical effectiveness in prostate and bladder cancer is yet to be evaluated. Zyflamend, like PC-SPES, is a combined CAM therapy used in prostate cancer. Acupuncture is popular among patients experiencing hot flushes who are receiving androgen-deprivation therapy for prostate cancer. Conclusive evidence for the use of CAM in prostate and bladder cancer is lacking and not without risk.</p></div></div>
]]></content:encoded><description>
 To provide an overview of the scientific and clinical studies underlying the most common vitamin and herbal preparations used in prostate and bladder cancer and evaluate the evidence behind them. A literature search was undertaken on PubMed using various keywords relating to the use of complementary and alternative medicine (CAM) in prostate and bladder cancer. Vitamin E and selenium supplementation can potentially have adverse effects by increasing the risk of prostate cancer. Initial clinical studies of pomegranate and green tea, investigating their chemotherapeutic properties in prostate and bladder cancer have yielded encouraging results. Curcumin, resveratrol, and silibinin have potential anticancer properties through multiple molecular targets; their clinical effectiveness in prostate and bladder cancer is yet to be evaluated. Zyflamend, like PC-SPES, is a combined CAM therapy used in prostate cancer. Acupuncture is popular among patients experiencing hot flushes who are receiving androgen-deprivation therapy for prostate cancer. Conclusive evidence for the use of CAM in prostate and bladder cancer is lacking and not without risk.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12015" xmlns="http://purl.org/rss/1.0/"><title>Accuracy of post-radiotherapy biopsy before salvage radical prostatectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12015</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Accuracy of post-radiotherapy biopsy before salvage radical prostatectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joshua J. Meeks, Marc Walker, Melanie Bernstein, Matthew Kent, James A. Eastham</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-13T06:32:36.292369-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12015</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12015</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12015</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12015-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12015-list-0001" class="bullet">
<li>To determine whether post-radiotherapy (RT) biopsy (PRB) adequately predicts the presence, location, and histological features of cancer in the salvage radical prostatectomy (SRP) specimen. Before salvage treatment, a PRB is required to confirm the presence of locally recurrent or persistent cancer and to determine the extent and location of the prostate cancer.</li>
</ul></div></div>
<div class="section" id="bju12015-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12015-list-0002" class="bullet">
<li>SRP was performed between 1998 and 2011 on 198 patients.</li>
<li>All patients underwent a PRB. PRB and SRP specimens were evaluated by a genitourinary pathologist. Patients had external-beam RT alone (EBRT; 71%) or brachytherapy with or without EBRT (29%).</li>
</ul></div></div>
<div class="section" id="bju12015-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12015-list-0003" class="bullet">
<li>Of the men undergoing SRP, 26 (14%) were clinical stage ≥T3, with 13% of PRBs with Gleason score ≥8.</li>
<li>Cancer was unilateral in 120 (61%) biopsies, with contralateral or bilateral prostate cancer at SRP in 49%. In the SRP specimen, cancer was multifocal in 57%.</li>
<li>Cancer was upgraded at SRP in 58% of men, with 20% having an increase in primary Gleason grade.</li>
<li>The accuracy of PRB varied by region from 62% to 76%, with undetected cancers ranging from 12% to 26% and most likely to occur at the mid-gland.</li>
</ul></div></div>
<div class="section" id="bju12015-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12015-list-0004" class="bullet">
<li>Radiation-recurrent prostate cancers were often multifocal, and biopsy missed up to 20% of tumours.</li>
<li>More than half of the cancers were upgraded at SRP, and many that were unilateral on PRB were bilateral at SRP.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To determine whether post-radiotherapy (RT) biopsy (PRB) adequately predicts the presence, location, and histological features of cancer in the salvage radical prostatectomy (SRP) specimen. Before salvage treatment, a PRB is required to confirm the presence of locally recurrent or persistent cancer and to determine the extent and location of the prostate cancer.



Patients and Methods

SRP was performed between 1998 and 2011 on 198 patients.
All patients underwent a PRB. PRB and SRP specimens were evaluated by a genitourinary pathologist. Patients had external-beam RT alone (EBRT; 71%) or brachytherapy with or without EBRT (29%).



Results

Of the men undergoing SRP, 26 (14%) were clinical stage ≥T3, with 13% of PRBs with Gleason score ≥8.
Cancer was unilateral in 120 (61%) biopsies, with contralateral or bilateral prostate cancer at SRP in 49%. In the SRP specimen, cancer was multifocal in 57%.
Cancer was upgraded at SRP in 58% of men, with 20% having an increase in primary Gleason grade.
The accuracy of PRB varied by region from 62% to 76%, with undetected cancers ranging from 12% to 26% and most likely to occur at the mid-gland.



Conclusions

Radiation-recurrent prostate cancers were often multifocal, and biopsy missed up to 20% of tumours.
More than half of the cancers were upgraded at SRP, and many that were unilateral on PRB were bilateral at SRP.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12009" xmlns="http://purl.org/rss/1.0/"><title>Zip-related genital injury</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Zip-related genital injury</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Herman S. Bagga, Gregory E. Tasian, James McGeady, Sarah D. Blaschko, Charles E. McCulloch, Jack W. McAninch, Benjamin N. Breyer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-13T06:31:21.22068-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12009</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12009</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12009-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12009-list-0001" class="bullet">
<li>To describe the epidemiology of genital injuries caused by trouser zips and to educate both consumers and the caregivers of patients who sustain such injuries.</li>
</ul></div></div>
<div class="section" id="bju12009-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12009-list-0002" class="bullet">
<li>The National Electronic Injury Surveillance System, a dataset validated to provide a probability sample of patients who present to emergency departments (EDs) in the USA with injuries, was analysed to characterize zip-related genital injuries occurring between 2002 and 2010.</li>
<li>A total of 523 cases were analysed to obtain national estimates.</li>
</ul></div></div>
<div class="section" id="bju12009-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12009-list-0003" class="bullet">
<li>Between 2002 and 2010, an estimated 17 616 patients presented to US EDs with trouser zip injuries to the genitals.</li> <li>The penis was almost always the only genital organ involved.</li>
<li>Zip injuries represented nearly one-fifth of all penile injuries.</li>
<li>Amongst adults, zips were the most frequent cause of penile injuries.</li>
<li>Annual zip-related genital injury incidence remained stable over the study period.</li>
</ul></div></div>
<div class="section" id="bju12009-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12009-list-0004" class="bullet">
<li>Zip-related genital injuries affect both paediatric and adult cohorts.</li>
<li>Practitioners should be familiar with various zip-detachment strategies for these populations.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To describe the epidemiology of genital injuries caused by trouser zips and to educate both consumers and the caregivers of patients who sustain such injuries.



Patients and Methods

The National Electronic Injury Surveillance System, a dataset validated to provide a probability sample of patients who present to emergency departments (EDs) in the USA with injuries, was analysed to characterize zip-related genital injuries occurring between 2002 and 2010.
A total of 523 cases were analysed to obtain national estimates.



Results

Between 2002 and 2010, an estimated 17 616 patients presented to US EDs with trouser zip injuries to the genitals. The penis was almost always the only genital organ involved.
Zip injuries represented nearly one-fifth of all penile injuries.
Amongst adults, zips were the most frequent cause of penile injuries.
Annual zip-related genital injury incidence remained stable over the study period.



Conclusions

Zip-related genital injuries affect both paediatric and adult cohorts.
Practitioners should be familiar with various zip-detachment strategies for these populations.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12028" xmlns="http://purl.org/rss/1.0/"><title>Botulinum toxin type A for the treatment of non-neurogenic overactive bladder: does using onabotulinumtoxinA (Botox®) or abobotulinumtoxinA (Dysport®) make a difference?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12028</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Botulinum toxin type A for the treatment of non-neurogenic overactive bladder: does using onabotulinumtoxinA (Botox®) or abobotulinumtoxinA (Dysport®) make a difference?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pravisha Ravindra, Benjamin L. Jackson, Richard J. Parkinson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-12T08:02:59.704772-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12028</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12028</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12028</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12028-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12028-list-0001" class="bullet">
<li>To compare the clinical effects of two different commercially available botulinum toxin type A products, onabotulinumtoxinA (Botox<sup>®</sup>; Allergan Inc., Irvine, CA, USA) and abobotulinumtoxinA (Dysport<sup>®</sup>; Ipsen Ltd, Slough, UK), on non-neurogenic overactive bladder (OAB).</li>
</ul></div></div>
<div class="section" id="bju12028-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12028-list-0002" class="bullet">
<li>We included 207 patients, who underwent treatment with botulinum toxin type A for non-neurogenic OAB from January 2009 to June 2012 at our institution, in a prospective database that recorded details of their presentation, treatment and outcomes.</li>
<li>In December 2009, our institution switched from using onabotulinumtoxinA to using abobotulinumtoxinA.</li>
</ul></div></div>
<div class="section" id="bju12028-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12028-list-0003" class="bullet">
<li>Results from the onabotulinumtoxinA cohort (n = 101) and the abobotulinumtoxinA cohort (n = 106) were compared.</li>
<li>Similar reductions in daytime frequency, nocturia and incontinence episodes were observed after treatment, with no difference in duration of effect.</li>
<li>The abobotulinumtoxinA cohort had almost twice the rate of symptomatic urinary retention (23 vs 42%) requiring intermittent self-catheterisation (ISC).</li>
</ul></div></div>
<div class="section" id="bju12028-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12028-list-0004" class="bullet">
<li>AbobotulinumtoxinA use was complicated by a significantly higher risk of requiring ISC.</li>
<li>The study suggests that these two toxins are not interchangeable at the doses used.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To compare the clinical effects of two different commercially available botulinum toxin type A products, onabotulinumtoxinA (Botox®; Allergan Inc., Irvine, CA, USA) and abobotulinumtoxinA (Dysport®; Ipsen Ltd, Slough, UK), on non-neurogenic overactive bladder (OAB).



Patients and Methods

We included 207 patients, who underwent treatment with botulinum toxin type A for non-neurogenic OAB from January 2009 to June 2012 at our institution, in a prospective database that recorded details of their presentation, treatment and outcomes.
In December 2009, our institution switched from using onabotulinumtoxinA to using abobotulinumtoxinA.



Results

Results from the onabotulinumtoxinA cohort (n = 101) and the abobotulinumtoxinA cohort (n = 106) were compared.
Similar reductions in daytime frequency, nocturia and incontinence episodes were observed after treatment, with no difference in duration of effect.
The abobotulinumtoxinA cohort had almost twice the rate of symptomatic urinary retention (23 vs 42%) requiring intermittent self-catheterisation (ISC).



Conclusions

AbobotulinumtoxinA use was complicated by a significantly higher risk of requiring ISC.
The study suggests that these two toxins are not interchangeable at the doses used.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12024" xmlns="http://purl.org/rss/1.0/"><title>Can transrectal needle biopsy be optimised to detect nearly all prostate cancer with a volume of ≥0.5 mL? A three-dimensional analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12024</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Can transrectal needle biopsy be optimised to detect nearly all prostate cancer with a volume of ≥0.5 mL? A three-dimensional analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kent Kanao, James A. Eastham, Peter T. Scardino, Victor E. Reuter, Samson W. Fine</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-12T08:02:54.489312-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12024</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12024</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12024</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12024-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12024-list-0001" class="bullet">
<li>To investigate whether transrectal needle biopsy can be optimised to detect nearly all prostate cancer with a tumour volume (TV) of ≥0.5 mL.</li>
</ul></div></div>
<div class="section" id="bju12024-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12024-list-0002" class="bullet">
<li>Retrospectively analysed 109 whole-mounted and entirely submitted radical prostatectomy specimens with prostate cancer.</li>
<li>All tumours in each prostate were outlined on whole-mount slides and digitally scanned to produce tumour maps. Tumour map images were exported to three-dimensional (3D) slicer software (<!--TODO: clickthrough URL--><a href="http://www.slicer.org" title="Link to external resource: http://www.slicer.org">http://www.slicer.org</a>) to develop a 3D-prostate cancer model.</li>
<li>In all, 20 transrectal biopsy schemes involving two to 40 cores and two to six anteriorly directed biopsy (ADBx) cores (including transition zone, TZ) were simulated, as well as models with various biopsy cutting lengths.</li>
<li>Detection rates for tumours of different volumes were determined for the various biopsy simulation schemes.</li>
</ul></div></div>
<div class="section" id="bju12024-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12024-list-0003" class="bullet">
<li>In 109 prostates, 800 tumours were detected, 90 with a TV of ≥0.5 mL (mean TV 0.24 mL).</li>
<li>Detection rate for tumours with a TV of ≥0.5 mL plateaued at 77% (69/90) using a 12-core (3 × 4) scheme, standard 17-mm biopsy cutting length without ADBx cores. In all, 20 of 21 (95%) tumours with a TV of ≥0.5 mL not detected by this scheme originated in the anterior peripheral zone or TZ.</li>
<li>Increasing the biopsy cutting length and depth/number of ADBx cores improved the detection rate for tumours with a TVof ≥0.5 mL in the 12-core scheme.</li>
<li>Using a 22-mm cutting length and a 12-core scheme with additional volume-adjusted ADBx cores, 100% of ≥0.5 mL tumours in prostates ≤ 50 mL in volume and 94.7% of ≥0.5 mL tumours in prostates &gt; 50 mL in volume were detected.</li>
</ul></div></div>
<div class="section" id="bju12024-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12024-list-0004" class="bullet">
<li>Our 3D-prostate cancer model analysis suggests that nearly all prostate cancers with a TV of ≥0.5 mL can be detected by 14–18 transrectal needle-biopsy cores.</li>
<li>Using longer biopsy cutting lengths and increasing the depth and number of ADBx cores (including TZ) according to prostate volume are necessary as well.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To investigate whether transrectal needle biopsy can be optimised to detect nearly all prostate cancer with a tumour volume (TV) of ≥0.5 mL.



Materials and Methods

Retrospectively analysed 109 whole-mounted and entirely submitted radical prostatectomy specimens with prostate cancer.
All tumours in each prostate were outlined on whole-mount slides and digitally scanned to produce tumour maps. Tumour map images were exported to three-dimensional (3D) slicer software (http://www.slicer.org) to develop a 3D-prostate cancer model.
In all, 20 transrectal biopsy schemes involving two to 40 cores and two to six anteriorly directed biopsy (ADBx) cores (including transition zone, TZ) were simulated, as well as models with various biopsy cutting lengths.
Detection rates for tumours of different volumes were determined for the various biopsy simulation schemes.



Results

In 109 prostates, 800 tumours were detected, 90 with a TV of ≥0.5 mL (mean TV 0.24 mL).
Detection rate for tumours with a TV of ≥0.5 mL plateaued at 77% (69/90) using a 12-core (3 × 4) scheme, standard 17-mm biopsy cutting length without ADBx cores. In all, 20 of 21 (95%) tumours with a TV of ≥0.5 mL not detected by this scheme originated in the anterior peripheral zone or TZ.
Increasing the biopsy cutting length and depth/number of ADBx cores improved the detection rate for tumours with a TVof ≥0.5 mL in the 12-core scheme.
Using a 22-mm cutting length and a 12-core scheme with additional volume-adjusted ADBx cores, 100% of ≥0.5 mL tumours in prostates ≤ 50 mL in volume and 94.7% of ≥0.5 mL tumours in prostates &gt; 50 mL in volume were detected.



Conclusions

Our 3D-prostate cancer model analysis suggests that nearly all prostate cancers with a TV of ≥0.5 mL can be detected by 14–18 transrectal needle-biopsy cores.
Using longer biopsy cutting lengths and increasing the depth and number of ADBx cores (including TZ) according to prostate volume are necessary as well.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11693.x" xmlns="http://purl.org/rss/1.0/"><title>Extent of lymphadenectomy does not improve the survival of patients with renal cell carcinoma and nodal metastases: biases associated with the handling of missing data</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11693.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Extent of lymphadenectomy does not improve the survival of patients with renal cell carcinoma and nodal metastases: biases associated with the handling of missing data</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maxine Sun, Quoc-Dien Trinh, Marco Bianchi, Jens Hansen, Firas Abdollah, Zhe Tian, Shahrokh F. Shariat, Francesco Montorsi, Paul Perrotte, Pierre I. Karakiewicz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-12T08:02:31.680207-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11693.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11693.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11693.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju90013-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11693-list-0001" class="bullet">
<li>A recent population-based analysis suggested a potential survival benefit with respect to performing lymph node dissection at nephrectomy in node-positive patients with RCC.</li>
<li>The findings of the present study failed to corroborate the association of a survival benefit with the performance of lymph node dissection at nephrectomy.</li>
</ul></div></div>
<div class="section" id="bju90013-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11693-list-0002" class="bullet">
<li>Previous studies showed no survival benefit with respect to performing lymph node dissection (LND) at nephrectomy, whereas a recent population-based analysis suggested otherwise, although the latter relied on imputation. To reconcile the findings of that study by critically evaluating the handling of missing data.</li>
</ul></div></div>
<div class="section" id="bju90013-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11693-list-0003" class="bullet">
<li>Study participants comprised patients diagnosed with non-metastatic renal cell carcinoma (RCC) of all stages who underwent LND at nephrectomy (<em>n</em> = 10 596).</li>
<li>Multivariable Cox regression models were performed to predict cancer-specific mortality (CSM), where the primary variable of interest was the extent of LND.</li>
<li>To examine differences in approaches with respect to handling missing data, separate analyses were performed: (i) imputed population; (ii) exclusion of patients with missing data; and (iii) inclusion of patients with missing data as a sub-category.</li>
</ul></div></div>
<div class="section" id="bju90013-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11693-list-0004" class="bullet">
<li>Overall, 2916 (28%) patients had missing tumour grade.</li>
<li>In multivariable analyses, our findings showed that increasing the extent of LND was associated with a significant protective effect on CSM in patients with pN1 after imputation (hazard ratio [HR], 0.82; <em>P</em> = 0.04).</li>
<li>By contrast, the extent of LND was no longer significantly associated with a lower risk of CSM after excluding patients with a missing tumour grade (HR, 0.83; <em>P</em> = 0.1) or when including patients with missing tumour grade as a sub-category (HR, 0.82; <em>P</em> = 0.05).</li>
</ul></div></div>
<div class="section" id="bju90013-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11693-list-0005" class="bullet">
<li>The findings of the present study failed to corroborate the association of a survival benefit with increasing extent of LND at nephrectomy.</li>
<li>The different methodologies employed to account for missing data may introduce important biases.</li>
<li>Such considerations are non-negligible with respect to the interpretation of results for investigators who rely on administrative cohorts.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

A recent population-based analysis suggested a potential survival benefit with respect to performing lymph node dissection at nephrectomy in node-positive patients with RCC.
The findings of the present study failed to corroborate the association of a survival benefit with the performance of lymph node dissection at nephrectomy.



Objective

Previous studies showed no survival benefit with respect to performing lymph node dissection (LND) at nephrectomy, whereas a recent population-based analysis suggested otherwise, although the latter relied on imputation. To reconcile the findings of that study by critically evaluating the handling of missing data.



Patients and Methods

Study participants comprised patients diagnosed with non-metastatic renal cell carcinoma (RCC) of all stages who underwent LND at nephrectomy (n = 10 596).
Multivariable Cox regression models were performed to predict cancer-specific mortality (CSM), where the primary variable of interest was the extent of LND.
To examine differences in approaches with respect to handling missing data, separate analyses were performed: (i) imputed population; (ii) exclusion of patients with missing data; and (iii) inclusion of patients with missing data as a sub-category.



Results

Overall, 2916 (28%) patients had missing tumour grade.
In multivariable analyses, our findings showed that increasing the extent of LND was associated with a significant protective effect on CSM in patients with pN1 after imputation (hazard ratio [HR], 0.82; P = 0.04).
By contrast, the extent of LND was no longer significantly associated with a lower risk of CSM after excluding patients with a missing tumour grade (HR, 0.83; P = 0.1) or when including patients with missing tumour grade as a sub-category (HR, 0.82; P = 0.05).



Conclusions

The findings of the present study failed to corroborate the association of a survival benefit with increasing extent of LND at nephrectomy.
The different methodologies employed to account for missing data may introduce important biases.
Such considerations are non-negligible with respect to the interpretation of results for investigators who rely on administrative cohorts.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11662.x" xmlns="http://purl.org/rss/1.0/"><title>Bipolar vs monopolar transurethral resection of the prostate: evaluation of the impact on overall sexual function in an international randomized controlled trial setting</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11662.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bipolar vs monopolar transurethral resection of the prostate: evaluation of the impact on overall sexual function in an international randomized controlled trial setting</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Charalampos Mamoulakis, Andreas Skolarikos, Michael Schulze, Cesare M. Scoffone, Jens J. Rassweiler, Gerasimos Alivizatos, Roberto M. Scarpa, Jean J.M.C.H. Rosette</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-12T08:02:25.271343-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11662.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11662.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11662.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11662-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11662-list-0001" class="bullet">
<li>The effect of TURP on overall sexual function and particularly erectile function (EF) is controversial with conflicting results based on a low level of evidence. The effects of monopolar and bipolar TURP (M-TURP and B-TURP, respectively) on EF are similar, as has been shown in a few non-focused randomized control trials (RCTs).</li>
<li>For the first time, the present study offers focused results of a comparative evaluation of the effects of B-TURP and M-TURP on overall sexual function, as quantified with the International Index of Erectile Function Questionnaire (IIEF-15) in an international, multicentre, double-blind RCT setting.</li>
</ul></div></div>
<div class="section" id="bju11662-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11662-list-0002" class="bullet">
<li>To compare monopolar and bipolar transurethral resection of the prostate (M-TURP and B-TURP, respectively) using a true bipolar system, for the first time in an international multicentre double-blind randomized controlled trial focusing on the overall sexual function quantified with the International Index of Erectile Function Questionnaire (IIEF-15). Other baseline/perioperative parameters potentially influencing erectile function (EF) after TURP were secondarily investigated.</li>
</ul></div></div>
<div class="section" id="bju11662-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11662-list-0003" class="bullet">
<li>From July 2006 to June 2009, consecutive TURP candidates with benign prostatic obstruction were prospectively recruited in four academic urological centres, randomized 1:1 into M-TURP/B-TURP arms and followed up at 6 weeks, 6 and 12 months after surgery. In all, 295 eligible patients were enrolled.</li>
<li>Overall sexual function was quantified using self-administered IIEF-15 at baseline and at each subsequent visit.</li>
<li>Total IIEF/domain scores were calculated and EF score classified erectile dysfunction severity. Differences in erectile dysfunction severity at each visit compared with baseline (EF evolution), classified patients into ‘improved’, ‘stable’ or ‘deteriorated’.</li>
<li>Pre-postoperative IIEF/domain scores and differences in the distribution of EF evolution were compared between arms throughout follow-up.</li>
</ul></div></div>
<div class="section" id="bju11662-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11662-list-0004" class="bullet">
<li>In all, 279 patients received the allocated intervention; 218/279 patients (78.1%) provided complete IIEF-15 data at baseline and were considered in sexual function analysis. Complete IIEF-15 data were available from 193/218 (88.5%), 186/218 (85.3%) and 179/218 (82.1%) patients at 6 weeks, 6 months and 12 months, respectively.</li>
<li>Sexual function did not differ significantly between arms during follow-up (scores: IIEF, <em>P</em> = 0.750; EF, <em>P</em> = 0.636; orgasmic function, <em>P</em> = 0.868; sexual desire, <em>P</em> = 0.735; intercourse satisfaction, <em>P</em> = 0.917; overall satisfaction, <em>P</em> = 0.927).</li>
<li>Resection type was not a predictor of any sexual function changes observed.</li>
<li>Distribution of EF evolution did not differ between arms at any time (M-TURP vs B-TURP at 12 months: improved, 23/87 [26.4%] vs 18/92 [19.6%]; stable, 53/87 [60.9%] vs 56/92 [60.8%]; deteriorated, 11/87 [12.7%] vs 18/92 [19.6%]; <em>P</em> = 0.323).</li>
</ul></div></div>
<div class="section" id="bju11662-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11662-list-0005" class="bullet">
<li>There were no differences between M-TURP/B-TURP in any aspect of sexual function.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The effect of TURP on overall sexual function and particularly erectile function (EF) is controversial with conflicting results based on a low level of evidence. The effects of monopolar and bipolar TURP (M-TURP and B-TURP, respectively) on EF are similar, as has been shown in a few non-focused randomized control trials (RCTs).
For the first time, the present study offers focused results of a comparative evaluation of the effects of B-TURP and M-TURP on overall sexual function, as quantified with the International Index of Erectile Function Questionnaire (IIEF-15) in an international, multicentre, double-blind RCT setting.



Objective

To compare monopolar and bipolar transurethral resection of the prostate (M-TURP and B-TURP, respectively) using a true bipolar system, for the first time in an international multicentre double-blind randomized controlled trial focusing on the overall sexual function quantified with the International Index of Erectile Function Questionnaire (IIEF-15). Other baseline/perioperative parameters potentially influencing erectile function (EF) after TURP were secondarily investigated.



Materials and Methods

From July 2006 to June 2009, consecutive TURP candidates with benign prostatic obstruction were prospectively recruited in four academic urological centres, randomized 1:1 into M-TURP/B-TURP arms and followed up at 6 weeks, 6 and 12 months after surgery. In all, 295 eligible patients were enrolled.
Overall sexual function was quantified using self-administered IIEF-15 at baseline and at each subsequent visit.
Total IIEF/domain scores were calculated and EF score classified erectile dysfunction severity. Differences in erectile dysfunction severity at each visit compared with baseline (EF evolution), classified patients into ‘improved’, ‘stable’ or ‘deteriorated’.
Pre-postoperative IIEF/domain scores and differences in the distribution of EF evolution were compared between arms throughout follow-up.



Results

In all, 279 patients received the allocated intervention; 218/279 patients (78.1%) provided complete IIEF-15 data at baseline and were considered in sexual function analysis. Complete IIEF-15 data were available from 193/218 (88.5%), 186/218 (85.3%) and 179/218 (82.1%) patients at 6 weeks, 6 months and 12 months, respectively.
Sexual function did not differ significantly between arms during follow-up (scores: IIEF, P = 0.750; EF, P = 0.636; orgasmic function, P = 0.868; sexual desire, P = 0.735; intercourse satisfaction, P = 0.917; overall satisfaction, P = 0.927).
Resection type was not a predictor of any sexual function changes observed.
Distribution of EF evolution did not differ between arms at any time (M-TURP vs B-TURP at 12 months: improved, 23/87 [26.4%] vs 18/92 [19.6%]; stable, 53/87 [60.9%] vs 56/92 [60.8%]; deteriorated, 11/87 [12.7%] vs 18/92 [19.6%]; P = 0.323).



Conclusion

There were no differences between M-TURP/B-TURP in any aspect of sexual function.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12053" xmlns="http://purl.org/rss/1.0/"><title>Evaluation of robotic and laparoscopic partial nephrectomy for small renal tumours (T1a)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12053</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evaluation of robotic and laparoscopic partial nephrectomy for small renal tumours (T1a)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Saied Froghi, Kamran Ahmed, Mohammad S. Khan, Prokar Dasgupta, Ben Challacombe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-11T08:28:23.717729-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12053</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12053</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12053</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12053-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12053-list-0001" class="bullet">
<li>To compare laparoscopic partial nephrectomy (LPN) with robotic PN (RPN) using meta-analytical techniques, since there has been a rise in the incidence of small renal masses (SRM; &lt;4 cm) minimally invasive approaches are becoming more popular in dealing with such pathologies.</li>
</ul></div></div>
<div class="section" id="bju12053-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12053-list-0002" class="bullet">
<li>A systematic review of the literature was performed to identify studies comparing LPN and RPN.</li>
<li>Comparative studies evaluating RPN and LPN that fulfilled the inclusion criteria were selected.</li>
<li>Data on preoperative, operative (operative time, estimated blood loss [EBL], and warm ischaemia time [WIT]), postoperative (length of stay [LOS]) variables and complications were collected.</li>
<li>A meta-analysis using random effect model was performed.</li>
<li>A further Bland–Altman analysis of some of the operative variables was done to compare their reproducibility and mean difference in techniques.</li>
</ul></div></div>
<div class="section" id="bju12053-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12053-list-0003" class="bullet">
<li>Six studies matched the selection criteria. In all, 256 patients were analysed (40% RPN and 60% LPN).</li>
<li>There was no significant different in EBL (<em>P</em> = 0.12, 95% confidence interval [CI] –12.01 to 104.26).</li>
<li>Similarly, there was no significant different in WIT between the groups (<em>P</em> = 0.23, 95% CI –15.22 to 3.70).</li>
<li>Also, LOS (<em>P</em> = 0.22, 95% CI –0.38 to 0.09) and overall postoperative complication rates were not significantly different between the groups (<em>P</em> = 0.84, 95% CI –0.05 to 0.06).</li>
</ul></div></div>
<div class="section" id="bju12053-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12053-list-0004" class="bullet">
<li>Despite multiple studies reporting better perioperative variables for RPN, the present study found no significant differences between RPN and LPN. This has implications for both the surgeon and the patient.</li>
<li>Lack of randomised controlled trials in addition to a lack of long-term oncological data for RPN are current limitations.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To compare laparoscopic partial nephrectomy (LPN) with robotic PN (RPN) using meta-analytical techniques, since there has been a rise in the incidence of small renal masses (SRM; &lt;4 cm) minimally invasive approaches are becoming more popular in dealing with such pathologies.



Materials and Methods

A systematic review of the literature was performed to identify studies comparing LPN and RPN.
Comparative studies evaluating RPN and LPN that fulfilled the inclusion criteria were selected.
Data on preoperative, operative (operative time, estimated blood loss [EBL], and warm ischaemia time [WIT]), postoperative (length of stay [LOS]) variables and complications were collected.
A meta-analysis using random effect model was performed.
A further Bland–Altman analysis of some of the operative variables was done to compare their reproducibility and mean difference in techniques.



Results

Six studies matched the selection criteria. In all, 256 patients were analysed (40% RPN and 60% LPN).
There was no significant different in EBL (P = 0.12, 95% confidence interval [CI] –12.01 to 104.26).
Similarly, there was no significant different in WIT between the groups (P = 0.23, 95% CI –15.22 to 3.70).
Also, LOS (P = 0.22, 95% CI –0.38 to 0.09) and overall postoperative complication rates were not significantly different between the groups (P = 0.84, 95% CI –0.05 to 0.06).



Conclusions

Despite multiple studies reporting better perioperative variables for RPN, the present study found no significant differences between RPN and LPN. This has implications for both the surgeon and the patient.
Lack of randomised controlled trials in addition to a lack of long-term oncological data for RPN are current limitations.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11763.x" xmlns="http://purl.org/rss/1.0/"><title>Comparison of laparoendoscopic single site (LESS) and conventional laparoscopic donor nephrectomy at a single institution</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11763.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of laparoendoscopic single site (LESS) and conventional laparoscopic donor nephrectomy at a single institution</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lambros Stamatakis, Miguel A. Mercado, Judy M. Choi, Edward J. Sanchez, A. Osama Gaber, Richard J. Knight, Wesley A. Mayer, Richard E. Link</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-11T08:28:16.978974-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11763.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11763.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11763.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11763-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11763-list-0001" class="bullet">
<li>Most transplant centres harvest living donor kidneys via a conventional laparoscopic surgical approach. Laparoendoscopic single-site donor nephrectomy (LESS-DN) is a relatively novel minimally invasive approach that allows the surgery to be performed via a single incision. This technique may be advantageous in decreasing surgical morbidity and improving cosmetic outcomes, thus plausibly reducing the barriers to kidney donation.</li>
<li>The study demonstrates the safety and feasibility of LESS-DN in a large consecutive series of kidney donors. Comparative analysis between LDN and LESS-DN showed that there was a significant decrease in intra-operative blood loss and allograft warm ischaemia time in the LESS-DN group, but also a significant increase in operating time. Other peri-operative outcomes were similar between the two approaches. Evaluation of the LESS-DN cases alone revealed that, the operating times did not significantly change through the course of the series. Using this outcome as a surrogate for technical difficulty suggests a relatively shallow learning curve for LESS-DN.</li>
</ul></div></div>
<div class="section" id="bju11763-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11763-list-0002" class="bullet">
<li>To present a comparative analysis of peri-operative outcomes for &gt;200 cases of conventional laparoscopic donor nephrectomy (LDN) and laparoendoscopic single site donor nephrectomy (LESS-DN).</li>
</ul></div></div>
<div class="section" id="bju11763-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11763-list-0003" class="bullet">
<li>From 2006 to 2011, 213 donor nephrectomies were performed by two surgeons (R.E.L and W.A.M.) at a tertiary transplant centre. The approach changed from conventional LDN to LESS-DN over the course of the series.</li>
<li>The two approaches were compared retrospectively and evaluated for differences in peri-operative outcomes.</li>
<li>Statistical significance was assessed using Student's <em>t</em>-test and chi-squared analysis.</li>
</ul></div></div>
<div class="section" id="bju11763-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11763-list-0004" class="bullet">
<li>A total of 111 patients underwent LDN and 102 patients underwent LESS-DN.</li>
<li>Total operating time was significantly longer in the LESS-DN group (206.1 vs 181.9 min, <em>P</em> &lt; 0.001), but LESS-DN resulted in less intra-operative blood loss (61.5 mL vs 85.9 mL, <em>P</em> &lt; 0.001) and shorter warm ischaemia times (4.4 vs 5.0 min, <em>P</em> = 0.01).</li>
<li>There were no significant differences in analgesic requirements, subjective pain scores, length of hospital stay, postoperative graft function, or donor's postoperative glomerular filtration rate between the two approaches.</li>
<li>Complication rates were low regardless of the approach, and there were no major complications (&gt;grade II) in the LESS-DN group.</li>
</ul></div></div>
<div class="section" id="bju11763-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11763-list-0005" class="bullet">
<li>In experienced hands, LESS-DN results in peri-operative outcomes similar to those of conventional LDN without compromising donor safety, while providing a desirable cosmetic result.</li>
<li>For surgeons familiar with LDN, transitioning to the LESS approach using this technique appears to have a relatively short learning curve.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Most transplant centres harvest living donor kidneys via a conventional laparoscopic surgical approach. Laparoendoscopic single-site donor nephrectomy (LESS-DN) is a relatively novel minimally invasive approach that allows the surgery to be performed via a single incision. This technique may be advantageous in decreasing surgical morbidity and improving cosmetic outcomes, thus plausibly reducing the barriers to kidney donation.
The study demonstrates the safety and feasibility of LESS-DN in a large consecutive series of kidney donors. Comparative analysis between LDN and LESS-DN showed that there was a significant decrease in intra-operative blood loss and allograft warm ischaemia time in the LESS-DN group, but also a significant increase in operating time. Other peri-operative outcomes were similar between the two approaches. Evaluation of the LESS-DN cases alone revealed that, the operating times did not significantly change through the course of the series. Using this outcome as a surrogate for technical difficulty suggests a relatively shallow learning curve for LESS-DN.



Objective

To present a comparative analysis of peri-operative outcomes for &gt;200 cases of conventional laparoscopic donor nephrectomy (LDN) and laparoendoscopic single site donor nephrectomy (LESS-DN).



Patients and Methods

From 2006 to 2011, 213 donor nephrectomies were performed by two surgeons (R.E.L and W.A.M.) at a tertiary transplant centre. The approach changed from conventional LDN to LESS-DN over the course of the series.
The two approaches were compared retrospectively and evaluated for differences in peri-operative outcomes.
Statistical significance was assessed using Student's t-test and chi-squared analysis.



Results

A total of 111 patients underwent LDN and 102 patients underwent LESS-DN.
Total operating time was significantly longer in the LESS-DN group (206.1 vs 181.9 min, P &lt; 0.001), but LESS-DN resulted in less intra-operative blood loss (61.5 mL vs 85.9 mL, P &lt; 0.001) and shorter warm ischaemia times (4.4 vs 5.0 min, P = 0.01).
There were no significant differences in analgesic requirements, subjective pain scores, length of hospital stay, postoperative graft function, or donor's postoperative glomerular filtration rate between the two approaches.
Complication rates were low regardless of the approach, and there were no major complications (&gt;grade II) in the LESS-DN group.



Conclusions

In experienced hands, LESS-DN results in peri-operative outcomes similar to those of conventional LDN without compromising donor safety, while providing a desirable cosmetic result.
For surgeons familiar with LDN, transitioning to the LESS approach using this technique appears to have a relatively short learning curve.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12059" xmlns="http://purl.org/rss/1.0/"><title>Trends in surgery for upper urinary tract calculi in the USA using the Nationwide Inpatient Sample: 1999–2009</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12059</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Trends in surgery for upper urinary tract calculi in the USA using the Nationwide Inpatient Sample: 1999–2009</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Khurshid R. Ghani, Jesse D. Sammon, Pierre I. Karakiewicz, Maxine Sun, Naeem Bhojani, Shyam Sukumar, James O. Peabody, Mani Menon, Quoc-Dien Trinh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-11T07:57:37.73973-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12059</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12059</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12059</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12059-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12059-list-0001" class="bullet">
<li>To determine trends in demographics and treatment for inpatient upper urinary tract calculi in the USA using a population-based cohort.</li>
</ul></div></div>
<div class="section" id="bju12059-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12059-list-0002" class="bullet">
<li>All patients with a primary or secondary diagnosis of kidney or ureteric calculus between 1999 and 2009 in the US Nationwide Inpatient Sample were extracted and weighted.</li>
<li>Temporal trend analyses were used to determine trends in gender, race and age presentation, as well as utilization rates of interventions.</li>
<li>Temporal trends were quantified using the estimated annual percent change (EAPC) using least squares linear regression analysis.</li>
</ul></div></div>
<div class="section" id="bju12059-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12059-list-0003" class="bullet">
<li>Overall, 2 109 455 patients were hospitalized with upper urinary tract calculi over the 11-year period. The majority of admissions were for ureteric calculi (63.4%).</li>
<li>Admissions for renal calculus increased by 12.1% during the study period (EAPC + 0.92%, <em>P</em> = 0.039, 95% CI: 0.17–1.66), whilst discharges for ureteric calculus remained stable.</li>
<li>A significant increase (25.4%) in hospitalizations for women was found (EAPC + 2.21%, <em>P</em> &lt; 0.001, 95% CI: 1.40–3.03); by 2006, more women than men were admitted to hospital (95 953 vs. 94 556, respectively).</li>
<li>There were significant increases in hospitalization for black, Hispanic and older patients.</li>
<li>Significant changes in the use of all studied interventions were found except for ureteroscopy, extracorporeal shockwave lithotripsy and nephrectomy.</li>
</ul></div></div>
<div class="section" id="bju12059-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12059-list-0004" class="bullet">
<li>In this nationally representative sample of inpatient discharges, significant increases were found in admissions for renal compared with ureteric calculi, and for black, Hispanic and older patients.</li>
<li>With regard to surgical intervention, the largest increase was found in the use of procedures for kidney calculi.</li>
<li>Women now comprise the majority in the inpatient management of stone disease.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To determine trends in demographics and treatment for inpatient upper urinary tract calculi in the USA using a population-based cohort.



Patients and Methods

All patients with a primary or secondary diagnosis of kidney or ureteric calculus between 1999 and 2009 in the US Nationwide Inpatient Sample were extracted and weighted.
Temporal trend analyses were used to determine trends in gender, race and age presentation, as well as utilization rates of interventions.
Temporal trends were quantified using the estimated annual percent change (EAPC) using least squares linear regression analysis.



Results

Overall, 2 109 455 patients were hospitalized with upper urinary tract calculi over the 11-year period. The majority of admissions were for ureteric calculi (63.4%).
Admissions for renal calculus increased by 12.1% during the study period (EAPC + 0.92%, P = 0.039, 95% CI: 0.17–1.66), whilst discharges for ureteric calculus remained stable.
A significant increase (25.4%) in hospitalizations for women was found (EAPC + 2.21%, P &lt; 0.001, 95% CI: 1.40–3.03); by 2006, more women than men were admitted to hospital (95 953 vs. 94 556, respectively).
There were significant increases in hospitalization for black, Hispanic and older patients.
Significant changes in the use of all studied interventions were found except for ureteroscopy, extracorporeal shockwave lithotripsy and nephrectomy.



Conclusions

In this nationally representative sample of inpatient discharges, significant increases were found in admissions for renal compared with ureteric calculi, and for black, Hispanic and older patients.
With regard to surgical intervention, the largest increase was found in the use of procedures for kidney calculi.
Women now comprise the majority in the inpatient management of stone disease.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11789.x" xmlns="http://purl.org/rss/1.0/"><title>Initial management of prostate-specific antigen-detected, low-risk prostate cancer and the risk of death from prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11789.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Initial management of prostate-specific antigen-detected, low-risk prostate cancer and the risk of death from prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ayal A. Aizer, Ming-Hui Chen, Jona Hattangadi, Anthony V. D'Amico</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-08T09:02:48.112465-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11789.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11789.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11789.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11789-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11789-list-0001" class="bullet">
<li>The recently published Prostate Cancer Intervention versus Observation Trial (PIVOT) did not identify differences in prostate cancer-specific mortality or all-cause mortality among patients with low-risk disease managed conservatively vs those managed definitively; however, recently published data suggest that older men may harbour more aggressive disease than is identified at biopsy owing to sampling error and undergrading. Whether older men with apparent low-risk disease are placed at risk of prostate cancer-specific mortality when managed conservatively remains unknown.</li>
<li>The study used population-level data to show that non-curative approaches for older men with low-risk prostate cancer do result in an increased risk of prostate cancer-specific mortality. Differences between our study and the PIVOT trial include the fact that we included a larger sample size, analysed the data using an ‘as-treated’ approach, and included a healthier cohort of men as evinced by lower 4-year all-cause mortality estimates in our study than in the PIVOT. Our results suggest that older men with apparent low-risk prostate cancer are at risk of undergrading, which probably explains the differences in prostate cancer-specific mortality observed between men managed conservatively vs those managed definitively. Our study suggests that alternative approaches to excluding occult, high grade prostate cancer are needed in such men.</li>
</ul></div></div>
<div class="section" id="bju11789-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11789-list-0002" class="bullet">
<li>To evaluate whether older age in men with low-risk prostate cancer increases the risk of prostate cancer-specific mortality (PCSM) when non-curative approaches are selected as initial management.</li>
</ul></div></div>
<div class="section" id="bju11789-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11789-list-0003" class="bullet">
<li>The study cohort consisted of 27 969 men, with a median age of 67 years, with prostate-specific antigen (PSA)-detected, low-risk prostate cancer (clinical category T1c, Gleason score ≤6, and PSA ≤10) identified by the Surveillance, Epidemiology and End Results programme between 2004 and 2007.</li>
<li>Fine and Gray's competing risk regression analysis was used to evaluate whether management with non-curative vs curative therapy was associated with an increased risk of PCSM after adjusting for PSA level, age at diagnosis and year of diagnosis.</li>
</ul></div></div>
<div class="section" id="bju11789-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11789-list-0004" class="bullet">
<li>After a median follow-up of 2.75 years, 1121 men died, 60 (5.4%) from prostate cancer.</li>
<li>Both older age (adjusted hazard ratio [AHR] 1.05; 95% confidence interval (CI) 1.02–1.08; <em>P</em> &lt; 0.001) and non-curative treatment (AHR 3.34; 95% CI 1.97–5.67; <em>P</em> &lt; 0.001) were significantly associated with an increased risk of PCSM.</li>
<li>Men &gt; the median age experienced increased estimates of PCSM when treated with non-curative as opposed to curative intent (<em>P</em> &lt; 0.001); this finding was not seen in men ≤ the median age (<em>P</em> = 0.17).</li>
</ul></div></div>
<div class="section" id="bju11789-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11789-list-0005" class="bullet">
<li>Pending prospective validation, our study suggests that non-curative approaches for older men with ‘low-risk’ prostate cancer result in an increased risk of PCSM, suggesting the need for alternative approaches to exclude occult, high grade prostate cancer in these men.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The recently published Prostate Cancer Intervention versus Observation Trial (PIVOT) did not identify differences in prostate cancer-specific mortality or all-cause mortality among patients with low-risk disease managed conservatively vs those managed definitively; however, recently published data suggest that older men may harbour more aggressive disease than is identified at biopsy owing to sampling error and undergrading. Whether older men with apparent low-risk disease are placed at risk of prostate cancer-specific mortality when managed conservatively remains unknown.
The study used population-level data to show that non-curative approaches for older men with low-risk prostate cancer do result in an increased risk of prostate cancer-specific mortality. Differences between our study and the PIVOT trial include the fact that we included a larger sample size, analysed the data using an ‘as-treated’ approach, and included a healthier cohort of men as evinced by lower 4-year all-cause mortality estimates in our study than in the PIVOT. Our results suggest that older men with apparent low-risk prostate cancer are at risk of undergrading, which probably explains the differences in prostate cancer-specific mortality observed between men managed conservatively vs those managed definitively. Our study suggests that alternative approaches to excluding occult, high grade prostate cancer are needed in such men.



Objective

To evaluate whether older age in men with low-risk prostate cancer increases the risk of prostate cancer-specific mortality (PCSM) when non-curative approaches are selected as initial management.



Patients and Methods

The study cohort consisted of 27 969 men, with a median age of 67 years, with prostate-specific antigen (PSA)-detected, low-risk prostate cancer (clinical category T1c, Gleason score ≤6, and PSA ≤10) identified by the Surveillance, Epidemiology and End Results programme between 2004 and 2007.
Fine and Gray's competing risk regression analysis was used to evaluate whether management with non-curative vs curative therapy was associated with an increased risk of PCSM after adjusting for PSA level, age at diagnosis and year of diagnosis.



Results

After a median follow-up of 2.75 years, 1121 men died, 60 (5.4%) from prostate cancer.
Both older age (adjusted hazard ratio [AHR] 1.05; 95% confidence interval (CI) 1.02–1.08; P &lt; 0.001) and non-curative treatment (AHR 3.34; 95% CI 1.97–5.67; P &lt; 0.001) were significantly associated with an increased risk of PCSM.
Men &gt; the median age experienced increased estimates of PCSM when treated with non-curative as opposed to curative intent (P &lt; 0.001); this finding was not seen in men ≤ the median age (P = 0.17).



Conclusion

Pending prospective validation, our study suggests that non-curative approaches for older men with ‘low-risk’ prostate cancer result in an increased risk of PCSM, suggesting the need for alternative approaches to exclude occult, high grade prostate cancer in these men.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12045" xmlns="http://purl.org/rss/1.0/"><title>Comparative assessment of three standardized robotic surgery training methods</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12045</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative assessment of three standardized robotic surgery training methods</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrew J. Hung, Isuru S. Jayaratna, Kara Teruya, Mihir M. Desai, Inderbir S. Gill, Alvin C. Goh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:02:29.424115-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12045</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12045</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12045</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Surgical Education</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12045-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12045-list-0001" class="bullet">
<li>To evaluate three standardized robotic surgery training methods, inanimate, virtual reality and <em>in vivo</em>, for their construct validity.</li>
<li>To explore the concept of cross-method validity, where the relative performance of each method is compared.</li>
</ul></div></div>
<div class="section" id="bju12045-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12045-list-0002" class="bullet">
<li>Robotic surgical skills were prospectively assessed in 49 participating surgeons who were classified as follows: ‘novice/trainee’: urology residents, previous experience &lt;30 cases (<em>n</em> = 38) and ‘experts’: faculty surgeons, previous experience ≥30 cases (<em>n</em> = 11).</li>
<li>Three standardized, validated training methods were used: (i) structured inanimate tasks; (ii) virtual reality exercises on the da Vinci Skills Simulator (Intuitive Surgical, Sunnyvale, CA, USA); and (iii) a standardized robotic surgical task in a live porcine model with performance graded by the Global Evaluative Assessment of Robotic Skills (GEARS) tool.</li>
<li>A Kruskal–Wallis test was used to evaluate performance differences between novices and experts (construct validity).</li>
<li>Spearman's correlation coefficient (ρ) was used to measure the association of performance across inanimate, simulation and <em>in vivo</em> methods (cross-method validity).</li>
</ul></div></div>
<div class="section" id="bju12045-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12045-list-0003" class="bullet">
<li>Novice and expert surgeons had previously performed a median (range) of 0 (0–20) and 300 (30–2000) robotic cases, respectively (<em>P</em> &lt; 0.001).</li>
<li>Construct validity: experts consistently outperformed residents with all three methods (<em>P</em> &lt; 0.001).</li>
<li>Cross-method validity: overall performance of inanimate tasks significantly correlated with virtual reality robotic performance (ρ = −0.7, <em>P</em> &lt; 0.001) and <em>in vivo</em> robotic performance based on GEARS (ρ = −0.8, <em>P</em> &lt; 0.0001).</li>
<li>Virtual reality performance and <em>in vivo</em> tissue performance were also found to be strongly correlated (ρ = 0.6, <em>P</em> &lt; 0.001).</li>
</ul></div></div>
<div class="section" id="bju12045-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12045-list-0004" class="bullet">
<li>We propose the novel concept of cross-method validity, which may provide a method of evaluating the relative value of various forms of skills education and assessment.</li>
<li>We externally confirmed the construct validity of each featured training tool.</li>
</ul></div></div>
]]></content:encoded><description>

Objectives

To evaluate three standardized robotic surgery training methods, inanimate, virtual reality and in vivo, for their construct validity.
To explore the concept of cross-method validity, where the relative performance of each method is compared.



Materials and Methods

Robotic surgical skills were prospectively assessed in 49 participating surgeons who were classified as follows: ‘novice/trainee’: urology residents, previous experience &lt;30 cases (n = 38) and ‘experts’: faculty surgeons, previous experience ≥30 cases (n = 11).
Three standardized, validated training methods were used: (i) structured inanimate tasks; (ii) virtual reality exercises on the da Vinci Skills Simulator (Intuitive Surgical, Sunnyvale, CA, USA); and (iii) a standardized robotic surgical task in a live porcine model with performance graded by the Global Evaluative Assessment of Robotic Skills (GEARS) tool.
A Kruskal–Wallis test was used to evaluate performance differences between novices and experts (construct validity).
Spearman's correlation coefficient (ρ) was used to measure the association of performance across inanimate, simulation and in vivo methods (cross-method validity).



Results

Novice and expert surgeons had previously performed a median (range) of 0 (0–20) and 300 (30–2000) robotic cases, respectively (P &lt; 0.001).
Construct validity: experts consistently outperformed residents with all three methods (P &lt; 0.001).
Cross-method validity: overall performance of inanimate tasks significantly correlated with virtual reality robotic performance (ρ = −0.7, P &lt; 0.001) and in vivo robotic performance based on GEARS (ρ = −0.8, P &lt; 0.0001).
Virtual reality performance and in vivo tissue performance were also found to be strongly correlated (ρ = 0.6, P &lt; 0.001).



Conclusions

We propose the novel concept of cross-method validity, which may provide a method of evaluating the relative value of various forms of skills education and assessment.
We externally confirmed the construct validity of each featured training tool.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12011" xmlns="http://purl.org/rss/1.0/"><title>Evolving ideas about the male refractory period</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolving ideas about the male refractory period</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kenneth R. Turley, David L. Rowland</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:02:23.401196-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12011-sec-9001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11637-list-0002" class="bullet">
<li>The male refractory period (MRP) continues to be a topic of discussion and debate within the field of sexual medicine. To date explanations rely on central descending (efferent) influences involving specific neurotransmitter systems. Herein we explore the issue of the male refractory period, identifying problems with current explanations, specifying the parameters of an adequate model, and suggesting possible mechanisms mediating this phenomenon.</li>
</ul></div></div>
<div class="section" id="bju12011-sec-9002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><ul id="bju11637-list-0003" class="bullet">
<li>We review the literature regarding existing explanations for the MRP and look to other systems of physiological regulation that might provide a model for the conceptualization of the MRP.</li>
</ul></div></div>
<div class="section" id="bju12011-sec-9003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11637-list-0004" class="bullet">
<li>Our approach differs from traditional explanations in that it emphasizes the possible roles of various peripheral, rather than central, feedback (afferent) systems that affect peripheral autonomic functioning and response.</li>
<li>Yet our approach is consistent with other peripheral regulatory feedback systems controlling autonomic response related to such processes as heart rate, respiration, and gut motility.</li>
</ul></div></div>
<div class="section" id="bju12011-sec-9004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11637-list-0005" class="bullet">
<li>Although direct empirical research supporting our approach is lacking, sufficient evidence exists to support the idea that such processes are not only possible but likely with respect to the male refractory period. We suggest several lines of research that might provide empirical support for this approach.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

The male refractory period (MRP) continues to be a topic of discussion and debate within the field of sexual medicine. To date explanations rely on central descending (efferent) influences involving specific neurotransmitter systems. Herein we explore the issue of the male refractory period, identifying problems with current explanations, specifying the parameters of an adequate model, and suggesting possible mechanisms mediating this phenomenon.



Methods

We review the literature regarding existing explanations for the MRP and look to other systems of physiological regulation that might provide a model for the conceptualization of the MRP.



Results

Our approach differs from traditional explanations in that it emphasizes the possible roles of various peripheral, rather than central, feedback (afferent) systems that affect peripheral autonomic functioning and response.
Yet our approach is consistent with other peripheral regulatory feedback systems controlling autonomic response related to such processes as heart rate, respiration, and gut motility.



Conclusion

Although direct empirical research supporting our approach is lacking, sufficient evidence exists to support the idea that such processes are not only possible but likely with respect to the male refractory period. We suggest several lines of research that might provide empirical support for this approach.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12001" xmlns="http://purl.org/rss/1.0/"><title>Long-term evaluation of survival, continence and potency (SCP) outcomes after robot-assisted radical prostatectomy (RARP)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12001</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Long-term evaluation of survival, continence and potency (SCP) outcomes after robot-assisted radical prostatectomy (RARP)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vincenzo Ficarra, Marco Borghesi, Nazareno Suardi, Geert De Naeyer, Giacomo Novara, Peter Schatteman, Ruben De Groote, Paul Carpentier, Alexander Mottrie</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:02:21.17482-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12001</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12001</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12001</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12001-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12001-list-0001" class="bullet">
<li>To report combined oncological and functional outcome in a series of patients who underwent robot-assisted radical prostatectomy (RARP) for clinically localised prostate cancer in a single European centre after 5-year minimum follow-up according to survival, continence and potency (SCP) outcomes.</li>
</ul></div></div>
<div class="section" id="bju12001-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12001-list-0002" class="bullet">
<li>We extracted from our prostate cancer database all consecutive patients with a minimum follow-up of 5 years after RARP. Biochemical failure was defined as a confirmed PSA concentration of &gt;0.2 ng/mL.</li>
<li>All patients alive at the last follow-up were evaluated for functional outcomes using the Expanded Prostate Cancer Index Composite (EPIC) and Sexual Health Inventory for Men (SHIM) questionnaires.</li>
<li>Oncological and functional outcomes were reported according to the SCP system. Specifically, patients were classified as using no pad (C0), using one pad for security (C1), and using ≥1 pad (C2) (not including the prior definition).</li>
<li>Patients potent (SHIM score of &gt;17) without any aids were classified as P0 category; patients potent (SHIM score of &gt;17) with use of phosphodiesterase type 5 inhibitorsas P1; and patients with erectile dysfunction (SHIM score of &lt;17) as P2 category. Patients who did not undergo a nerve-sparing technique, who were not potent preoperatively, who were not interested in erections, or who did not have sexual partners were classified as Px category.</li>
</ul></div></div>
<div class="section" id="bju12001-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12001-list-0003" class="bullet">
<li>The 3-, 5- and 7-year biochemical recurrence-free survival rates were 96.3%; 89.6% and 88.3%, respectively.</li>
<li>At follow-up, 146 (79.8%) were fully continent (C0), 20 (10.9%) still used a safety pad (C1) and 17 (9.3%) were incontinent using ≥1 pad (C2).</li>
<li>Excluding Px patients, 52 patients (47.3%) were classified as P0; 41 patients (37.3%) were classified as P1 and 17 patients (15.5%) were P2.</li>
<li>In patients preoperatively continent and potent, who received a nerve-sparing technique and did not require any adjuvant therapy, oncological and functional success was attained by 77 (80.2%) patients.</li>
<li>In the subgroup of 67 patients not evaluable for potency recovery (Px), oncological and continence outcomes were attained in 46 patients (68.7%).</li>
</ul></div></div>
<div class="section" id="bju12001-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12001-list-0004" class="bullet">
<li>Oncological and functional success was attained in a high percentage of patients who underwent RARP at ≥5 years follow-up.</li>
<li>Interestingly, this study confirmed that excellent oncological and functional outcomes can be obtained in the ‘best’ category of patients, i.e. those preoperatively continent and potent and with tumour characteristics suitable for a nerve-sparing technique.</li>
</ul></div></div>
]]></content:encoded><description>

Objective

To report combined oncological and functional outcome in a series of patients who underwent robot-assisted radical prostatectomy (RARP) for clinically localised prostate cancer in a single European centre after 5-year minimum follow-up according to survival, continence and potency (SCP) outcomes.



Patients and Methods

We extracted from our prostate cancer database all consecutive patients with a minimum follow-up of 5 years after RARP. Biochemical failure was defined as a confirmed PSA concentration of &gt;0.2 ng/mL.
All patients alive at the last follow-up were evaluated for functional outcomes using the Expanded Prostate Cancer Index Composite (EPIC) and Sexual Health Inventory for Men (SHIM) questionnaires.
Oncological and functional outcomes were reported according to the SCP system. Specifically, patients were classified as using no pad (C0), using one pad for security (C1), and using ≥1 pad (C2) (not including the prior definition).
Patients potent (SHIM score of &gt;17) without any aids were classified as P0 category; patients potent (SHIM score of &gt;17) with use of phosphodiesterase type 5 inhibitorsas P1; and patients with erectile dysfunction (SHIM score of &lt;17) as P2 category. Patients who did not undergo a nerve-sparing technique, who were not potent preoperatively, who were not interested in erections, or who did not have sexual partners were classified as Px category.



Results

The 3-, 5- and 7-year biochemical recurrence-free survival rates were 96.3%; 89.6% and 88.3%, respectively.
At follow-up, 146 (79.8%) were fully continent (C0), 20 (10.9%) still used a safety pad (C1) and 17 (9.3%) were incontinent using ≥1 pad (C2).
Excluding Px patients, 52 patients (47.3%) were classified as P0; 41 patients (37.3%) were classified as P1 and 17 patients (15.5%) were P2.
In patients preoperatively continent and potent, who received a nerve-sparing technique and did not require any adjuvant therapy, oncological and functional success was attained by 77 (80.2%) patients.
In the subgroup of 67 patients not evaluable for potency recovery (Px), oncological and continence outcomes were attained in 46 patients (68.7%).



Conclusions

Oncological and functional success was attained in a high percentage of patients who underwent RARP at ≥5 years follow-up.
Interestingly, this study confirmed that excellent oncological and functional outcomes can be obtained in the ‘best’ category of patients, i.e. those preoperatively continent and potent and with tumour characteristics suitable for a nerve-sparing technique.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11696.x" xmlns="http://purl.org/rss/1.0/"><title>Psychological needs when diagnosed with testicular cancer: findings from a population-based study with long-term follow-up</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11696.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Psychological needs when diagnosed with testicular cancer: findings from a population-based study with long-term follow-up</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Johanna Skoogh, Gunnar Steineck, Boo Johansson, Ulrica Wilderäng, Ulrika Stierner, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:02:16.711056-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11696.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11696.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11696.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11696-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11696-list-0001" class="bullet">
<li>There are few large-scale follow-up studies regarding psychological reactions among men diagnosed with testicular cancer; therefore, our knowledge is sparse about the psychological consequences of being diagnosed with and treated for testicular cancer. Moreover, we know little about what kind of psychological support the men would prefer and benefit from.</li>
<li>Our study shows that most patients with testicular cancer, regardless of the seriousness of the disease, experience a psychological crisis at diagnosis. Furthermore, we found that most men wish that psychological support, including information about stress and crises reactions and psychological counselling, was offered at diagnosis. Our study highlights the need not only to provide patients with testicular cancer with the best physical treatment but also to take into account the psychological consequences of being diagnosed and offer the men psychological support.</li>
</ul></div></div>
<div class="section" id="bju11696-sec-1002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11696-list-0002" class="bullet">
<li>To investigate the psychological needs of patients diagnosed with testicular cancer.</li>
</ul></div></div>
<div class="section" id="bju11696-sec-1003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11696-list-0003" class="bullet">
<li>We identified 1192 eligible men diagnosed with non-seminomatous testicular cancer, treated according to the bi-national cancer-care programmes SWENOTECA I–IV between 1981 and 2004.</li>
<li>Using a study-specific questionnaire we asked the survivors if they had experienced some kind of crisis attributable to their cancer diagnosis. We also asked if they were and, if not, if they wish they had been offered information about crisis and stress reactions and professional counselling.</li>
</ul></div></div>
<div class="section" id="bju11696-sec-1004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11696-list-0004" class="bullet">
<li>We obtained information from 974/1192 (82%) testicular cancer survivors diagnosed at a mean of 11 years before follow-up.</li>
<li>Sixty-three percent reported that they had experienced a crisis owing to their diagnosis. For most men (76%) the crisis was at its worst at the time of diagnosis and treatment.</li>
<li>Between 1981 and 2004, 145 men (15%) reported that they received information about common stress and crisis reactions and 348 (36%) reported that they were offered counselling.</li>
<li>Of the men not informed about stress and crisis reactions and not offered counselling, 353/514 (69%) and 251/403 (62%), respectively, wish they had been. The percentage who reported that they wish that they had been informed or offered counselling did not differ significantly depending on civil status, age at diagnosis or stage of disease.</li>
</ul></div></div>
<div class="section" id="bju11696-sec-1005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11696-list-0005" class="bullet">
<li>The vast majority of Swedish testicular cancer survivors reported that they experienced a crisis because of their cancer diagnosis.</li>
<li>Moreover, regardless of stage of disease, most men reported a need for psychological support at the time of diagnosis and treatment that was not satisfactorily met by the healthcare provision.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

There are few large-scale follow-up studies regarding psychological reactions among men diagnosed with testicular cancer; therefore, our knowledge is sparse about the psychological consequences of being diagnosed with and treated for testicular cancer. Moreover, we know little about what kind of psychological support the men would prefer and benefit from.
Our study shows that most patients with testicular cancer, regardless of the seriousness of the disease, experience a psychological crisis at diagnosis. Furthermore, we found that most men wish that psychological support, including information about stress and crises reactions and psychological counselling, was offered at diagnosis. Our study highlights the need not only to provide patients with testicular cancer with the best physical treatment but also to take into account the psychological consequences of being diagnosed and offer the men psychological support.



Objective

To investigate the psychological needs of patients diagnosed with testicular cancer.



Patients and Methods

We identified 1192 eligible men diagnosed with non-seminomatous testicular cancer, treated according to the bi-national cancer-care programmes SWENOTECA I–IV between 1981 and 2004.
Using a study-specific questionnaire we asked the survivors if they had experienced some kind of crisis attributable to their cancer diagnosis. We also asked if they were and, if not, if they wish they had been offered information about crisis and stress reactions and professional counselling.



Results

We obtained information from 974/1192 (82%) testicular cancer survivors diagnosed at a mean of 11 years before follow-up.
Sixty-three percent reported that they had experienced a crisis owing to their diagnosis. For most men (76%) the crisis was at its worst at the time of diagnosis and treatment.
Between 1981 and 2004, 145 men (15%) reported that they received information about common stress and crisis reactions and 348 (36%) reported that they were offered counselling.
Of the men not informed about stress and crisis reactions and not offered counselling, 353/514 (69%) and 251/403 (62%), respectively, wish they had been. The percentage who reported that they wish that they had been informed or offered counselling did not differ significantly depending on civil status, age at diagnosis or stage of disease.



Conclusions

The vast majority of Swedish testicular cancer survivors reported that they experienced a crisis because of their cancer diagnosis.
Moreover, regardless of stage of disease, most men reported a need for psychological support at the time of diagnosis and treatment that was not satisfactorily met by the healthcare provision.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11670.x" xmlns="http://purl.org/rss/1.0/"><title>Assessing the accuracy and generalizability of the preoperative and postoperative Karakiewicz nomograms for renal cell carcinoma: results from a multicentre European and US study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11670.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Assessing the accuracy and generalizability of the preoperative and postoperative Karakiewicz nomograms for renal cell carcinoma: results from a multicentre European and US study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luca Cindolo, Paolo Chiodini, Sabine Brookman-May, Ottavio De Cobelli, Matthias May, Stefano Squillacciotti, Cosimo De Nunzio, Andrea Tubaro, Ioan Coman, Bodgan Feciche, Michael Truss, Manfred P. Wirth, Orietta Dalpiaz, Thomas F. Chromecki, Shahrock F. Shariat, Manuel Sanchez-Chapado, Maria Carmen Santiago Martin, Bernardo Rocco, Luigi Salzano, Giuseppe Lotrecchiano, Francesco Berardinelli, Luigi Schips</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:01:04.255174-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11670.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11670.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11670.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11670-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11670-list-0001" class="bullet">
<li>The preoperative and postoperative Karakiewicz models for RCC are considered among the best prognostic tools available for clinical counseling. Nevertheless, their predictive acuracy was externally validated only in two papers: by the same author and in an independent sample of Asian patients. However, these models have not been externally validated in truly independent multicentre series of patients.</li>
<li>Our study demonstrated that these models 1) provide robust prognostic information; 2) were robustly built; 3) are useful also in population far from the original series. The present results are the first to show the validity and generalizability of Karakiewicz nomograms, which are based on surgical series from European centres, for large-, mid- and small-volume European and American centres.</li>
</ul></div></div>
<div class="section" id="bju11670-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11670-list-0002" class="bullet">
<li>To assess the accuracy and generalizability of the pre- and postoperative Karakiewicz nomograms for predicting cancer-specific survival (CSS) in patients with renal cell carcinoma (RCC).</li>
</ul></div></div>
<div class="section" id="bju11670-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11670-list-0003" class="bullet">
<li>This retrospective study included 3231 patients from European and US centres, who were treated by radical or partial nephrectomy for RCC between 1992 and 2010.</li>
<li>Prognostic scores for each patient were calculated and the primary endpoint was CSS.</li>
<li>Discriminating ability was assessed by Harrell's c-index for censored data. The ‘validation by calibration’ method proposed by Van Houwelingen was used for checking the calibration of covariate effects. Calibration was graphically explored.</li>
</ul></div></div>
<div class="section" id="bju11670-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11670-list-0004" class="bullet">
<li>Local and systemic symptoms were present in 23.2% and 9.1% of the patients, respectively.</li>
<li>The median follow-up (FU) was 49 months. At the last FU, 408 cancer-related deaths were recorded, Kaplan–Meier estimates of CSS (with 95% confidence intervals [CIs]) at 5 and 10 years were 0.86 (0.84–0.87) and 0.77 (0.75–0.80), respectively.</li>
<li>Both nomograms discriminated well. Stratified c-indices for CSS were 0.784 (95% CI 0.753–0.814) for the preoperative nomogram, and 0.842 (95% CI 0.816–0.867) for the postoperative one, with a significant difference between the two values (<em>P</em> &lt; 0.001).</li>
<li>The covariate-based predictions on our data for both nomograms were valid. The calibration plots showed no relevant departures from ideal predictions.</li>
</ul></div></div>
<div class="section" id="bju11670-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11670-list-0005" class="bullet">
<li>The results suggest that the postoperative Karakiewicz nomogram discriminates substantially better than the preoperative one.</li>
<li>These nomogram-based predictions may be used as benchmark data for pretreatment and postoperative decision-making in patients at various stages of RCC.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The preoperative and postoperative Karakiewicz models for RCC are considered among the best prognostic tools available for clinical counseling. Nevertheless, their predictive acuracy was externally validated only in two papers: by the same author and in an independent sample of Asian patients. However, these models have not been externally validated in truly independent multicentre series of patients.
Our study demonstrated that these models 1) provide robust prognostic information; 2) were robustly built; 3) are useful also in population far from the original series. The present results are the first to show the validity and generalizability of Karakiewicz nomograms, which are based on surgical series from European centres, for large-, mid- and small-volume European and American centres.



Objective

To assess the accuracy and generalizability of the pre- and postoperative Karakiewicz nomograms for predicting cancer-specific survival (CSS) in patients with renal cell carcinoma (RCC).



Patients and Methods

This retrospective study included 3231 patients from European and US centres, who were treated by radical or partial nephrectomy for RCC between 1992 and 2010.
Prognostic scores for each patient were calculated and the primary endpoint was CSS.
Discriminating ability was assessed by Harrell's c-index for censored data. The ‘validation by calibration’ method proposed by Van Houwelingen was used for checking the calibration of covariate effects. Calibration was graphically explored.



Results

Local and systemic symptoms were present in 23.2% and 9.1% of the patients, respectively.
The median follow-up (FU) was 49 months. At the last FU, 408 cancer-related deaths were recorded, Kaplan–Meier estimates of CSS (with 95% confidence intervals [CIs]) at 5 and 10 years were 0.86 (0.84–0.87) and 0.77 (0.75–0.80), respectively.
Both nomograms discriminated well. Stratified c-indices for CSS were 0.784 (95% CI 0.753–0.814) for the preoperative nomogram, and 0.842 (95% CI 0.816–0.867) for the postoperative one, with a significant difference between the two values (P &lt; 0.001).
The covariate-based predictions on our data for both nomograms were valid. The calibration plots showed no relevant departures from ideal predictions.



Conclusions

The results suggest that the postoperative Karakiewicz nomogram discriminates substantially better than the preoperative one.
These nomogram-based predictions may be used as benchmark data for pretreatment and postoperative decision-making in patients at various stages of RCC.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11497.x" xmlns="http://purl.org/rss/1.0/"><title>Trends in the surgical management of localized renal masses: thermal ablation, partial and radical nephrectomy in the USA, 1998–2008</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11497.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Trends in the surgical management of localized renal masses: thermal ablation, partial and radical nephrectomy in the USA, 1998–2008</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeffrey M. Woldrich, Kerrin Palazzi, Sean P. Stroup, Roger L. Sur, J. Kellogg Parson, David Chang, Ithaar H. Derweesh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T08:00:43.591376-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11497.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11497.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11497.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11497-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11497-list-0001" class="bullet">
<li>Treatment options for small renal masses include radical nephrectomy (RN), and nephron sparing modalities (NSM) such as partial nephrectomy (PN), and thermal ablation (Cryo- and radiofrequency ablation, C/RFA). Prior studies had demonstrated gross underutilization of PN; however overall treatment trends for C/RFA had not been well studied using a population-based cohort. In this study, which examined management trends of localized renal masses in the USA, we identified an increased prevalence of RN, PN and C/RFA over the study period, with PN increasing the most rapidly, and with RN continuing to account for the vast majority of procedures.</li>
<li>This is the first study to examine surgical management of renal masses in patients with non-dialysis dependent chronic renal insufficiency. Although nephron sparing modalities were increasingly utilized over the study period, it is particularly concerning that patients with pre-existing non-dialysis dependent chronic renal insufficiency are receiving less nephron sparing approaches. Further investigations are required to confirm these findings and to identify impediments to the dissemination of nephron sparing modalities.</li>
</ul></div></div>
<div class="section" id="bju11497-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11497-list-0002" class="bullet">
<li>To evaluate the diffusion of nephron-sparing modalities (NSM) for the treatment of renal neoplasms in the USA over the last decade and to identify the factors associated with renal procedure selection.</li>
</ul></div></div>
<div class="section" id="bju11497-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11497-list-0003" class="bullet">
<li>The Nationwide Inpatient Sample was utlized to identify patients undergoing cryo/radiofrequency ablation (C/RFA), radical nephrectomy (RN) and partial nephrectomy (PN) from 1998 to 2008.</li>
<li>Annual trends in procedure prevalence were determined.</li>
<li>Multivariate analyses were performed to query the influence of age, race, sex and comorbid disease on surgery selection.</li>
</ul></div></div>
<div class="section" id="bju11497-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11497-list-0004" class="bullet">
<li>We identified 443 853 procedures performed during the study period: 25 599 C/RFA, 79 568 PN and 338 687 RN.</li>
<li>The prevalence per 100 000 hospital admissions in 1998 was 3.7 for C/RFA, nine for PN and 87.1 for RN. All procedures increased over the study period, by 1.05, 3.1 and 2.2/100 000 admissions per year, respectively (all <em>P</em> &lt; 0.001).</li>
<li>Diabetes, urban, teaching and large capacity hospitals were associated with NSM (either C/RFA or PN) compared to RN (all <em>P</em> ≤ 0.011). Age ≥70 years, female, hypertension, diabetes, chronic kidney disease (CKD) and region outside the Northeast favoured C/RFA over PN (all <em>P</em> ≤ 0.026).</li>
<li>Compared to those without CKD, patients with CKD had an almost twofold higher probability of undergoing RN than NSM (odds ratio, 1.88; 95% confidence interval, 1.7–2.1). Despite increasing NSM utilization over the study period, most patients with CKD still received RN.</li>
</ul></div></div>
<div class="section" id="bju11497-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11497-list-0005" class="bullet">
<li>Although the prevalence of NSM is increasing, RN is more common.</li>
<li>The low utilization of NSM in patients with pre-existing CKD warrants further investigation.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Treatment options for small renal masses include radical nephrectomy (RN), and nephron sparing modalities (NSM) such as partial nephrectomy (PN), and thermal ablation (Cryo- and radiofrequency ablation, C/RFA). Prior studies had demonstrated gross underutilization of PN; however overall treatment trends for C/RFA had not been well studied using a population-based cohort. In this study, which examined management trends of localized renal masses in the USA, we identified an increased prevalence of RN, PN and C/RFA over the study period, with PN increasing the most rapidly, and with RN continuing to account for the vast majority of procedures.
This is the first study to examine surgical management of renal masses in patients with non-dialysis dependent chronic renal insufficiency. Although nephron sparing modalities were increasingly utilized over the study period, it is particularly concerning that patients with pre-existing non-dialysis dependent chronic renal insufficiency are receiving less nephron sparing approaches. Further investigations are required to confirm these findings and to identify impediments to the dissemination of nephron sparing modalities.



Objective

To evaluate the diffusion of nephron-sparing modalities (NSM) for the treatment of renal neoplasms in the USA over the last decade and to identify the factors associated with renal procedure selection.



Patients and Methods

The Nationwide Inpatient Sample was utlized to identify patients undergoing cryo/radiofrequency ablation (C/RFA), radical nephrectomy (RN) and partial nephrectomy (PN) from 1998 to 2008.
Annual trends in procedure prevalence were determined.
Multivariate analyses were performed to query the influence of age, race, sex and comorbid disease on surgery selection.



Results

We identified 443 853 procedures performed during the study period: 25 599 C/RFA, 79 568 PN and 338 687 RN.
The prevalence per 100 000 hospital admissions in 1998 was 3.7 for C/RFA, nine for PN and 87.1 for RN. All procedures increased over the study period, by 1.05, 3.1 and 2.2/100 000 admissions per year, respectively (all P &lt; 0.001).
Diabetes, urban, teaching and large capacity hospitals were associated with NSM (either C/RFA or PN) compared to RN (all P ≤ 0.011). Age ≥70 years, female, hypertension, diabetes, chronic kidney disease (CKD) and region outside the Northeast favoured C/RFA over PN (all P ≤ 0.026).
Compared to those without CKD, patients with CKD had an almost twofold higher probability of undergoing RN than NSM (odds ratio, 1.88; 95% confidence interval, 1.7–2.1). Despite increasing NSM utilization over the study period, most patients with CKD still received RN.



Conclusions

Although the prevalence of NSM is increasing, RN is more common.
The low utilization of NSM in patients with pre-existing CKD warrants further investigation.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12025" xmlns="http://purl.org/rss/1.0/"><title>Prognosis is deteriorating for upper tract urothelial cancer: data for England 1985–2010</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12025</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Prognosis is deteriorating for upper tract urothelial cancer: data for England 1985–2010</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maike F. Eylert, Luke Hounsome, Julia Verne, Amit Bahl, Edward R. Jefferies, Raj A. Persad</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:51:25.943777-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12025</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12025</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12025</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12025-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12025-list-0001" class="bullet">
<li>To ascertain current trends in the incidence and mortality rates for upper tract urothelial cancer (UTUC) and identify any relationship with age, stage at presentation, social deprivation and treatment method.</li>
</ul></div></div>
<div class="section" id="bju12025-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12025-list-0002" class="bullet">
<li>We used national databases to collect the data: incidence, stage and survival data from the National Cancer Data Repository (NCDR) and British Association of Urological Surgeons (BAUS) audit database; mortality data from the Office for National Statistics (ONS); and treatment method data from the Hospital Episodes Statistics (HES).</li>
</ul></div></div>
<div class="section" id="bju12025-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12025-list-0003" class="bullet">
<li>The incidence of UTUC is increasing (from 1985 to 2009 it increased by 38% in men and 77% in women). It affects mainly those aged &gt;60 years, and diagnoses are increasingly made in those aged &gt;80 years. Diagnoses at advanced stage have increased from 45 to 80%.</li>
<li>Mortality has risen faster than incidence; the overall 5-year survival rate has dropped from 60 to 48%. Survival is worst in stage IV disease and in patients aged ≥80 years; when analysed by age or stage group, survival rates are unchanged.</li> <li>Nephroureterectomy has increased by 75%, but endoscopic treatment, which only became available part way through the study period, now accounts for 11% of surgical interventions for UTUC, mainly in stage I disease and in the elderly.</li>
</ul></div></div>
<div class="section" id="bju12025-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12025-list-0004" class="bullet">
<li>Despite sharing its risk factors with bladder cancer, current incidence and mortality trends for UTUC contrast with those in bladder cancer. Increasing use of cross-sectional imaging may explain some of the identified increased incidence. Higher incidence specifically in people &gt;80 years, together with stage migration to more advanced cancers, are likely to have caused at least some of the observed increased mortality.</li>
<li>Further study is required to answer the questions of whether there are other hitherto unidentified aetiological or prognostic factors; whether less aggressive treatment of UTUCs in the elderly is always justified; and whether the rising frequency of minimally invasive treatment means suboptimum oncological management.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To ascertain current trends in the incidence and mortality rates for upper tract urothelial cancer (UTUC) and identify any relationship with age, stage at presentation, social deprivation and treatment method.



Patients and Methods

We used national databases to collect the data: incidence, stage and survival data from the National Cancer Data Repository (NCDR) and British Association of Urological Surgeons (BAUS) audit database; mortality data from the Office for National Statistics (ONS); and treatment method data from the Hospital Episodes Statistics (HES).



Results

The incidence of UTUC is increasing (from 1985 to 2009 it increased by 38% in men and 77% in women). It affects mainly those aged &gt;60 years, and diagnoses are increasingly made in those aged &gt;80 years. Diagnoses at advanced stage have increased from 45 to 80%.
Mortality has risen faster than incidence; the overall 5-year survival rate has dropped from 60 to 48%. Survival is worst in stage IV disease and in patients aged ≥80 years; when analysed by age or stage group, survival rates are unchanged. Nephroureterectomy has increased by 75%, but endoscopic treatment, which only became available part way through the study period, now accounts for 11% of surgical interventions for UTUC, mainly in stage I disease and in the elderly.



Conclusions

Despite sharing its risk factors with bladder cancer, current incidence and mortality trends for UTUC contrast with those in bladder cancer. Increasing use of cross-sectional imaging may explain some of the identified increased incidence. Higher incidence specifically in people &gt;80 years, together with stage migration to more advanced cancers, are likely to have caused at least some of the observed increased mortality.
Further study is required to answer the questions of whether there are other hitherto unidentified aetiological or prognostic factors; whether less aggressive treatment of UTUCs in the elderly is always justified; and whether the rising frequency of minimally invasive treatment means suboptimum oncological management.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11775.x" xmlns="http://purl.org/rss/1.0/"><title>Laparoendoscopic single-site nephroureterectomy for upper urinary tract urothelial carcinoma: outcomes of an international multi-institutional study of 101 patients</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11775.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Laparoendoscopic single-site nephroureterectomy for upper urinary tract urothelial carcinoma: outcomes of an international multi-institutional study of 101 patients</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sung Yul Park, Koon Ho Rha, Riccardo Autorino, Ithaar Derweesh, Evangelos Liastikos, Yao Chou Tsai, Ill Young Seo, Ugo Nagele, Aly M. Abdel-Karim, Thomas Herrmann, Deok Hyun Han, Soroush Rais-Bahrami, Seung Wook Lee, Kyu Shik Kim, Paolo Fornara, Panagiotis Kallidonis, Christopher Springer, Salah Élsalmy, Shih-Chieh Jeff Chueh, Chen-Hsun Ho, Kamol Panumatrassamee, Ryan Kopp, Jens-Uwe Stolzenburg, Lee Richstone, Jae Hoon Chung, Tae Young Shin, Francesco Greco, Jihad H. Kaouk</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:51:20.527622-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11775.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11775.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11775.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11775-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11775-list-0001" class="bullet">
<li>LESS-NU may be an alternative minimally-invasive treatment option for patients eligible to undergo laparoscopic surgery for upper urinary tract urothelial carcinoma.</li>
<li>The true benefits of LESS-NU remain to be determined and require randomized control trials in the future. Despite encouraging early findings, clinical trials still are warranted before this procedure is adopted widely, and longer follow-up is needed to determine its oncological durability.</li>
</ul></div></div>
<div class="section" id="bju11775-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11775-list-0002" class="bullet">
<li>To report a large multi-institutional series of laparoendoscopic single-site (LESS) nephroureterectomy (NU).</li>
</ul></div></div>
<div class="section" id="bju11775-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11775-list-0003" class="bullet">
<li>Data on all cases of LESS-NU performed between 2008 and 2012 at 15 institutions were retrospectively gathered.</li>
<li>The main demographic data and perioperative outcomes were analysed.</li>
</ul></div></div>
<div class="section" id="bju11775-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11775-list-0004" class="bullet">
<li>The study included 101 patients whose mean (<span class="smallCaps">sd</span>) age was 66.4 (9.9) years and mean (<span class="smallCaps">sd</span>) body mass index was 24.8 (4) kg/m<sup>2</sup>, and of whom 29.7% had undergone previous abdominal/pelvic surgery.</li>
<li>The mean (<span class="smallCaps">sd</span>) operating time was 221.4 (73.7) min, estimated blood loss 231.7 (348.0) mL.</li>
<li>A robot-assisted LESS technique was applied in 25.7% of cases. An extra trocar was inserted in 28.7% of cases to complete the procedure. Conversion to open surgery was necessary in three cases (3.0%). There was no bladder cuff excision in 20.8% of cases, and excision was carried out using a variety of techniques in the remaining cases.</li>
<li>Six intra-operative complications occurred (5.9%). The mean (<span class="smallCaps">sd</span>) length of hospital stay was 6.3 (3.5) days. The overall postoperative complication rate was 10.0%, and most of the complications were low grade (Clavien grades 1 and 2).</li>
<li>The mean tumour size was 3.1 (1.9) cm. Pathological staging was pTis in two patients, pTa in 12 patients, pT1 in 42 patients, pT2 in 20 patients, pT3 in 23 patients and pT4 in two patients. Pathological grade was high in 71 and low in 30 patients.</li>
<li>At a mean follow-up of 14 months, six patients (5.9%) had died. Disease recurrence (including distant and bladder recurrence) was detected in 22.8% of patients, with a mean time to recurrence of 11.5 months.</li>
</ul></div></div>
<div class="section" id="bju11775-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11775-list-0005" class="bullet">
<li>This study reports the largest multi-institutional experience of LESS-NU to date.</li>
<li>Peri-operative outcomes mirror those of published standard laparoscopy series.</li>
<li>Despite encouraging early findings, longer follow-up is needed to determine the oncological efficacy of the procedure.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

LESS-NU may be an alternative minimally-invasive treatment option for patients eligible to undergo laparoscopic surgery for upper urinary tract urothelial carcinoma.
The true benefits of LESS-NU remain to be determined and require randomized control trials in the future. Despite encouraging early findings, clinical trials still are warranted before this procedure is adopted widely, and longer follow-up is needed to determine its oncological durability.


 Objective

To report a large multi-institutional series of laparoendoscopic single-site (LESS) nephroureterectomy (NU).



Materials and Methods

Data on all cases of LESS-NU performed between 2008 and 2012 at 15 institutions were retrospectively gathered.
The main demographic data and perioperative outcomes were analysed.



Results

The study included 101 patients whose mean (sd) age was 66.4 (9.9) years and mean (sd) body mass index was 24.8 (4) kg/m2, and of whom 29.7% had undergone previous abdominal/pelvic surgery.
The mean (sd) operating time was 221.4 (73.7) min, estimated blood loss 231.7 (348.0) mL.
A robot-assisted LESS technique was applied in 25.7% of cases. An extra trocar was inserted in 28.7% of cases to complete the procedure. Conversion to open surgery was necessary in three cases (3.0%). There was no bladder cuff excision in 20.8% of cases, and excision was carried out using a variety of techniques in the remaining cases.
Six intra-operative complications occurred (5.9%). The mean (sd) length of hospital stay was 6.3 (3.5) days. The overall postoperative complication rate was 10.0%, and most of the complications were low grade (Clavien grades 1 and 2).
The mean tumour size was 3.1 (1.9) cm. Pathological staging was pTis in two patients, pTa in 12 patients, pT1 in 42 patients, pT2 in 20 patients, pT3 in 23 patients and pT4 in two patients. Pathological grade was high in 71 and low in 30 patients.
At a mean follow-up of 14 months, six patients (5.9%) had died. Disease recurrence (including distant and bladder recurrence) was detected in 22.8% of patients, with a mean time to recurrence of 11.5 months.



Conclusions

This study reports the largest multi-institutional experience of LESS-NU to date.
Peri-operative outcomes mirror those of published standard laparoscopy series.
Despite encouraging early findings, longer follow-up is needed to determine the oncological efficacy of the procedure.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11731.x" xmlns="http://purl.org/rss/1.0/"><title>Quantitative measurement of the androgen receptor in prepuces of boys with and without hypospadias</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11731.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Quantitative measurement of the androgen receptor in prepuces of boys with and without hypospadias</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Renate Pichler, Gabriel Djedovic, Helmut Klocker, Isabel Heidegger, Alexander Strasak, Wolfgang Loidl, Jasmin Bektic, Viktor Skradski, Wolfgang Horninger, Josef Oswald</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:51:17.194237-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11731.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11731.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11731.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Paediatrics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11731-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11731-list-0001" class="bullet">
<li>Despite diverse anatomical and histological trials in humans and animal models, the aetiology of hypospadias remains unknown and currently there is no clear molecular explanation about the emergence of this disease; however, genetic, endocrine and environmental mechanisms have been suggested.</li>
<li>The aim of the present study was to quantify and compare the androgen receptor (AR; mRNA and protein) levels in 40 prepuces of boys with and without hypospadias using quantitative real-time polymerase chain reaction, Western Blot and standardised, automated immunohistochemistry. AR mRNA (<em>P</em> = 0.013) and AR protein (<em>P</em> = 0.014) was significantly elevated in the prepuces of boys with hypospadias compared with boys without hypospadias. Altogether our data indicate that elevated AR mRNA and protein levels can be considered as a biochemical response of an AR signalling defect as an identified cause in boys with hypospadias. Additionally, nuclear staining intensity for AR-protein in specimens of boys with hypospadias was higher than in boys with phimosis.</li>
</ul></div></div>
<div class="section" id="bju11731-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11731-list-0002" class="bullet">
<li>To address the role of the androgen receptor (AR) on mRNA and protein levels in prepuces of boys with and without hypospadias.</li>
</ul></div></div>
<div class="section" id="bju11731-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11731-list-0003" class="bullet">
<li>Data from 40 foreskin specimens of consecutive circumcised boys (20 with vs 20 without hypospadias) were enrolled in this prospective study. After surgery, samples were fixed in formaldehyde and frozen in liquid nitrogen. Total RNA was isolated from frozen tissue and transcribed to complementary DNA.</li>
<li>The amount of AR mRNA was measured by quantitative real-time polymerase chain reaction and Western Blot and standardised, automated immunohistochemistry were used to assess AR protein levels.</li>
</ul></div></div>
<div class="section" id="bju11731-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11731-list-0004" class="bullet">
<li>The mean age at time of surgery was 61.8 and 30.9 months in boys without and with hypospadias, respectively.</li>
<li>There was penile, coronal and sine hypospadias in seven (35%), nine (45%), and four (20%) boys, respectively.</li> <li>AR mRNA was significantly elevated in the prepuces of boys with hypospadias compared with boys without hypospadias, at a mean (<span class="smallCaps">sd</span>) of 28.33 (5.39) vs 15.31 (1.85) (<em>P</em> = 0.013).</li>
<li>Furthermore, the amount of AR protein was higher in boys with, compared with boys without hypospadias, at a mean (<span class="smallCaps">sd</span>) of 133.25 (6.17) vs 100 (4.45) (<em>P</em> = 0.014).</li>
</ul></div></div>
<div class="section" id="bju11731-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11731-list-0005" class="bullet">
<li>Different AR mRNA expression and protein levels seem to be an indication of an AR signalling defect as a cause in boys with hypospadias.</li>
<li>Decreased AR DNA binding and functional capability may result in a compensatory up-regulation of both AR mRNA and protein.</li>
<li>Further studies are necessary to perform structural analysis of the AR and to corroborate these preliminary findings.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Despite diverse anatomical and histological trials in humans and animal models, the aetiology of hypospadias remains unknown and currently there is no clear molecular explanation about the emergence of this disease; however, genetic, endocrine and environmental mechanisms have been suggested.
The aim of the present study was to quantify and compare the androgen receptor (AR; mRNA and protein) levels in 40 prepuces of boys with and without hypospadias using quantitative real-time polymerase chain reaction, Western Blot and standardised, automated immunohistochemistry. AR mRNA (P = 0.013) and AR protein (P = 0.014) was significantly elevated in the prepuces of boys with hypospadias compared with boys without hypospadias. Altogether our data indicate that elevated AR mRNA and protein levels can be considered as a biochemical response of an AR signalling defect as an identified cause in boys with hypospadias. Additionally, nuclear staining intensity for AR-protein in specimens of boys with hypospadias was higher than in boys with phimosis.


 Objective

To address the role of the androgen receptor (AR) on mRNA and protein levels in prepuces of boys with and without hypospadias.



Patients and Methods

Data from 40 foreskin specimens of consecutive circumcised boys (20 with vs 20 without hypospadias) were enrolled in this prospective study. After surgery, samples were fixed in formaldehyde and frozen in liquid nitrogen. Total RNA was isolated from frozen tissue and transcribed to complementary DNA.
The amount of AR mRNA was measured by quantitative real-time polymerase chain reaction and Western Blot and standardised, automated immunohistochemistry were used to assess AR protein levels.



Results

The mean age at time of surgery was 61.8 and 30.9 months in boys without and with hypospadias, respectively.
There was penile, coronal and sine hypospadias in seven (35%), nine (45%), and four (20%) boys, respectively. AR mRNA was significantly elevated in the prepuces of boys with hypospadias compared with boys without hypospadias, at a mean (sd) of 28.33 (5.39) vs 15.31 (1.85) (P = 0.013).
Furthermore, the amount of AR protein was higher in boys with, compared with boys without hypospadias, at a mean (sd) of 133.25 (6.17) vs 100 (4.45) (P = 0.014).



Conclusions

Different AR mRNA expression and protein levels seem to be an indication of an AR signalling defect as a cause in boys with hypospadias.
Decreased AR DNA binding and functional capability may result in a compensatory up-regulation of both AR mRNA and protein.
Further studies are necessary to perform structural analysis of the AR and to corroborate these preliminary findings.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11723.x" xmlns="http://purl.org/rss/1.0/"><title>To treat or not to treat: is the way forward clearer in low-risk prostate cancer?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11723.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">To treat or not to treat: is the way forward clearer in low-risk prostate cancer?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vincent J. Gnanapragasam</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:51:03.846551-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11723.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11723.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11723.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11695.x" xmlns="http://purl.org/rss/1.0/"><title>Predictors of biochemical failure in patients undergoing prostate whole-gland salvage cryotherapy: a novel risk stratification model</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11695.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Predictors of biochemical failure in patients undergoing prostate whole-gland salvage cryotherapy: a novel risk stratification model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philippe E. Spiess, David A. Levy, Vladimir Mouraviev, Louis L. Pisters, J. Stephen Jones</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:50:59.85034-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11695.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11695.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11695.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11695-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11695-list-0001" class="bullet">
<li>Previous studies have identified the most important prognostic factors of the likely outcomes of salvage prostate whole-gland ablation, including initial clinical stage, biopsy Gleason score, and PSA (total and doubling time). There is potential for further optimization of candidate selection for salvage cryoablation with curative intent and nadir PSA achieved after whole-gland cryotherapy may provide additional prognostic value.</li>
<li>The study shows that the most important prognostic factors of biochemical progression-free survival for patients who have undergone whole-gland salvage prostate cryotherapy are nadir PSA achieved after therapy and pre-therapy biopsy Gleason score. Based on these two prognostic variables, we have identified risk stratification groups (low, intermediate and high) which help predict the expected outcomes of salvage whole-gland prostate cryotherapy in a given patient. This risk stratification constitutes a useful clinical tool in defining which patients maybe best suited for this local salvage treatment method.</li>
</ul></div></div>
<div class="section" id="bju11695-sec-1002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11695-list-0002" class="bullet">
<li>To assess the prognostic variables predicting the risk of biochemical progression-free survival (bPFS) after salvage prostate whole-gland cryotherapy using the Phoenix definition of bPFS.</li>
</ul></div></div>
<div class="section" id="bju11695-sec-1003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11695-list-0003" class="bullet">
<li>A total of 132 patients underwent prostate whole-gland salvage cryotherapy with curative intent. No patient underwent neoadjuvant/adjuvant hormonal ablative therapy, and all had extended post-salvage prostate-specific antigen (PSA) follow-up data.</li>
<li>Cox univariate and multivariate logistic regression analyses of potential predictors of bPFS were conducted.</li>
<li>Kaplan–Meier analyses of bPFS was also performed.</li>
</ul></div></div>
<div class="section" id="bju11695-sec-1004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11695-list-0004" class="bullet">
<li>At a mean (range) follow-up of 4.3 (0.9–12.7) years, the median (range) post-cryotherapy nadir PSA achieved was 0.17 (0–33.9) ng/mL.</li>
<li>On multivariate analysis, predictors of bPFS were nadir PSA post-cryotherapy and pre-salvage biopsy Gleason score (<em>P</em> &lt; 0.001 and 0.009, respectively).</li>
<li>Risk stratification groups (low, intermediate and high) were developed based on the presence of zero, one or two adverse risk factors, the risk factors being either a nadir PSA &gt;2.5 ng/mL or biopsy Gleason score ≥7, with the Kaplan–Meier bPFS curves of these risk groups being significantly different (<em>P =</em> 0.02 and &lt;0.001, respectively).</li>
</ul></div></div>
<div class="section" id="bju11695-sec-1005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11695-list-0005" class="bullet">
<li>Post-salvage nadir PSA and pre-salvage biopsy Gleason score are important predictors of outcome in this patient cohort.</li>
<li>Low-, intermediate- and high-risk groups can be determined based on these variables and can define patients best suited for prostate cryotherapy.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Previous studies have identified the most important prognostic factors of the likely outcomes of salvage prostate whole-gland ablation, including initial clinical stage, biopsy Gleason score, and PSA (total and doubling time). There is potential for further optimization of candidate selection for salvage cryoablation with curative intent and nadir PSA achieved after whole-gland cryotherapy may provide additional prognostic value.
The study shows that the most important prognostic factors of biochemical progression-free survival for patients who have undergone whole-gland salvage prostate cryotherapy are nadir PSA achieved after therapy and pre-therapy biopsy Gleason score. Based on these two prognostic variables, we have identified risk stratification groups (low, intermediate and high) which help predict the expected outcomes of salvage whole-gland prostate cryotherapy in a given patient. This risk stratification constitutes a useful clinical tool in defining which patients maybe best suited for this local salvage treatment method.


 Objective

To assess the prognostic variables predicting the risk of biochemical progression-free survival (bPFS) after salvage prostate whole-gland cryotherapy using the Phoenix definition of bPFS.



Patients and Methods

A total of 132 patients underwent prostate whole-gland salvage cryotherapy with curative intent. No patient underwent neoadjuvant/adjuvant hormonal ablative therapy, and all had extended post-salvage prostate-specific antigen (PSA) follow-up data.
Cox univariate and multivariate logistic regression analyses of potential predictors of bPFS were conducted.
Kaplan–Meier analyses of bPFS was also performed.



Results

At a mean (range) follow-up of 4.3 (0.9–12.7) years, the median (range) post-cryotherapy nadir PSA achieved was 0.17 (0–33.9) ng/mL.
On multivariate analysis, predictors of bPFS were nadir PSA post-cryotherapy and pre-salvage biopsy Gleason score (P &lt; 0.001 and 0.009, respectively).
Risk stratification groups (low, intermediate and high) were developed based on the presence of zero, one or two adverse risk factors, the risk factors being either a nadir PSA &gt;2.5 ng/mL or biopsy Gleason score ≥7, with the Kaplan–Meier bPFS curves of these risk groups being significantly different (P = 0.02 and &lt;0.001, respectively).



Conclusions

Post-salvage nadir PSA and pre-salvage biopsy Gleason score are important predictors of outcome in this patient cohort.
Low-, intermediate- and high-risk groups can be determined based on these variables and can define patients best suited for prostate cryotherapy.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11653.x" xmlns="http://purl.org/rss/1.0/"><title>Tumour expression of bladder cancer-associated urinary proteins</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11653.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tumour expression of bladder cancer-associated urinary proteins</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mårten Lindén, Ulrika Segersten, Marcus Runeson, Kenneth Wester, Christer Busch, Ulf Pettersson, Sara Bergström Lind, Per-Uno Malmström</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T07:50:57.812593-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11653.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11653.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11653.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11653-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11653-list-1001" class="bullet">
<li>The current basis for diagnosis and prognosis in urinary bladder cancer is based on the pathologists' assessment of a biopsy of the tumour. Urinary biomarkers are preferable as they can be non-invasively sampled. Urinary cytology is the only test with widespread use but is hampered by poor reproducibility and low sensitivity.</li>
<li>By studying the protein expression in bladder tumour tissue samples of proteins previously found in elevated levels in the urine of patients with bladder cancer, we have been able to show that these proteins originate from the tumour. The immunoreactivity of three of the investigated proteins increased with higher stage. Also a serine peptidase inhibitor was found to be predictive of progression from non-muscle-invasive to muscle-invasive tumours.</li>
</ul></div></div>
<div class="section" id="bju11653-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11653-list-0001" class="bullet">
<li>To analyse the expression of five bladder cancer-associated urinary proteins and investigate if expression is related to the malignant phenotype of the tumour.</li>
<li>To explore the possible prognostic value of these proteins.</li>
</ul></div></div>
<div class="section" id="bju11653-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11653-list-0002" class="bullet">
<li>Urine samples, 16 from patients with bladder cancer and 26 from controls, were used in Western Blotting experiments.</li>
<li>Tissue microarrays with bladder tissue from 344 patients diagnosed with bladder cancer between 1984 and 2005 was used in immunohistochemistry experiments.</li>
<li>The proteins apolipoprotein E (APOE), fibrinogen β chain precursor (FGB), leucine-rich α2-glycoprotein (LRG1), polymerase (RNA) I polypeptide E (POLR1E), α1-antitrypsin (SERPINA1) and topoisomerase 2A (TOP2A) were probed with antibodies validated by the Human Protein Atlas.</li>
</ul></div></div>
<div class="section" id="bju11653-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11653-list-0003" class="bullet">
<li>Increased expressions of APOE, FGB and POLR1E were correlated with increased tumour stage (<em>P</em> &lt; 0.001).</li>
<li>Expression of SERPINA1 in Ta and T1 tumours was found to increase the risk of tumour progression (hazard ratio 2.57, 95% confidence interval 1.13–5.87; <em>P</em> = 0.025)</li>
</ul></div></div>
<div class="section" id="bju11653-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11653-list-0004" class="bullet">
<li>All proteins previously detected in urine from patients with bladder cancer were also expressed in bladder cancer tissue.</li>
<li>The expression of APOE, FGB and POLR1E increased with stage and they are potential diagnostic markers.</li>
<li>SERPINA1 was identified as a prognostic marker candidate.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The current basis for diagnosis and prognosis in urinary bladder cancer is based on the pathologists' assessment of a biopsy of the tumour. Urinary biomarkers are preferable as they can be non-invasively sampled. Urinary cytology is the only test with widespread use but is hampered by poor reproducibility and low sensitivity.
By studying the protein expression in bladder tumour tissue samples of proteins previously found in elevated levels in the urine of patients with bladder cancer, we have been able to show that these proteins originate from the tumour. The immunoreactivity of three of the investigated proteins increased with higher stage. Also a serine peptidase inhibitor was found to be predictive of progression from non-muscle-invasive to muscle-invasive tumours.


 Objectives

To analyse the expression of five bladder cancer-associated urinary proteins and investigate if expression is related to the malignant phenotype of the tumour.
To explore the possible prognostic value of these proteins.



Patients and Methods

Urine samples, 16 from patients with bladder cancer and 26 from controls, were used in Western Blotting experiments.
Tissue microarrays with bladder tissue from 344 patients diagnosed with bladder cancer between 1984 and 2005 was used in immunohistochemistry experiments.
The proteins apolipoprotein E (APOE), fibrinogen β chain precursor (FGB), leucine-rich α2-glycoprotein (LRG1), polymerase (RNA) I polypeptide E (POLR1E), α1-antitrypsin (SERPINA1) and topoisomerase 2A (TOP2A) were probed with antibodies validated by the Human Protein Atlas.



Results

Increased expressions of APOE, FGB and POLR1E were correlated with increased tumour stage (P &lt; 0.001).
Expression of SERPINA1 in Ta and T1 tumours was found to increase the risk of tumour progression (hazard ratio 2.57, 95% confidence interval 1.13–5.87; P = 0.025)



Conclusions

All proteins previously detected in urine from patients with bladder cancer were also expressed in bladder cancer tissue.
The expression of APOE, FGB and POLR1E increased with stage and they are potential diagnostic markers.
SERPINA1 was identified as a prognostic marker candidate.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12006" xmlns="http://purl.org/rss/1.0/"><title>Effects of drug cessation after flexible-dose fesoterodine in patients with overactive bladder</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of drug cessation after flexible-dose fesoterodine in patients with overactive bladder</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vik Khullar, Linda Cardozo, Con J. Kelleher, Timothy Hall, John Ryan, Caty Ebel Bitoun, Amanda Darekar, Daniel Arumi, Adrian Wagg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T05:57:59.203978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12006-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12006-list-0001" class="bullet">
<li>To determine the course of overactive bladder (OAB) symptoms after 4 weeks of no treatment following a 12-week study of the efficacy and safety of flexible-dose fesoterodine in patients with OAB who were enrolled in the UK healthcare system. There are limited data available on the natural time course of OAB symptoms after the cessation of treatment.</li>
</ul></div></div>
<div class="section" id="bju12006-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><ul id="bju12006-list-0002" class="bullet">
<li>In the open-label UK Study Assessing Flexible-dose Fesoterodine in Adults trial, patients aged ≥18 years with self-reported OAB symptoms for ≥3 months, a mean of at least eight micturitions per 24 h and three or more urgency episodes per 24 h on a 3-day bladder diary at baseline, and at least moderate bladder-related problems reported on the Patient Perception of Bladder Condition (PPBC) at baseline, were treated with fesoterodine for 12 weeks.</li>
<li>All patients received fesoterodine 4 mg once daily for the first 4 weeks, at which time they could choose to increase the dose to 8 mg once daily, based on a discussion of treatment efficacy and tolerability with the investigator, or they could remain on fesoterodine 4 mg for the remaining 8 weeks.</li>
<li>The 12-week treatment period was followed by a 4-week follow-up period of no fesoterodine treatment.</li>
<li>Patients completed 3-day bladder diaries and the PPBC at baseline, week 4, end of treatment (week 12) and end of the follow-up period (week 16); the King's Health Questionnaire at baseline, end of treatment (week 12) and end of the follow-up period (week 16); and the Benefit, Satisfaction and Willingness to Continue questionnaire at week 12.</li>
</ul></div></div>
<div class="section" id="bju12006-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12006-list-0003" class="bullet">
<li>After 12 weeks of fesoterodine treatment, patients had clinically meaningful improvements in bladder diary variables and King's Health Questionnaire domains; 79% (254/322) of patients reported an improvement on the PPBC.</li>
<li>After 4 weeks of no treatment, most patients deteriorated back to week 4 levels or worse on all bladder diary and patient-reported outcomes.</li>
<li>Patients who expressed a benefit from fesoterodine treatment, satisfaction with their treatment or a willingness to continue treatment showed greater improvement from baseline to week 12 and greater deterioration from week 12 to week 16 than patients who did not respond positively on the Benefit, Satisfaction and Willingness to Continue questionnaire.</li>
<li>Both men and women showed a meaningful deterioration in bladder diary variables and patient-reported outcomes at week 16; baseline symptom severity, age and week 4 dose escalation status did not appear to affect outcome deterioration at week 16.</li>
</ul></div></div>
<div class="section" id="bju12006-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12006-list-0004" class="bullet">
<li>At 4 weeks after fesoterodine was discontinued, patients showed an increase in the frequency of OAB symptoms, an increase in the severity of bladder-related problems and a reduction in health-related quality of life.</li>
<li>Many patients with OAB who respond to antimuscarinics may require treatment for more than 12 weeks because symptoms recur as early as 4 weeks after the cessation of therapy.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To determine the course of overactive bladder (OAB) symptoms after 4 weeks of no treatment following a 12-week study of the efficacy and safety of flexible-dose fesoterodine in patients with OAB who were enrolled in the UK healthcare system. There are limited data available on the natural time course of OAB symptoms after the cessation of treatment.



Patients and methods

In the open-label UK Study Assessing Flexible-dose Fesoterodine in Adults trial, patients aged ≥18 years with self-reported OAB symptoms for ≥3 months, a mean of at least eight micturitions per 24 h and three or more urgency episodes per 24 h on a 3-day bladder diary at baseline, and at least moderate bladder-related problems reported on the Patient Perception of Bladder Condition (PPBC) at baseline, were treated with fesoterodine for 12 weeks.
All patients received fesoterodine 4 mg once daily for the first 4 weeks, at which time they could choose to increase the dose to 8 mg once daily, based on a discussion of treatment efficacy and tolerability with the investigator, or they could remain on fesoterodine 4 mg for the remaining 8 weeks.
The 12-week treatment period was followed by a 4-week follow-up period of no fesoterodine treatment.
Patients completed 3-day bladder diaries and the PPBC at baseline, week 4, end of treatment (week 12) and end of the follow-up period (week 16); the King's Health Questionnaire at baseline, end of treatment (week 12) and end of the follow-up period (week 16); and the Benefit, Satisfaction and Willingness to Continue questionnaire at week 12.



Results

After 12 weeks of fesoterodine treatment, patients had clinically meaningful improvements in bladder diary variables and King's Health Questionnaire domains; 79% (254/322) of patients reported an improvement on the PPBC.
After 4 weeks of no treatment, most patients deteriorated back to week 4 levels or worse on all bladder diary and patient-reported outcomes.
Patients who expressed a benefit from fesoterodine treatment, satisfaction with their treatment or a willingness to continue treatment showed greater improvement from baseline to week 12 and greater deterioration from week 12 to week 16 than patients who did not respond positively on the Benefit, Satisfaction and Willingness to Continue questionnaire.
Both men and women showed a meaningful deterioration in bladder diary variables and patient-reported outcomes at week 16; baseline symptom severity, age and week 4 dose escalation status did not appear to affect outcome deterioration at week 16.



Conclusions

At 4 weeks after fesoterodine was discontinued, patients showed an increase in the frequency of OAB symptoms, an increase in the severity of bladder-related problems and a reduction in health-related quality of life.
Many patients with OAB who respond to antimuscarinics may require treatment for more than 12 weeks because symptoms recur as early as 4 weeks after the cessation of therapy.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11649.x" xmlns="http://purl.org/rss/1.0/"><title>Impact of renal function on eligibility for chemotherapy and survival in patients who have undergone radical nephro-ureterectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11649.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impact of renal function on eligibility for chemotherapy and survival in patients who have undergone radical nephro-ureterectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Evanguelos Xylinas, Michael Rink, Vitaly Margulis, Thomas Clozel, Richard K. Lee, Evi Comploj, Giacomo Novara, Jay D. Raman, Yair Lotan, Alon Weizer, Morgan Roupret, Armin Pycha, Douglas S. Scherr, Christian Seitz, Vincenzo Ficarra, Quoc-Dien Trinh, Pierre I. Karakiewicz, Francesco Montorsi, Marc Zerbib, Shahrokh F. Shariat, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T12:57:19.822479-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11649.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11649.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11649.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11649-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11649-list-1001" class="bullet">
<li>Radical nephroureterectomy (RNU), the standard of care treatment for high-risk urothelial carcinoma of the upper tract (UTUC), results in loss of a renal unit. Loss of renal function decreases eligibility for systemic chemotherapies and results in decreased overall survival in various malignancies.</li>
<li>The study shows that only a small proportion of patients had a preoperative renal function that would allow cisplatin-based chemotherapy. Moreover, eGFR significantly decreased after RNU, thereby lowering the rate of cisplatin eligibility to only 16 and 52% of patients based on the thresholds of 60 and 45 mL/min/1.73 m<sup>2</sup>, respectively. Taken together with the rest of the literature, the findings of the study support the use of cisplatin-based chemotherapy, when indicated, in the neoadjuvant rather than adjuvant setting.</li>
</ul></div></div>
<div class="section" id="bju11649-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11649-list-0001" class="bullet">
<li>To report (i) the estimated glomerular filtration rate (eGFR) changes in patients undergoing radical nephro-ureterectomy (RNU) for upper tract urothelial carcinoma (UTUC); (ii) the rate of change in eGFR in patients eligible for cisplatin-based chemotherapy; and (iii) the association of preoperative, postoperative and rate of change of renal function variables with survival outcomes.</li>
</ul></div></div>
<div class="section" id="bju11649-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patient and Methods</h4><div class="para"><ul id="bju11649-list-0002" class="bullet">
<li>We performed a retrospective analysis of 666 patients treated with RNU for UTUC at seven international institutions from 1994 to 2007.</li>
<li>The eGFR was calculated at baseline and at 3–6 months (Modification of Diet in Renal Disease formula (MDRD) and Chronic Kidney Disease Epidemiology Collaboration formula (CKD-EP) equations).</li>
</ul></div></div>
<div class="section" id="bju11649-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11649-list-0003" class="bullet">
<li>The median (interquartile range) eGFR decreased by 18.2 (8–12)% after RNU. A total of 37% of patients had a preoperative eGFR ≥ 60 mL/min/1.73 m<sup>2</sup>, which decreased to 16% after RNU (<em>P</em> &lt; 0.001); 72% of patients had a preoperative eGFR ≥ 45 mL/min/1.73 m<sup>2</sup>, which decreased to 52% after RNU (<em>P</em> &lt; 0.001). The distributions were similar when analyses were restricted to patients with locally advanced disease (pT3–pT4) and/or lymph node metastasis. Patients older than the median age of 70 years were more likely to have a decrease in eGFR after RNU (<em>P</em> &lt; 0.001).</li>
<li>None of the renal function variables was associated with clinical outcomes such as disease recurrence, cancer-specific and overall mortality; however, when analyses were restricted to patients who had no adjuvant chemotherapy and did not experience disease recurrence (<em>n</em> = 431), a preoperative eGFR ≥ 60 mL/min/1.73 m<sup>2</sup> (<em>P</em> = 0.03) and a postoperative eGFR ≥ 45 mL/min/1.73 m<sup>2</sup> (<em>P</em> = 0.04) were associated with better overall survival in univariable analyses.</li>
</ul></div></div>
<div class="section" id="bju11649-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11649-list-0004" class="bullet">
<li>In patients who had UTUC, eGFR was low and furthermore, it significantly decreased after RNU.</li> <li>Renal function did not affect cancer-specific outcomes after RNU.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Radical nephroureterectomy (RNU), the standard of care treatment for high-risk urothelial carcinoma of the upper tract (UTUC), results in loss of a renal unit. Loss of renal function decreases eligibility for systemic chemotherapies and results in decreased overall survival in various malignancies.
The study shows that only a small proportion of patients had a preoperative renal function that would allow cisplatin-based chemotherapy. Moreover, eGFR significantly decreased after RNU, thereby lowering the rate of cisplatin eligibility to only 16 and 52% of patients based on the thresholds of 60 and 45 mL/min/1.73 m2, respectively. Taken together with the rest of the literature, the findings of the study support the use of cisplatin-based chemotherapy, when indicated, in the neoadjuvant rather than adjuvant setting.


 Objective

To report (i) the estimated glomerular filtration rate (eGFR) changes in patients undergoing radical nephro-ureterectomy (RNU) for upper tract urothelial carcinoma (UTUC); (ii) the rate of change in eGFR in patients eligible for cisplatin-based chemotherapy; and (iii) the association of preoperative, postoperative and rate of change of renal function variables with survival outcomes.



Patient and Methods

We performed a retrospective analysis of 666 patients treated with RNU for UTUC at seven international institutions from 1994 to 2007.
The eGFR was calculated at baseline and at 3–6 months (Modification of Diet in Renal Disease formula (MDRD) and Chronic Kidney Disease Epidemiology Collaboration formula (CKD-EP) equations).



Results

The median (interquartile range) eGFR decreased by 18.2 (8–12)% after RNU. A total of 37% of patients had a preoperative eGFR ≥ 60 mL/min/1.73 m2, which decreased to 16% after RNU (P &lt; 0.001); 72% of patients had a preoperative eGFR ≥ 45 mL/min/1.73 m2, which decreased to 52% after RNU (P &lt; 0.001). The distributions were similar when analyses were restricted to patients with locally advanced disease (pT3–pT4) and/or lymph node metastasis. Patients older than the median age of 70 years were more likely to have a decrease in eGFR after RNU (P &lt; 0.001).
None of the renal function variables was associated with clinical outcomes such as disease recurrence, cancer-specific and overall mortality; however, when analyses were restricted to patients who had no adjuvant chemotherapy and did not experience disease recurrence (n = 431), a preoperative eGFR ≥ 60 mL/min/1.73 m2 (P = 0.03) and a postoperative eGFR ≥ 45 mL/min/1.73 m2 (P = 0.04) were associated with better overall survival in univariable analyses.



Conclusions

In patients who had UTUC, eGFR was low and furthermore, it significantly decreased after RNU. Renal function did not affect cancer-specific outcomes after RNU.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12029" xmlns="http://purl.org/rss/1.0/"><title>Impact of the European Randomized Study of Screening for Prostate Cancer (ERSPC) on prostate-specific antigen (PSA) testing by Dutch general practitioners</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12029</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impact of the European Randomized Study of Screening for Prostate Cancer (ERSPC) on prostate-specific antigen (PSA) testing by Dutch general practitioners</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Saskia Meer, Boudewijn J. Kollen, Willem H. Hirdes, Martijn G. Steffens, Josette E.H.M. Hoekstra-Weebers, Rien M. Nijman, Marco H. Blanker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T12:41:53.878751-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12029</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12029</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12029</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12029-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12029-list-0001" class="bullet">
<li>To determine the impact of the European Randomized Study of Screening for Prostate Cancer (ERSPC) publication in 2009 on prostate-specific antigen (PSA) level testing by Dutch general practitioners (GPs) in men aged ≥40 years.</li>
</ul></div></div>
<div class="section" id="bju12029-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12029-list-0002" class="bullet">
<li>Retrospective study with a Dutch insurance company database (containing PSA test claims) and a large district hospital-laboratory database (containing PSA-test results).</li>
<li>The difference in primary PSA-testing rate as well as follow-up testing before and after the ERSPC was tested using the chi-square test with statistical significance at <em>P</em> &lt; 0.05.</li>
</ul></div></div>
<div class="section" id="bju12029-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12029-list-0003" class="bullet">
<li>Decline in PSA tests 4 months after ERSPC publication, especially for men aged ≥60 years.</li>
<li>Primary testing as well as follow-up testing decreased, both for PSA levels of &lt;4 ng/mL as well as for PSA levels of 4–10 ng/mL.</li>
<li>Follow-up testing after a PSA level result of &gt;10 ng/mL moderately increased (<em>P</em> = 0.171).</li>
<li>Referral to a urologist after a PSA level result of &gt;4 ng/mL decreased slightly after the ERSPC publication (<em>P</em> = 0.044).</li>
</ul></div></div>
<div class="section" id="bju12029-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12029-list-0004" class="bullet">
<li>After the ERSPC publication primary PSA testing as well as follow-up testing decreased.</li>
<li>Follow-up testing seemed not to be adequate after an abnormal PSA result. The reasons for this remain unclear.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To determine the impact of the European Randomized Study of Screening for Prostate Cancer (ERSPC) publication in 2009 on prostate-specific antigen (PSA) level testing by Dutch general practitioners (GPs) in men aged ≥40 years.



Materials and Methods

Retrospective study with a Dutch insurance company database (containing PSA test claims) and a large district hospital-laboratory database (containing PSA-test results).
The difference in primary PSA-testing rate as well as follow-up testing before and after the ERSPC was tested using the chi-square test with statistical significance at P &lt; 0.05.



Results

Decline in PSA tests 4 months after ERSPC publication, especially for men aged ≥60 years.
Primary testing as well as follow-up testing decreased, both for PSA levels of &lt;4 ng/mL as well as for PSA levels of 4–10 ng/mL.
Follow-up testing after a PSA level result of &gt;10 ng/mL moderately increased (P = 0.171).
Referral to a urologist after a PSA level result of &gt;4 ng/mL decreased slightly after the ERSPC publication (P = 0.044).



Conclusions

After the ERSPC publication primary PSA testing as well as follow-up testing decreased.
Follow-up testing seemed not to be adequate after an abnormal PSA result. The reasons for this remain unclear.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12014" xmlns="http://purl.org/rss/1.0/"><title>Gender-specific effect of smoking on upper tract urothelial carcinoma outcomes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gender-specific effect of smoking on upper tract urothelial carcinoma outcomes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael Rink, Evanguelos Xylinas, Quoc-Dien Trinh, Yair Lotan, Vitaly Margulis, Jay D. Raman, Margit Fisch, Richard K. Lee, Felix K. Chun, Joual Abdennabi, Christian Seitz, Armin Pycha, Alexandre R. Zlotta, Pierre I. Karakiewicz, Marko Babjuk, Douglas S. Scherr, Shahrokh F. Shariat, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T12:40:40.238524-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12014</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12014</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12014-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12014-list-0001" class="bullet">
<li>To evaluate the gender-specific differential effects of smoking habits and cumulative smoking exposure on outcomes in patients with upper tract urothelial carcinoma (UTUC) treated with radical nephroureterectomy (RNU).</li>
</ul></div></div>
<div class="section" id="bju12014-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12014-list-0002" class="bullet">
<li>A total of 864 consecutive patients, comprising 553 (64%) men and 311 (36%) women, from five international institutions underwent RNU without neoadjuvant chemotherapy.</li>
<li>Smoking history included smoking status (current, former or never), quantity of cigarettes per day (CPD), smoking duration in years and years since smoking cessation. Cumulative smoking exposure was categorized as light short-term (≤19 CPD and ≤19.9 years), moderate (all combinations except light short-term and heavy long-term), and heavy long-term (≥20 CPD and ≥20 years).</li>
<li>Uni- and multivariable competing risk regression models were used to assess the associations with outcomes.</li>
</ul></div></div>
<div class="section" id="bju12014-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12014-list-0003" class="bullet">
<li>Overall, 244 (28.2%), 297 (34.4%) and 323 (37.4%) patients were never, former and current smokers, respectively.</li>
<li>There were no differences in smoking status, quantity and duration between the genders.</li> <li>In female ever smokers, 30 (9.6%), 121 (38.9%) and 67 (21.5%) were light short-term, moderate and heavy long-term smokers, respectively. Compared with men, female current smokers were more likely to experience disease recurrence in univariable analysis (<em>P</em> = 0.013).</li>
<li>In heavy long-term smokers, female gender was significantly associated with disease recurrence (hazard ratio [HR] 1.7; <em>P</em> = 0.03) and cancer-specific mortality (HR 2.0; <em>P</em> = 0.009) in multivariable analysis that adjusted for standard clinico-pathological features.</li>
<li>In female patients only, smoking quantity, duration and cumulative exposure were associated with disease recurrence and cancer-specific mortality on multivariable analyses (<em>P</em> ≤ 0.025).</li>
</ul></div></div>
<div class="section" id="bju12014-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12014-list-0004" class="bullet">
<li>The impact of smoking on UTUC outcomes after RNU is gender-specific.</li>
<li>Females who are current and heavy long-term smokers experience worse outcomes than their male counterparts.</li>
<li>Further research is needed to elucidate the molecular mechanisms underlying the gender-specific differential effect of smoking on UTUC outcomes.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the gender-specific differential effects of smoking habits and cumulative smoking exposure on outcomes in patients with upper tract urothelial carcinoma (UTUC) treated with radical nephroureterectomy (RNU).



Patients and Methods

A total of 864 consecutive patients, comprising 553 (64%) men and 311 (36%) women, from five international institutions underwent RNU without neoadjuvant chemotherapy.
Smoking history included smoking status (current, former or never), quantity of cigarettes per day (CPD), smoking duration in years and years since smoking cessation. Cumulative smoking exposure was categorized as light short-term (≤19 CPD and ≤19.9 years), moderate (all combinations except light short-term and heavy long-term), and heavy long-term (≥20 CPD and ≥20 years).
Uni- and multivariable competing risk regression models were used to assess the associations with outcomes.



Results

Overall, 244 (28.2%), 297 (34.4%) and 323 (37.4%) patients were never, former and current smokers, respectively.
There were no differences in smoking status, quantity and duration between the genders. In female ever smokers, 30 (9.6%), 121 (38.9%) and 67 (21.5%) were light short-term, moderate and heavy long-term smokers, respectively. Compared with men, female current smokers were more likely to experience disease recurrence in univariable analysis (P = 0.013).
In heavy long-term smokers, female gender was significantly associated with disease recurrence (hazard ratio [HR] 1.7; P = 0.03) and cancer-specific mortality (HR 2.0; P = 0.009) in multivariable analysis that adjusted for standard clinico-pathological features.
In female patients only, smoking quantity, duration and cumulative exposure were associated with disease recurrence and cancer-specific mortality on multivariable analyses (P ≤ 0.025).



Conclusions

The impact of smoking on UTUC outcomes after RNU is gender-specific.
Females who are current and heavy long-term smokers experience worse outcomes than their male counterparts.
Further research is needed to elucidate the molecular mechanisms underlying the gender-specific differential effect of smoking on UTUC outcomes.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11689.x" xmlns="http://purl.org/rss/1.0/"><title>Identification of the variables associated with pain during transrectal ultrasonography-guided prostate biopsy in the era of periprostatic nerve block: the role of transrectal probe configuration</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11689.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Identification of the variables associated with pain during transrectal ultrasonography-guided prostate biopsy in the era of periprostatic nerve block: the role of transrectal probe configuration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ayman S. Moussa, Ahmed El-Shafei, Ed Diaz, Tianming Gao, Osama M. Zaytoun, Khaled Fareed, James C. Ulchaker, J. Stephen Jones</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T12:40:22.874173-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11689.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11689.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11689.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11687-sec-0016" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11689-list-0001" class="bullet">
<li>Currently, peri-prostatic nerve block (PPNB) is the most effective method to reduce pain during TRUS biopsy. Although the advance in PPNB allowed a better tolerability of the procedure by most of patients, a minority of men still find the procedure unacceptably painful.</li>
<li>We found in this study that the probe design and the needle guide affect pain encountered during different steps of TRUS guided PBx.</li>
</ul></div></div>
<div class="section" id="bju11689-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11689-list-0002" class="bullet">
<li>To identify the different factors that are associated with pain perceived during transrectal ultrasonography (TRUS)-guided prostate biopsy (PBx), with special focus on the role of transrectal probe configuration.</li>
</ul></div></div>
<div class="section" id="bju11689-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11689-list-0003" class="bullet">
<li>We analysed prospective data on 1114 patients undergoing TRUS-guided PBx at our institute from January 2007 to August 2010.</li>
<li>Patients completed questionnaires based on a 10-point visual analogue pain scale related to the consecutive steps of PBx: probe insertion, application of periprostatic nerve block (PPNB) and the obtaining of PBx cores.</li>
<li>The variables of interest were age, prostate volume, DRE findings, number of previous biopsies, probe type and the number of retrieved cores.</li>
<li>All variables were correlated to pain scores using multivariate regression analysis.</li>
</ul></div></div>
<div class="section" id="bju11689-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11689-list-0004" class="bullet">
<li>At the probe insertion step, end-fire probes were more painful than side-fire probes.</li>
<li>The Siemens G50<sup>TM</sup> with metal, short plastic and long plastic needle guides (Siemens, Munich, Germany) had higher pain scores than the B&amp;K probe (Bruel &amp; Kjaer Medical, Copenhagen, Denmark; <em>P</em> = 0.09, 0.008 and 0.003, respectively).</li>
<li>For pain at the PPNB application step, all G50<sup>TM</sup> guide subtypes and the Sonoline Prima probe (Siemens) had higher pain scores than the B&amp;K probe, but this only reached statistical significance for the G50<sup>TM</sup> probe with short plastic guide (<em>P</em> = 0.03).</li>
<li>On obtaining PBx cores, all G50<sup>TM</sup> subtypes had higher pain scores when compared with the B&amp;K probe (<em>P</em> = 0.59, 0.38 and 0.69, respectively).</li>
</ul></div></div>
<div class="section" id="bju11689-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11689-list-0005" class="bullet">
<li>The probe design and needle guide affect pain during each step of TRUS-guided PBx.</li>
<li>Both the B&amp;K and Sonoline Prima probes caused less pain when compared with the G50<sup>TM</sup> probe, regardless of needle guide.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Currently, peri-prostatic nerve block (PPNB) is the most effective method to reduce pain during TRUS biopsy. Although the advance in PPNB allowed a better tolerability of the procedure by most of patients, a minority of men still find the procedure unacceptably painful.
We found in this study that the probe design and the needle guide affect pain encountered during different steps of TRUS guided PBx.


 Objective

To identify the different factors that are associated with pain perceived during transrectal ultrasonography (TRUS)-guided prostate biopsy (PBx), with special focus on the role of transrectal probe configuration.



Patients and Methods

We analysed prospective data on 1114 patients undergoing TRUS-guided PBx at our institute from January 2007 to August 2010.
Patients completed questionnaires based on a 10-point visual analogue pain scale related to the consecutive steps of PBx: probe insertion, application of periprostatic nerve block (PPNB) and the obtaining of PBx cores.
The variables of interest were age, prostate volume, DRE findings, number of previous biopsies, probe type and the number of retrieved cores.
All variables were correlated to pain scores using multivariate regression analysis.



Results

At the probe insertion step, end-fire probes were more painful than side-fire probes.
The Siemens G50TM with metal, short plastic and long plastic needle guides (Siemens, Munich, Germany) had higher pain scores than the B&amp;K probe (Bruel &amp; Kjaer Medical, Copenhagen, Denmark; P = 0.09, 0.008 and 0.003, respectively).
For pain at the PPNB application step, all G50TM guide subtypes and the Sonoline Prima probe (Siemens) had higher pain scores than the B&amp;K probe, but this only reached statistical significance for the G50TM probe with short plastic guide (P = 0.03).
On obtaining PBx cores, all G50TM subtypes had higher pain scores when compared with the B&amp;K probe (P = 0.59, 0.38 and 0.69, respectively).



Conclusions

The probe design and needle guide affect pain during each step of TRUS-guided PBx.
Both the B&amp;K and Sonoline Prima probes caused less pain when compared with the G50TM probe, regardless of needle guide.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11798.x" xmlns="http://purl.org/rss/1.0/"><title>Perioperative and early oncological outcomes after robot-assisted radical prostatectomy (RARP) in morbidly obese patients: a propensity score-matched study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11798.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Perioperative and early oncological outcomes after robot-assisted radical prostatectomy (RARP) in morbidly obese patients: a propensity score-matched study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Haidar Abdul-Muhsin, Camilo Giedelman, Srinivas Samavedi, Oscar Schatloff, Rafael Coelho, Bernardo Rocco, Kenneth Palmer, George Ebra, Vipul Patel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-05T11:09:52.682402-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2013.11798.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2013.11798.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11798.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11798-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11798-list-0001" class="bullet">
<li>To evaluate the perioperative and pathological outcomes associated with robot-assisted radical prostatectomy (RARP) in morbidly obese men.</li>
</ul></div></div> <div class="section" id="bju11798-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11798-list-0002" class="bullet">
<li>Between January 2008 and March 2012, 3041 patients underwent RARP at our institution by a single surgeon (V.P.).</li>
<li>In all, 44 patients were considered morbidly obese with a body mass index (BMI) of ≥40 kg/m<sup>2</sup>.</li>
<li>A propensity score-matched analysis was conducted using multivariable analysis to identify comparable groups of patients with a BMI of ≥40 and &lt;40 kg/m<sup>2</sup>.</li>
<li>Perioperative, pathological outcomes and complications were compared between the two matched groups.</li>
</ul></div></div>
<div class="section" id="bju11798-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11798-list-0003" class="bullet">
<li>There was no significant difference in operative time. However, the mean estimated blood loss was higher in morbidly obese patients, at a mean (<span class="smallCaps">sd</span>) of 113 (41) vs 130 (27) mL (<em>P</em> = 0.049).</li>
<li>Anastomosis was more difficult in morbidly obese patients (<em>P</em> = 0.001).</li>
<li>There were no significant differences in laterality, ease of nerve sparing, or transfusion rate between the groups.</li>
<li>There were no intraoperative complications in either group. Postoperative pathological outcomes were similar between the groups.</li>
<li>Differences in positive surgical margins and ease of nerve sparing approached statistical significance (<em>P</em> = 0.097, <em>P</em> = 0.075 respectively). Postoperative complication rates, pain scores, length of stay and indwelling catheter duration were similar in the groups.</li>
</ul></div></div>
<div class="section" id="bju11798-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11798-list-0004" class="bullet">
<li>RARP in morbidly obese patients is technically demanding. However, it can be accomplished with acceptable morbidity and resource use.</li>
<li>In the hands of an experienced surgeon, it is a safe procedure and offers beneficial clinical outcomes.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the perioperative and pathological outcomes associated with robot-assisted radical prostatectomy (RARP) in morbidly obese men.

 
Patients and Methods

Between January 2008 and March 2012, 3041 patients underwent RARP at our institution by a single surgeon (V.P.).
In all, 44 patients were considered morbidly obese with a body mass index (BMI) of ≥40 kg/m2.
A propensity score-matched analysis was conducted using multivariable analysis to identify comparable groups of patients with a BMI of ≥40 and &lt;40 kg/m2.
Perioperative, pathological outcomes and complications were compared between the two matched groups.



Results

There was no significant difference in operative time. However, the mean estimated blood loss was higher in morbidly obese patients, at a mean (sd) of 113 (41) vs 130 (27) mL (P = 0.049).
Anastomosis was more difficult in morbidly obese patients (P = 0.001).
There were no significant differences in laterality, ease of nerve sparing, or transfusion rate between the groups.
There were no intraoperative complications in either group. Postoperative pathological outcomes were similar between the groups.
Differences in positive surgical margins and ease of nerve sparing approached statistical significance (P = 0.097, P = 0.075 respectively). Postoperative complication rates, pain scores, length of stay and indwelling catheter duration were similar in the groups.



Conclusions

RARP in morbidly obese patients is technically demanding. However, it can be accomplished with acceptable morbidity and resource use.
In the hands of an experienced surgeon, it is a safe procedure and offers beneficial clinical outcomes.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12032" xmlns="http://purl.org/rss/1.0/"><title>A comparison of patient and tumour characteristics in two UK bladder cancer cohorts separated by 20 years</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12032</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A comparison of patient and tumour characteristics in two UK bladder cancer cohorts separated by 20 years</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard T. Bryan, Maurice P. Zeegers, Eline H. Roekel, Deborah Bird, Margaret R. Grant, Janet A. Dunn, Sarah Bathers, Gulnaz Iqbal, Humera S. Khan, Stuart I. Collins, Andrew Howman, Nayneeta S. Deshmukh, Nicholas D. James, Kar Keung Cheng, D. Michael A. Wallace</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:47:27.356123-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12032</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12032</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12032</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12032-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12032-list-0001" class="bullet">
<li>To compare patient and tumour characteristics at presentation from two large bladder cancer cohorts, with recruitment separated by 15–20 years</li>
<li>To identify significant differences in the West Midlands' urothelial cancer of the bladder (UCB) population during this period.</li>
</ul></div></div>
<div class="section" id="bju12032-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12032-list-0002" class="bullet">
<li>Data were collected prospectively from 1478 patients newly diagnosed with UCB in the West Midlands from January 1991 to June 1992 (Cohort 1), and from 1168 patients newly diagnosed with UBC within the same region from December 2005 to April 2011 (Cohort 2).</li>
<li>Gender, age, smoking history, and tumour grade, stage, type, multiplicity and size at presentation were compared using a Pearson chi-square test or Cochran–Armitage trend test, as appropriate.</li>
</ul></div></div>
<div class="section" id="bju12032-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Result</h4><div class="para"><ul id="bju12032-list-0003" class="bullet">
<li>Cohort 2 had a higher proportion of male patients (<em>P</em> = 0.021), elderly patients (<em>P</em> &lt; 0.001), grade 3 tumours (<em>P</em> &lt; 0.001), Ta/T1 tumours (<em>P</em> = 0.008), multiple tumours (<em>P</em> &lt; 0.001), and tumours of ≤2 cm in diameter (<em>P</em> &lt; 0.001).</li>
</ul></div></div>
<div class="section" id="bju12032-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12032-list-0004" class="bullet">
<li>There were significant differences between the cohorts.</li>
<li>These differences are potentially explained by an ageing population, changes in grading practices, improved awareness of important symptoms, improved cystoscopic technology, and reductions in treatment delays.</li>
<li>Regional cohorts remain important for identifying changes in tumour and patient characteristics that may influence disease management in the UK and beyond.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To compare patient and tumour characteristics at presentation from two large bladder cancer cohorts, with recruitment separated by 15–20 years
To identify significant differences in the West Midlands' urothelial cancer of the bladder (UCB) population during this period.



Patients and Methods

Data were collected prospectively from 1478 patients newly diagnosed with UCB in the West Midlands from January 1991 to June 1992 (Cohort 1), and from 1168 patients newly diagnosed with UBC within the same region from December 2005 to April 2011 (Cohort 2).
Gender, age, smoking history, and tumour grade, stage, type, multiplicity and size at presentation were compared using a Pearson chi-square test or Cochran–Armitage trend test, as appropriate.



Result

Cohort 2 had a higher proportion of male patients (P = 0.021), elderly patients (P &lt; 0.001), grade 3 tumours (P &lt; 0.001), Ta/T1 tumours (P = 0.008), multiple tumours (P &lt; 0.001), and tumours of ≤2 cm in diameter (P &lt; 0.001).



Conclusions

There were significant differences between the cohorts.
These differences are potentially explained by an ageing population, changes in grading practices, improved awareness of important symptoms, improved cystoscopic technology, and reductions in treatment delays.
Regional cohorts remain important for identifying changes in tumour and patient characteristics that may influence disease management in the UK and beyond.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11799.x" xmlns="http://purl.org/rss/1.0/"><title>Upgrading of Gleason score and prostate volume: a clinicopathological analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11799.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Upgrading of Gleason score and prostate volume: a clinicopathological analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kwang Hyun Kim, Sey Kiat Lim, Tae-Young Shin, Joo Yong Lee, Byung Ha Chung, Koon Ho Rha, Sung Joon Hong</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:47:23.533859-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2013.11799.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2013.11799.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2013.11799.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11799-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11799-list-0001" class="bullet">
<li>To more clearly elucidate the association between prostate volume and Gleason score (GS) upgrading.</li>
</ul></div></div>
<div class="section" id="bju11799-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patient and Methods</h4><div class="para"><ul id="bju11799-list-0002" class="bullet">
<li>We reviewed 451 patients with prostate cancer with a GS of 6 on biopsy, who underwent radical prostatectomy without neoadjuvant treatment.</li>
<li>As a preoperative variable, we assessed the independent effect of prostate volume on GS upgrading.</li>
<li>To evaluate the association between prostate volume and GS upgrading, we developed multivariate models with volumetric pathological variables, including postoperative tumour volume and percent tumour volume (tumour volume as a percentage of prostate volume).</li>
</ul></div></div>
<div class="section" id="bju11799-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11799-list-0003" class="bullet">
<li>GS upgrading was observed in 194 patients (43.0%).</li>
<li>As a preoperative variable, smaller prostate volume was an independent predictor of GS upgrading.</li>
<li>In regression analysis, prostate volume and postoperative tumour volume were inversely correlated.</li>
<li>On multivariate analysis including volumetric pathological variables, tumour volume was a strong independent factor influencing GS upgrading, and prostate volume lost statistical significance after adjusting for tumour volume.</li>
<li>Percent tumour volume was inversely correlated with GS upgrading after adjusting for tumour volume.</li>
</ul></div></div>
<div class="section" id="bju11799-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11799-list-0004" class="bullet">
<li>Smaller prostate volume was an independent predictor of GS upgrading as a preoperative variable.</li>
<li>The inverse relationship between prostate volume and GS upgrading seems to be attributable to cancer biology, which was represented by tumour volume in our study. Percent tumour volume was also inversely associated with GS upgrading.</li>
<li>These results suggest that biological factors and sampling error both play important roles in GS upgrading.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To more clearly elucidate the association between prostate volume and Gleason score (GS) upgrading.



Patient and Methods

We reviewed 451 patients with prostate cancer with a GS of 6 on biopsy, who underwent radical prostatectomy without neoadjuvant treatment.
As a preoperative variable, we assessed the independent effect of prostate volume on GS upgrading.
To evaluate the association between prostate volume and GS upgrading, we developed multivariate models with volumetric pathological variables, including postoperative tumour volume and percent tumour volume (tumour volume as a percentage of prostate volume).



Results

GS upgrading was observed in 194 patients (43.0%).
As a preoperative variable, smaller prostate volume was an independent predictor of GS upgrading.
In regression analysis, prostate volume and postoperative tumour volume were inversely correlated.
On multivariate analysis including volumetric pathological variables, tumour volume was a strong independent factor influencing GS upgrading, and prostate volume lost statistical significance after adjusting for tumour volume.
Percent tumour volume was inversely correlated with GS upgrading after adjusting for tumour volume.



Conclusions

Smaller prostate volume was an independent predictor of GS upgrading as a preoperative variable.
The inverse relationship between prostate volume and GS upgrading seems to be attributable to cancer biology, which was represented by tumour volume in our study. Percent tumour volume was also inversely associated with GS upgrading.
These results suggest that biological factors and sampling error both play important roles in GS upgrading.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11776.x" xmlns="http://purl.org/rss/1.0/"><title>Comparative effectiveness, costs and trends in treatment of small renal masses from 2005 to 2007</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11776.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative effectiveness, costs and trends in treatment of small renal masses from 2005 to 2007</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Keith J. Kowalczyk, Toni K. Choueiri, Nathanael D. Hevelone, Quoc-Dien Trinh, Stuart R. Lipsitz, Paul L. Nguyen, John H. Lynch, Jim C. Hu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:47:20.830035-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11776.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11776.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11776.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11776-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11776-list-0001" class="bullet">
<li>Retrospective data have suggested an increased survival benefit for patients undergoing partial nephrectomy compared to radical nephrectomy, possibly as a result of the avoidance of long-term renalin sufficiency and subsequent sequelae. However, recent level-one evidence has questioned this benefit. Both retrospective studies and randomized controlled trials are not without limitations.</li>
<li>There are few population-based data available with respect to the outcomes of partial nephrectomy vs radical nephrectomy. Additionally, there are no population-based studies analyzing the surgical approach (minimally-invasive vs open), as well as other modalities, such as ablation and surveillance. Finally, there is very little information available on the potential differences in cost for each approach. The present study comprises the first comprehensive population-based analysis of the trends, outcomes and costs of all treatment modalities for T1a renal masses from 2005 to 2007.</li>
</ul></div></div>
<div class="section" id="bju11776-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11776-list-0002" class="bullet">
<li>To perform a comprehensive analysis of the outcomes and costs for treatments for small renal masses (SRM) using a population-based approach. Partial nephrectomy may be associated with improved survival, although level-one evidence has questioned this survival advantage.</li>
</ul></div></div>
<div class="section" id="bju11776-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11776-list-0003" class="bullet">
<li>Using Surveillance, Epidemiology and End Results–Medicare data, we identified 1682 subjects who were diagnosed with SRM from 2005 to 2007.</li>
<li>Treatment included open radical nephrectomy (ORN; <em>n</em> = 404), minimally-invasive radical nephrectomy (MIRN; <em>n</em> = 535), open partial nephrectomy (OPN; <em>n</em> = 330), minimally-invasive partial nephrectomy (MIPN; <em>n</em> = 160), ablation (<em>n</em> = 211) and surveillance (<em>n</em> = 42).</li>
<li>Postoperative complications, renal insufficiency diagnosis, overall mortality, cancer-specific mortality and postoperative costs were compared.</li>
<li>Covariates were balanced before outcomes analysis using propensity score methods.</li>
</ul></div></div>
<div class="section" id="bju11776-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11776-list-0004" class="bullet">
<li>Although the use of nephron-sparing surgery (NSS) increased over the study period, radical nephrectomy remained the predominant approach for SRM in 2007.</li>
<li>Minimally-invasive approaches had shorter lengths of stay (<em>P</em> &lt; 0.001), whereas open approaches had more overall complications, respiratory complications and intensive care unit admissions (all <em>P</em> &lt; 0.003).</li>
<li>MIRN and ORN were associated with more peri-operative medical complications, acute renal failure, haemodialysis use and long-term chronic renal insufficiency diagnosis vs NSS (all <em>P</em> &lt; 0.001).</li>
<li>Ablation, MIRN and ORN were associated with the highest overall mortality rates (<em>P</em> &lt; 0.001), whereas MIRN and ORN were associated with the highest cancer-specific mortality rates (<em>P</em> &lt; 0.001).</li>
<li>Treatment costs were lowest for surveillance ($2911) followed by ablation ($10 730), MIRN ($15 373), MIPN ($15 695), OPN ($16 986) and ORN ($17 803).</li>
</ul></div></div>
<div class="section" id="bju11776-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11776-list-0005" class="bullet">
<li>Although not the predominant treatment approach for SRM over the study period, the use of NSS increased and was associated with improved survival, fewer complications and less renal insufficiency.</li>
<li>Minimally-invasive approaches confer lower costs.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Retrospective data have suggested an increased survival benefit for patients undergoing partial nephrectomy compared to radical nephrectomy, possibly as a result of the avoidance of long-term renalin sufficiency and subsequent sequelae. However, recent level-one evidence has questioned this benefit. Both retrospective studies and randomized controlled trials are not without limitations.
There are few population-based data available with respect to the outcomes of partial nephrectomy vs radical nephrectomy. Additionally, there are no population-based studies analyzing the surgical approach (minimally-invasive vs open), as well as other modalities, such as ablation and surveillance. Finally, there is very little information available on the potential differences in cost for each approach. The present study comprises the first comprehensive population-based analysis of the trends, outcomes and costs of all treatment modalities for T1a renal masses from 2005 to 2007.


 Objective

To perform a comprehensive analysis of the outcomes and costs for treatments for small renal masses (SRM) using a population-based approach. Partial nephrectomy may be associated with improved survival, although level-one evidence has questioned this survival advantage.



Patients and Methods

Using Surveillance, Epidemiology and End Results–Medicare data, we identified 1682 subjects who were diagnosed with SRM from 2005 to 2007.
Treatment included open radical nephrectomy (ORN; n = 404), minimally-invasive radical nephrectomy (MIRN; n = 535), open partial nephrectomy (OPN; n = 330), minimally-invasive partial nephrectomy (MIPN; n = 160), ablation (n = 211) and surveillance (n = 42).
Postoperative complications, renal insufficiency diagnosis, overall mortality, cancer-specific mortality and postoperative costs were compared.
Covariates were balanced before outcomes analysis using propensity score methods.



Results

Although the use of nephron-sparing surgery (NSS) increased over the study period, radical nephrectomy remained the predominant approach for SRM in 2007.
Minimally-invasive approaches had shorter lengths of stay (P &lt; 0.001), whereas open approaches had more overall complications, respiratory complications and intensive care unit admissions (all P &lt; 0.003).
MIRN and ORN were associated with more peri-operative medical complications, acute renal failure, haemodialysis use and long-term chronic renal insufficiency diagnosis vs NSS (all P &lt; 0.001).
Ablation, MIRN and ORN were associated with the highest overall mortality rates (P &lt; 0.001), whereas MIRN and ORN were associated with the highest cancer-specific mortality rates (P &lt; 0.001).
Treatment costs were lowest for surveillance ($2911) followed by ablation ($10 730), MIRN ($15 373), MIPN ($15 695), OPN ($16 986) and ORN ($17 803).



Conclusions

Although not the predominant treatment approach for SRM over the study period, the use of NSS increased and was associated with improved survival, fewer complications and less renal insufficiency.
Minimally-invasive approaches confer lower costs.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11741.x" xmlns="http://purl.org/rss/1.0/"><title>De novo erectile dysfunction after anterior urethroplasty: a systematic review and meta-analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11741.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">De novo erectile dysfunction after anterior urethroplasty: a systematic review and meta-analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarah D. Blaschko, Melissa T. Sanford, Nadya M. Cinman, Jack W. McAninch, Benjamin N. Breyer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:47:14.952857-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11741.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11741.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11741.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11741-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11741-list-0001" class="bullet">
<li>Erectile dysfunction has been associated with urethroplasty operations, but the incidence of erectile dysfunction after anterior urethroplasty operations is largely unknown.</li>
<li>A 1% incidence of <em>de novo</em> erectile dysfunction after anterior urethropathy was found with systematic review and meta analysis of 36 studies with 2323 patients. In most cases the erectile dysfunction was transient and resolved within six to twelve months.</li>
</ul></div></div>
<div class="section" id="bju11741-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11741-list-0002" class="bullet">
<li>To evaluate the likelihood of developing <em>de novo</em> erectile dysfunction (ED) after anterior urethroplasty and to determine if this likelihood is influenced by age, stricture length, number of previous procedures or timing of evaluation.</li>
</ul></div></div>
<div class="section" id="bju11741-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11741-list-0003" class="bullet">
<li>PubMed, Embase, Cochrane, and Google Scholar databases were searched for the terms ‘urethroplasty’, ‘urethral obstruction’, ‘urethral stricture’, ‘sexual function’, ‘erection’, ‘erectile function’, ‘erectile dysfunction’, ‘impotence’ and ‘sexual dysfunction’.</li>
<li>Two reviewers evaluated articles for inclusion based on predetermined criteria.</li>
</ul></div></div>
<div class="section" id="bju11741-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11741-list-0004" class="bullet">
<li>In a meta-analysis of 36 studies with a total of 2323 patients, <em>de novo</em> ED was rare, with an incidence of 1%.</li>
<li>In studies that assessed postoperative erectile function at more than one time point, ED was transient and resolved at between 6 and 12 months in 86% of cases.</li>
</ul></div></div>
<div class="section" id="bju11741-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11741-list-0005" class="bullet">
<li>Men should be counselled regarding the possibility of transient or permanent <em>de novo</em> ED after anterior urethroplasty procedures.</li>
<li>Increasing mean age was associated with an increased likelihood of <em>de novo</em> ED, but this was not statistically significant.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Erectile dysfunction has been associated with urethroplasty operations, but the incidence of erectile dysfunction after anterior urethroplasty operations is largely unknown.
A 1% incidence of de novo erectile dysfunction after anterior urethropathy was found with systematic review and meta analysis of 36 studies with 2323 patients. In most cases the erectile dysfunction was transient and resolved within six to twelve months.


 Objective

To evaluate the likelihood of developing de novo erectile dysfunction (ED) after anterior urethroplasty and to determine if this likelihood is influenced by age, stricture length, number of previous procedures or timing of evaluation.



Materials and Methods

PubMed, Embase, Cochrane, and Google Scholar databases were searched for the terms ‘urethroplasty’, ‘urethral obstruction’, ‘urethral stricture’, ‘sexual function’, ‘erection’, ‘erectile function’, ‘erectile dysfunction’, ‘impotence’ and ‘sexual dysfunction’.
Two reviewers evaluated articles for inclusion based on predetermined criteria.



Results

In a meta-analysis of 36 studies with a total of 2323 patients, de novo ED was rare, with an incidence of 1%.
In studies that assessed postoperative erectile function at more than one time point, ED was transient and resolved at between 6 and 12 months in 86% of cases.



Conclusions

Men should be counselled regarding the possibility of transient or permanent de novo ED after anterior urethroplasty procedures.
Increasing mean age was associated with an increased likelihood of de novo ED, but this was not statistically significant.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12031" xmlns="http://purl.org/rss/1.0/"><title>Distribution of phosphodiesterase type 5 (PDE5) in the lateral wall of the guinea pig urinary bladder</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12031</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Distribution of phosphodiesterase type 5 (PDE5) in the lateral wall of the guinea pig urinary bladder</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mohammad S. Rahnama'i, Gommert A. Koeveringe, Ramona Hohnen, Samsya Ona, Philip E.V. Kerrebroeck, Stefan G.G. Wachter</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:37:34.29933-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12031</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12031</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12031</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12031-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12031-list-0001" class="bullet">
<li>To study PDE5 localisation by visualising the product of phosphodiesterase type 5 (PDE5) inhibition, namely cGMP, to determine the site of action of inhibitors in the urinary bladder.</li>
</ul></div></div>
<div class="section" id="bju12031-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju12031-list-0002" class="bullet">
<li>Bladders of nine male guinea pigs were dissected and treated in wells containing 2 mL Krebs' solution and 1 μM of the specific PDE5 inhibitor vardenafil at 36 °C for 30 min.</li>
<li>After stimulating tissues with 100 μM of the nitric oxide (NO) donor diethylamine-NONOate for 10 min, the tissues were snap-frozen and 9–10 μm sections were cut.</li>
<li>Sections were examined for cGMP immunoreactivity and also stained for vimentin, a marker for interstitial cells and the neuromarkers protein gene product 9.5 (PGP9.5), synaptic vesicle protein 2 (SV2), neurofilament (NF) and calcitonin gene-related peptide (CGRP), using the two-step indirect immunohistochemistry technique.</li>
</ul></div></div> <div class="section" id="bju12031-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12031-list-0003" class="bullet">
<li>After PDE5 inhibition, cGMP was found to be present in the urothelium, suburothelial interstitial cells and endothelium of blood vessels.</li>
<li>cGMP was not expressed in nerves positive for CGRP, NF and SV2, and was expressed only in very few efferent nerves positive for PGP9.5.</li>
</ul></div></div>
<div class="section" id="bju12031-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12031-list-0004" class="bullet">
<li>Our data show that the possible sites of action of PDE5 inhibition in the bladder are the urothelium, suburothelial interstitial cells and blood vessels, rather than the bladder nerve fibres.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To study PDE5 localisation by visualising the product of phosphodiesterase type 5 (PDE5) inhibition, namely cGMP, to determine the site of action of inhibitors in the urinary bladder.



Materials and Methods

Bladders of nine male guinea pigs were dissected and treated in wells containing 2 mL Krebs' solution and 1 μM of the specific PDE5 inhibitor vardenafil at 36 °C for 30 min.
After stimulating tissues with 100 μM of the nitric oxide (NO) donor diethylamine-NONOate for 10 min, the tissues were snap-frozen and 9–10 μm sections were cut.
Sections were examined for cGMP immunoreactivity and also stained for vimentin, a marker for interstitial cells and the neuromarkers protein gene product 9.5 (PGP9.5), synaptic vesicle protein 2 (SV2), neurofilament (NF) and calcitonin gene-related peptide (CGRP), using the two-step indirect immunohistochemistry technique.

 
Results

After PDE5 inhibition, cGMP was found to be present in the urothelium, suburothelial interstitial cells and endothelium of blood vessels.
cGMP was not expressed in nerves positive for CGRP, NF and SV2, and was expressed only in very few efferent nerves positive for PGP9.5.



Conclusion

Our data show that the possible sites of action of PDE5 inhibition in the bladder are the urothelium, suburothelial interstitial cells and blood vessels, rather than the bladder nerve fibres.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12004" xmlns="http://purl.org/rss/1.0/"><title>Effect of remote ischaemic preconditioning on renal protection in patients undergoing laparoscopic partial nephrectomy: a ‘blinded’ randomised controlled trial</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of remote ischaemic preconditioning on renal protection in patients undergoing laparoscopic partial nephrectomy: a ‘blinded’ randomised controlled trial</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jiwei Huang, YongHui Chen, Baijun Dong, Wen Kong, Jin Zhang, Wei Xue, DongMing Liu, Yiran Huang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:37:24.834595-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12004</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12004</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12004-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12004-list-0001" class="bullet">
<li>To evaluate whether remote ischaemic preconditioning (RIPC) reduces renal injury in patients undergoing laparoscopic partial nephrectomy (LPN).</li>
</ul></div></div>
<div class="section" id="bju12004-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><ul id="bju12004-list-0002" class="bullet">
<li>In all, 82 patients undergoing LPN were randomly assigned to either the RIPC or control group, with 40 and 38 patients, respectively completing 6-months follow-up.</li>
<li>RIPC was conducted after induction of anaesthesia, which consisted of three 5-min cycles of right lower limb ischaemia and 5 min of reperfusion during each cycle.</li>
<li>The primary outcome was the absolute change in glomerular filtration rate (GFR) of the affected kidney by renal scintigraphy from baseline to 6 months.</li>
<li>The secondary outcomes included urinary retinol-binding protein (RBP) levels measured at 24 and 48 h, serum creatinine, and estimated GFR (eGFR) at 1 and 6 months, and changes in GFR by renal scintigraphy.</li>
</ul></div></div>
<div class="section" id="bju12004-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12004-list-0003" class="bullet">
<li>There were no differences in the change of GFR of the affected kidney at 6 months, while it was significantly decreased by 15.0% in the control group vs 8.8% in the RIPC group at 1 month (<em>P</em> = 0.034).</li>
<li>The urinary RBP levels increased 8.4-fold at 24 h in the control group compared with a lower increase of 3.9-fold in the RIPC group (<em>P</em> &lt; 0.001).</li>
<li>There were no differences in the serum creatinine level or eGFR at 1 and 6 months between the two groups.</li>
</ul></div></div>
<div class="section" id="bju12004-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12004-list-0004" class="bullet">
<li>In patients undergoing LPN, RIPC using transient lower limb ischaemia may reduce renal impairment in the short term, but failed in the longer term despite a non-significant trend in favour of RIPC.</li>
<li>These novel data support the need for a larger study of RIPC during LPN surgery.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate whether remote ischaemic preconditioning (RIPC) reduces renal injury in patients undergoing laparoscopic partial nephrectomy (LPN).



Patients and methods

In all, 82 patients undergoing LPN were randomly assigned to either the RIPC or control group, with 40 and 38 patients, respectively completing 6-months follow-up.
RIPC was conducted after induction of anaesthesia, which consisted of three 5-min cycles of right lower limb ischaemia and 5 min of reperfusion during each cycle.
The primary outcome was the absolute change in glomerular filtration rate (GFR) of the affected kidney by renal scintigraphy from baseline to 6 months.
The secondary outcomes included urinary retinol-binding protein (RBP) levels measured at 24 and 48 h, serum creatinine, and estimated GFR (eGFR) at 1 and 6 months, and changes in GFR by renal scintigraphy.



Results

There were no differences in the change of GFR of the affected kidney at 6 months, while it was significantly decreased by 15.0% in the control group vs 8.8% in the RIPC group at 1 month (P = 0.034).
The urinary RBP levels increased 8.4-fold at 24 h in the control group compared with a lower increase of 3.9-fold in the RIPC group (P &lt; 0.001).
There were no differences in the serum creatinine level or eGFR at 1 and 6 months between the two groups.



Conclusions

In patients undergoing LPN, RIPC using transient lower limb ischaemia may reduce renal impairment in the short term, but failed in the longer term despite a non-significant trend in favour of RIPC.
These novel data support the need for a larger study of RIPC during LPN surgery.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11652.x" xmlns="http://purl.org/rss/1.0/"><title>Is there a difference between women with or without detrusor overactivity complaining of symptoms of overactive bladder?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11652.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Is there a difference between women with or without detrusor overactivity complaining of symptoms of overactive bladder?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ilias Giarenis, Heleni Mastoroudes, Sushma Srikrishna, Dudley Robinson, Linda Cardozo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:37:22.132308-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11652.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11652.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11652.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11652-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11652-list-1001" class="bullet">
<li>Overactive bladder syndrome (OAB) is a highly prevalent medical condition, which is linked to the urodynamic observation of detrusor overactivity (DO). Urodynamics detect DO in about half of female patients with OAB.</li>
<li>Our study detects significant differences between female patients with OAB with and without DO. DO could be considered as a more severe form in the wide OAB spectrum and the two terms should not be used interchangeably. The detected differences should be taken into account in the design of studies for the assessment of new selective or combination treatments of OAB and in the provision of treatment in everyday clinical practice.</li>
</ul></div></div>
<div class="section" id="bju11652-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11652-list-0001" class="bullet">
<li>To determine if there are differences between female patients complaining of symptoms of overactive bladder (OAB) with and without detrusor overactivity (DO).</li>
</ul></div></div>
<div class="section" id="bju11652-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11652-list-0002" class="bullet">
<li>The present study was a cross-sectional study of consecutive women attending a one-stop urodynamic assessment clinic with OAB symptoms.</li>
<li>The King's Health Questionnaire (KHQ) and a 3-day bladder diary incorporating the Patient's Perception of Intensity of Urgency Scale (PPIUS) were used to assess symptoms and health-related quality of life (HRQoL).</li>
<li>The participants underwent multichannel urodynamics (UDS) according to the International Continence Society (ICS) recommendations.</li>
<li>Patients whose symptom of urgency was not reproduced during the laboratory test underwent a 4-h ambulatory UDS test.</li>
</ul></div></div>
<div class="section" id="bju11652-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11652-list-0003" class="bullet">
<li>Of the 556 patients who were included in the study, 43% were diagnosed with DO by either laboratory (227/556) or ambulatory UDS (11/39).</li>
<li>There was no difference between the groups in age, body mass index (BMI), menopausal status or the presence of prolapse.</li>
<li>Patients with DO had a smaller functional bladder capacity (<em>P</em> &lt; 0.001), higher urgency episode frequency (<em>P</em> &lt; 0.001) and larger maximum and mean urge ratings (<em>P</em> &lt; 0.001).</li>
<li>No significant differences were found in daytime or nocturnal micturitions between the groups.</li>
<li>The presence of DO had a more negative impact on the quality of life, with a statistically significant difference between the groups in six of the domains of the KHQ.</li>
</ul></div></div>
<div class="section" id="bju11652-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11652-list-0004" class="bullet">
<li>The present study detects objective and subjective differences between female patients with OAB with and without DO.</li>
<li>Women with DO experience more significant impairment to their quality of life and have a greater degree of bladder dysfunction.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Overactive bladder syndrome (OAB) is a highly prevalent medical condition, which is linked to the urodynamic observation of detrusor overactivity (DO). Urodynamics detect DO in about half of female patients with OAB.
Our study detects significant differences between female patients with OAB with and without DO. DO could be considered as a more severe form in the wide OAB spectrum and the two terms should not be used interchangeably. The detected differences should be taken into account in the design of studies for the assessment of new selective or combination treatments of OAB and in the provision of treatment in everyday clinical practice.


 Objective

To determine if there are differences between female patients complaining of symptoms of overactive bladder (OAB) with and without detrusor overactivity (DO).



Patients and Methods

The present study was a cross-sectional study of consecutive women attending a one-stop urodynamic assessment clinic with OAB symptoms.
The King's Health Questionnaire (KHQ) and a 3-day bladder diary incorporating the Patient's Perception of Intensity of Urgency Scale (PPIUS) were used to assess symptoms and health-related quality of life (HRQoL).
The participants underwent multichannel urodynamics (UDS) according to the International Continence Society (ICS) recommendations.
Patients whose symptom of urgency was not reproduced during the laboratory test underwent a 4-h ambulatory UDS test.



Results

Of the 556 patients who were included in the study, 43% were diagnosed with DO by either laboratory (227/556) or ambulatory UDS (11/39).
There was no difference between the groups in age, body mass index (BMI), menopausal status or the presence of prolapse.
Patients with DO had a smaller functional bladder capacity (P &lt; 0.001), higher urgency episode frequency (P &lt; 0.001) and larger maximum and mean urge ratings (P &lt; 0.001).
No significant differences were found in daytime or nocturnal micturitions between the groups.
The presence of DO had a more negative impact on the quality of life, with a statistically significant difference between the groups in six of the domains of the KHQ.



Conclusions

The present study detects objective and subjective differences between female patients with OAB with and without DO.
Women with DO experience more significant impairment to their quality of life and have a greater degree of bladder dysfunction.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11493.x" xmlns="http://purl.org/rss/1.0/"><title>How does robot-assisted radical prostatectomy (RARP) compare with open surgery in men with high-risk prostate cancer?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11493.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">How does robot-assisted radical prostatectomy (RARP) compare with open surgery in men with high-risk prostate cancer?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sanoj Punnen, Maxwell V. Meng, Matthew R. Cooperberg, Kirsten L. Greene, Janet E. Cowan, Peter R. Carroll</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T06:37:10.702983-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11493.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11493.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11493.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11493-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11493-list-0001" class="bullet">
<li>Previous studies have shown that robot-assisted radical prostatectomy (RARP) can be performed in men with high-risk prostate cancer with similar outcomes to that of open surgery. However, most of the literature consists of small case series and compares RARP outcomes to open outcomes from the literature.</li>
<li>This study compared a cohort of high-risk patients undergoing open RP and RARP at a single institution with good follow up. We found no difference in positive margin rates or likelihood of prostate cancer recurrence. This adds to the growing evidence that RARP is a safe option for men with high-risk disease.</li>
</ul></div></div>
<div class="section" id="bju11493-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11493-list-0002" class="bullet">
<li>To compare oncological outcomes in high-risk patients who underwent open retropubic radical prostatectomy (RRP) and robot-assisted RP (RARP) at a single institution. Despite equivalent oncological outcomes between open RRP and RARP, the use of RARP in men with high-risk tumours has been debated.</li>
</ul></div></div>
<div class="section" id="bju11493-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11493-list-0003" class="bullet">
<li>A retrospective analysis of high-risk patients treated with open RRP or RARP at UCSF from 2002 to 2011 was conducted.</li>
<li>The relationship between surgical approach and positive margin rate was assessed by multivariate logistic regression</li>
<li>Cox proportional hazards regression assessed the effect of surgical approach on time to tumour recurrence.</li>
</ul></div></div>
<div class="section" id="bju11493-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11493-list-0004" class="bullet">
<li>In all, 177 open RRP and 233 RARP patients made up the final cohort for analyses. The mean (SD) age was 61.6 (6.6) years and the median (range) follow-up was 27 (2–112) months.</li>
<li>RARP patients had less blood loss (median 200 vs 400 mL, <em>P</em> &lt; 0.01) and underwent complete bilateral nerve sparing more often (54% vs 34%, <em>P</em> &lt; 0.01) than those undergoing open RRP.</li>
<li>There were no differences by approach in pathological grade, stage, or positive margin rates. However, there was a trend towards higher positive margin rates with RARP early on.</li>
<li>Recurrence-free survival was similar at 2 years (84% and 79%) and 4 years (68% and 66%) after open RRP and RARP, respectively (log-rank <em>P</em> = 0.53).</li>
</ul></div></div>
<div class="section" id="bju11493-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11493-list-0005" class="bullet">
<li>This study is novel in that it assesses outcomes of open RRP vs RARP in a cohort of high-risk men at a single institution.</li>
<li>RARP appears to be a feasible option for men with high-risk prostate cancer and displayed equivalent oncological outcomes compared with open RRP.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Previous studies have shown that robot-assisted radical prostatectomy (RARP) can be performed in men with high-risk prostate cancer with similar outcomes to that of open surgery. However, most of the literature consists of small case series and compares RARP outcomes to open outcomes from the literature.
This study compared a cohort of high-risk patients undergoing open RP and RARP at a single institution with good follow up. We found no difference in positive margin rates or likelihood of prostate cancer recurrence. This adds to the growing evidence that RARP is a safe option for men with high-risk disease.


 Objective

To compare oncological outcomes in high-risk patients who underwent open retropubic radical prostatectomy (RRP) and robot-assisted RP (RARP) at a single institution. Despite equivalent oncological outcomes between open RRP and RARP, the use of RARP in men with high-risk tumours has been debated.



Patients and Methods

A retrospective analysis of high-risk patients treated with open RRP or RARP at UCSF from 2002 to 2011 was conducted.
The relationship between surgical approach and positive margin rate was assessed by multivariate logistic regression
Cox proportional hazards regression assessed the effect of surgical approach on time to tumour recurrence.



Results

In all, 177 open RRP and 233 RARP patients made up the final cohort for analyses. The mean (SD) age was 61.6 (6.6) years and the median (range) follow-up was 27 (2–112) months.
RARP patients had less blood loss (median 200 vs 400 mL, P &lt; 0.01) and underwent complete bilateral nerve sparing more often (54% vs 34%, P &lt; 0.01) than those undergoing open RRP.
There were no differences by approach in pathological grade, stage, or positive margin rates. However, there was a trend towards higher positive margin rates with RARP early on.
Recurrence-free survival was similar at 2 years (84% and 79%) and 4 years (68% and 66%) after open RRP and RARP, respectively (log-rank P = 0.53).



Conclusions

This study is novel in that it assesses outcomes of open RRP vs RARP in a cohort of high-risk men at a single institution.
RARP appears to be a feasible option for men with high-risk prostate cancer and displayed equivalent oncological outcomes compared with open RRP.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12012" xmlns="http://purl.org/rss/1.0/"><title>Current clinical practice gaps in the treatment of intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC) with emphasis on the use of bacillus Calmette-Guérin (BCG): results of an international individual patient data survey (IPDS)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Current clinical practice gaps in the treatment of intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC) with emphasis on the use of bacillus Calmette-Guérin (BCG): results of an international individual patient data survey (IPDS)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Alfred Witjes, Joan Palou, Mark Soloway, Donald Lamm, Ashish M. Kamat, Maurizio Brausi, Raj Persad, Roger Buckley, Marc Colombel, Andreas Böhle</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T07:55:48.875712-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12012</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12012</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12012-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12012-list-0001" class="bullet">
<li>To examine the management of intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC), particularly with regard to the use of bacillus Calmette-Guérin (BCG) therapy, in North America and Europe.</li>
<li>To compare NMIBC management practices to European Association of Urology (EAU) and American Urological Association (AUA) guideline recommendations for the management of intermediate- and high-risk NMIBC.</li>
</ul></div></div>
<div class="section" id="bju12012-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12012-list-0002" class="bullet">
<li>In all, 102 urologists from Europe and North America participated in this retrospective on-line chart review, which was conducted between 1 April 2011 and 30 April 2012.</li>
<li>Participants selected the charts of the first 10 intermediate- (defined as multiple or recurrent low-grade tumours) or high-risk (defined as any T1 and/or high-grade/G3 tumours and/or carcinoma <em>in situ</em>) patients who underwent transurethral resection of bladder tumour in 2009.</li>
<li>Physicians retrospectively reviewed the charts and completed an on-line survey consisting of questions related to diagnosis, planned treatment, treatment status and follow-up.</li>
<li>In all, 971 patients (197 intermediate-risk; 774 high-risk) were included in the analysis; frequency counts and associated percentages were used to analyse treatment variables.</li>
</ul></div></div>
<div class="section" id="bju12012-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12012-list-0003" class="bullet">
<li>In all, 47% of intermediate-risk patients received EAU or AUA guideline-recommended intravesical therapy: intravesical chemotherapy, BCG induction therapy or BCG induction plus maintenance.</li>
<li>Of the high-risk patients, 50% received maintenance BCG as recommended by the EAU and the AUA; although not recommended for high-risk NMIBC, 12.5% received intravesical chemotherapy.</li>
<li>Of patients prescribed maintenance BCG, 93% were scheduled for at least 1 year of therapy.</li>
<li>Notably, only 15% discontinued BCG maintenance and, of these discontinuations, 65% were due to reasons unrelated to BCG-associated adverse events.</li>
</ul></div></div>
<div class="section" id="bju12012-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12012-list-0004" class="bullet">
<li>There is significant non-adherence to EAU and AUA guideline recommendations for BCG use in intermediate- and high-risk NMIBC.</li>
<li>However, most of those patients prescribed BCG maintenance therapy are scheduled for at least 1 year of therapy, as recommended by current guidelines for NMIBC management, and BCG maintenance discontinuation is low.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To examine the management of intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC), particularly with regard to the use of bacillus Calmette-Guérin (BCG) therapy, in North America and Europe.
To compare NMIBC management practices to European Association of Urology (EAU) and American Urological Association (AUA) guideline recommendations for the management of intermediate- and high-risk NMIBC.



Patients and Methods

In all, 102 urologists from Europe and North America participated in this retrospective on-line chart review, which was conducted between 1 April 2011 and 30 April 2012.
Participants selected the charts of the first 10 intermediate- (defined as multiple or recurrent low-grade tumours) or high-risk (defined as any T1 and/or high-grade/G3 tumours and/or carcinoma in situ) patients who underwent transurethral resection of bladder tumour in 2009.
Physicians retrospectively reviewed the charts and completed an on-line survey consisting of questions related to diagnosis, planned treatment, treatment status and follow-up.
In all, 971 patients (197 intermediate-risk; 774 high-risk) were included in the analysis; frequency counts and associated percentages were used to analyse treatment variables.



Results

In all, 47% of intermediate-risk patients received EAU or AUA guideline-recommended intravesical therapy: intravesical chemotherapy, BCG induction therapy or BCG induction plus maintenance.
Of the high-risk patients, 50% received maintenance BCG as recommended by the EAU and the AUA; although not recommended for high-risk NMIBC, 12.5% received intravesical chemotherapy.
Of patients prescribed maintenance BCG, 93% were scheduled for at least 1 year of therapy.
Notably, only 15% discontinued BCG maintenance and, of these discontinuations, 65% were due to reasons unrelated to BCG-associated adverse events.



Conclusions

There is significant non-adherence to EAU and AUA guideline recommendations for BCG use in intermediate- and high-risk NMIBC.
However, most of those patients prescribed BCG maintenance therapy are scheduled for at least 1 year of therapy, as recommended by current guidelines for NMIBC management, and BCG maintenance discontinuation is low.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12008" xmlns="http://purl.org/rss/1.0/"><title>Ureteroscopic management of upper tract urothelial carcinoma (UTUC) in patients with Lynch Syndrome (hereditary nonpolyposis colorectal cancer syndrome)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ureteroscopic management of upper tract urothelial carcinoma (UTUC) in patients with Lynch Syndrome (hereditary nonpolyposis colorectal cancer syndrome)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Scott G. Hubosky, Bruce M. Boman, Sarah Charles, Marluce Bibbo, Demetrius H. Bagley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T07:55:40.333525-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12008</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12008</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12008-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12008-list-0001" class="bullet">
<li>To report our experience with ureteroscopic laser ablation of upper tract urothelial carcinoma (UTUC) in patients with Lynch Syndrome (LS), as defined by a documented germline mutation in the <em>MSH-2</em> gene.</li>
<li>To increase awareness among urologists about UTUC in this unique patient population and refer to genetic counselling when appropriate.</li>
</ul></div></div>
<div class="section" id="bju12008-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12008-list-0002" class="bullet">
<li>Demographic, clinical and pathological data on 13 consecutive patients with UTUC and documented <em>MSH-2</em> mutation comprising 15 involved renal units were retrospectively collected.</li>
<li>Ureteroscopic evaluations involved biopsy and laser treatment with combination holmium/neodymium yttrium aluminum garnet (YAG) lasers.</li>
<li>Tumours were graded from 1 to 3 according to the 1973 World Health Organisation classification by a single pathologist evaluating cell block preparations.</li>
</ul></div></div>
<div class="section" id="bju12008-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12008-list-0003" class="bullet">
<li>The mean patient age at initial presentation was 56.5 years, with six of 13 patients having metachronous bilateral UT disease.</li>
<li>The mean follow-up was 59 months with a mean number of surveillances of 12.</li> <li>Of 15 affected renal units, 10/15 (67%) of initial tumours involved the ureter with mean lesion size of 17.5 mm, while five of 15 (33%) involved the intrarenal collecting system with mean lesion size of 25 mm.</li>
<li>Ureteroscopy cleared 13/15 (87%) lesions and four of those 13 (31%) needed staged procedures. Renal preservation rate was 14/15 (93%) with one nephroureterectomy and one segmental ureterectomy performed.</li>
<li>One patient developed metastatic UTUC after 40 months surveillance. No patient presented with bladder tumours but seven of the 13 (54%) developed them within 10 months of the initial ureteroscopy.</li>
</ul></div></div>
<div class="section" id="bju12008-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12008-list-0004" class="bullet">
<li>Patients with LS who develop UTUC present at younger ages and appear to be more likely to have bilateral UT disease over their lifetimes vs sporadic UTUC patients.</li>
<li>Ureteroscopic laser ablation offers a good renal preservation rate with reasonable cancer control in patients willing to undergo endoscopic surveillance.</li>
<li>Development of new bladder tumours is common.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To report our experience with ureteroscopic laser ablation of upper tract urothelial carcinoma (UTUC) in patients with Lynch Syndrome (LS), as defined by a documented germline mutation in the MSH-2 gene.
To increase awareness among urologists about UTUC in this unique patient population and refer to genetic counselling when appropriate.



Patients and Methods

Demographic, clinical and pathological data on 13 consecutive patients with UTUC and documented MSH-2 mutation comprising 15 involved renal units were retrospectively collected.
Ureteroscopic evaluations involved biopsy and laser treatment with combination holmium/neodymium yttrium aluminum garnet (YAG) lasers.
Tumours were graded from 1 to 3 according to the 1973 World Health Organisation classification by a single pathologist evaluating cell block preparations.



Results

The mean patient age at initial presentation was 56.5 years, with six of 13 patients having metachronous bilateral UT disease.
The mean follow-up was 59 months with a mean number of surveillances of 12. Of 15 affected renal units, 10/15 (67%) of initial tumours involved the ureter with mean lesion size of 17.5 mm, while five of 15 (33%) involved the intrarenal collecting system with mean lesion size of 25 mm.
Ureteroscopy cleared 13/15 (87%) lesions and four of those 13 (31%) needed staged procedures. Renal preservation rate was 14/15 (93%) with one nephroureterectomy and one segmental ureterectomy performed.
One patient developed metastatic UTUC after 40 months surveillance. No patient presented with bladder tumours but seven of the 13 (54%) developed them within 10 months of the initial ureteroscopy.



Conclusions

Patients with LS who develop UTUC present at younger ages and appear to be more likely to have bilateral UT disease over their lifetimes vs sporadic UTUC patients.
Ureteroscopic laser ablation offers a good renal preservation rate with reasonable cancer control in patients willing to undergo endoscopic surveillance.
Development of new bladder tumours is common.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11508.x" xmlns="http://purl.org/rss/1.0/"><title>Population-based trends in urinary diversion among patients undergoing radical cystectomy for bladder cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11508.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Population-based trends in urinary diversion among patients undergoing radical cystectomy for bladder cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Simon P. Kim, Nilay D. Shah, Christopher J. Weight, R. Houston Thompson, Jeffrey K. Wang, R. Jeffrey Karnes, Leona C. Han, Jeanette Y. Ziegenfuss, Igor Frank, Matthew K. Tollefson, Stephen A. Boorjian</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T07:55:24.027295-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11508.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11508.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11508.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11508-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11508-list-0001" class="bullet">
<li>Variations in the type of urinary diversion exist for patients undergoing radical cystectomy.</li>
<li>Although its use has been increasing from 2001 to 2008, patients who are older, female, and primary insured by Medicaid are less likely to receive continent diversions. Furthermore, patients treated surgically at high-volume and teaching hospitals are more likely to receive continent diversions.</li>
</ul></div></div>
<div class="section" id="bju11508-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11508-list-0002" class="bullet">
<li>To describe the contemporary trends in urinary diversion among patients undergoing radical cystectomy (RC) for bladder cancer; and elucidate whether socioeconomic disparities persist in the type of diversion performed in the USA from a population-based cohort.</li>
</ul></div></div>
<div class="section" id="bju11508-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11508-list-0003" class="bullet">
<li>Using the Nationwide Inpatient Sample, we identified patients who underwent RC for bladder cancer between 2001 and 2008.</li>
<li>Multivariable regression models were used to identify patient and hospital covariates associated with continent urinary diversion and enumerate predicted probabilities for statistically significant variables over time.</li>
</ul></div></div>
<div class="section" id="bju11508-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11508-list-0004" class="bullet">
<li>Overall, 55 635 (92%) patients undergoing RC for bladder cancer received incontinent urinary diversion, while 4552 (8%) patients received continent diversion from 2001 to 2008.</li>
<li>Receipt of continent urinary diversion increased from 6.6% in 2001–2002 to 9.4% in 2007–2008 (<em>P</em> &lt; 0.001 for trend).</li>
<li>Patients who were older (odds ratio [OR] 0.93; <em>P</em> &lt; 0.001), female (OR 0.52; <em>P</em> &lt; 0.001) and insured by Medicaid (OR 0.54; <em>P</em> = 0.002) were less likely to receive continent urinary diversion.</li>
<li>However, patients treated at teaching (OR 2.14; <em>P</em> &lt; 0.001) and high-volume hospitals (OR 2.39; <em>P</em> = 0.04) had higher odds of continent urinary diversion.</li>
<li>Predicted probabilities of continent diversion remained lower for female patients, Medicaid insurance status, and non-teaching and medium/low-volume hospitals over time.</li>
</ul></div></div>
<div class="section" id="bju11508-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11508-list-0005" class="bullet">
<li>In this nationally representative sample of hospitals from 2001 to 2008, the use of continent diversion in RC gradually increased.</li>
<li>Although variations in urinary diversion exist by hospital teaching status, case volume, patient gender and primary health insurance, increased attention in expanding the use of continent diversions may help reduce these disparities for patients undergoing RC for bladder cancer.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Variations in the type of urinary diversion exist for patients undergoing radical cystectomy.
Although its use has been increasing from 2001 to 2008, patients who are older, female, and primary insured by Medicaid are less likely to receive continent diversions. Furthermore, patients treated surgically at high-volume and teaching hospitals are more likely to receive continent diversions.


 Objective

To describe the contemporary trends in urinary diversion among patients undergoing radical cystectomy (RC) for bladder cancer; and elucidate whether socioeconomic disparities persist in the type of diversion performed in the USA from a population-based cohort.



Patients and Methods

Using the Nationwide Inpatient Sample, we identified patients who underwent RC for bladder cancer between 2001 and 2008.
Multivariable regression models were used to identify patient and hospital covariates associated with continent urinary diversion and enumerate predicted probabilities for statistically significant variables over time.



Results

Overall, 55 635 (92%) patients undergoing RC for bladder cancer received incontinent urinary diversion, while 4552 (8%) patients received continent diversion from 2001 to 2008.
Receipt of continent urinary diversion increased from 6.6% in 2001–2002 to 9.4% in 2007–2008 (P &lt; 0.001 for trend).
Patients who were older (odds ratio [OR] 0.93; P &lt; 0.001), female (OR 0.52; P &lt; 0.001) and insured by Medicaid (OR 0.54; P = 0.002) were less likely to receive continent urinary diversion.
However, patients treated at teaching (OR 2.14; P &lt; 0.001) and high-volume hospitals (OR 2.39; P = 0.04) had higher odds of continent urinary diversion.
Predicted probabilities of continent diversion remained lower for female patients, Medicaid insurance status, and non-teaching and medium/low-volume hospitals over time.



Conclusions

In this nationally representative sample of hospitals from 2001 to 2008, the use of continent diversion in RC gradually increased.
Although variations in urinary diversion exist by hospital teaching status, case volume, patient gender and primary health insurance, increased attention in expanding the use of continent diversions may help reduce these disparities for patients undergoing RC for bladder cancer.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11736.x" xmlns="http://purl.org/rss/1.0/"><title>Efficacy of adding behavioural treatment or antimuscarinic drug therapy to α-blocker therapy in men with nocturia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11736.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Efficacy of adding behavioural treatment or antimuscarinic drug therapy to α-blocker therapy in men with nocturia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Theodore M. Johnson, Alayne D. Markland, Patricia S. Goode, Camille P. Vaughan, Janet L. Colli, Joseph G. Ouslander, David T. Redden, Gerald McGwin, Kathryn L. Burgio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-28T10:55:34.124596-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11736.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11736.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11736.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11736-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11736-list-0001" class="bullet">
<li>Nocturia is a common and bothersome lower urinary tract symptom, particularly in men. Many single drug therapies have limited benefit.</li>
<li>For men who have persistent nocturia despite alpha-blocker therapy, the addition of behavioural and exercise therapy is statistically superior to anticholinergic therapy.</li>
</ul></div></div>
<div class="section" id="bju11736-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11736-list-0002" class="bullet">
<li>To compare reductions in nocturia resulting from adding either behavioural treatment or antimuscarinic drug therapy to α-adrenergic antagonist (α-blocker) therapy in men.</li>
</ul></div></div>
<div class="section" id="bju11736-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11736-list-0003" class="bullet">
<li>Participants were men who had continuing urinary frequency &gt;8 voids/day) and urgency after 4 weeks of α-blocker therapy run-in and who had ≥1 nightly episode of nocturia.</li>
<li>Participants received individually titrated drug therapy (extended-release oxybutynin) or multicomponent behavioural treatment (pelvic floor muscle training, delayed voiding and urge suppression techniques).</li>
<li>Seven-day bladder diaries were used to calculate reductions in mean nocturia.</li>
</ul></div></div>
<div class="section" id="bju11736-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11736-list-0004" class="bullet">
<li>A total of 127 men aged 42–88 years with ≥1 nocturia episode per night were included in the study.</li>
<li>There were 76 men who had a mean of ≥2 nocturia episodes.</li>
<li>Among those with ≥1 nocturia episode, behavioural treatment reduced nightly nocturia by a mean of 0.97 episodes and was significantly more effective than drug therapy (mean reduction = 0.56 episodes; <em>P</em> = 0.01).</li>
<li>Participants with ≥2 episodes nocturia at baseline also showed larger changes with behavioural treatment compared with antimuscarinic therapy (mean reduction = 1.26 vs 0.61; <em>P</em> = 0.008).</li>
</ul></div></div>
<div class="section" id="bju11736-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11736-list-0005" class="bullet">
<li>Both behavioural treatment and drug therapy reduced nocturia in men with ≥1 episode of nocturia/night when added to α-blocker therapy.</li>
<li>These results were similar even when only those with ≥2 episodes of nocturia were considered.</li>
<li>The addition of behavioural treatment was statistically better than bladder-relaxant therapy for nocturia.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Nocturia is a common and bothersome lower urinary tract symptom, particularly in men. Many single drug therapies have limited benefit.
For men who have persistent nocturia despite alpha-blocker therapy, the addition of behavioural and exercise therapy is statistically superior to anticholinergic therapy.


 Objective

To compare reductions in nocturia resulting from adding either behavioural treatment or antimuscarinic drug therapy to α-adrenergic antagonist (α-blocker) therapy in men.



Patients and Methods

Participants were men who had continuing urinary frequency &gt;8 voids/day) and urgency after 4 weeks of α-blocker therapy run-in and who had ≥1 nightly episode of nocturia.
Participants received individually titrated drug therapy (extended-release oxybutynin) or multicomponent behavioural treatment (pelvic floor muscle training, delayed voiding and urge suppression techniques).
Seven-day bladder diaries were used to calculate reductions in mean nocturia.



Results

A total of 127 men aged 42–88 years with ≥1 nocturia episode per night were included in the study.
There were 76 men who had a mean of ≥2 nocturia episodes.
Among those with ≥1 nocturia episode, behavioural treatment reduced nightly nocturia by a mean of 0.97 episodes and was significantly more effective than drug therapy (mean reduction = 0.56 episodes; P = 0.01).
Participants with ≥2 episodes nocturia at baseline also showed larger changes with behavioural treatment compared with antimuscarinic therapy (mean reduction = 1.26 vs 0.61; P = 0.008).



Conclusions

Both behavioural treatment and drug therapy reduced nocturia in men with ≥1 episode of nocturia/night when added to α-blocker therapy.
These results were similar even when only those with ≥2 episodes of nocturia were considered.
The addition of behavioural treatment was statistically better than bladder-relaxant therapy for nocturia.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11690.x" xmlns="http://purl.org/rss/1.0/"><title>Can one blood draw replace transrectal ultrasonography-estimated prostate volume to predict prostate cancer risk?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11690.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Can one blood draw replace transrectal ultrasonography-estimated prostate volume to predict prostate cancer risk?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sigrid V. Carlsson, Mari T. Peltola, Daniel Sjoberg, Fritz H. Schröder, Jonas Hugosson, Kim Pettersson, Peter T. Scardino, Andrew J. Vickers, Hans Lilja, Monique J. Roobol</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-28T08:55:38.891683-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11690.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11690.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11690.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11690-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11690-list-0002" class="bullet">
<li>Previous studies have shown that a statistical model based on a panel of kallikrein markers in blood (total, free and intact PSA and kallikrein-related peptidase 2) can predict prostate cancer on biopsy.</li>
<li>The current study explores the relationship between the above-mentioned panel and prostate volume, and whether this panel could be an alternative for clinical measures such as DRE and TRUS in predicting prostate cancer on biopsy.</li>
</ul></div></div>
<div class="section" id="bju11690-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11690-list-0003" class="bullet">
<li>To explore whether a panel of kallikrein markers in blood: total, free and intact prostate-specific antigen (PSA) and kallikrein-related peptidase 2, could be used as a non-invasive alternative for predicting prostate cancer on biopsy in a screening setting.</li>
</ul></div></div>
<div class="section" id="bju11690-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects and Methods</h4><div class="para"><ul id="bju11690-list-0004" class="bullet">
<li>The study cohort comprised previously unscreened men who underwent sextant biopsy owing to elevated PSA (≥3 ng/mL) in two different centres of the European Randomized Study of Screening for Prostate Cancer, Rotterdam (<em>n</em> = 2914) and Göteborg (<em>n</em> = 740).</li>
<li>A statistical model, based on kallikrein markers, was compared with one based on established clinical factors for the prediction of biopsy outcome.</li>
</ul></div></div>
<div class="section" id="bju11690-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11690-list-0005" class="bullet">
<li>The clinical tests were found to be no better than blood markers, with an area under the curve in favour of the blood measurements of 0.766 vs. 0.763 in Rotterdam and 0.809 vs. 0.774 in Göteborg.</li>
<li>Adding digital rectal examination (DRE) or DRE plus transrectal ultrasonography (TRUS) volume to the markers improved discrimination, although the increases were small. Results were similar for predicting high-grade cancer.</li>
<li>There was a strong correlation between the blood measurements and TRUS-estimated prostate volume (Spearman's correlation 0.60 in Rotterdam and 0.57 in Göteborg).</li>
</ul></div></div>
<div class="section" id="bju11690-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11690-list-0006" class="bullet">
<li>In previously unscreened men, each with indication for biopsy, a statistical model based on kallikrein levels was similar to a clinical model in predicting prostate cancer in a screening setting, outside the day-to-day clinical practice.</li>
<li>Whether a clinical approach can be replaced by laboratory analyses or used in combination with decision models (nomograms) is a clinical judgment that may vary from clinician to clinician depending on how they weigh the different advantages and disadvantages (harms, costs, time, invasiveness) of both approaches.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Previous studies have shown that a statistical model based on a panel of kallikrein markers in blood (total, free and intact PSA and kallikrein-related peptidase 2) can predict prostate cancer on biopsy.
The current study explores the relationship between the above-mentioned panel and prostate volume, and whether this panel could be an alternative for clinical measures such as DRE and TRUS in predicting prostate cancer on biopsy.


 Objective

To explore whether a panel of kallikrein markers in blood: total, free and intact prostate-specific antigen (PSA) and kallikrein-related peptidase 2, could be used as a non-invasive alternative for predicting prostate cancer on biopsy in a screening setting.



Subjects and Methods

The study cohort comprised previously unscreened men who underwent sextant biopsy owing to elevated PSA (≥3 ng/mL) in two different centres of the European Randomized Study of Screening for Prostate Cancer, Rotterdam (n = 2914) and Göteborg (n = 740).
A statistical model, based on kallikrein markers, was compared with one based on established clinical factors for the prediction of biopsy outcome.



Results

The clinical tests were found to be no better than blood markers, with an area under the curve in favour of the blood measurements of 0.766 vs. 0.763 in Rotterdam and 0.809 vs. 0.774 in Göteborg.
Adding digital rectal examination (DRE) or DRE plus transrectal ultrasonography (TRUS) volume to the markers improved discrimination, although the increases were small. Results were similar for predicting high-grade cancer.
There was a strong correlation between the blood measurements and TRUS-estimated prostate volume (Spearman's correlation 0.60 in Rotterdam and 0.57 in Göteborg).



Conclusions

In previously unscreened men, each with indication for biopsy, a statistical model based on kallikrein levels was similar to a clinical model in predicting prostate cancer in a screening setting, outside the day-to-day clinical practice.
Whether a clinical approach can be replaced by laboratory analyses or used in combination with decision models (nomograms) is a clinical judgment that may vary from clinician to clinician depending on how they weigh the different advantages and disadvantages (harms, costs, time, invasiveness) of both approaches.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12026" xmlns="http://purl.org/rss/1.0/"><title>Construction of predictive models for recurrence and progression in &gt;1000 patients with non-muscle-invasive bladder cancer (NMIBC) from a single centre</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12026</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Construction of predictive models for recurrence and progression in &gt;1000 patients with non-muscle-invasive bladder cancer (NMIBC) from a single centre</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bedeir Ali-El-Dein, Prasanna Sooriakumaran, Quoc-Dien Trinh, Tamer S. Barakat, Adel Nabeeh, El-Housseiny I. Ibrahiem</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-27T11:34:05.41835-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12026</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12026</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12026</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12026-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12026-list-0001" class="bullet">
<li>To construct predictive models based on the objectively calculated risks of progression and recurrence of non-muscle-invasive bladder cancer (NMIBC) in a large cohort of patients from a single centre.</li>
</ul></div></div>
<div class="section" id="bju12026-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12026-list-0002" class="bullet">
<li>Between October 1984 and March 2009 a cohort of 1019 patients (877 males; 142 females; median age 44 years) with histologically confirmed NMIBC was included in this study.</li>
<li>Among these patients, 74% received bacillus Calmette-Guérin (BCG)-based therapy. Complete transurethral resection of bladder tumour of all visible tumours was carried out in all patients, and the stage and grade were determined.</li>
<li>Univariate analysis and multivariate Cox regression were used to identify predictors of recurrence and progression. The studied predictors included age, sex, stage, grade, associated carcinoma <em>in situ</em>, tumour size, multiplicity, macroscopic appearance of the tumour, history of recurrence and type of adjuvant intravesical therapy.</li>
<li>Multivariate logistic regression models were used to develop the 12- and 60-month recurrence and progression predictive models. The predictive accuracy of the models was assessed for discrimination as well as calibration.</li>
</ul></div></div>
<div class="section" id="bju12026-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12026-list-0003" class="bullet">
<li>The median (range) follow-up was 44 (6–254) months.</li>
<li>On multivariate analysis, stage, multiplicity, history of recurrence and adjuvant intravesical therapy were significantly associated with recurrence, whereas for progression only tumour grade and size were significant independent predictors.</li>
<li>The constructed nomograms had a 64.9% and 69.4% chance of correctly distinguishing between two patients, one destined to have a recurrence and one not at 12 and 60 months, respectively.</li>
<li>The constructed nomograms had a 70.2% and 73.5% chance of correctly distinguishing between two patients, one destined to progress and one not at 12 and 60 months, respectively. All predictive models were well calibrated.</li>
</ul></div></div>
<div class="section" id="bju12026-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12026-list-0004" class="bullet">
<li>Based on multivariate analysis of the studied prognostic factors nomograms for predicting recurrence and progression in NMIBC were constructed.</li>
<li>Most of the studied patients had received BCG-based therapy, making these models more closely applicable to contemporary practice than others.</li>
<li>These predictive models have reasonable discriminative ability and are well calibrated, but require external validation before they can be applied to other populations.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To construct predictive models based on the objectively calculated risks of progression and recurrence of non-muscle-invasive bladder cancer (NMIBC) in a large cohort of patients from a single centre.



Patients and Methods

Between October 1984 and March 2009 a cohort of 1019 patients (877 males; 142 females; median age 44 years) with histologically confirmed NMIBC was included in this study.
Among these patients, 74% received bacillus Calmette-Guérin (BCG)-based therapy. Complete transurethral resection of bladder tumour of all visible tumours was carried out in all patients, and the stage and grade were determined.
Univariate analysis and multivariate Cox regression were used to identify predictors of recurrence and progression. The studied predictors included age, sex, stage, grade, associated carcinoma in situ, tumour size, multiplicity, macroscopic appearance of the tumour, history of recurrence and type of adjuvant intravesical therapy.
Multivariate logistic regression models were used to develop the 12- and 60-month recurrence and progression predictive models. The predictive accuracy of the models was assessed for discrimination as well as calibration.



Results

The median (range) follow-up was 44 (6–254) months.
On multivariate analysis, stage, multiplicity, history of recurrence and adjuvant intravesical therapy were significantly associated with recurrence, whereas for progression only tumour grade and size were significant independent predictors.
The constructed nomograms had a 64.9% and 69.4% chance of correctly distinguishing between two patients, one destined to have a recurrence and one not at 12 and 60 months, respectively.
The constructed nomograms had a 70.2% and 73.5% chance of correctly distinguishing between two patients, one destined to progress and one not at 12 and 60 months, respectively. All predictive models were well calibrated.



Conclusions

Based on multivariate analysis of the studied prognostic factors nomograms for predicting recurrence and progression in NMIBC were constructed.
Most of the studied patients had received BCG-based therapy, making these models more closely applicable to contemporary practice than others.
These predictive models have reasonable discriminative ability and are well calibrated, but require external validation before they can be applied to other populations.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12016" xmlns="http://purl.org/rss/1.0/"><title>Surgical correction of vesico-ureteric reflux for recurrent febrile urinary tract infections after kidney transplantation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Surgical correction of vesico-ureteric reflux for recurrent febrile urinary tract infections after kidney transplantation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ayhan Dinckan, Ibrahim Aliosmanoglu, Huseyin Kocak, Filiz Gunseren, Ayhan Mesci, Zeki Ertug, Selcuk Yucel, Gultekin Suleymanlar, Alihan Gurkan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-27T11:33:53.672407-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12016-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12016-list-0001" class="bullet">
<li>To evaluate the outcome of anti-reflux revision surgery in patients diagnosed with at least a grade 3 reflux at voiding cysto-urethrography in patients with recurrent urinary tract infection (UTI) after renal transplantation.</li>
</ul></div></div>
<div class="section" id="bju12016-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12016-list-0002" class="bullet">
<li>We identified 60 patients with a diagnosis of recurrent febrile UTI and post-transplantation vesico-ureteric reflux (VUR) who underwent open surgical correction of reflux.</li>
<li>Patient characteristics, including the aetiology of end-stage renal disease, age, time to VUR correction, type of VUR correction, serum creatinine levels, and number of UTIs before and after correction were documented.</li>
</ul></div></div>
<div class="section" id="bju12016-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12016-list-0003" class="bullet">
<li>The median (range) age of the patients was 31.5 (9–65) years. A total of 30 patients underwent uretero-ureterostomy or pyelo-ureterostomy and 30 underwent extravesical or intravesical ureteric reimplantation.</li>
<li>The median (range) creatinine levels before and after correction were 1.5 (0.8–4.5) mg/dL and 1.3 (0.7–4.5) mg/dL (<em>P</em> &lt; 0.05), respectively.</li>
<li>The median (range) number of UTI episodes reported before the correction surgery was 4 (3–12), whereas number of UTI episodes after the surgery was 1 (0–12), the difference being significant (<em>P</em> &lt; 0.05).</li>
</ul></div></div>
<div class="section" id="bju12016-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12016-list-0004" class="bullet">
<li>Open surgical correction of post-transplant VUR is an effective and safe method of decreasing UTI episodes and stopping reflux.</li>
<li>Surgical correction of reflux may prolong the life of the renal graft.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the outcome of anti-reflux revision surgery in patients diagnosed with at least a grade 3 reflux at voiding cysto-urethrography in patients with recurrent urinary tract infection (UTI) after renal transplantation.



Patients and Methods

We identified 60 patients with a diagnosis of recurrent febrile UTI and post-transplantation vesico-ureteric reflux (VUR) who underwent open surgical correction of reflux.
Patient characteristics, including the aetiology of end-stage renal disease, age, time to VUR correction, type of VUR correction, serum creatinine levels, and number of UTIs before and after correction were documented.



Results

The median (range) age of the patients was 31.5 (9–65) years. A total of 30 patients underwent uretero-ureterostomy or pyelo-ureterostomy and 30 underwent extravesical or intravesical ureteric reimplantation.
The median (range) creatinine levels before and after correction were 1.5 (0.8–4.5) mg/dL and 1.3 (0.7–4.5) mg/dL (P &lt; 0.05), respectively.
The median (range) number of UTI episodes reported before the correction surgery was 4 (3–12), whereas number of UTI episodes after the surgery was 1 (0–12), the difference being significant (P &lt; 0.05).



Conclusions

Open surgical correction of post-transplant VUR is an effective and safe method of decreasing UTI episodes and stopping reflux.
Surgical correction of reflux may prolong the life of the renal graft.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12033" xmlns="http://purl.org/rss/1.0/"><title>Lack of predictive correlation between peripheral arterial tone and colour flow Doppler parameters in men with erectile dysfunction</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12033</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Lack of predictive correlation between peripheral arterial tone and colour flow Doppler parameters in men with erectile dysfunction</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Catherine M. Seager, Jianbo Li, Daniel A. Shoskes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-22T10:08:46.169185-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12033</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12033</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12033</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12033-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12033-list-0001" class="bullet">
<li>To evaluate whether peripheral arterial tone (PAT) can predict the results of penile colour flow Doppler in the evaluation of erectile dysfunction (ED).</li>
</ul></div></div>
<div class="section" id="bju12033-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12033-list-0002" class="bullet">
<li>Fifty men presenting to an ED clinic were tested with an Endo-PAT2000 machine (Itamar Medical, Caesarea, Israel), which assessed augmentation index (AI), a measure of arterial stiffness, and reactive hyperaemia index (RHI), a measure of endothelial vasodilatation.</li>
<li>Penile haemodynamics were measured and used to identify both arterial insufficiency (abnormal peak systolic velocity [PSV]) and veno-occlusive disease (abnormal end diastolic velocity [EDV]) after pharmacological erection with prostaglandin E1 using colour flow Doppler.</li>
<li>Between-group comparisons were carried out using a Wilcoxon rank-sum test for continuous variables and a chi-squared test for categorical variables. Simple and multivariable logistic regression analyses were used to analyse the correlation between outcome measures.</li>
</ul></div></div>
<div class="section" id="bju12033-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12033-list-0003" class="bullet">
<li>Using Doppler analysis, 58% of patients were found to have arterial insufficiency (abnormal PSV) and 48% had veno-occlussive disease (abnormal EDV).</li>
<li>Using the Endo-PAT machine, 44% of patients were found to have increased arterial stiffness (abnormal AI) and 54% had decreased endothelial relaxation (abnormal RHI).</li>
<li>Neither AI nor RHI were correlated with PSV or EDV. The closest association was between high AI and low PSV, with a sensitivity of 0.55 and specificity of 0.71.</li>
</ul></div></div>
<div class="section" id="bju12033-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12033-list-0004" class="bullet">
<li>In our patient cohort, PAT did not reliably predict the results of penile Doppler.</li>
<li>The two tests appear to measure different although potentially complementary aspects of the local and systemic vasculature.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate whether peripheral arterial tone (PAT) can predict the results of penile colour flow Doppler in the evaluation of erectile dysfunction (ED).



Patients and Methods

Fifty men presenting to an ED clinic were tested with an Endo-PAT2000 machine (Itamar Medical, Caesarea, Israel), which assessed augmentation index (AI), a measure of arterial stiffness, and reactive hyperaemia index (RHI), a measure of endothelial vasodilatation.
Penile haemodynamics were measured and used to identify both arterial insufficiency (abnormal peak systolic velocity [PSV]) and veno-occlusive disease (abnormal end diastolic velocity [EDV]) after pharmacological erection with prostaglandin E1 using colour flow Doppler.
Between-group comparisons were carried out using a Wilcoxon rank-sum test for continuous variables and a chi-squared test for categorical variables. Simple and multivariable logistic regression analyses were used to analyse the correlation between outcome measures.



Results

Using Doppler analysis, 58% of patients were found to have arterial insufficiency (abnormal PSV) and 48% had veno-occlussive disease (abnormal EDV).
Using the Endo-PAT machine, 44% of patients were found to have increased arterial stiffness (abnormal AI) and 54% had decreased endothelial relaxation (abnormal RHI).
Neither AI nor RHI were correlated with PSV or EDV. The closest association was between high AI and low PSV, with a sensitivity of 0.55 and specificity of 0.71.



Conclusions

In our patient cohort, PAT did not reliably predict the results of penile Doppler.
The two tests appear to measure different although potentially complementary aspects of the local and systemic vasculature.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12005" xmlns="http://purl.org/rss/1.0/"><title>Refractory chronic pelvic pain syndrome in men: can transcutaneous electrical nerve stimulation help?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12005</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Refractory chronic pelvic pain syndrome in men: can transcutaneous electrical nerve stimulation help?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marc P. Schneider, Marc Tellenbach, Livio Mordasini, George N. Thalmann, Thomas M. Kessler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-22T10:08:41.564669-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12005</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12005</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12005</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12005-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12005-list-0001" class="bullet">
<li>To evaluate the effect of transcutaneous electrical nerve stimulation (TENS) for treating men with refractory chronic pelvic pain syndrome (CPPS).</li>
</ul></div></div>
<div class="section" id="bju12005-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12005-list-0002" class="bullet">
<li>A consecutive series of 60 men treated with TENS for refractory CPPS was evaluated prospectively at an academic tertiary referral centre.</li>
<li>The effects of treatment were evaluated by a pain diary and by the quality of life item of the National Institutes of Health Chronic Prostatitis Symptom Index at baseline, after 12 weeks of TENS treatment, and at last known follow-up.</li>
<li>Adverse events related to TENS were also assessed.</li>
</ul></div></div>
<div class="section" id="bju12005-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12005-list-0003" class="bullet">
<li>The mean (95% confidence interval, CI; range) age of the 60 men was 46.9 (43.5–50.3; 21–82) years.</li>
<li>TENS was successful after 12 weeks of treatment in 29 (48%) patients and a positive effect was sustained during a mean (95%, CI; range) follow-up of 43.6 (33.2–56; 6–88) months in 21 patients. After 12 weeks of TENS treatment, mean (95% CI) pain visual analogue scale decreased significantly (<em>P</em> &lt; 0.001) from 6.6 (6.3–6.9) to 3.9 (3.2–4.6).</li>
<li>Patients' quality of life changed significantly after TENS treatment (<em>P</em> &lt; 0.001). Before TENS, all 60 patients felt mostly dissatisfied (<em>n</em> = 17; 28%), unhappy (<em>n</em> = 28; 47%) or terrible (<em>n</em> = 15; 25%). After 12 weeks of TENS treatment, 29 (48%) patients felt mostly satisfied (<em>n</em> = 5), pleased (<em>n</em> = 18) or delighted (<em>n</em> = 6).</li>
<li>No adverse events related to TENS were noted.</li>
</ul></div></div>
<div class="section" id="bju12005-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju12005-list-0004" class="bullet">
<li>TENS may be an effective and safe treatment for refractory CPPS in men, warranting randomized, placebo-controlled trials.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To evaluate the effect of transcutaneous electrical nerve stimulation (TENS) for treating men with refractory chronic pelvic pain syndrome (CPPS).



Patients and Methods

A consecutive series of 60 men treated with TENS for refractory CPPS was evaluated prospectively at an academic tertiary referral centre.
The effects of treatment were evaluated by a pain diary and by the quality of life item of the National Institutes of Health Chronic Prostatitis Symptom Index at baseline, after 12 weeks of TENS treatment, and at last known follow-up.
Adverse events related to TENS were also assessed.



Results

The mean (95% confidence interval, CI; range) age of the 60 men was 46.9 (43.5–50.3; 21–82) years.
TENS was successful after 12 weeks of treatment in 29 (48%) patients and a positive effect was sustained during a mean (95%, CI; range) follow-up of 43.6 (33.2–56; 6–88) months in 21 patients. After 12 weeks of TENS treatment, mean (95% CI) pain visual analogue scale decreased significantly (P &lt; 0.001) from 6.6 (6.3–6.9) to 3.9 (3.2–4.6).
Patients' quality of life changed significantly after TENS treatment (P &lt; 0.001). Before TENS, all 60 patients felt mostly dissatisfied (n = 17; 28%), unhappy (n = 28; 47%) or terrible (n = 15; 25%). After 12 weeks of TENS treatment, 29 (48%) patients felt mostly satisfied (n = 5), pleased (n = 18) or delighted (n = 6).
No adverse events related to TENS were noted.



Conclusion

TENS may be an effective and safe treatment for refractory CPPS in men, warranting randomized, placebo-controlled trials.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11747.x" xmlns="http://purl.org/rss/1.0/"><title>Antidiuretic effect of antimuscarinic agents in rat model depends on C-fibre afferent nerves in the bladder</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11747.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Antidiuretic effect of antimuscarinic agents in rat model depends on C-fibre afferent nerves in the bladder</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nozomu Watanabe, Hironobu Akino, Tetsuyuki Kurokawa, Minekatu Taga, Ryusei Yokokawa, Kazuya Tanase, Keiko Nagase, Osamu Yokoyama</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-22T10:08:37.677629-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11747.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11747.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11747.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11747-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11747-list-0001" class="bullet">
<li>Antichollnergic agents are anticipated to diminish storage symptoms, as well as nocturia. Nevertheless, the effect of this treatment on polyuria related to nocturia is not clear. By subgroup analysis of the data set from a phase III clinical trial of antimuscarinic agent for OAB patients in Japan, imidafenacin was found to improve nocturia with a reduction in nocturnal polyuria.</li>
<li>This study adds the effects and underlying mechanism of antimuscarinic agents decreasing urine production through inhibition of C-fibre in the bladder of water-leaded rats.</li>
</ul></div></div>
<div class="section" id="bju11747-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11747-list-0002" class="bullet">
<li>To evaluate the effects and underlying mechanisms of antimuscarinic agents used to decrease in urine production in water-loaded rats.</li>
</ul></div></div>
<div class="section" id="bju11747-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects and Methods</h4><div class="para"><ul id="bju11747-list-0003" class="bullet">
<li>Urine production was measured using a cystostomy catheter in female Sprague–Dawley rats every 2 h.</li>
<li>The effect of the antimuscarinic agents atropine, tolterodine and imidafenacin on urine production was investigated under water-loaded conditions, which were induced by i.p. injection of 15 mL saline.</li>
<li>Blood samples were collected to determine the levels of antidiuretic hormone (ADH), aldosterone (ALD), atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) before, and 2 and 8 h after, antimuscarinic agent administration.</li>
<li>To induce desensitization of C-fibre afferent nerves, resiniferatoxin (RTX)was injected s.c. or intravesically 2 days before experiments.</li>
</ul></div></div>
<div class="section" id="bju11747-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11747-list-0004" class="bullet">
<li>Urine production increased and reached its maximum 2 h after 15 mL saline injection.</li>
<li>Imidafenacin and tolterodine decreased urine production in water-loaded rats, but ADH, ALD, ANP and BNP levels were not different between imidafenacin-treated and vehicle-treated rats.</li>
<li>The inhibitory effect on urine production was not found in RTX-treated rats.</li>
<li>Atropine did not reduce urine production.</li>
</ul></div></div>
<div class="section" id="bju11747-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11747-list-0005" class="bullet">
<li>These results suggest that antimuscarinic agents decrease urine volume through C-fibres in the bladder; thus, antimuscarinics with inhibitory effects on C-fibres could be beneficial for nocturia with nocturnal polyuria.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Antichollnergic agents are anticipated to diminish storage symptoms, as well as nocturia. Nevertheless, the effect of this treatment on polyuria related to nocturia is not clear. By subgroup analysis of the data set from a phase III clinical trial of antimuscarinic agent for OAB patients in Japan, imidafenacin was found to improve nocturia with a reduction in nocturnal polyuria.
This study adds the effects and underlying mechanism of antimuscarinic agents decreasing urine production through inhibition of C-fibre in the bladder of water-leaded rats.


 Objective

To evaluate the effects and underlying mechanisms of antimuscarinic agents used to decrease in urine production in water-loaded rats.



Subjects and Methods

Urine production was measured using a cystostomy catheter in female Sprague–Dawley rats every 2 h.
The effect of the antimuscarinic agents atropine, tolterodine and imidafenacin on urine production was investigated under water-loaded conditions, which were induced by i.p. injection of 15 mL saline.
Blood samples were collected to determine the levels of antidiuretic hormone (ADH), aldosterone (ALD), atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) before, and 2 and 8 h after, antimuscarinic agent administration.
To induce desensitization of C-fibre afferent nerves, resiniferatoxin (RTX)was injected s.c. or intravesically 2 days before experiments.



Results

Urine production increased and reached its maximum 2 h after 15 mL saline injection.
Imidafenacin and tolterodine decreased urine production in water-loaded rats, but ADH, ALD, ANP and BNP levels were not different between imidafenacin-treated and vehicle-treated rats.
The inhibitory effect on urine production was not found in RTX-treated rats.
Atropine did not reduce urine production.



Conclusion

These results suggest that antimuscarinic agents decrease urine volume through C-fibres in the bladder; thus, antimuscarinics with inhibitory effects on C-fibres could be beneficial for nocturia with nocturnal polyuria.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11766.x" xmlns="http://purl.org/rss/1.0/"><title>Does obesity affect the accuracy of prostate-specific antigen (PSA) for predicting prostate cancer among men undergoing prostate biopsy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11766.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Does obesity affect the accuracy of prostate-specific antigen (PSA) for predicting prostate cancer among men undergoing prostate biopsy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jong J. Oh, Seong J. Jeong, Byung K. Lee, Chang W. Jeong, Seok-Soo Byun, Sung K. Hong, Sang E. Lee</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-21T08:47:24.89477-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11766.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11766.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11766.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11766-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11766-list-0001" class="bullet">
<li>As most urologist known, obesity significantly lowers serum PSA levels. So there is some concern about delayed diagnosis of prostate cancer in obese men.</li>
<li>In the present study, we found that the accuracy level of PSA for detecting prostate cancer was not significantly different between different obesity levels. A well-designed study adjusting for several factors, e.g. diet, exercise, medication and comorbidity, which may possibly compensate for the associated effects on PSA levels, is needed for confirmation of the present findings.</li>
</ul></div></div>
<div class="section" id="bju11766-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11766-list-0002" class="bullet">
<li>To investigate prostate-specific antigen (PSA) accuracy in detecting prostate cancer according to body mass index (BMI) in Asian men with a PSA level of &lt;30 ng/mL using contemporary multicore (≥12) prostate biopsy.</li>
</ul></div></div>
<div class="section" id="bju11766-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11766-list-0003" class="bullet">
<li>We reviewed the records of 3471 patients, whose initial PSA levels were &lt;30 ng/mL, who underwent multicore (≥12) transrectal ultrasound-guided prostate biopsy between January 2004 and May 2011.</li>
<li>BMI was categorised as performed previously for the Asian population: &lt;23, 23–24.9, 25–29.9, and ≥30 kg/m<sup>2</sup>. PSA accuracy for detecting prostate cancer in each BMI group was assessed based on the receiver operating characteristics-derived area under the curve.</li>
</ul></div></div>
<div class="section" id="bju11766-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11766-list-0004" class="bullet">
<li>The mean age and median PSA level were inversely associated with BMI; the median PSA level in each BMI category was 7.84, 7.75, 7.33 and 5.79 ng/mL, respectively (<em>P</em> &lt; 0.001).</li> <li>In all, prostate cancer was detected from biopsy in 1102 (31.7%) patients.</li>
<li>The PSA accuracy for predicting prostate cancer in all patients was estimated to be 0.607, and PSA accuracies in each BMI category were 0.638, 0.572, 0.613 and 0.544, respectively; there was no significant difference among the groups in terms of PSA accuracy.</li>
</ul></div></div>
<div class="section" id="bju11766-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11766-list-0005" class="bullet">
<li>The accuracy of PSA in predicting prostate cancer did not change regardless of BMI category in Asian men.</li>
<li>However, as patients with higher BMIs had lower PSA levels than those with lower BMIs, it can therefore be suggested that the PSA threshold should be lower in obese men to discriminate between prostate cancer and benign conditions in the real clinical situation.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

As most urologist known, obesity significantly lowers serum PSA levels. So there is some concern about delayed diagnosis of prostate cancer in obese men.
In the present study, we found that the accuracy level of PSA for detecting prostate cancer was not significantly different between different obesity levels. A well-designed study adjusting for several factors, e.g. diet, exercise, medication and comorbidity, which may possibly compensate for the associated effects on PSA levels, is needed for confirmation of the present findings.


 Objective

To investigate prostate-specific antigen (PSA) accuracy in detecting prostate cancer according to body mass index (BMI) in Asian men with a PSA level of &lt;30 ng/mL using contemporary multicore (≥12) prostate biopsy.



Patients and Methods

We reviewed the records of 3471 patients, whose initial PSA levels were &lt;30 ng/mL, who underwent multicore (≥12) transrectal ultrasound-guided prostate biopsy between January 2004 and May 2011.
BMI was categorised as performed previously for the Asian population: &lt;23, 23–24.9, 25–29.9, and ≥30 kg/m2. PSA accuracy for detecting prostate cancer in each BMI group was assessed based on the receiver operating characteristics-derived area under the curve.



Results

The mean age and median PSA level were inversely associated with BMI; the median PSA level in each BMI category was 7.84, 7.75, 7.33 and 5.79 ng/mL, respectively (P &lt; 0.001). In all, prostate cancer was detected from biopsy in 1102 (31.7%) patients.
The PSA accuracy for predicting prostate cancer in all patients was estimated to be 0.607, and PSA accuracies in each BMI category were 0.638, 0.572, 0.613 and 0.544, respectively; there was no significant difference among the groups in terms of PSA accuracy.



Conclusions

The accuracy of PSA in predicting prostate cancer did not change regardless of BMI category in Asian men.
However, as patients with higher BMIs had lower PSA levels than those with lower BMIs, it can therefore be suggested that the PSA threshold should be lower in obese men to discriminate between prostate cancer and benign conditions in the real clinical situation.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12007" xmlns="http://purl.org/rss/1.0/"><title>Urodynamic evaluation: can it prevent the need for surgical intervention in women with apparent pure stress urinary incontinence?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12007</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Urodynamic evaluation: can it prevent the need for surgical intervention in women with apparent pure stress urinary incontinence?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maurizio Serati, Elena Cattoni, Gabriele Siesto, Andrea Braga, Paola Sorice, Simona Cantaluppi, Antonella Cromi, Fabio Ghezzi, Domenico Vitobello, Pierfrancesco Bolis, Stefano Salvatore</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-20T07:12:42.323034-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12007</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12007</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12007</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12007-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju12007-list-0001" class="bullet">
<li>To identify how many patients with symptoms of pure stress urinary incontinence (SUI) do not require any surgical treatment on the basis of urodynamics (UDS) and how many patients still do not require surgery 1 year after UDS.</li>
<li>To assess the outcomes of these patients at 12-month follow-up.</li>
</ul></div></div>
<div class="section" id="bju12007-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><ul id="bju12007-list-0002" class="bullet">
<li>Women with pure SUI received UDS and were prospectively divided into four groups, comprising women with: urodynamic stress incontinence (USI); detrusor overactivity (DO); USI + DO; and inconclusive UDS.</li>
<li>Women with USI underwent a Tension Free Vaginal Tape (Obturator) (TVT-O) procedure (Gynecare; Ethicon Inc., Somerville, NJ, USA), whereas women with DO ±/− USI were recommended 24-week antimuscarinic therapy.</li>
<li>Follow-up was scheduled at 3 and 12 months. To define subjective outcomes, all patients completed the International Consultation on Incontinence Questionnaire – short form, the Patient Global Impression – Improvement and the Urinary Distress Inventory.</li>
<li>Patients were considered cured if they presented a negative stress test, a score reduction of at least 80% on the Urinary Distress Inventory and a response of ‘much better’ or ‘very much better’ on the Patient Global Impression – Improvement.</li>
</ul></div></div>
<div class="section" id="bju12007-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12007-list-0003" class="bullet">
<li>Of the 263 women with pure SUI, 74.5% had a urodynamic diagnosis of USI, 10.6% had DO, 8% had USI + DO and 6.8% had inconclusive UDS.</li>
<li>At 12-month follow-up, 165/181 (91.6%) women in group 1 were considered cured post-TVT-O; in the other groups, 33/67 (49.2%) patients were considered cured simply as a result of taking antimuscarinics; 13 of these 67 patients required TVT-O.</li>
</ul></div></div>
<div class="section" id="bju12007-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12007-list-0004" class="bullet">
<li>UDS is able to show that several patients with symptoms of pure SUI present an underlying DO and do not require surgery, even 1 year after UDS.</li>
<li>In these patients, antimuscarinic treatment appears to ensure a good rate of cure; thus, UDS could lead to the avoidance of several surgical procedures.</li>
</ul></div></div>
]]></content:encoded><description>
 Objectives

To identify how many patients with symptoms of pure stress urinary incontinence (SUI) do not require any surgical treatment on the basis of urodynamics (UDS) and how many patients still do not require surgery 1 year after UDS.
To assess the outcomes of these patients at 12-month follow-up.



Patients and methods

Women with pure SUI received UDS and were prospectively divided into four groups, comprising women with: urodynamic stress incontinence (USI); detrusor overactivity (DO); USI + DO; and inconclusive UDS.
Women with USI underwent a Tension Free Vaginal Tape (Obturator) (TVT-O) procedure (Gynecare; Ethicon Inc., Somerville, NJ, USA), whereas women with DO ±/− USI were recommended 24-week antimuscarinic therapy.
Follow-up was scheduled at 3 and 12 months. To define subjective outcomes, all patients completed the International Consultation on Incontinence Questionnaire – short form, the Patient Global Impression – Improvement and the Urinary Distress Inventory.
Patients were considered cured if they presented a negative stress test, a score reduction of at least 80% on the Urinary Distress Inventory and a response of ‘much better’ or ‘very much better’ on the Patient Global Impression – Improvement.



Results

Of the 263 women with pure SUI, 74.5% had a urodynamic diagnosis of USI, 10.6% had DO, 8% had USI + DO and 6.8% had inconclusive UDS.
At 12-month follow-up, 165/181 (91.6%) women in group 1 were considered cured post-TVT-O; in the other groups, 33/67 (49.2%) patients were considered cured simply as a result of taking antimuscarinics; 13 of these 67 patients required TVT-O.



Conclusions

UDS is able to show that several patients with symptoms of pure SUI present an underlying DO and do not require surgery, even 1 year after UDS.
In these patients, antimuscarinic treatment appears to ensure a good rate of cure; thus, UDS could lead to the avoidance of several surgical procedures.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12027" xmlns="http://purl.org/rss/1.0/"><title>Prostate volume in male patients with spinal cord injury: a question of nerves?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12027</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Prostate volume in male patients with spinal cord injury: a question of nerves?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jürgen Pannek, Peter Bartel, Konrad Göcking, Angela Frotzler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:26:04.304029-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12027</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12027</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12027</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12027-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12027-list-0001" class="bullet">
<li>To assess the influence of standardized complete surgical deafferentation of the lower urinary tract by sacral deafferentation (SDAF) and sacral anterior root stimulation (SARS) on prostate volume in men with spinal cord injury (SCI).</li>
</ul></div></div>
<div class="section" id="bju12027-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju12027-list-0002" class="bullet">
<li>In a prospective study, the prostate volume of men with SCI who underwent SDAF/SARS was measured using transrectal ultrasonography.</li>
<li>The prostate volumes of these men were compared with those of men with complete SCI but who did not undergo SDAF/SARS, those of men with incomplete SCI, and those of a historical sample of able-bodied men.</li>
</ul></div></div>
<div class="section" id="bju12027-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12027-list-0003" class="bullet">
<li>The median [25th;75th percentile] prostate volume of men who underwent SDAF/SARS (20.0 [14.0; 29.0]) and of men with complete SCI who did not undergo SDAF/SARS (20.0 [16.5; 29.0]) was significantly smaller than in the reference group (25.0 [5.0; 84.0]).</li>
<li>The mean prostate volume was associated with age in the reference group (<em>r</em> = 0.185; <em>P</em> &lt; 0.001) and in men with incomplete SCI (<em>r</em> = 0.284; <em>P</em> = 0.031), but not in men with complete SCI, irrespective of SDAF/SARS.</li>
</ul></div></div>
<div class="section" id="bju12027-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12027-list-0004" class="bullet">
<li>The prostate volume of men with complete SCI was significantly smaller than that of able-bodied men.</li>
<li>Our data imply that sustained central innervation of the prostate plays an important role in prostate growth.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To assess the influence of standardized complete surgical deafferentation of the lower urinary tract by sacral deafferentation (SDAF) and sacral anterior root stimulation (SARS) on prostate volume in men with spinal cord injury (SCI).



Patients and Methods

In a prospective study, the prostate volume of men with SCI who underwent SDAF/SARS was measured using transrectal ultrasonography.
The prostate volumes of these men were compared with those of men with complete SCI but who did not undergo SDAF/SARS, those of men with incomplete SCI, and those of a historical sample of able-bodied men.



Results

The median [25th;75th percentile] prostate volume of men who underwent SDAF/SARS (20.0 [14.0; 29.0]) and of men with complete SCI who did not undergo SDAF/SARS (20.0 [16.5; 29.0]) was significantly smaller than in the reference group (25.0 [5.0; 84.0]).
The mean prostate volume was associated with age in the reference group (r = 0.185; P &lt; 0.001) and in men with incomplete SCI (r = 0.284; P = 0.031), but not in men with complete SCI, irrespective of SDAF/SARS.



Conclusions

The prostate volume of men with complete SCI was significantly smaller than that of able-bodied men.
Our data imply that sustained central innervation of the prostate plays an important role in prostate growth.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12003" xmlns="http://purl.org/rss/1.0/"><title>A 9-year experience of renal injury at an Australian level 1 trauma centre</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12003</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A 9-year experience of renal injury at an Australian level 1 trauma centre</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jennifer J. Shoobridge, Matthew F. Bultitude, Jim Koukounaras, Katherine E. Martin, Peter L. Royce, Niall M. Corcoran</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:25:55.007247-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/bju.12003</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/bju.12003</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fbju.12003</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju12003-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju12003-list-0001" class="bullet">
<li>To detail the 9-year experience of renal trauma at a modern Level 1 trauma centre and report on patterns of injury, management and complications.</li>
</ul></div></div>
<div class="section" id="bju12003-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><ul id="bju12003-list-0002" class="bullet">
<li>We analysed 338 patients with renal injuries who presented to our institution over a 9-year period.</li>
<li>Data on demographics, clinical presentation, management and complications were recorded.</li>
</ul></div></div>
<div class="section" id="bju12003-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju12003-list-0003" class="bullet">
<li>Males comprised 74.9% of patients with renal injuries and the highest incidence was amongst those aged 20–24 years.</li>
<li>Blunt injuries comprised 96.2% (<em>n</em> = 325) of all the renal injuries, with road trauma being the predominant mechanism accounting for 72.5% of injuries.</li>
<li>The distribution of injury grade was; 21.6% grade 1 (<em>n</em> = 73), 24.3% grade 2 (<em>n</em> = 82), 24.9% grade 3 (<em>n</em> = 84), 16.6% grade 4 (<em>n</em> = 56), and 12.7% grade 5 (<em>n</em> = 43).</li>
<li>Conservative management was successful in all grade 1 and 2 renal injuries, and 94.9%, 90.7% and 35.1% of grade 3, 4 and 5 injuries respectively.</li>
<li>All but one of the 13 patients with penetrating injuries were successfully managed conservatively.</li>
</ul></div></div>
<div class="section" id="bju12003-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju12003-list-0004" class="bullet">
<li>Road trauma is the greatest cause of renal injury.</li>
<li>Most haemodynamically stable patients are successfully managed conservatively.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To detail the 9-year experience of renal trauma at a modern Level 1 trauma centre and report on patterns of injury, management and complications.



Patients and methods

We analysed 338 patients with renal injuries who presented to our institution over a 9-year period.
Data on demographics, clinical presentation, management and complications were recorded.



Results

Males comprised 74.9% of patients with renal injuries and the highest incidence was amongst those aged 20–24 years.
Blunt injuries comprised 96.2% (n = 325) of all the renal injuries, with road trauma being the predominant mechanism accounting for 72.5% of injuries.
The distribution of injury grade was; 21.6% grade 1 (n = 73), 24.3% grade 2 (n = 82), 24.9% grade 3 (n = 84), 16.6% grade 4 (n = 56), and 12.7% grade 5 (n = 43).
Conservative management was successful in all grade 1 and 2 renal injuries, and 94.9%, 90.7% and 35.1% of grade 3, 4 and 5 injuries respectively.
All but one of the 13 patients with penetrating injuries were successfully managed conservatively.



Conclusions

Road trauma is the greatest cause of renal injury.
Most haemodynamically stable patients are successfully managed conservatively.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11787.x" xmlns="http://purl.org/rss/1.0/"><title>Increasing importance of truly informed consent: the role of written patient information</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11787.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Increasing importance of truly informed consent: the role of written patient information</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roger Kirby, Ben Challacombe, Simon Hughes, Simon Chowdhury, Prokar Dasgupta</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:25:11.946282-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11787.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11787.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11787.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Comment</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11779.x" xmlns="http://purl.org/rss/1.0/"><title>Changing paradigms in the investigation of an elevated PSA level</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11779.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Changing paradigms in the investigation of an elevated PSA level</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roger Kirby, Uday Patel, Ben Challacombe, Prokar Dasgupta</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:23:19.737032-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11779.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11779.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11779.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Comment</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11671.x" xmlns="http://purl.org/rss/1.0/"><title>The learning curve for laparoscopic extended pelvic lymphadenectomy for intermediate- and high-risk prostate cancer: implications for compliance with existing guidelines</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11671.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The learning curve for laparoscopic extended pelvic lymphadenectomy for intermediate- and high-risk prostate cancer: implications for compliance with existing guidelines</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher G. Eden, Evangelos Zacharakis, Simon Bott</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:23:07.939739-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11671.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11671.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11671.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11671-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11671-list-0001" class="bullet">
<li>To investigate the learning curve for performing extended pelvic lymphadenectomy (ePLND) during laparoscopic radical prostatectomy (LRP) in patients with intermediate- and high-risk prostate cancer.</li>
</ul></div></div>
<div class="section" id="bju11671-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and methods</h4><div class="para"><ul id="bju11671-list-0002" class="bullet">
<li>In all, 500 patients underwent ePLND for intermediate- or high-risk prostate cancer by one surgeon during a 48-month period. A transperitoneal laparoscopic approach was used in all patients to allow adequate access to the internal iliac vessels.</li>
<li>The variables chosen as being the most important discriminators of the quality of ePLND were operating time, complication rate and lymph node (LN) yield.</li>
<li>The learning curves for ePLND were calculated using the cumulative sum and cumulative average methods and the number of procedures performed until attainment of acceptable failure rates (competence levels) was calculated. LN parameters were compared with the results from the preceding 311 cases where limited PLND was undertaken.</li>
</ul></div></div>
<div class="section" id="bju11671-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11671-list-0003" class="bullet">
<li>The median (range) preoperative PSA level was 8.0(1–62.5) ng/mL and biopsy Gleason score was 7(6–10). In all, 64% of patients had intermediate-risk and 36% had high-risk prostate cancer. There were no intraoperative blood transfusions and no conversions to open surgery. The median (range) blood loss was 200(10–1400) mL and the postoperative transfusion rate was 1.6%.</li>
<li>The operating time fell at a steady rate of 2.7% after the 15th case and plateaued after 130 patients. At competence levels of 5% and 10%, the learning curve for all complications ended after 346 and 136 patients, respectively.</li>
<li>At a 5% competence level the learning curve for PLND-specific complications was 40 cases and there was no learning curve at a 10% competence level.</li>
<li>The overall complication rate was 7.2% of which almost half (47%) were deemed to be PLND-specific. The cumulative average of the LN counts plateaued after 150 procedures. Furthermore, the median LN count after ePLND was more than double that of the authors' historical standard PLND controls (14 vs 6, <em>P</em> &lt; 0.001) and increased with experience up to the end of the series (9 to 20).</li>
<li>The likelihood of LN involvement (LNI) correlated with biopsy and pathological Gleason grade, clinical and pathological stage and d'Amico risk group.</li>
</ul></div></div>
<div class="section" id="bju11671-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11671-list-0004" class="bullet">
<li>This study suggests a learning curve of ≈130 cases for operating time, 136 cases for all complications, 40 cases for PLND-specific complications and 150 cases for LN yield.</li>
<li>The risk of LNI for patients with intermediate- and high-risk prostate cancer was 8.4% and 19.4%, respectively, which suggests that a significant proportion would benefit from ePLND. It also shows that ePLND can be safely incorporated into LRP, and therefore also into robot-assisted RP, in a high-volume setting.</li>
</ul></div></div>
]]></content:encoded><description>
 Objective

To investigate the learning curve for performing extended pelvic lymphadenectomy (ePLND) during laparoscopic radical prostatectomy (LRP) in patients with intermediate- and high-risk prostate cancer.



Patients and methods

In all, 500 patients underwent ePLND for intermediate- or high-risk prostate cancer by one surgeon during a 48-month period. A transperitoneal laparoscopic approach was used in all patients to allow adequate access to the internal iliac vessels.
The variables chosen as being the most important discriminators of the quality of ePLND were operating time, complication rate and lymph node (LN) yield.
The learning curves for ePLND were calculated using the cumulative sum and cumulative average methods and the number of procedures performed until attainment of acceptable failure rates (competence levels) was calculated. LN parameters were compared with the results from the preceding 311 cases where limited PLND was undertaken.



Results

The median (range) preoperative PSA level was 8.0(1–62.5) ng/mL and biopsy Gleason score was 7(6–10). In all, 64% of patients had intermediate-risk and 36% had high-risk prostate cancer. There were no intraoperative blood transfusions and no conversions to open surgery. The median (range) blood loss was 200(10–1400) mL and the postoperative transfusion rate was 1.6%.
The operating time fell at a steady rate of 2.7% after the 15th case and plateaued after 130 patients. At competence levels of 5% and 10%, the learning curve for all complications ended after 346 and 136 patients, respectively.
At a 5% competence level the learning curve for PLND-specific complications was 40 cases and there was no learning curve at a 10% competence level.
The overall complication rate was 7.2% of which almost half (47%) were deemed to be PLND-specific. The cumulative average of the LN counts plateaued after 150 procedures. Furthermore, the median LN count after ePLND was more than double that of the authors' historical standard PLND controls (14 vs 6, P &lt; 0.001) and increased with experience up to the end of the series (9 to 20).
The likelihood of LN involvement (LNI) correlated with biopsy and pathological Gleason grade, clinical and pathological stage and d'Amico risk group.



Conclusions

This study suggests a learning curve of ≈130 cases for operating time, 136 cases for all complications, 40 cases for PLND-specific complications and 150 cases for LN yield.
The risk of LNI for patients with intermediate- and high-risk prostate cancer was 8.4% and 19.4%, respectively, which suggests that a significant proportion would benefit from ePLND. It also shows that ePLND can be safely incorporated into LRP, and therefore also into robot-assisted RP, in a high-volume setting.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11667.x" xmlns="http://purl.org/rss/1.0/"><title>Phase II clinical trial of cediranib in patients with metastatic castration-resistant prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11667.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Phase II clinical trial of cediranib in patients with metastatic castration-resistant prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">William L. Dahut, Ravi A. Madan, Joyson J. Karakunnel, David Adelberg, James L. Gulley, Ismail B. Turkbey, Cindy H. Chau, Shawn D. Spencer, Marcia Mulquin, John Wright, Howard L. Parnes, Seth M. Steinberg, Peter L. Choyke, William D. Figg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-18T11:22:56.723549-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11667.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11667.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11667.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11667-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11667-list-0001" class="bullet">
<li>Recent advances in the treatment of metastatic castration-resistant prostate cancer (CRPC) have resulted in improved outcomes; however, the effects have not proved to be long term, highlighting the need for new therapies, particularly in patients with docetaxel-refractory metastatic CRPC. Angiogenesis has been shown to play an important role in the development and progression of prostate cancer. Although targeting angiogenesis appears to be a rational and therapeutic approach for metastatic CRPC, identifying the appropriate subgroups that may benefit from anti-angiogenic therapy remains a challenge.</li>
<li>The study demonstrates the potential use of dynamic contrast-enhanced (DCE)-MRI variables as pharmacodynamic endpoints in predicting the clinical outcomes associated with anti-angiogenic agents such as cediranib. Further investigation into the potential predictive value of DCE-MRI variables as biomarkers for antiangiogenic therapy is warranted.</li>
</ul></div></div>
<div class="section" id="bju11667-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11667-list-0002" class="bullet">
<li>To assess the efficacy and toxicity of cediranib, a highly potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, in patients with metastatic castration-resistant prostate cancer (CRPC) previously treated with docetaxel-based therapy.</li>
</ul></div></div>
<div class="section" id="bju11667-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11667-list-0003" class="bullet">
<li>The study used a Simon two-stage trial design, which required at least two of 12 patients in the first cohort to be progression-free at 6 months.</li>
<li>We enrolled a total of 35 evaluable patients who all received cediranib 20 mg orally daily.</li>
<li>In a second cohort, 23 additional patients received prednisone 10 mg daily with cediranib.</li>
<li>Endpoints included tumour response, progression-free survival (PFS), overall survival (OS), vascular permeability via dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI), and toxicity.</li>
</ul></div></div>
<div class="section" id="bju11667-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11667-list-0004" class="bullet">
<li>A total of 59 patients were enrolled, of whom 67% had received two or more previous chemotherapy regimens.</li>
<li>Six of 39 patients with measurable disease had confirmed partial responses and one had an unconfirmed partial response.</li>
<li>At 6 months, 43.9% of patients were progression-free; the median PFS and OS periods for all patients were 3.7 months and 10.1 months, respectively.</li>
<li>We found that the DCE-MRI variables baseline transport constant (K<sub>trans</sub>) and rate constant at day 28 were significantly associated with PFS in univariate analyses, but only baseline K<sub>trans</sub> remained significant when considered jointly.</li>
<li>The most frequent toxicities were hypertension, fatigue, anorexia and weight loss; the addition of prednisone reduced the incidence of constitutional toxicities.</li>
</ul></div></div>
<div class="section" id="bju11667-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11667-list-0005" class="bullet">
<li>This study demonstrated that cediranib was generally well tolerated with some anti-tumour activity in highly pretreated patients with metastatic CRPC who had progressive disease after docetaxel-based therapy.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Recent advances in the treatment of metastatic castration-resistant prostate cancer (CRPC) have resulted in improved outcomes; however, the effects have not proved to be long term, highlighting the need for new therapies, particularly in patients with docetaxel-refractory metastatic CRPC. Angiogenesis has been shown to play an important role in the development and progression of prostate cancer. Although targeting angiogenesis appears to be a rational and therapeutic approach for metastatic CRPC, identifying the appropriate subgroups that may benefit from anti-angiogenic therapy remains a challenge.
The study demonstrates the potential use of dynamic contrast-enhanced (DCE)-MRI variables as pharmacodynamic endpoints in predicting the clinical outcomes associated with anti-angiogenic agents such as cediranib. Further investigation into the potential predictive value of DCE-MRI variables as biomarkers for antiangiogenic therapy is warranted.


 Objective

To assess the efficacy and toxicity of cediranib, a highly potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, in patients with metastatic castration-resistant prostate cancer (CRPC) previously treated with docetaxel-based therapy.



Patients and Methods

The study used a Simon two-stage trial design, which required at least two of 12 patients in the first cohort to be progression-free at 6 months.
We enrolled a total of 35 evaluable patients who all received cediranib 20 mg orally daily.
In a second cohort, 23 additional patients received prednisone 10 mg daily with cediranib.
Endpoints included tumour response, progression-free survival (PFS), overall survival (OS), vascular permeability via dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI), and toxicity.



Results

A total of 59 patients were enrolled, of whom 67% had received two or more previous chemotherapy regimens.
Six of 39 patients with measurable disease had confirmed partial responses and one had an unconfirmed partial response.
At 6 months, 43.9% of patients were progression-free; the median PFS and OS periods for all patients were 3.7 months and 10.1 months, respectively.
We found that the DCE-MRI variables baseline transport constant (Ktrans) and rate constant at day 28 were significantly associated with PFS in univariate analyses, but only baseline Ktrans remained significant when considered jointly.
The most frequent toxicities were hypertension, fatigue, anorexia and weight loss; the addition of prednisone reduced the incidence of constitutional toxicities.



Conclusion

This study demonstrated that cediranib was generally well tolerated with some anti-tumour activity in highly pretreated patients with metastatic CRPC who had progressive disease after docetaxel-based therapy.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11748.x" xmlns="http://purl.org/rss/1.0/"><title>Predicting progression of bladder urothelial carcinoma using microRNA expression</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11748.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Predicting progression of bladder urothelial carcinoma using microRNA expression</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eran Rosenberg, Jack Baniel, Yael Spector, Alexander Faerman, Eti Meiri, Ranit Aharonov, David Margel, Yaron Goren, Ofer Nativ</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-06T09:55:52.504391-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11748.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11748.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11748.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11748-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11748-list-0001" class="bullet">
<li>Recurrence and progression prediction in urothelial cancer is currently based on clinical and pathological factors: tumour grade, tumour stage, number of lesions, tumour size, previous recurrence rate, and presence of concomitant carcinoma in situ. These factors are not specific enough to predict progression and ∼50% of patients diagnosed as high risk in fact do not progress within 3 years. Patient follow-up is both expensive and unpleasant (frequent invasive cystoscopies). Molecular biomarkers, including microRNAs have been studied to provide additional prognostic information for these patients, but to date no molecular biomarker has become the ‘gold standard’ for patient diagnosis and follow-up.</li>
<li>We used Rosetta Genomics’ highly specific microRNA expression profiling platforms to study the prognostic role of microRNAs in bladder cancer. Using microdissection we chose specific tumour microRNAs to study in order to avoid background contamination. Tumour progression was associated with altered levels of microRNAs. In particular, high expression levels of miR-29c* were associated with a good prognosis. The study found that the use of microRNAs for determining progression and invasiveness for patients with urothelial cancer could potentially have a substantial impact on the treatment and follow-up individual patients.</li>
</ul></div></div>
<div class="section" id="bju11748-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11748-list-0002" class="bullet">
<li>To identify microRNAs that could be useful as prognostic markers for non-muscle-invasive (NMI) bladder carcinoma.</li>
</ul></div></div>
<div class="section" id="bju11748-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11748-list-0003" class="bullet">
<li>Formalin-fixed, paraffin-embedded samples of 108 NMI bladder carcinomas, and 29 carcinomas invading bladder muscle were collected, and microRNA expression levels were measured using microarrays.</li>
<li>For 19 samples, microdissection was performed to compare microRNA expression between the tumour and surrounding tissue.</li>
<li>MicroRNAs that were found to be unrelated to the tumour itself were excluded as potential prognostic markers.</li>
</ul></div></div>
<div class="section" id="bju11748-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11748-list-0004" class="bullet">
<li>Expression profiles identified microRNAs that were differentially expressed in NMI tumours from patients who later progressed to carcinoma invading bladder muscle compared with NMI tumours from patients that did not progress.</li>
<li>The microRNA profile of tumours invading the bladder muscle was more similar to that of NMI tumours from patients who later progressed, than to that of the same-stage NMI tumours from patients who did not later progress.</li>
<li>The expression level of one microRNA, miR-29c*, was significantly under-expressed in tumours that progressed and could be used to stratify patients with T1 disease into risk groups.</li>
</ul></div></div>
<div class="section" id="bju11748-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11748-list-0005" class="bullet">
<li>MicroRNAs can be useful biomarkers for prognosis in patients with urothelial carcinoma.</li>
<li>In our study, expression levels of several microRNAs, including miR-29c* identified high- and low-risk groups. These biomarkers show promise for the stratification of patients with bladder cancer.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Recurrence and progression prediction in urothelial cancer is currently based on clinical and pathological factors: tumour grade, tumour stage, number of lesions, tumour size, previous recurrence rate, and presence of concomitant carcinoma in situ. These factors are not specific enough to predict progression and ∼50% of patients diagnosed as high risk in fact do not progress within 3 years. Patient follow-up is both expensive and unpleasant (frequent invasive cystoscopies). Molecular biomarkers, including microRNAs have been studied to provide additional prognostic information for these patients, but to date no molecular biomarker has become the ‘gold standard’ for patient diagnosis and follow-up.
We used Rosetta Genomics’ highly specific microRNA expression profiling platforms to study the prognostic role of microRNAs in bladder cancer. Using microdissection we chose specific tumour microRNAs to study in order to avoid background contamination. Tumour progression was associated with altered levels of microRNAs. In particular, high expression levels of miR-29c* were associated with a good prognosis. The study found that the use of microRNAs for determining progression and invasiveness for patients with urothelial cancer could potentially have a substantial impact on the treatment and follow-up individual patients.


 Objective

To identify microRNAs that could be useful as prognostic markers for non-muscle-invasive (NMI) bladder carcinoma.



Patients and Methods

Formalin-fixed, paraffin-embedded samples of 108 NMI bladder carcinomas, and 29 carcinomas invading bladder muscle were collected, and microRNA expression levels were measured using microarrays.
For 19 samples, microdissection was performed to compare microRNA expression between the tumour and surrounding tissue.
MicroRNAs that were found to be unrelated to the tumour itself were excluded as potential prognostic markers.



Results

Expression profiles identified microRNAs that were differentially expressed in NMI tumours from patients who later progressed to carcinoma invading bladder muscle compared with NMI tumours from patients that did not progress.
The microRNA profile of tumours invading the bladder muscle was more similar to that of NMI tumours from patients who later progressed, than to that of the same-stage NMI tumours from patients who did not later progress.
The expression level of one microRNA, miR-29c*, was significantly under-expressed in tumours that progressed and could be used to stratify patients with T1 disease into risk groups.



Conclusions

MicroRNAs can be useful biomarkers for prognosis in patients with urothelial carcinoma.
In our study, expression levels of several microRNAs, including miR-29c* identified high- and low-risk groups. These biomarkers show promise for the stratification of patients with bladder cancer.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11751.x" xmlns="http://purl.org/rss/1.0/"><title>Pathological response to neoadjuvant chemotherapy for muscle-invasive micropapillary bladder cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11751.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pathological response to neoadjuvant chemotherapy for muscle-invasive micropapillary bladder cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joshua J. Meeks, Jennifer M. Taylor, Kazuhito Matsushita, Harry W. Herr, S. Machele Donat, Bernard H. Bochner, Guido Dalbagni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T05:43:09.702606-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11751.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11751.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11751.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11751-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11751-list-0001" class="bullet">
<li>Micropapillary bladder cancer is a high grade variant with poor prognosis. There is no consensus about patients with micropapillary bladder cancer receiving neoadjuvant chemotherapy, but many suggest that radical cystectomy should not be delayed.</li>
<li>Data from this study suggest that patients with micropapillary bladder cancer have a similar rate of response to neoadjuvant chemotherapy to that of patients with urothelial carcinoma. If these patients have pT0 disease, their survival is significantly improved at 2 years.</li>
</ul></div></div>
<div class="section" id="bju11751-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11751-list-0002" class="bullet">
<li>To describe the pathological outcomes of patients with muscle-invasive micropapillary bladder cancer who have undergone neoadjuvant chemotherapy.</li>
</ul></div></div>
<div class="section" id="bju11751-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11751-list-0003" class="bullet">
<li>A total of 82 patients with muscle-invasive micropapillary bladder cancer were treated between 1997 and 2010.</li>
<li>After excluding those with metastatic disease, micropapillary histology only at radical cystectomy (RC), and chemo-radiation as primary treatment, 44 patients remained. All patients had ≥cT2 disease before chemotherapy/surgery.</li>
<li>The median follow-up after RC was 28 months.</li>
<li>Neoadjuvant chemotherapy was initiated in 29 (66%) patients and all patients underwent RC (93%) or partial cystectomy (7%).</li>
</ul></div></div>
<div class="section" id="bju11751-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11751-list-0004" class="bullet">
<li>Micropapillary histology was diagnosed at first transurethral resection in 37 (84%) patients.</li> <li>Final RC pathology revealed pT0 in 15 (34%) patients and positive lymph nodes in 13 (31%) patients.</li>
<li>Down-staging to pT0 occurred in 13 (45%) of those who received neoadjuvant chemotherapy compared with two (13%) of those who did not (<em>P</em> = 0.049).</li>
<li>Patients with pT0 disease with micropapillary histology had higher overall survival rates (25 vs. 92%) and lower rates of bladder cancer recurrence (21 vs. 79%) at the 24-month follow-up.</li>
</ul></div></div>
<div class="section" id="bju11751-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11751-list-0005" class="bullet">
<li>Almost half of the patients responded completely to neoadjuvant chemotherapy with a pT0 rate of 45%; therefore, patients with the micropapillary variant of urothelial carcinoma should not be excluded from consideration for neoadjuvant chemotherapy.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Micropapillary bladder cancer is a high grade variant with poor prognosis. There is no consensus about patients with micropapillary bladder cancer receiving neoadjuvant chemotherapy, but many suggest that radical cystectomy should not be delayed.
Data from this study suggest that patients with micropapillary bladder cancer have a similar rate of response to neoadjuvant chemotherapy to that of patients with urothelial carcinoma. If these patients have pT0 disease, their survival is significantly improved at 2 years.


 Objective

To describe the pathological outcomes of patients with muscle-invasive micropapillary bladder cancer who have undergone neoadjuvant chemotherapy.



Patients and Methods

A total of 82 patients with muscle-invasive micropapillary bladder cancer were treated between 1997 and 2010.
After excluding those with metastatic disease, micropapillary histology only at radical cystectomy (RC), and chemo-radiation as primary treatment, 44 patients remained. All patients had ≥cT2 disease before chemotherapy/surgery.
The median follow-up after RC was 28 months.
Neoadjuvant chemotherapy was initiated in 29 (66%) patients and all patients underwent RC (93%) or partial cystectomy (7%).



Results

Micropapillary histology was diagnosed at first transurethral resection in 37 (84%) patients. Final RC pathology revealed pT0 in 15 (34%) patients and positive lymph nodes in 13 (31%) patients.
Down-staging to pT0 occurred in 13 (45%) of those who received neoadjuvant chemotherapy compared with two (13%) of those who did not (P = 0.049).
Patients with pT0 disease with micropapillary histology had higher overall survival rates (25 vs. 92%) and lower rates of bladder cancer recurrence (21 vs. 79%) at the 24-month follow-up.



Conclusions

Almost half of the patients responded completely to neoadjuvant chemotherapy with a pT0 rate of 45%; therefore, patients with the micropapillary variant of urothelial carcinoma should not be excluded from consideration for neoadjuvant chemotherapy.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11721.x" xmlns="http://purl.org/rss/1.0/"><title>The true risk of blood transfusion after nephrectomy for renal masses: a population-based study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11721.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The true risk of blood transfusion after nephrectomy for renal masses: a population-based study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gino J. Vricella, Antonio Finelli, Shabbir M.H. Alibhai, Lee E. Ponsky, Robert Abouassaly</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-31T09:45:22.718395-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11721.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11721.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11721.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11721-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11721-list-0001" class="bullet">
<li>There is a paucity of population-based analyses of expected outcomes after renal surgery for kidney cancer. Reported blood transfusion rates after nephrectomy show considerable variability, probably as a result of the referral patterns that influence reports from tertiary academic medical centres.</li>
<li>With emerging data on the inferior outcomes in patients undergoing allogeneic blood transfusion, we aimed to evaluate the patient, surgeon and hospital factors that influence the receipt of a blood transfusion after nephrectomy. A more detailed understanding of these factors may help in preoperative patient counselling and informed consent.</li>
</ul></div></div>
<div class="section" id="bju11721-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11721-list-0002" class="bullet">
<li>To examine blood transfusion rates after nephrectomy for renal masses at the population-level.</li>
</ul></div></div>
<div class="section" id="bju11721-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11721-list-0003" class="bullet">
<li>We performed a population-based, retrospective observational study using a national discharge abstract database.</li>
<li>The study cohort consisted of 10 902 patients who were treated by radical nephrectomy (RN) or partial nephrectomy (PN) for a renal mass between 1 April 2003 and 31 March 2008.</li>
<li>The association between blood transfusion and various explanatory variables was examined using the chi-squared test and multivariable logistic regression.</li>
</ul></div></div>
<div class="section" id="bju11721-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11721-list-0004" class="bullet">
<li>The overall blood transfusion rate was 18.1%.</li>
<li>Transfusions occurred after 28.2%, 12.7%, 9.2% and 8.6% of open RN, open PN, laparoscopic RN and laparoscopic PN, respectively (<em>P</em> &lt; 0.001).</li>
<li>Transfusion rates were found to be strongly associated with age and comorbidity, such that patients aged &lt;50 years with Charlson scores of 0 were transfused 11.2% and 14.5% of the time compared to 28.2% and 40.7% in patients aged ≥80 years with Charlson scores of ≥3, respectively (<em>P</em> &lt; 0.001).</li>
<li>On multivariable logistic regression, age (<em>P</em> &lt; 0.001), Charlson score (<em>P</em> &lt; 0.001), procedure type (<em>P</em> &lt; 0.001), surgeon (<em>P</em> &lt; 0.001) and hospital volume quartile (<em>P</em> &lt; 0.001) were all found to be associated with the rate of blood transfusions, whereas year of surgery, sex and income quintile were not.</li>
</ul></div></div>
<div class="section" id="bju11721-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11721-list-0005" class="bullet">
<li>The transfusion rate after nephrectomy in general clinical practice is higher than that reported in the urological literature.</li>
<li>Patient and provider factors appear to contribute to the considerable variability that exists in the observed transfusion rate.</li>
<li>A more detailed understanding of these factors may help with respect to preoperative patient counselling and informed consent.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

There is a paucity of population-based analyses of expected outcomes after renal surgery for kidney cancer. Reported blood transfusion rates after nephrectomy show considerable variability, probably as a result of the referral patterns that influence reports from tertiary academic medical centres.
With emerging data on the inferior outcomes in patients undergoing allogeneic blood transfusion, we aimed to evaluate the patient, surgeon and hospital factors that influence the receipt of a blood transfusion after nephrectomy. A more detailed understanding of these factors may help in preoperative patient counselling and informed consent.


 Objective

To examine blood transfusion rates after nephrectomy for renal masses at the population-level.



Patients and Methods

We performed a population-based, retrospective observational study using a national discharge abstract database.
The study cohort consisted of 10 902 patients who were treated by radical nephrectomy (RN) or partial nephrectomy (PN) for a renal mass between 1 April 2003 and 31 March 2008.
The association between blood transfusion and various explanatory variables was examined using the chi-squared test and multivariable logistic regression.



Results

The overall blood transfusion rate was 18.1%.
Transfusions occurred after 28.2%, 12.7%, 9.2% and 8.6% of open RN, open PN, laparoscopic RN and laparoscopic PN, respectively (P &lt; 0.001).
Transfusion rates were found to be strongly associated with age and comorbidity, such that patients aged &lt;50 years with Charlson scores of 0 were transfused 11.2% and 14.5% of the time compared to 28.2% and 40.7% in patients aged ≥80 years with Charlson scores of ≥3, respectively (P &lt; 0.001).
On multivariable logistic regression, age (P &lt; 0.001), Charlson score (P &lt; 0.001), procedure type (P &lt; 0.001), surgeon (P &lt; 0.001) and hospital volume quartile (P &lt; 0.001) were all found to be associated with the rate of blood transfusions, whereas year of surgery, sex and income quintile were not.



Conclusions

The transfusion rate after nephrectomy in general clinical practice is higher than that reported in the urological literature.
Patient and provider factors appear to contribute to the considerable variability that exists in the observed transfusion rate.
A more detailed understanding of these factors may help with respect to preoperative patient counselling and informed consent.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11738.x" xmlns="http://purl.org/rss/1.0/"><title>Extracorporeal shockwave lithotripsy to distal ureteric stones: the transgluteal approach significantly increases stone-free rates</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11738.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Extracorporeal shockwave lithotripsy to distal ureteric stones: the transgluteal approach significantly increases stone-free rates</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Simon Phipps, Carolann Stephenson, David Tolley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T08:03:05.131559-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11738.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11738.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11738.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Upper Urinary Tract</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11738-sec-0006" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11738-list-0001" class="bullet">
<li>Shockwave lithotripsy (SWL) can be used to treat stones at any position within the ureter, as long as the stone is radio-opaque and there is a path for the shockwave to reach the stone. However the results of SWL to distal ureteric calculi, with the patient in a prone position, were inferior to those of treating stones within the upper ureter.</li>
<li>The transguteal approach allows the lithotripsy shockwave to reach the lower ureter via the greater selatle foramen. This study shows that this approach for SWL to distal ureteric calculi is more effective than the prone approach.</li>
</ul></div></div>
<div class="section" id="bju11738-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11738-list-0002" class="bullet">
<li>To compare the outcomes of extracorporeal shockwave lithotripsy (ESWL) for distal ureteric stones treated using the prone and transgluteal (supine) approaches in a tertiary referral stone unit using a fourth generation lithotriptor.</li>
</ul></div></div>
<div class="section" id="bju11738-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11738-list-0003" class="bullet">
<li>We selected consecutive patients undergoing ESWL to distal ureteric stones over 1 year, during which we changed our treatment protocol from a prone to transgluteal (supine) approach.</li>
<li>Patients were treated using the Sonolith Vision Lithotriptor (Technomed Medical Systems, Vaulx-en-Velin, France).</li>
<li>Outcome was assessed using plain abdominal film of kidney, ureter and bladder (KUB) X-ray taken at 2 weeks then monthly as required.</li>
<li>Treatment success was defined as complete clearance of stone fragments and treatment failure was defined as persistence of stone fragments beyond 3 months or the need for ureteroscopy.</li>
</ul></div></div>
<div class="section" id="bju11738-sec-0009" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11738-list-0004" class="bullet">
<li>A total of 38 patients were treated in the prone position and 72 patients using a transgluteal approach.</li>
<li>Patient and stone characteristics were identical in both groups. The mean (range) stone size was 7.8 (4–16) mm.</li>
<li>The proportions of patients who were stone-free after one treatment session within the prone and transgluteal treatment groups were 40 and 78%, respectively (&lt;0.001).</li>
<li>The overall success rates for treatment within the prone and transgluteal groups were 63 and 92%, respectively (&lt;0.001).</li>
</ul></div></div>
<div class="section" id="bju11738-sec-0010" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11738-list-0005" class="bullet">
<li>Transgluteal ESWL to stones within the distal ureter leads to significantly higher stone-free rates than treatment using the prone approach.</li>
<li>The majority of patients are rendered stone-free after one session of treatment and the overall success rates are similar to those of ureteroscopic management.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Shockwave lithotripsy (SWL) can be used to treat stones at any position within the ureter, as long as the stone is radio-opaque and there is a path for the shockwave to reach the stone. However the results of SWL to distal ureteric calculi, with the patient in a prone position, were inferior to those of treating stones within the upper ureter.
The transguteal approach allows the lithotripsy shockwave to reach the lower ureter via the greater selatle foramen. This study shows that this approach for SWL to distal ureteric calculi is more effective than the prone approach.


 Objective

To compare the outcomes of extracorporeal shockwave lithotripsy (ESWL) for distal ureteric stones treated using the prone and transgluteal (supine) approaches in a tertiary referral stone unit using a fourth generation lithotriptor.



Patients and Methods

We selected consecutive patients undergoing ESWL to distal ureteric stones over 1 year, during which we changed our treatment protocol from a prone to transgluteal (supine) approach.
Patients were treated using the Sonolith Vision Lithotriptor (Technomed Medical Systems, Vaulx-en-Velin, France).
Outcome was assessed using plain abdominal film of kidney, ureter and bladder (KUB) X-ray taken at 2 weeks then monthly as required.
Treatment success was defined as complete clearance of stone fragments and treatment failure was defined as persistence of stone fragments beyond 3 months or the need for ureteroscopy.



Results

A total of 38 patients were treated in the prone position and 72 patients using a transgluteal approach.
Patient and stone characteristics were identical in both groups. The mean (range) stone size was 7.8 (4–16) mm.
The proportions of patients who were stone-free after one treatment session within the prone and transgluteal treatment groups were 40 and 78%, respectively (&lt;0.001).
The overall success rates for treatment within the prone and transgluteal groups were 63 and 92%, respectively (&lt;0.001).



Conclusions

Transgluteal ESWL to stones within the distal ureter leads to significantly higher stone-free rates than treatment using the prone approach.
The majority of patients are rendered stone-free after one session of treatment and the overall success rates are similar to those of ureteroscopic management.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11759.x" xmlns="http://purl.org/rss/1.0/"><title>Serum receptor activator of nuclear factor κB ligand (RANKL) levels predict biochemical recurrence in patients undergoing radical prostatectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11759.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Serum receptor activator of nuclear factor κB ligand (RANKL) levels predict biochemical recurrence in patients undergoing radical prostatectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tilman Todenhöfer, Jörg Hennenlotter, Philipp Leidenberger, Alexander Wald, Andrea Hohneder, Ursula Kühs, Johannes Mischinger, Stefan Aufderklamm, Georgios Gakis, Gunnar Blumenstock, Arnulf Stenzl, Christian Schwentner</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:42:54.71664-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11759.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11759.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11759.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11759-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11759-list-0001" class="bullet">
<li>There is increasing evidence that the receptor activator of nuclear factor κB ligand (RANKL) pathway not only contributes to the development of bone metastases, but also influences tumour biology in earlier stages of cancer.</li>
<li>The study shows that preoperative serum levels of RANKL and its inhibitor osteoprotegerin (OPG) have a prognostic impact in patients undergoing radical prostatectomy for clinically localized prostate cancer. Both high levels of RANKL and a higher RANKL/OPG ratio are independent predictors of early biochemical recurrence in these patients.</li>
</ul></div></div>
<div class="section" id="bju11759-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11759-list-0002" class="bullet">
<li>To assess the prognostic impact of proteins of the receptor activator of nuclear factor κB (RANKL) pathway in serum samples from patients undergoing radical prostatectomy.</li>
</ul></div></div>
<div class="section" id="bju11759-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11759-list-0003" class="bullet">
<li>We retrospectively determined soluble RANKL (sRANKL) and osteoprotegerin (OPG) by ELISA in serum samples of 178 patients undergoing radical prostatectomy between 2004 and 2006.</li>
<li>Clinical and patient follow-up data were analysed using the Wilcoxon–Mann–Whitney test, the Kaplan–Maier method, and single variable or multifactorial Cox proportional hazards analysis.</li>
</ul></div></div>
<div class="section" id="bju11759-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11759-list-0004" class="bullet">
<li>Higher serum sRANKL levels (<em>P</em> = 0.01), lower serum OPG levels (<em>P</em> = 0.01) and a higher sRANKL/OPG ratio (<em>P</em> = 0.004) were significant risk factors for biochemical recurrence (BCR).</li>
<li>In multifactorial analysis, adjusted for the common risk factors for BCR, sRANKL and sRANKL/OPG ratio were confirmed as independent prognostic factors.</li>
<li>Neither sRANKL nor OPG showed a clear association with histopathological factors such as pT stage, pN Gleason score or resection margin status, nor were they associated with prostate-specific antigen level.</li>
</ul></div></div>
<div class="section" id="bju11759-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11759-list-0005" class="bullet">
<li>Greater activity of the RANKL pathway in the serum of patients with prostate cancer undergoing radical prostatectomy is a risk factor for BCR.</li>
<li>The RANKL pathway seems to contribute to the biological behaviour of prostate cancer even at the organ-confined stage of the disease.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

There is increasing evidence that the receptor activator of nuclear factor κB ligand (RANKL) pathway not only contributes to the development of bone metastases, but also influences tumour biology in earlier stages of cancer.
The study shows that preoperative serum levels of RANKL and its inhibitor osteoprotegerin (OPG) have a prognostic impact in patients undergoing radical prostatectomy for clinically localized prostate cancer. Both high levels of RANKL and a higher RANKL/OPG ratio are independent predictors of early biochemical recurrence in these patients.


 Objective

To assess the prognostic impact of proteins of the receptor activator of nuclear factor κB (RANKL) pathway in serum samples from patients undergoing radical prostatectomy.



Patients and Methods

We retrospectively determined soluble RANKL (sRANKL) and osteoprotegerin (OPG) by ELISA in serum samples of 178 patients undergoing radical prostatectomy between 2004 and 2006.
Clinical and patient follow-up data were analysed using the Wilcoxon–Mann–Whitney test, the Kaplan–Maier method, and single variable or multifactorial Cox proportional hazards analysis.



Results

Higher serum sRANKL levels (P = 0.01), lower serum OPG levels (P = 0.01) and a higher sRANKL/OPG ratio (P = 0.004) were significant risk factors for biochemical recurrence (BCR).
In multifactorial analysis, adjusted for the common risk factors for BCR, sRANKL and sRANKL/OPG ratio were confirmed as independent prognostic factors.
Neither sRANKL nor OPG showed a clear association with histopathological factors such as pT stage, pN Gleason score or resection margin status, nor were they associated with prostate-specific antigen level.



Conclusions

Greater activity of the RANKL pathway in the serum of patients with prostate cancer undergoing radical prostatectomy is a risk factor for BCR.
The RANKL pathway seems to contribute to the biological behaviour of prostate cancer even at the organ-confined stage of the disease.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11753.x" xmlns="http://purl.org/rss/1.0/"><title>Comparison of musculoskeletal anatomic relationships, determined by magnetic resonance imaging, in postpubertal female patients with and without classic bladder exstrophy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11753.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of musculoskeletal anatomic relationships, determined by magnetic resonance imaging, in postpubertal female patients with and without classic bladder exstrophy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ifeanyi Anusionwu, Aylin Tekes, Andrew A. Stec, John P. Gearhart, E. James Wright</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:42:47.578948-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11753.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11753.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11753.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Paediatrics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11753-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11753-list-0001" class="bullet">
<li>Several studies in the paediatric literature have characterized the pelvic musculoskeletal anatomy of infants and children with bladder exstrophy using MRI and three-dimensional CT. The pelvic floor anatomy of female patients with bladder exstrophy who have undergone somatic growth and puberty is less well described.</li>
<li>This study uses MRI to characterize comprehensively the pelvic anatomy of postpubertal females with classic bladder exstrophy by measuring 15 pelvic floor variables previously described in younger children with bladder exstrophy.</li>
</ul></div></div>
<div class="section" id="bju11753-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11753-list-0002" class="bullet">
<li>To characterize pelvic musculoskeletal anatomy in postpubertal females with classic bladder exstrophy, and to compare this with females without bladder exstrophy.</li>
</ul></div></div>
<div class="section" id="bju11753-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11753-list-0003" class="bullet">
<li>The authors reviewed the medical records of all females in our institutional review board-approved bladder exstrophy database of 1078 patients and identified those with classic bladder exstrophy who underwent pelvic magnetic resonance imaging (MRI) after the age of 12 years.</li>
<li>Indications for MRI included haematuria, adnexal lesion, perineal fistula, non-pelvic cancer staging, abdominal wall hernia and vaginal stenosis.</li>
<li>Age- and race-matched female patients without exstrophy who underwent MRI evaluation for similar indications were included for comparison.</li>
<li>The MRI protocol included axial, sagittal and coronal T1- and/or T2-weighted imaging.</li>
</ul></div></div>
<div class="section" id="bju11753-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11753-list-0004" class="bullet">
<li>The study included 30 patients with a median (range) age of 22.5 (12–55) years at time of MRI. Ten patients had bladder exstrophy while 20 control patients did not.</li>
<li>A smaller percentage of levator ani was located in the anterior compartment of the pelvis in patients with bladder exstrophy compared with controls.</li>
<li>The iliac wing angle, puborectalis angle, ileococcygeous angle, levator ani width, symphyseal diastasis, erectile body diastasis, posterior bladder neck distance and posterior anal distance was greater in patients with bladder exstrophy than in those without.</li>
<li>The ischial angle and obturator internus angle were narrower in patients with bladder exstrophy than in those without, and there was no significant difference between levator ani surface area, sacral anal angle, sacral bladder neck angle and bladder neck erectile body distance between the two patient groups.</li>
</ul></div></div>
<div class="section" id="bju11753-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11753-list-0005" class="bullet">
<li>In postpubertal females with bladder exstrophy, significant deviations from normal pelvimetry exist, including posterior location of the majority of the levator ani muscle, a wider ileococcygeous angle and a wider symphyseal diastasis.</li>
<li>These differences are similar to those described in previous comparisons of younger children with bladder exstrophy and control children.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Several studies in the paediatric literature have characterized the pelvic musculoskeletal anatomy of infants and children with bladder exstrophy using MRI and three-dimensional CT. The pelvic floor anatomy of female patients with bladder exstrophy who have undergone somatic growth and puberty is less well described.
This study uses MRI to characterize comprehensively the pelvic anatomy of postpubertal females with classic bladder exstrophy by measuring 15 pelvic floor variables previously described in younger children with bladder exstrophy.


 Objective

To characterize pelvic musculoskeletal anatomy in postpubertal females with classic bladder exstrophy, and to compare this with females without bladder exstrophy.



Patients and Methods

The authors reviewed the medical records of all females in our institutional review board-approved bladder exstrophy database of 1078 patients and identified those with classic bladder exstrophy who underwent pelvic magnetic resonance imaging (MRI) after the age of 12 years.
Indications for MRI included haematuria, adnexal lesion, perineal fistula, non-pelvic cancer staging, abdominal wall hernia and vaginal stenosis.
Age- and race-matched female patients without exstrophy who underwent MRI evaluation for similar indications were included for comparison.
The MRI protocol included axial, sagittal and coronal T1- and/or T2-weighted imaging.



Results

The study included 30 patients with a median (range) age of 22.5 (12–55) years at time of MRI. Ten patients had bladder exstrophy while 20 control patients did not.
A smaller percentage of levator ani was located in the anterior compartment of the pelvis in patients with bladder exstrophy compared with controls.
The iliac wing angle, puborectalis angle, ileococcygeous angle, levator ani width, symphyseal diastasis, erectile body diastasis, posterior bladder neck distance and posterior anal distance was greater in patients with bladder exstrophy than in those without.
The ischial angle and obturator internus angle were narrower in patients with bladder exstrophy than in those without, and there was no significant difference between levator ani surface area, sacral anal angle, sacral bladder neck angle and bladder neck erectile body distance between the two patient groups.



Conclusions

In postpubertal females with bladder exstrophy, significant deviations from normal pelvimetry exist, including posterior location of the majority of the levator ani muscle, a wider ileococcygeous angle and a wider symphyseal diastasis.
These differences are similar to those described in previous comparisons of younger children with bladder exstrophy and control children.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11719.x" xmlns="http://purl.org/rss/1.0/"><title>Congenital completely buried penis in boys: anatomical basis and surgical technique</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11719.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Congenital completely buried penis in boys: anatomical basis and surgical technique</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xing Liu, Da-wei He, Yi Hua, De-ying Zhang, Guang-hui Wei</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:41:31.845981-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11719.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11719.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11719.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Paediatrics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11719-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11719-list-0001" class="bullet">
<li>Surgical correction of the congenital completely buried penis (CCBP) is a difficult challenge and there is no unanimous consensus about the surgical ‘gold standard’ and patient eligibility for surgery.</li>
<li>In the present study, dysgenetic fundiform ligaments were found to be attached to the distal or middle shaft of the penis. This abnormality can be successfully corrected by releasing the fundiform ligament and mobilising the scrotal skin to cover the length of the penile shaft. The study shows that the paucity and traction of the penile skin and an abnormal fundiform ligament are important anatomical defects in CCBP. Dorsal curve and severe shortage of penile skin in erectile conditions are the main indications for surgical correction.</li>
</ul></div></div>
<div class="section" id="bju11719-sec-0009" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11719-list-0002" class="bullet">
<li>To present our experience of anatomical findings for congenital completely buried penis (CCBP), which has no unanimous consensus regarding the ‘gold standard’ for surgical correction and patient eligibility, by providing our surgical technique and illustrations.</li>
</ul></div></div>
<div class="section" id="bju11719-sec-0010" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11719-list-0003" class="bullet">
<li>Between February 2006 and February 2011, 22 children with a median (range) age of 4.2 (2.5–5.8) years, with CCBP underwent surgical correction by one surgeon.</li>
<li>Toilet training and photographs of morning erections by parents were advised before surgery.</li>
<li>The abnormal anatomical structure of buried penis during the operation was observed. The technique consisted of the release of the fundiform ligament, fixation of the subcutaneous penile skin at the base of the degloved penis, penoscrotal Z-plasty and mobilisation of the penile and scrotal skin to cover the penile shaft.</li>
</ul></div></div>
<div class="section" id="bju11719-sec-0011" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11719-list-0004" class="bullet">
<li>In reflex erectile conditions, CCBP presents varying degrees of dorsal curve and shortage of penile skin.</li>
<li>Dysgenetic fundiform ligaments were found to be attached to the distal or middle shaft of the penis in all patients.</li>
<li>All wounds healed well and the cosmetic outcome was good at 6-month follow-up after the repair.</li>
</ul></div></div>
<div class="section" id="bju11719-sec-0012" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11719-list-0005" class="bullet">
<li>The appearance of the dorsal curve in CCBP mainly results from the traction of penile dorsal skin and the abnormal attachment of the fundiform ligament to the shaft. This abnormality can be successfully corrected by releasing the abnormal fundiform ligament and mobilising scrotal skin to cover the length of the penile shaft.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Surgical correction of the congenital completely buried penis (CCBP) is a difficult challenge and there is no unanimous consensus about the surgical ‘gold standard’ and patient eligibility for surgery.
In the present study, dysgenetic fundiform ligaments were found to be attached to the distal or middle shaft of the penis. This abnormality can be successfully corrected by releasing the fundiform ligament and mobilising the scrotal skin to cover the length of the penile shaft. The study shows that the paucity and traction of the penile skin and an abnormal fundiform ligament are important anatomical defects in CCBP. Dorsal curve and severe shortage of penile skin in erectile conditions are the main indications for surgical correction.


 Objective

To present our experience of anatomical findings for congenital completely buried penis (CCBP), which has no unanimous consensus regarding the ‘gold standard’ for surgical correction and patient eligibility, by providing our surgical technique and illustrations.



Patients and Methods

Between February 2006 and February 2011, 22 children with a median (range) age of 4.2 (2.5–5.8) years, with CCBP underwent surgical correction by one surgeon.
Toilet training and photographs of morning erections by parents were advised before surgery.
The abnormal anatomical structure of buried penis during the operation was observed. The technique consisted of the release of the fundiform ligament, fixation of the subcutaneous penile skin at the base of the degloved penis, penoscrotal Z-plasty and mobilisation of the penile and scrotal skin to cover the penile shaft.



Results

In reflex erectile conditions, CCBP presents varying degrees of dorsal curve and shortage of penile skin.
Dysgenetic fundiform ligaments were found to be attached to the distal or middle shaft of the penis in all patients.
All wounds healed well and the cosmetic outcome was good at 6-month follow-up after the repair.



Conclusion

The appearance of the dorsal curve in CCBP mainly results from the traction of penile dorsal skin and the abnormal attachment of the fundiform ligament to the shaft. This abnormality can be successfully corrected by releasing the abnormal fundiform ligament and mobilising scrotal skin to cover the length of the penile shaft.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11697.x" xmlns="http://purl.org/rss/1.0/"><title>Haematuria after prostate brachytherapy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11697.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Haematuria after prostate brachytherapy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael S. Leapman, Simon J. Hall, Nelson N. Stone, Richard G. Stock</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:40:55.208513-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11697.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11697.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11697.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11697-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11697-list-0001" class="bullet">
<li>Previous descriptions of haematuria after brachytherapy are limited.</li>
<li>This study characterizes the long-term incidence and associated clinical risk factors of haematuria after prostate brachytherapy.</li>
</ul></div></div>
<div class="section" id="bju11697-sec-1002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11697-list-0002" class="bullet">
<li>To characterize the incidence and clinical history of gross haematuria after prostate brachytherapy.</li>
<li>To identify treatment risk factors for the development of gross haematuria in this setting.</li>
</ul></div></div>
<div class="section" id="bju11697-sec-1003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11697-list-0003" class="bullet">
<li>We reviewed haematuria outcomes collected prospectively in 2454 patients treated with transperineal prostate brachytherapy over a 20-year period at a single institution.</li>
<li>Patients were followed for a median of 5.9 years.</li>
<li>The association of haematuria with age, pretreatment PSA, ethnicity, clinical tumour stage, Gleason score, prostate volume, isotope (iodine 125 or palladium 103), biologically effective dose (BED), external beam radiation, androgen deprivation, development of urinary retention and occurrence of biochemical failure was investigated.</li>
</ul></div></div> <div class="section" id="bju11697-sec-1004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11697-list-0004" class="bullet">
<li>A total of 218 men (8.9%) reported gross haematuria at a median time of 772.2 days after implantation.</li>
<li>Haematuria was associated with prostate volume &gt;40 cm<sup>3</sup> (<em>P</em> &lt; 0.01), use of external beam radiation (<em>P</em> &lt; 0.01), Gleason score &gt;7 (<em>P</em> = 0.037), Asian ethnicity (<em>P</em> &lt; 0.001), BED &gt;200 Gy (<em>P</em> = 0.01), and freedom from biochemical failure (<em>P</em> = 0.004).</li>
<li>On multivariate analysis, prostate volume &gt;40 cm<sup>3</sup> (<em>P</em> = 0.002), external beam radiation, (<em>P</em> = 0.001), and freedom from biochemical failure (<em>P</em> = 0.035) were predictors of haematuria.</li>
</ul></div></div>
<div class="section" id="bju11697-sec-1005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11697-list-0005" class="bullet">
<li>Late gross haematuria was observed in a small proportion of men after brachytherapy and may occur with considerable latency.</li>
<li>Larger prostate glands, freedom from biochemical failure and external beam radiation are risk factors.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Previous descriptions of haematuria after brachytherapy are limited.
This study characterizes the long-term incidence and associated clinical risk factors of haematuria after prostate brachytherapy.


 Objective

To characterize the incidence and clinical history of gross haematuria after prostate brachytherapy.
To identify treatment risk factors for the development of gross haematuria in this setting.



Patients and Methods

We reviewed haematuria outcomes collected prospectively in 2454 patients treated with transperineal prostate brachytherapy over a 20-year period at a single institution.
Patients were followed for a median of 5.9 years.
The association of haematuria with age, pretreatment PSA, ethnicity, clinical tumour stage, Gleason score, prostate volume, isotope (iodine 125 or palladium 103), biologically effective dose (BED), external beam radiation, androgen deprivation, development of urinary retention and occurrence of biochemical failure was investigated.

 
Results

A total of 218 men (8.9%) reported gross haematuria at a median time of 772.2 days after implantation.
Haematuria was associated with prostate volume &gt;40 cm3 (P &lt; 0.01), use of external beam radiation (P &lt; 0.01), Gleason score &gt;7 (P = 0.037), Asian ethnicity (P &lt; 0.001), BED &gt;200 Gy (P = 0.01), and freedom from biochemical failure (P = 0.004).
On multivariate analysis, prostate volume &gt;40 cm3 (P = 0.002), external beam radiation, (P = 0.001), and freedom from biochemical failure (P = 0.035) were predictors of haematuria.



Conclusions

Late gross haematuria was observed in a small proportion of men after brachytherapy and may occur with considerable latency.
Larger prostate glands, freedom from biochemical failure and external beam radiation are risk factors.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11765.x" xmlns="http://purl.org/rss/1.0/"><title>Extended vs standard lymph node dissection in robot-assisted radical prostatectomy for intermediate- or high-risk prostate cancer: a propensity-score-matching analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11765.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Extended vs standard lymph node dissection in robot-assisted radical prostatectomy for intermediate- or high-risk prostate cancer: a propensity-score-matching analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kwang Hyun Kim, Sey Kiat Lim, Ha Yan Kim, Tae-Young Shin, Joo Yong Lee, Young Deuk Choi, Byung Ha Chung, Sung Joon Hong, Koon Ho Rha</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:36:05.460908-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11765.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11765.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11765.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11765-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11765-list-0001" class="bullet">
<li>Although lymph node dissection (LND) is known as the most accurate method of nodal staging, the therapeutic role of LND remains undetermined. This is mainly because of the lack of randomized prospective studies and the fact that retrospective analyses often result in bias and misinterpretation.</li>
<li>To overcome the limitation of retrospective analysis, we matched preoperative variables using propensity scores and compared the outcomes between patients treated with robot-assisted eLND and sLND. In the matched cohort, robot-asssited eLND achieved an increased detection rate of lymph node metastases; however, the therapeutic benefit was not statistically significant between the two groups on short-term follow-up.</li>
</ul></div></div>
<div class="section" id="bju11765-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11765-list-0002" class="bullet">
<li>To compare the pathological and biochemical outcomes between extended lymph node dissection (eLND) and standard lymph node dissection (sLND) in patients undergoing robot-assisted radical prostatectomy for intermediate- or high-risk prostate cancer.</li>
</ul></div></div>
<div class="section" id="bju11765-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11765-list-0003" class="bullet">
<li>A total of 905 patients underwent robot-assisted radical prostatectomy and lymph node dissection (LND) by a single surgeon between June 2006 and January 2011. Of these, 170 patients who underwent robot-assisted eLND and 294 patients who underwent robot-assisted sLND for intermediate- or high-risk prostate cancer were included in the study.</li>
<li>Propensity-score matching was performed using the preoperative variables which included age, body mass index, prostate-specific antigen, clinical stage, biopsy Gleason score 1 and 2, total number of biopsied cores, number of positive cores and prostate volumes.</li>
<li>Pathological and biochemical outcomes were assessed according to the extent of LND.</li>
</ul></div></div>
<div class="section" id="bju11765-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11765-list-0004" class="bullet">
<li>The median (range) follow-up period was 36 (12–77) months and the median number of lymph nodes removed was 21 and 12 in the eLND and sLND groups, respectively.</li>
<li>Propensity-score matching resulted in 141 patients in each group. Although patients who underwent eLND had a higher clinical stage, biopsy Gleason score and number of positive cores than those treated with sLND in the entire cohort, there were no preoperative between-group differences in the matched cohort.</li>
<li>In the matched cohort, lymph node metastases were detected at a significantly higher rate in the eLND than in the sLND group (12.1 vs. 5.0%, <em>P =</em> 0.033).</li>
<li>In the matched cohort, the 3-year biochemical recurrence-free survival rates were 77.8 and 73.5% in the eLND and sLND groups, respectively, which was not significant (hazard ratio 0.85, <em>P =</em> 0.497).</li>
</ul></div></div>
<div class="section" id="bju11765-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11765-list-0005" class="bullet">
<li>Robot-assisted eLND achieved an increased lymph node yield and higher detection rate of lymph node metastases; however, robotic eLND did not alter biochemical outcomes in a short-term follow-up.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Although lymph node dissection (LND) is known as the most accurate method of nodal staging, the therapeutic role of LND remains undetermined. This is mainly because of the lack of randomized prospective studies and the fact that retrospective analyses often result in bias and misinterpretation.
To overcome the limitation of retrospective analysis, we matched preoperative variables using propensity scores and compared the outcomes between patients treated with robot-assisted eLND and sLND. In the matched cohort, robot-asssited eLND achieved an increased detection rate of lymph node metastases; however, the therapeutic benefit was not statistically significant between the two groups on short-term follow-up.


 Objective

To compare the pathological and biochemical outcomes between extended lymph node dissection (eLND) and standard lymph node dissection (sLND) in patients undergoing robot-assisted radical prostatectomy for intermediate- or high-risk prostate cancer.



Patients and Methods

A total of 905 patients underwent robot-assisted radical prostatectomy and lymph node dissection (LND) by a single surgeon between June 2006 and January 2011. Of these, 170 patients who underwent robot-assisted eLND and 294 patients who underwent robot-assisted sLND for intermediate- or high-risk prostate cancer were included in the study.
Propensity-score matching was performed using the preoperative variables which included age, body mass index, prostate-specific antigen, clinical stage, biopsy Gleason score 1 and 2, total number of biopsied cores, number of positive cores and prostate volumes.
Pathological and biochemical outcomes were assessed according to the extent of LND.



Results

The median (range) follow-up period was 36 (12–77) months and the median number of lymph nodes removed was 21 and 12 in the eLND and sLND groups, respectively.
Propensity-score matching resulted in 141 patients in each group. Although patients who underwent eLND had a higher clinical stage, biopsy Gleason score and number of positive cores than those treated with sLND in the entire cohort, there were no preoperative between-group differences in the matched cohort.
In the matched cohort, lymph node metastases were detected at a significantly higher rate in the eLND than in the sLND group (12.1 vs. 5.0%, P = 0.033).
In the matched cohort, the 3-year biochemical recurrence-free survival rates were 77.8 and 73.5% in the eLND and sLND groups, respectively, which was not significant (hazard ratio 0.85, P = 0.497).



Conclusion

Robot-assisted eLND achieved an increased lymph node yield and higher detection rate of lymph node metastases; however, robotic eLND did not alter biochemical outcomes in a short-term follow-up.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11762.x" xmlns="http://purl.org/rss/1.0/"><title>Bladder preservation in the treatment of muscle-invasive bladder cancer (MIBC): a review of the literature and a practical approach to therapy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11762.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bladder preservation in the treatment of muscle-invasive bladder cancer (MIBC): a review of the literature and a practical approach to therapy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zachary L. Smith, John P. Christodouleas, Stephen M. Keefe, S. Bruce Malkowicz, Thomas J. Guzzo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:36:01.151402-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11762.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11762.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11762.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11762-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><p>Bladder preservation therapies for muscle-invasive bladder cancer (MIBC) have been developed to address the needs of two cohorts: patients with severe medical co-morbidities for whom radical cystectomy is too high risk and patients with limited disease who wish to avoid aggressive surgery. There are multiple bladder preservation options, although the trimodal approach of maximal transurethral resection with chemoradiotherapy is the most strongly supported. While outcomes are worse for patients unfit for surgery than those otherwise fit for surgery, bladder preservation approaches still offer curative potential.</p></div><div class="para"><p>We present a comprehensive review of the literature and outline a practical approach to bladder preservation therapy for MIBC. This review aims to help urologists easily navigate through the decision tree of therapeutic options.</p></div></div>
<div class="section" id="bju11762-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><ul id="bju11762-list-0001" class="bullet">
<li>Radical cystectomy (RC) is associated with considerable morbidity. Aside from the perioperative period, RC with urinary diversion poses great potential for long-term complications and morbidity.</li>
<li>Bladder preservation therapies for muscle-invasive bladder cancer (MIBC) have been developed to address the needs of two cohorts: patients with severe medical co-morbidities for whom a radical surgery is too high risk and patients with limited disease who wish to avoid radical surgery.</li>
<li>The goal of achieving complete response to treatment while maintaining bladder form and function has led to the development of multimodal approaches to this disease.</li>
<li>There are multiple bladder preservation options, although the trimodal approach of maximal transurethral resection with chemoradiotherapy is the most strongly supported.</li>
<li>In medically operable patients (‘fit’ for surgery), there is abundant evidence to support trimodal therapy as an acceptable treatment option for highly selected patients with MIBC with favourable pathological parameters.</li>
<li>While outcomes are worse for medically inoperable patients (‘unfit’ for surgery), bladder preservation approaches still offer curative potential. However, prospective trials comparing the above regimens to RC are still needed to better define their role in the treatment of MIBC.</li>
<li>We present a comprehensive review of the literature and outline a practical approach to bladder preservation therapy for MIBC.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?
Bladder preservation therapies for muscle-invasive bladder cancer (MIBC) have been developed to address the needs of two cohorts: patients with severe medical co-morbidities for whom radical cystectomy is too high risk and patients with limited disease who wish to avoid aggressive surgery. There are multiple bladder preservation options, although the trimodal approach of maximal transurethral resection with chemoradiotherapy is the most strongly supported. While outcomes are worse for patients unfit for surgery than those otherwise fit for surgery, bladder preservation approaches still offer curative potential.
We present a comprehensive review of the literature and outline a practical approach to bladder preservation therapy for MIBC. This review aims to help urologists easily navigate through the decision tree of therapeutic options.

 
Radical cystectomy (RC) is associated with considerable morbidity. Aside from the perioperative period, RC with urinary diversion poses great potential for long-term complications and morbidity.
Bladder preservation therapies for muscle-invasive bladder cancer (MIBC) have been developed to address the needs of two cohorts: patients with severe medical co-morbidities for whom a radical surgery is too high risk and patients with limited disease who wish to avoid radical surgery.
The goal of achieving complete response to treatment while maintaining bladder form and function has led to the development of multimodal approaches to this disease.
There are multiple bladder preservation options, although the trimodal approach of maximal transurethral resection with chemoradiotherapy is the most strongly supported.
In medically operable patients (‘fit’ for surgery), there is abundant evidence to support trimodal therapy as an acceptable treatment option for highly selected patients with MIBC with favourable pathological parameters.
While outcomes are worse for medically inoperable patients (‘unfit’ for surgery), bladder preservation approaches still offer curative potential. However, prospective trials comparing the above regimens to RC are still needed to better define their role in the treatment of MIBC.
We present a comprehensive review of the literature and outline a practical approach to bladder preservation therapy for MIBC.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11714.x" xmlns="http://purl.org/rss/1.0/"><title>Factors influencing intracytoplasmic sperm injection (ICSI) outcome in men with azoospermia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11714.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Factors influencing intracytoplasmic sperm injection (ICSI) outcome in men with azoospermia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amr Abdel Raheem, Nagla Rushwan, Giulio Garaffa, Evangelos Zacharakis, Alpesh Doshi, Carleen Heath, Paul Serhal, Joyce C. Harper, Nim A. Christopher, David Ralph</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:35:56.497102-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11714.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11714.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11714.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11714-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11714-list-0001" class="bullet">
<li>The management of patients with non-obstructive azoospermia (NOA) and some cases of obstructive azoospermia involves testicular sperm extraction (TESE or micro-dissection TESE) combined with intracytoplasmic sperm injection (ICSI). Several studies have investigated the effect of the male age, the cause of azoospermia, testicular histopathology, the type of sperm used, and the use of pentoxyphilline, on the ICSI cycle outcome in men with azoospermia.</li>
<li>The present study showed that none of these factors influenced the ICSI outcome in men with azoospermia, thus once sperm is found in an azoospermic male, no other male factor seems to influence the ICSI outcome. To our knowledge this is the first study to comment on the outcome of ICSI in men with NOA based on testicular histopathology.</li>
</ul></div></div>
<div class="section" id="bju11714-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11714-list-0002" class="bullet">
<li>To access the effect of: male age, the cause of azoospermia (obstructive azoospermia vs non-obstructive azoospermia [NOA]), testicular histopathology, the type of sperm used (fresh vs frozen-thawed), and the use of pentoxyphilline on the intracytoplasmic sperm injection (ICSI) cycle outcome in men with azoospermia.</li>
<li>To our knowledge this is the first study to comment on the outcome of ICSI in men with NOA based on testicular histopathology.</li>
</ul></div></div>
<div class="section" id="bju11714-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11714-list-0003" class="bullet">
<li>A retrospective analysis of 137 testicular sperm extraction-ICSI cycles performed between 2001–2010, involving 103 men with azoospermia, with 26 couples having repeat cycles.</li>
</ul></div></div>
<div class="section" id="bju11714-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11714-list-0004" class="bullet">
<li>Analysis of the results did not show any statistically significant differences in the fertilization, embryo cleavage, clinical pregnancy, live birth and miscarriage rates in relation to the male age, cuase of azoospermia, testicular histopathology, type of sperm used and the use of pentoxyphilline.</li>
</ul></div></div>
<div class="section" id="bju11714-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11714-list-0005" class="bullet">
<li>Once sperm is found in a man with azoospermia, no other male factor seems to influence the ICSI outcome.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The management of patients with non-obstructive azoospermia (NOA) and some cases of obstructive azoospermia involves testicular sperm extraction (TESE or micro-dissection TESE) combined with intracytoplasmic sperm injection (ICSI). Several studies have investigated the effect of the male age, the cause of azoospermia, testicular histopathology, the type of sperm used, and the use of pentoxyphilline, on the ICSI cycle outcome in men with azoospermia.
The present study showed that none of these factors influenced the ICSI outcome in men with azoospermia, thus once sperm is found in an azoospermic male, no other male factor seems to influence the ICSI outcome. To our knowledge this is the first study to comment on the outcome of ICSI in men with NOA based on testicular histopathology.


 Objectives

To access the effect of: male age, the cause of azoospermia (obstructive azoospermia vs non-obstructive azoospermia [NOA]), testicular histopathology, the type of sperm used (fresh vs frozen-thawed), and the use of pentoxyphilline on the intracytoplasmic sperm injection (ICSI) cycle outcome in men with azoospermia.
To our knowledge this is the first study to comment on the outcome of ICSI in men with NOA based on testicular histopathology.



Patients and Methods

A retrospective analysis of 137 testicular sperm extraction-ICSI cycles performed between 2001–2010, involving 103 men with azoospermia, with 26 couples having repeat cycles.



Results

Analysis of the results did not show any statistically significant differences in the fertilization, embryo cleavage, clinical pregnancy, live birth and miscarriage rates in relation to the male age, cuase of azoospermia, testicular histopathology, type of sperm used and the use of pentoxyphilline.



Conclusion

Once sperm is found in a man with azoospermia, no other male factor seems to influence the ICSI outcome.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11737.x" xmlns="http://purl.org/rss/1.0/"><title>A molecular complex of bovine milk protein and oleic acid selectively kills cancer cells in vitro and inhibits tumour growth in an orthotopic rat bladder tumour model</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11737.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A molecular complex of bovine milk protein and oleic acid selectively kills cancer cells in vitro and inhibits tumour growth in an orthotopic rat bladder tumour model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zhengwen Xiao, Allan Mak, Karen Koch, Ronald B. Moore</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T07:35:52.583523-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11737.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11737.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11737.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11737-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11737-list-0001" class="bullet">
<li>Novel intravesical therapies are needed for superficial bladder cancer that reduce the risk of infection associated with Bacillus Calmette–Guérin (BCG) and further destabilization of the urothelium associated with cytotoxic chemotherapy. Experimental therapies to date have included photodynamic therapy, oncolytic viruses, gene therapy (antisense oligonucleotides and silencing RNA), cytokine therapy, death receptor agonists (tumour-necrosis-factor-related apoptosis-inducing ligand and anti-DR5 monoclonal antibody), naturally occurring substances (curcumin and deguelin) and human α-lactalbumin made lethal to tumour cells (HAMLET). HAMLET, a natural occurring product in milk, induces apoptosis in urothelial cancer cells but has limitations in clinical application because of its human source. A previous study in patients with bladder cancer has demonstrated that intravesical HAMLET (daily for 5 days before tumour resection) caused selective apoptotic tumour cell death. BAMLET, the bovine equivalent of HAMLET, is a complex of bovine α-lactalbumin and oleic acid (bLAC) that has been shown <em>in vitro</em> to accumulate in the endolysosomal compartment of tumour cells and induce leakage of lysosomal cathepsins into the cytosol followed by activation of the pro-apoptotic protein Bax.</li>
<li>This is the first <em>in vivo</em> study to show that BAMLET (bLAC) induces apoptosis in urothelial cancer cells and controls the growth of high risk urothelial cancer in a syngeneic rat orthotopic model. This same bladder cancer model system has been used to test other novel therapies, including BCG, and therefore provides a relative comparison of its effectiveness with other intravesical therapies.</li>
</ul></div></div>
<div class="section" id="bju11737-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11737-list-0002" class="bullet">
<li>To investigate the efficacy of a complex of bovine α-lactalbumin and oleic acid (bLAC) to kill urothelial cancer cells <em>in vitro</em> and inhibit tumour growth and progression in a high risk bladder tumour model.</li>
</ul></div></div>
<div class="section" id="bju11737-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11737-list-0003" class="bullet">
<li>The cytotoxicity of bLAC to a large panel of urothelial cell cancer (UCC) cells was tested by the MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide) assay, using bLA, the folded α-lactalbumin without oleic acid, as a control.</li>
<li>The mechanism of bLAC-inducing cell death was evaluated by annexin V staining, TUNEL (terminal deoxynucleotidyl transferase mediated nick end labelling) assay and sub-G<sub>1</sub> DNA analysis.</li>
<li>The selective bLAC cytotoxicity was examined using multicellular spheroids consisting of UCC and non-transformed fibroblasts.</li>
<li>Rats bearing orthotopic tumour received intravesical instillations (twice weekly, for 3 weeks) of bLAC, bLA, BCG or saline, starting 6 days after UCC (AY-27) cell inoculation. Animals were monitored for survival, toxicity and tumour growth control.</li>
</ul></div></div>
<div class="section" id="bju11737-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11737-list-0004" class="bullet">
<li>A dose-dependent bLAC-inducing apoptotic-like cell death was shown in UCC cells tested, including cells refractory to classic apoptosis-inducing agents, whereas bLA showed little cytotoxicity.</li>
<li>bLAC selectively destroyed cancer cells in spheroids.</li>
<li>Intravesical bLAC therapy demonstrated marked reduction in tumour growth/progression and significantly prolonged animal survival vs saline instillations (<em>P</em> = 0.004, log-rank test) and showed comparable efficacy with BCG (standard) therapy.</li>
</ul></div></div>
<div class="section" id="bju11737-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11737-list-0005" class="bullet">
<li>The findings identify bLAC as a new candidate for UCC therapy and suggests that topical administration of bLAC alone or with BCG to prevent progression of bladder cancer warrants further exploration.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Novel intravesical therapies are needed for superficial bladder cancer that reduce the risk of infection associated with Bacillus Calmette–Guérin (BCG) and further destabilization of the urothelium associated with cytotoxic chemotherapy. Experimental therapies to date have included photodynamic therapy, oncolytic viruses, gene therapy (antisense oligonucleotides and silencing RNA), cytokine therapy, death receptor agonists (tumour-necrosis-factor-related apoptosis-inducing ligand and anti-DR5 monoclonal antibody), naturally occurring substances (curcumin and deguelin) and human α-lactalbumin made lethal to tumour cells (HAMLET). HAMLET, a natural occurring product in milk, induces apoptosis in urothelial cancer cells but has limitations in clinical application because of its human source. A previous study in patients with bladder cancer has demonstrated that intravesical HAMLET (daily for 5 days before tumour resection) caused selective apoptotic tumour cell death. BAMLET, the bovine equivalent of HAMLET, is a complex of bovine α-lactalbumin and oleic acid (bLAC) that has been shown in vitro to accumulate in the endolysosomal compartment of tumour cells and induce leakage of lysosomal cathepsins into the cytosol followed by activation of the pro-apoptotic protein Bax.
This is the first in vivo study to show that BAMLET (bLAC) induces apoptosis in urothelial cancer cells and controls the growth of high risk urothelial cancer in a syngeneic rat orthotopic model. This same bladder cancer model system has been used to test other novel therapies, including BCG, and therefore provides a relative comparison of its effectiveness with other intravesical therapies.


 Objective

To investigate the efficacy of a complex of bovine α-lactalbumin and oleic acid (bLAC) to kill urothelial cancer cells in vitro and inhibit tumour growth and progression in a high risk bladder tumour model.



Materials and Methods

The cytotoxicity of bLAC to a large panel of urothelial cell cancer (UCC) cells was tested by the MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide) assay, using bLA, the folded α-lactalbumin without oleic acid, as a control.
The mechanism of bLAC-inducing cell death was evaluated by annexin V staining, TUNEL (terminal deoxynucleotidyl transferase mediated nick end labelling) assay and sub-G1 DNA analysis.
The selective bLAC cytotoxicity was examined using multicellular spheroids consisting of UCC and non-transformed fibroblasts.
Rats bearing orthotopic tumour received intravesical instillations (twice weekly, for 3 weeks) of bLAC, bLA, BCG or saline, starting 6 days after UCC (AY-27) cell inoculation. Animals were monitored for survival, toxicity and tumour growth control.



Results

A dose-dependent bLAC-inducing apoptotic-like cell death was shown in UCC cells tested, including cells refractory to classic apoptosis-inducing agents, whereas bLA showed little cytotoxicity.
bLAC selectively destroyed cancer cells in spheroids.
Intravesical bLAC therapy demonstrated marked reduction in tumour growth/progression and significantly prolonged animal survival vs saline instillations (P = 0.004, log-rank test) and showed comparable efficacy with BCG (standard) therapy.



Conclusion

The findings identify bLAC as a new candidate for UCC therapy and suggests that topical administration of bLAC alone or with BCG to prevent progression of bladder cancer warrants further exploration.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11757.x" xmlns="http://purl.org/rss/1.0/"><title>Contemporaneous comparison of open vs minimally-invasive radical prostatectomy for high-risk prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11757.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Contemporaneous comparison of open vs minimally-invasive radical prostatectomy for high-risk prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Phillip M. Pierorazio, Jeffrey K. Mullins, John B. Eifler, Kipp Voth, Elias S. Hyams, Misop Han, Christian P. Pavlovich, Trinity J. Bivalacqua, Alan W. Partin, Mohamad E. Allaf, Edward M. Schaeffer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T07:02:16.004036-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11757.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11757.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11757.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11757-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11757-list-0001" class="bullet">
<li>The ideal treatment for men with high-risk prostate cancer is controversial, although most physicians agree that a multimodal approach, including radiation and hormone therapy with or without surgery, offers the best chance of cancer control. Minimally-invasive radical prostatectomy has emerged as a treatment option for clinically localized cancer; however, critics argue that the open approach may afford advantages of tactile feedback and a better lymph node dissection.</li>
<li>The present study demonstrates that open and minimally-invasive radical prostatectomy offer equivalent short-term outcomes for men with high-risk prostate cancer at a highly experienced centre.</li>
</ul></div></div>
<div class="section" id="bju11757-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11757-list-0002" class="bullet">
<li>To analyze pathological and short-term oncological outcomes in men undergoing open and minimally-invasive radical prostatectomy (MIRP) for high-risk prostate cancer (HRPC; prostate-specific antigen level [PSA] &gt;20 ng/mL, ≥ cT2c, Gleason score 8–10) in a contemporaneous series.</li>
</ul></div></div>
<div class="section" id="bju11757-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11757-list-0003" class="bullet">
<li>In total, 913 patients with HRPC were identified in the Johns Hopkins Radical Prostatectomy Database subsequent to the inception of MIRP at this institution (2002–2011)</li>
<li>Of these, 743 (81.4%) underwent open radical retropubic prostatectomy (ORRP), 105 (11.5%) underwent robot-assisted laparoscopic radical prostatectomy (RALRP) and 65 (7.1%) underwent laparoscopic radical prostatectomy (LRP) for HRPC.</li>
<li>Appropriate comparative tests were used to evaluate patient and prostate cancer characteristics.</li>
<li>Proportional hazards regression models were used to predict biochemical recurrence.</li>
</ul></div></div>
<div class="section" id="bju11757-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11757-list-0004" class="bullet">
<li>Age, race, body mass index, preoperative PSA level, clinical stage, number of positive cores and Gleason score at final pathology were similar between ORRP and MIRP.</li>
<li>On average, men undergoing MIRP had smaller prostates and more organ-confined (pT2) disease (<em>P</em> = 0.02).</li>
<li>The number of surgeons and surgeon experience were greatest for the ORRP cohort.</li>
<li>Overall surgical margin rate was 29.4%, 34.3% and 27.7% (<em>P</em> = 0.52) and 1.9%, 2.9% and 6.2% (<em>P</em> = 0.39) for pT2 disease in men undergoing ORRP, RALRP and LRP, respectively.</li>
<li>Biochemical recurrence-free survival among ORRP, RALRP and LRP was 56.3%, 67.8% and 41.1%, respectively, at 3 years (<em>P</em> = 0.6) and the approach employed did not predict biochemical recurrence in regression models.</li>
</ul></div></div>
<div class="section" id="bju11757-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11757-list-0005" class="bullet">
<li>At an experienced centre, MIRP is comparable to open radical prostatectomy for HRPC with respect to surgical margin status and biochemical recurrence.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The ideal treatment for men with high-risk prostate cancer is controversial, although most physicians agree that a multimodal approach, including radiation and hormone therapy with or without surgery, offers the best chance of cancer control. Minimally-invasive radical prostatectomy has emerged as a treatment option for clinically localized cancer; however, critics argue that the open approach may afford advantages of tactile feedback and a better lymph node dissection.
The present study demonstrates that open and minimally-invasive radical prostatectomy offer equivalent short-term outcomes for men with high-risk prostate cancer at a highly experienced centre.


 Objectives

To analyze pathological and short-term oncological outcomes in men undergoing open and minimally-invasive radical prostatectomy (MIRP) for high-risk prostate cancer (HRPC; prostate-specific antigen level [PSA] &gt;20 ng/mL, ≥ cT2c, Gleason score 8–10) in a contemporaneous series.



Patients and Methods

In total, 913 patients with HRPC were identified in the Johns Hopkins Radical Prostatectomy Database subsequent to the inception of MIRP at this institution (2002–2011)
Of these, 743 (81.4%) underwent open radical retropubic prostatectomy (ORRP), 105 (11.5%) underwent robot-assisted laparoscopic radical prostatectomy (RALRP) and 65 (7.1%) underwent laparoscopic radical prostatectomy (LRP) for HRPC.
Appropriate comparative tests were used to evaluate patient and prostate cancer characteristics.
Proportional hazards regression models were used to predict biochemical recurrence.



Results

Age, race, body mass index, preoperative PSA level, clinical stage, number of positive cores and Gleason score at final pathology were similar between ORRP and MIRP.
On average, men undergoing MIRP had smaller prostates and more organ-confined (pT2) disease (P = 0.02).
The number of surgeons and surgeon experience were greatest for the ORRP cohort.
Overall surgical margin rate was 29.4%, 34.3% and 27.7% (P = 0.52) and 1.9%, 2.9% and 6.2% (P = 0.39) for pT2 disease in men undergoing ORRP, RALRP and LRP, respectively.
Biochemical recurrence-free survival among ORRP, RALRP and LRP was 56.3%, 67.8% and 41.1%, respectively, at 3 years (P = 0.6) and the approach employed did not predict biochemical recurrence in regression models.



Conclusions

At an experienced centre, MIRP is comparable to open radical prostatectomy for HRPC with respect to surgical margin status and biochemical recurrence.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11715.x" xmlns="http://purl.org/rss/1.0/"><title>Fourteen-year oncological and functional outcomes of high-intensity focused ultrasound in localized prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11715.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fourteen-year oncological and functional outcomes of high-intensity focused ultrasound in localized prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roman Ganzer, Hans-Martin Fritsche, Andreas Brandtner, Johannes Bründl, Daniel Koch, Wolf F. Wieland, Andreas Blana</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T07:02:08.891153-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11715.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11715.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11715.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11715-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11715-list-0001" class="bullet">
<li>High-intensity focused ultrasound (HIFU) is an alternative treatment option for localized prostate cancer (PCa), which is applied for over 15 years. There are conflicting recommendations for HIFU among urological societies, which can be explained by the lack of prospective controlled studies, reports on preselected patient populations and limited follow-up providing little information on overall and cancer-specific survival.</li>
<li>We report on a large, unselected consecutive patient series of patients who have undergone primary HIFU for clinically localized PCa with the longest follow-up in current literature. Our results improve the understanding of the oncological efficacy, morbidity and side effects of primary HIFU.</li>
</ul></div></div>
<div class="section" id="bju11715-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11715-list-0002" class="bullet">
<li>To assess the safety, functional and oncological long-term outcomes of high-intensity focused ultrasound (HIFU) as a primary treatment option for localized prostate cancer (PCa).</li>
</ul></div></div>
<div class="section" id="bju11715-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11715-list-0003" class="bullet">
<li>We conducted a retrospective single-centre study on 538 consecutive patients who underwent primary HIFU for clinically localized PCa between November 1997 and September 2009.</li>
<li>Factors assessed were: biochemical disease-free survival (BDFS) according to Phoenix criteria (prostate-specific antigen nadir + 2 ng/mL); metastatic-free, overall and PCa-specific survival; salvage treatment; side effects; potency; and continence status.</li>
</ul></div></div>
<div class="section" id="bju11715-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11715-list-0004" class="bullet">
<li>The mean (<span class="smallCaps">sd</span>; range) follow-up was 8.1 (2.9; 2.1–14.0) years.</li>
<li>The actuarial BDFS rates at 5 and 10 years were 81 and 61%, respectively. The 5-year BDFS rates for low-, intermediate- and high-risk patients were 88, 83 and 48%, while the 10-year BDFS rates were 71, 63 and 32%, respectively.</li>
<li>Metastatic disease was reported in 0.4, 5.7 and 15.4% of low-, intermediate- and high-risk patients, respectively.</li>
<li>The salvage treatment rate was 18%.</li>
<li>Seventy-five (13.9%) patients died. PCa-specific death was registered in 18 (3.3%) patients (0, 3.8 and 11% in the low-, intermediate- and high-risk groups, respectively).</li>
<li>Side effects included bladder outlet obstruction (28.3%), Grade I, II and III stress urinary incontinence (13.8, 2.4 and 0.7%, respectively) and recto-urethral fistula (0.7%). Preserved potency was 25.4% (in previously potent patients).</li>
</ul></div></div>
<div class="section" id="bju11715-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11715-list-0005" class="bullet">
<li>The study demonstrates the efficacy and safety of HIFU for localized PCa.</li>
<li>HIFU is a therapeutic option for patients of advanced age, in the low- or intermediate-risk groups, and with a life expectancy of ∼10 years.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

High-intensity focused ultrasound (HIFU) is an alternative treatment option for localized prostate cancer (PCa), which is applied for over 15 years. There are conflicting recommendations for HIFU among urological societies, which can be explained by the lack of prospective controlled studies, reports on preselected patient populations and limited follow-up providing little information on overall and cancer-specific survival.
We report on a large, unselected consecutive patient series of patients who have undergone primary HIFU for clinically localized PCa with the longest follow-up in current literature. Our results improve the understanding of the oncological efficacy, morbidity and side effects of primary HIFU.


 Objective

To assess the safety, functional and oncological long-term outcomes of high-intensity focused ultrasound (HIFU) as a primary treatment option for localized prostate cancer (PCa).



Patients and Methods

We conducted a retrospective single-centre study on 538 consecutive patients who underwent primary HIFU for clinically localized PCa between November 1997 and September 2009.
Factors assessed were: biochemical disease-free survival (BDFS) according to Phoenix criteria (prostate-specific antigen nadir + 2 ng/mL); metastatic-free, overall and PCa-specific survival; salvage treatment; side effects; potency; and continence status.



Results

The mean (sd; range) follow-up was 8.1 (2.9; 2.1–14.0) years.
The actuarial BDFS rates at 5 and 10 years were 81 and 61%, respectively. The 5-year BDFS rates for low-, intermediate- and high-risk patients were 88, 83 and 48%, while the 10-year BDFS rates were 71, 63 and 32%, respectively.
Metastatic disease was reported in 0.4, 5.7 and 15.4% of low-, intermediate- and high-risk patients, respectively.
The salvage treatment rate was 18%.
Seventy-five (13.9%) patients died. PCa-specific death was registered in 18 (3.3%) patients (0, 3.8 and 11% in the low-, intermediate- and high-risk groups, respectively).
Side effects included bladder outlet obstruction (28.3%), Grade I, II and III stress urinary incontinence (13.8, 2.4 and 0.7%, respectively) and recto-urethral fistula (0.7%). Preserved potency was 25.4% (in previously potent patients).



Conclusions

The study demonstrates the efficacy and safety of HIFU for localized PCa.
HIFU is a therapeutic option for patients of advanced age, in the low- or intermediate-risk groups, and with a life expectancy of ∼10 years.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11659.x" xmlns="http://purl.org/rss/1.0/"><title>Cost-effectiveness of single-dose tamsulosin and dutasteride combination therapy compared with tamsulosin monotherapy in patients with benign prostatic hyperplasia in the UK</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11659.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cost-effectiveness of single-dose tamsulosin and dutasteride combination therapy compared with tamsulosin monotherapy in patients with benign prostatic hyperplasia in the UK</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Walker, Scott Doyle, John Posnett, Manjit Hunjan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T07:01:58.559308-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11659.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11659.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11659.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11659-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11659-list-1001" class="bullet">
<li>UK clinical guidelines for treating male patients with moderate to severe LUTS associated with BPH recommend treatment with an alpha-blocker (such as tamsulosin) in cases where conservative management options have not been successful or are not appropriate. An alpha-blocker plus 5-alpha-reductase inhibitor (such as dutasteride) is recommended for those patients with moderate to severe symptoms and prostate volume &gt;30 mL.</li>
<li>The present study evaluates the cost-effectiveness of a new, single-dose combination of tamsulosin and dutasteride (Combodart®) from the perspective of the UK National Health Service. The results show that the combination therapy has a high probability of being cost-effective compared with either monotherapy, and compared with the two therapies taken separately. The probability of the combination therapy being cost-effective at an incremental cost-effectiveness ratio threshold in the range £25 000–£30 000 per quality-adjusted life year is 78–88%.</li>
</ul></div></div>
<div class="section" id="bju11659-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11659-list-0001" class="bullet">
<li>To estimate the long-term cost-effectiveness of single-dose dutasteride/tamsulosin combination therapy as a first-line treatment for benign prostatic hyperplasia (BPH) from the perspective of the UK National Health Service (NHS).</li>
</ul></div></div>
<div class="section" id="bju11659-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><ul id="bju11659-list-0002" class="bullet">
<li>A Markov state transition model was developed to estimate healthcare costs and patient outcomes, measured by quality-adjusted life years (QALYs), for patients aged ≥50 years with diagnosed BPH and moderate to severe symptoms.</li>
<li>Costs and outcomes were estimated for two treatment comparators: oral, daily, single-dose combination therapy (dutasteride 0.5 mg + tamsulosin 0.4 mg), and oral daily tamsulosin (0.4 mg) over a period up to 25 years.</li>
<li>The efficacy of comparators was taken from results of the Combination of Avodart and Tamsulosin (CombAT) trial.</li>
</ul></div></div>
<div class="section" id="bju11659-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11659-list-0003" class="bullet">
<li>Cumulative discounted costs per patient were higher with combination therapy than with tamsulosin, but QALYs were also higher.</li>
<li>After 25 years, the incremental cost-effectiveness ratio for combination therapy was £12 219, well within the threshold range (£20 000–£30 000 per QALY) typically applied in the NHS.</li>
<li>Probabilistic sensitivity analysis showed that the probability of combination therapy being cost-effective given the threshold range is between 78% and 88%.</li>
</ul></div></div>
<div class="section" id="bju11659-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11659-list-0004" class="bullet">
<li>Single-dose combination dutasteride/tamsulosin therapy has a high probability of being cost-effective in comparison to tamsulosin monotherapy in the UK‘s NHS.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

UK clinical guidelines for treating male patients with moderate to severe LUTS associated with BPH recommend treatment with an alpha-blocker (such as tamsulosin) in cases where conservative management options have not been successful or are not appropriate. An alpha-blocker plus 5-alpha-reductase inhibitor (such as dutasteride) is recommended for those patients with moderate to severe symptoms and prostate volume &gt;30 mL.
The present study evaluates the cost-effectiveness of a new, single-dose combination of tamsulosin and dutasteride (Combodart®) from the perspective of the UK National Health Service. The results show that the combination therapy has a high probability of being cost-effective compared with either monotherapy, and compared with the two therapies taken separately. The probability of the combination therapy being cost-effective at an incremental cost-effectiveness ratio threshold in the range £25 000–£30 000 per quality-adjusted life year is 78–88%.


 Objective

To estimate the long-term cost-effectiveness of single-dose dutasteride/tamsulosin combination therapy as a first-line treatment for benign prostatic hyperplasia (BPH) from the perspective of the UK National Health Service (NHS).



Methods

A Markov state transition model was developed to estimate healthcare costs and patient outcomes, measured by quality-adjusted life years (QALYs), for patients aged ≥50 years with diagnosed BPH and moderate to severe symptoms.
Costs and outcomes were estimated for two treatment comparators: oral, daily, single-dose combination therapy (dutasteride 0.5 mg + tamsulosin 0.4 mg), and oral daily tamsulosin (0.4 mg) over a period up to 25 years.
The efficacy of comparators was taken from results of the Combination of Avodart and Tamsulosin (CombAT) trial.



Results

Cumulative discounted costs per patient were higher with combination therapy than with tamsulosin, but QALYs were also higher.
After 25 years, the incremental cost-effectiveness ratio for combination therapy was £12 219, well within the threshold range (£20 000–£30 000 per QALY) typically applied in the NHS.
Probabilistic sensitivity analysis showed that the probability of combination therapy being cost-effective given the threshold range is between 78% and 88%.



Conclusion

Single-dose combination dutasteride/tamsulosin therapy has a high probability of being cost-effective in comparison to tamsulosin monotherapy in the UK‘s NHS.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11788.x" xmlns="http://purl.org/rss/1.0/"><title>Standardized comparison of robot-assisted limited and extended pelvic lymphadenectomy for prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11788.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Standardized comparison of robot-assisted limited and extended pelvic lymphadenectomy for prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bertram E. Yuh, Nora H. Ruel, Rosa Mejia, Giacomo Novara, Timothy G. Wilson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:06:49.484243-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11788.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11788.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11788.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11788-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11788-list-0001" class="bullet">
<li>Extended pelvic lymphadenectomy is the present standard of care according to European Association of Urology guidelines. Extended dissection improves staging, removes more metastatic lymph nodes, and potentially has therapeutic benefits. Previous reports have examined the morbidity of extended dissection compared with a more limited dissection in the open and laparoscopic setting. While some have suggested an increased complication rate with extended node dissection, others have not.</li>
<li>This represents the first study focused on comparing the complications associated with the extent of node dissection using the modified Clavien system and Martin criteria in the literature on robot-assisted surgery. In a single surgeon series, we found no statistically significant differences in complications. With careful anatomic dissection, robot-assisted extended lymph node dissection can be performed safely and effectively, although operating time and length of hospital of stay are slightly increased.</li>
</ul></div></div>
<div class="section" id="bju11788-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11788-list-0002" class="bullet">
<li>To compare the perioperative course of patients undergoing robot-assisted limited lymph node dissection (LLND) or extended lymph node dissection (ELND) for prostate cancer.</li>
<li>To examine the differential lymph node counts and rates of detection of lymph node metastases.</li>
</ul></div></div>
<div class="section" id="bju11788-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11788-list-0003" class="bullet">
<li>Between 2008 and 2012, 406 consecutive patients with D'Amico intermediate- or high-risk prostate cancer underwent either bilateral LLND (<em>n</em> = 204) or ELND (<em>n</em> = 202) and robot-assisted laparoscopic radical prostatectomy by a single surgeon.</li>
<li>The region of dissection was the obturator fossa for LLND, while ELND included, in addition, the common iliac, external iliac and internal iliac lymph nodes.</li>
<li>All complications within 90 days of surgery were recorded according to a modified Clavien system.</li>
<li>Clinical variables were summarized and compared. Logistic regression was used to identify predictors of complications.</li>
</ul></div></div>
<div class="section" id="bju11788-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11788-list-0004" class="bullet">
<li>There were no differences in demographics when comparing patients who underwent ELND with those who underwent LLND.</li>
<li>The median operating time was 3.0 h for the ELND cohort and 2.8 h in the LLND cohort (<em>P</em> &lt; 0.001). Intraoperative blood loss was 200 mL in both cohorts. Hospital stay was longer for a small percentage of patients in the ELND cohort, with 75% of ELND patients and 85% of LLND patients staying 1 day (<em>P</em> = 0.004).</li>
<li>No significant difference was found in the overall or major complication rates between LLND (21.6% overall; 6.9% major) and ELND (22.8% overall; 4.5% major). No difference was seen in the symptomatic lymphocele rate between LLND and ELND, 2.9 vs 2.5%, respectively.</li>
<li>Overall, the lymph-node-positive rate was 12% compared with 4% for the ELND and LLND groups, respectively (<em>P</em> = 0.002).</li>
<li>A higher Charlson comorbidity index score was associated with the development of major complications.</li>
</ul></div></div>
<div class="section" id="bju11788-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11788-list-0005" class="bullet">
<li>ELND at the time of robot-assisted radical prostatectomy can be performed safely with minimal additional morbidity.</li>
<li>Long-term oncological and functional outcomes require further study.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Extended pelvic lymphadenectomy is the present standard of care according to European Association of Urology guidelines. Extended dissection improves staging, removes more metastatic lymph nodes, and potentially has therapeutic benefits. Previous reports have examined the morbidity of extended dissection compared with a more limited dissection in the open and laparoscopic setting. While some have suggested an increased complication rate with extended node dissection, others have not.
This represents the first study focused on comparing the complications associated with the extent of node dissection using the modified Clavien system and Martin criteria in the literature on robot-assisted surgery. In a single surgeon series, we found no statistically significant differences in complications. With careful anatomic dissection, robot-assisted extended lymph node dissection can be performed safely and effectively, although operating time and length of hospital of stay are slightly increased.


 Objectives

To compare the perioperative course of patients undergoing robot-assisted limited lymph node dissection (LLND) or extended lymph node dissection (ELND) for prostate cancer.
To examine the differential lymph node counts and rates of detection of lymph node metastases.



Patients and Methods

Between 2008 and 2012, 406 consecutive patients with D'Amico intermediate- or high-risk prostate cancer underwent either bilateral LLND (n = 204) or ELND (n = 202) and robot-assisted laparoscopic radical prostatectomy by a single surgeon.
The region of dissection was the obturator fossa for LLND, while ELND included, in addition, the common iliac, external iliac and internal iliac lymph nodes.
All complications within 90 days of surgery were recorded according to a modified Clavien system.
Clinical variables were summarized and compared. Logistic regression was used to identify predictors of complications.



Results

There were no differences in demographics when comparing patients who underwent ELND with those who underwent LLND.
The median operating time was 3.0 h for the ELND cohort and 2.8 h in the LLND cohort (P &lt; 0.001). Intraoperative blood loss was 200 mL in both cohorts. Hospital stay was longer for a small percentage of patients in the ELND cohort, with 75% of ELND patients and 85% of LLND patients staying 1 day (P = 0.004).
No significant difference was found in the overall or major complication rates between LLND (21.6% overall; 6.9% major) and ELND (22.8% overall; 4.5% major). No difference was seen in the symptomatic lymphocele rate between LLND and ELND, 2.9 vs 2.5%, respectively.
Overall, the lymph-node-positive rate was 12% compared with 4% for the ELND and LLND groups, respectively (P = 0.002).
A higher Charlson comorbidity index score was associated with the development of major complications.



Conclusions

ELND at the time of robot-assisted radical prostatectomy can be performed safely with minimal additional morbidity.
Long-term oncological and functional outcomes require further study.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11777.x" xmlns="http://purl.org/rss/1.0/"><title>Osteoporosis knowledge, health beliefs, and healthy bone behaviours in patients on androgen-deprivation therapy (ADT) for prostate cancer</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11777.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Osteoporosis knowledge, health beliefs, and healthy bone behaviours in patients on androgen-deprivation therapy (ADT) for prostate cancer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michelle Nadler, Shabbir Alibhai, Pamela Catton, Charles Catton, Matthew J. To, Jennifer M. Jones</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:06:41.039872-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11777.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11777.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11777.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11777-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11777-list-0001" class="bullet">
<li>There is an increase in use and duration of androgen-deprivation therapy (ADT) in patients with prostate cancer. ADT can cause decreased bone mineral density and lean muscle loss, putting these patients at increased risk of fracture. Guidelines exist for the prevention and management of bone loss in this population; however, data suggests that most patients are not receiving proper screening, evaluation, or treatment for bone loss. Research to date suggests that patients on ADT are unaware of the risks and side-effects of ADT and that most are not engaging in important preventative behaviours, e.g. calcium and vitamin D intake.</li>
<li>To our knowledge, there are no studies in patients on ADT specifically assessing patients' osteoporosis (OP) knowledge, self-efficacy, and feelings of susceptibility towards OP and their relationships to engagement in recommended healthy bone behaviours. We think that these data will aid in the development of health promotion uptake strategies that are directly targeted to this patient population.</li>
</ul></div></div>
<div class="section" id="bju11777-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11777-list-0002" class="bullet">
<li>To describe in patients with prostate cancer, receiving androgen-deprivation therapy (ADT): (i) knowledge, self-efficacy (SE), and health beliefs about osteoporosis (OP); (ii) current engagement in healthy bone behaviours (HBBs).</li>
<li>To explore the relationships between knowledge, SE, and health beliefs, and engagement in HBBs.</li>
</ul></div></div>
<div class="section" id="bju11777-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11777-list-0003" class="bullet">
<li>175 patients receiving ADT by injection completed questionnaires assessing current HBBs, OP knowledge, SE, and health beliefs (motivation, perceived susceptibility, and seriousness).</li>
<li>Descriptive statistics and independent samples <em>t</em>-tests were used to assess relationships between knowledge, SE, health beliefs, and engagement in HBBs.</li>
</ul></div></div>
<div class="section" id="bju11777-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11777-list-0004" class="bullet">
<li>Only 38% of patients had undergone a dual X-ray absorptiometry scan in the past 2 years. OP knowledge was low (mean [<span class="smallCaps">sd</span>, range] 9.6 [4.4, 0–19]) and perceived SE moderate (84.7 [24.5, 0–120]). Health motivation was fairly high (23.6 [3.1, 6–30]), but perceived susceptibility (16.8 [4.3]) and seriousness (16.8 [4.2]) of OP were low.</li>
<li>Few patients met the recommendations for vitamin D intake (42%) and exercise (31%), and 15% were at risk of over-supplementation of calcium.</li>
<li>Patients taking calcium supplements (<em>P</em> = 0.04), and meeting guidelines for vitamin D (<em>P</em> = 0.008) and for exercise (<em>P</em> = 0.002) had significantly greater knowledge than those who did not.</li>
<li>Patients who were engaging in less than four of five HBBs had lower knowledge (<em>P</em> &lt; 0.001) and health motivation (<em>P</em> = 0.01) than those who were engaging in four or all five HBBs.</li>
</ul></div></div>
<div class="section" id="bju11777-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11777-list-0005" class="bullet">
<li>Most patients who are receiving ADT are not receiving appropriate screening, lack basic information about bone health, and are not engaging in the appropriate HBBs.</li>
<li>These findings support the application of the Health Belief Model in this population: interventions that teach patients about the implications of bone loss, encourage proper uptake of HBBs, and promote feelings of SE could increase engagement in HBBs to prevent and manage bone loss.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

There is an increase in use and duration of androgen-deprivation therapy (ADT) in patients with prostate cancer. ADT can cause decreased bone mineral density and lean muscle loss, putting these patients at increased risk of fracture. Guidelines exist for the prevention and management of bone loss in this population; however, data suggests that most patients are not receiving proper screening, evaluation, or treatment for bone loss. Research to date suggests that patients on ADT are unaware of the risks and side-effects of ADT and that most are not engaging in important preventative behaviours, e.g. calcium and vitamin D intake.
To our knowledge, there are no studies in patients on ADT specifically assessing patients' osteoporosis (OP) knowledge, self-efficacy, and feelings of susceptibility towards OP and their relationships to engagement in recommended healthy bone behaviours. We think that these data will aid in the development of health promotion uptake strategies that are directly targeted to this patient population.


 Objectives

To describe in patients with prostate cancer, receiving androgen-deprivation therapy (ADT): (i) knowledge, self-efficacy (SE), and health beliefs about osteoporosis (OP); (ii) current engagement in healthy bone behaviours (HBBs).
To explore the relationships between knowledge, SE, and health beliefs, and engagement in HBBs.



Patients and Methods

175 patients receiving ADT by injection completed questionnaires assessing current HBBs, OP knowledge, SE, and health beliefs (motivation, perceived susceptibility, and seriousness).
Descriptive statistics and independent samples t-tests were used to assess relationships between knowledge, SE, health beliefs, and engagement in HBBs.



Results

Only 38% of patients had undergone a dual X-ray absorptiometry scan in the past 2 years. OP knowledge was low (mean [sd, range] 9.6 [4.4, 0–19]) and perceived SE moderate (84.7 [24.5, 0–120]). Health motivation was fairly high (23.6 [3.1, 6–30]), but perceived susceptibility (16.8 [4.3]) and seriousness (16.8 [4.2]) of OP were low.
Few patients met the recommendations for vitamin D intake (42%) and exercise (31%), and 15% were at risk of over-supplementation of calcium.
Patients taking calcium supplements (P = 0.04), and meeting guidelines for vitamin D (P = 0.008) and for exercise (P = 0.002) had significantly greater knowledge than those who did not.
Patients who were engaging in less than four of five HBBs had lower knowledge (P &lt; 0.001) and health motivation (P = 0.01) than those who were engaging in four or all five HBBs.



Conclusions

Most patients who are receiving ADT are not receiving appropriate screening, lack basic information about bone health, and are not engaging in the appropriate HBBs.
These findings support the application of the Health Belief Model in this population: interventions that teach patients about the implications of bone loss, encourage proper uptake of HBBs, and promote feelings of SE could increase engagement in HBBs to prevent and manage bone loss.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11680.x" xmlns="http://purl.org/rss/1.0/"><title>Multiple cores of Gleason score 6 correlate with favourable findings at radical prostatectomy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11680.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Multiple cores of Gleason score 6 correlate with favourable findings at radical prostatectomy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carla L. Ellis, Patrick C. Walsh, Alan W. Partin, Jonathan I. Epstein</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:06:32.73297-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11680.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11680.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11680.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11680-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11680-list-0001" class="bullet">
<li>Previous studies have reported variable outcomes at radical prostatectomy (RP) with Gleason score 6 (GS6) on biopsy. It has been shown that a significant proportion of patients with GS6 disease at biopsy are upgraded to Gleason score 7 or higher after RP, increasing the risk of an adverse outcome. However, such studies have focused on clinical parameters such as PSA, prostate volume and biopsy cancer volume, in concert with GS6, to predict clinically significant upgrading.</li>
<li>The present study is the first to use a significant number of patients with the aim of specifically analyzing the outcome at RP (i.e. percentage organ-confined, margin status, overall grade and biochemical recurrence) and making a direct correlation with the number of positive cores to show that the overall prognosis is favourable.</li>
</ul></div></div>
<div class="section" id="bju11680-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11680-list-0002" class="bullet">
<li>To establish whether the good prognosis of Gleason score 6 (GS6) is maintained in the setting of multiple involved cores.</li>
</ul></div></div>
<div class="section" id="bju11680-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11680-list-0003" class="bullet">
<li>In total, 6156 men (from 1 April 2000 to 30 April 2007) with GS6 on biopsy underwent radical prostatectomy (RP) at our institution.</li>
<li>The number of positive cores was correlated with the outcome at RP.</li>
</ul></div></div>
<div class="section" id="bju11680-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11680-list-0004" class="bullet">
<li>More positive cores correlated with less organ-confined disease (<em>P</em> &lt; 0.001), positive margins (<em>P</em> &lt; 0.012), increasing RP grade (<em>P</em> &lt; 0.001) and increased seminal vesicles/lymph node involvement (<em>P</em> = 0.012).</li>
<li>For men with data available, the actuarial risk of being biochemically free of disease at 5 years was 93.2% when ≤6 cores were positive (812 men followed to 5 years) vs 89.1% if &gt;6 cores were positive (41 men followed to 2 years) (<em>P</em> = 0.6).</li>
<li>Although the predicted ‘cure rate’ of &gt;75% probability of a tumour showing no evidence of biochemical recurrence at 10 years after RP was statistically different between cases with ≤6 vs &gt;6 positive cores (<em>P</em> &lt; 0.0001), the outcome in both groups was still favourable (90.5% vs 84%).</li>
<li>Partin-like tables were generated factoring in the number of positive cores to predict organ-confined disease as a guide for urologists to perform nerve-sparing surgery.</li>
<li>For example, with T1c disease, there was a ≥75% probability of organ-confined disease with one to three positive cores regardless of prostate-specific antigen (PSA) level, and the same probability was present with four to six positive cores and a PSA level of 0–4 ng/mL.</li>
</ul></div></div>
<div class="section" id="bju11680-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11680-list-0005" class="bullet">
<li>A low Gleason score on biopsy is a powerful prognostic finding, such that this favourable outcome is maintained even in the setting of multiple positive cores with GS6.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Previous studies have reported variable outcomes at radical prostatectomy (RP) with Gleason score 6 (GS6) on biopsy. It has been shown that a significant proportion of patients with GS6 disease at biopsy are upgraded to Gleason score 7 or higher after RP, increasing the risk of an adverse outcome. However, such studies have focused on clinical parameters such as PSA, prostate volume and biopsy cancer volume, in concert with GS6, to predict clinically significant upgrading.
The present study is the first to use a significant number of patients with the aim of specifically analyzing the outcome at RP (i.e. percentage organ-confined, margin status, overall grade and biochemical recurrence) and making a direct correlation with the number of positive cores to show that the overall prognosis is favourable.


 Objective

To establish whether the good prognosis of Gleason score 6 (GS6) is maintained in the setting of multiple involved cores.



Patients and Methods

In total, 6156 men (from 1 April 2000 to 30 April 2007) with GS6 on biopsy underwent radical prostatectomy (RP) at our institution.
The number of positive cores was correlated with the outcome at RP.



Results

More positive cores correlated with less organ-confined disease (P &lt; 0.001), positive margins (P &lt; 0.012), increasing RP grade (P &lt; 0.001) and increased seminal vesicles/lymph node involvement (P = 0.012).
For men with data available, the actuarial risk of being biochemically free of disease at 5 years was 93.2% when ≤6 cores were positive (812 men followed to 5 years) vs 89.1% if &gt;6 cores were positive (41 men followed to 2 years) (P = 0.6).
Although the predicted ‘cure rate’ of &gt;75% probability of a tumour showing no evidence of biochemical recurrence at 10 years after RP was statistically different between cases with ≤6 vs &gt;6 positive cores (P &lt; 0.0001), the outcome in both groups was still favourable (90.5% vs 84%).
Partin-like tables were generated factoring in the number of positive cores to predict organ-confined disease as a guide for urologists to perform nerve-sparing surgery.
For example, with T1c disease, there was a ≥75% probability of organ-confined disease with one to three positive cores regardless of prostate-specific antigen (PSA) level, and the same probability was present with four to six positive cores and a PSA level of 0–4 ng/mL.



Conclusion

A low Gleason score on biopsy is a powerful prognostic finding, such that this favourable outcome is maintained even in the setting of multiple positive cores with GS6.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11780.x" xmlns="http://purl.org/rss/1.0/"><title>A benedictory ode to urological live surgery</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11780.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A benedictory ode to urological live surgery</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amrith R. Rao, Omer Karim</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:01:17.414491-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11780.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11780.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11780.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Comment</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11739.x" xmlns="http://purl.org/rss/1.0/"><title>Actinobaculum schaalii, a commensal of the urogenital area</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11739.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Actinobaculum schaalii, a commensal of the urogenital area</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anne B. Olsen, Pernille K. Andersen, Steffen Bank, Karen Marie Søby, Lars Lund, Jørgen Prag</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:01:11.91053-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11739.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11739.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11739.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11739-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11739-list-0001" class="bullet">
<li>Actinobaculum schaalii is considered to be a part of the normai flora in the genital and urinary tract area. It has been associated to urinary tract infection (UTI), sepsis, osteomyelitis, endocarditis and Foumier's gangrene. So far it has mainly been isolated from urine, blood and pus, and predominantly in elderly patients.</li>
<li>This study examined the habitat of <em>A. schaalii</em> by collecting samples from skin and urine in patients with kidney or ureter stones before and after treatment with Extracorporeal Shock Wave Lithotripsy (ESWL). Additionally faeces and vaginal swabs from routine specimen in patients not undergoing ESWL and without known urinary calculi were also analysed.</li>
<li>The study does not find <em>A. schaalii</em> in faeces but shows it to be presents on skin and mucosa in the genital area. <em>A. schaalii</em> is also shown a possible pathogen in the stone-patient group undergoing ESWL.</li>
</ul></div></div>
<div class="section" id="bju11739-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11739-list-0002" class="bullet">
<li>To study the habitat of <em>Actinobaculum schaalii</em> by examing groin swabs, faeces samples and vaginal swabs, and to determine whether it is a common uropathogen in patients with kidney or ureter stones.</li>
</ul></div></div>
<div class="section" id="bju11739-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11739-list-0003" class="bullet">
<li>A quantitative real-time PCR assay was used to analyse all samples, which were collected between 2010 and 2011.</li>
<li>A total of 38 patients (24 men and 14 women), with kidney or ureter stones and undergoing extracorporeal shock wave lithotripsy (ESWL), provided urine samples and had groin swabs taken. In addition, 30 faecal samples and 19 vaginal swabs that had been sent for routine microbiological examinations from patients outside the ESWL group were analysed.</li>
<li>A chi-squared test was used to analyse the differences between patient groups, studying samples from urine, faeces samples, groin swabs and vaginal swabs.</li>
</ul></div></div>
<div class="section" id="bju11739-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11739-list-0004" class="bullet">
<li><em>Actinobaculum schaalii</em> was found in the urine samples from 14 (37%) patients undergoing ESWL, and in both urine and groin swabs from seven (18%) patients.</li>
<li><em>Actinobaculum schaalii</em> was not found in faeces samples but it was found in six (32%) of the vaginal swabs, predominantly in patients &gt;50 years (<em>P</em> = 0.06).</li>
</ul></div></div>
<div class="section" id="bju11739-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11739-list-0005" class="bullet">
<li>The study indicates that <em>A. schaalii</em> is a commensal found on skin, urine and vaginal mucosa in the human urogenital area and supports other investigations in its finding that the elderly are at greatest risk of being colonized with <em>A</em>. <em>schaalii</em>.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Actinobaculum schaalii is considered to be a part of the normai flora in the genital and urinary tract area. It has been associated to urinary tract infection (UTI), sepsis, osteomyelitis, endocarditis and Foumier's gangrene. So far it has mainly been isolated from urine, blood and pus, and predominantly in elderly patients.
This study examined the habitat of A. schaalii by collecting samples from skin and urine in patients with kidney or ureter stones before and after treatment with Extracorporeal Shock Wave Lithotripsy (ESWL). Additionally faeces and vaginal swabs from routine specimen in patients not undergoing ESWL and without known urinary calculi were also analysed.
The study does not find A. schaalii in faeces but shows it to be presents on skin and mucosa in the genital area. A. schaalii is also shown a possible pathogen in the stone-patient group undergoing ESWL.


 Objective

To study the habitat of Actinobaculum schaalii by examing groin swabs, faeces samples and vaginal swabs, and to determine whether it is a common uropathogen in patients with kidney or ureter stones.



Patients and Methods

A quantitative real-time PCR assay was used to analyse all samples, which were collected between 2010 and 2011.
A total of 38 patients (24 men and 14 women), with kidney or ureter stones and undergoing extracorporeal shock wave lithotripsy (ESWL), provided urine samples and had groin swabs taken. In addition, 30 faecal samples and 19 vaginal swabs that had been sent for routine microbiological examinations from patients outside the ESWL group were analysed.
A chi-squared test was used to analyse the differences between patient groups, studying samples from urine, faeces samples, groin swabs and vaginal swabs.



Results

Actinobaculum schaalii was found in the urine samples from 14 (37%) patients undergoing ESWL, and in both urine and groin swabs from seven (18%) patients.
Actinobaculum schaalii was not found in faeces samples but it was found in six (32%) of the vaginal swabs, predominantly in patients &gt;50 years (P = 0.06).



Conclusion

The study indicates that A. schaalii is a commensal found on skin, urine and vaginal mucosa in the human urogenital area and supports other investigations in its finding that the elderly are at greatest risk of being colonized with A. schaalii.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11562.x" xmlns="http://purl.org/rss/1.0/"><title>International online survey: female ejaculation has a positive impact on women's and their partners' sexual lives</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11562.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">International online survey: female ejaculation has a positive impact on women's and their partners' sexual lives</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Florian Wimpissinger, Christopher Springer, Walter Stackl</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:01:09.412511-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11562.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11562.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11562.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Sexual Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11562-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11562-list-1001" class="bullet">
<li>Genital secretions during female orgasm (female ejaculation) have been a matter of controversy for centuries. Scientific work on this essential part of female sexual function has been able to differentiate between female ejaculation, urinary incontinence and vaginal transudate. According to earlier studies, less than 50% of women actually do ejaculate during sexual stimulation. Few affected women discuss female ejaculation with their physician – partly because of its physiological nature, partly through embarrassment.</li>
<li>To gain knowledge on the characteristics of female ejaculation and its impact on women's sexual lives, an online questionnaire has been designed and published internationally. In this way, data from 320 women who perceive ejaculation could be acquired. Most women and their partners perceive female ejaculation as an enrichment of their sexual lives.</li>
</ul></div></div>
<div class="section" id="bju11562-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11562-list-0001" class="bullet">
<li>To study characteristics of female ejaculation as perceived by healthy women.</li>
<li>To evaluate whether fluid emission during sexual activity has an impact on women's or their partners' sexual lives.</li>
</ul></div></div>
<div class="section" id="bju11562-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11562-list-0002" class="bullet">
<li>An online questionnaire consisting of 23 questions addressing the participants' characteristics, aspects of perceived female ejaculation, and its impact on women's and their partners' lives was published internationally on various online platforms.</li>
</ul></div></div>
<div class="section" id="bju11562-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11562-list-0003" class="bullet">
<li>Over a period of 18 months, 320 women from all over the world were included in the study (excluding women below the age of 18 years and double entries).</li>
<li>The women's mean age was 34.1 years (±11.1) and their mean age at first ejaculation was 25.4 years.</li> <li>Most women ejaculate a few times a week. The volume of ejaculation is approximately 2 oz (29.1%), and the fluid is usually clear as water (83.1%).</li>
<li>For most women (78.8%) and their partners (90.0%), female ejaculation is an enrichment of their sexual lives, whereas 14 women (4.4%) stated that their partners were unaware of their potential ejaculation.</li>
</ul></div></div>
<div class="section" id="bju11562-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11562-list-0004" class="bullet">
<li>Perceived female ejaculation – and its onset – occurs in women of all ages.</li>
<li>Most women who ejaculate do so on a regular basis.</li>
<li>Female ejaculation is an enrichment of the sexual lives of women as well as their partners.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Genital secretions during female orgasm (female ejaculation) have been a matter of controversy for centuries. Scientific work on this essential part of female sexual function has been able to differentiate between female ejaculation, urinary incontinence and vaginal transudate. According to earlier studies, less than 50% of women actually do ejaculate during sexual stimulation. Few affected women discuss female ejaculation with their physician – partly because of its physiological nature, partly through embarrassment.
To gain knowledge on the characteristics of female ejaculation and its impact on women's sexual lives, an online questionnaire has been designed and published internationally. In this way, data from 320 women who perceive ejaculation could be acquired. Most women and their partners perceive female ejaculation as an enrichment of their sexual lives.


 Objective

To study characteristics of female ejaculation as perceived by healthy women.
To evaluate whether fluid emission during sexual activity has an impact on women's or their partners' sexual lives.



Materials and Methods

An online questionnaire consisting of 23 questions addressing the participants' characteristics, aspects of perceived female ejaculation, and its impact on women's and their partners' lives was published internationally on various online platforms.



Results

Over a period of 18 months, 320 women from all over the world were included in the study (excluding women below the age of 18 years and double entries).
The women's mean age was 34.1 years (±11.1) and their mean age at first ejaculation was 25.4 years. Most women ejaculate a few times a week. The volume of ejaculation is approximately 2 oz (29.1%), and the fluid is usually clear as water (83.1%).
For most women (78.8%) and their partners (90.0%), female ejaculation is an enrichment of their sexual lives, whereas 14 women (4.4%) stated that their partners were unaware of their potential ejaculation.



Conclusions

Perceived female ejaculation – and its onset – occurs in women of all ages.
Most women who ejaculate do so on a regular basis.
Female ejaculation is an enrichment of the sexual lives of women as well as their partners.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11746.x" xmlns="http://purl.org/rss/1.0/"><title>Effect of melatonin on chronic bladder-ischaemia-associated changes in rat bladder function</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11746.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of melatonin on chronic bladder-ischaemia-associated changes in rat bladder function</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Masanori Nomiya, David Mark Burmeister, Norifumi Sawada, Lysanne Campeau, Mona Zarifpour, Osamu Yamaguchi, Karl-Erik Andersson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T12:00:55.625542-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11746.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11746.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11746.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11746-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11746-list-0001" class="bullet">
<li>There are many studies showing melatonin's potent endogenous free radical scavenging and antioxidative properties, which protect against oxidative insult, but there is no information about the effect of chronic treatment with melatonin on oxidative-stress-related bladder dysfunction caused by chronic ischaemia.</li>
<li>The model used in this study shows that functional and morphological changes caused by chronic bladder ischaemia and oxidative stress were protected by chronic treatment with melatonin, resulting in improvement of bladder hyperactivity.</li>
</ul></div></div>
<div class="section" id="bju11746-sec-1002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11746-list-0002" class="bullet">
<li>To investigate the potential therapeutic benefit of melatonin for chronic ischaemia-related bladder dysfunction.</li>
</ul></div></div>
<div class="section" id="bju11746-sec-1003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11746-list-0003" class="bullet">
<li>Adult male Sprague–Dawley rats were divided into control, arterial injury (AI), AI with low-dose melatonin treatment (AI-ML) and AI with high-dose melatonin treatment (AI-MH) groups. The AI, AI-ML and AI-MH groups underwent a procedure to induce endothelial injury of the iliac arteries and received a 2% cholesterol diet after AI.</li>
<li>The rats in the AI-ML and AI-MH groups were treated with melatonin 2.5 or 20 mg/kg/day orally for 8 weeks after AI. The control group received a regular diet. After 8 weeks, urodynamic investigations were performed.</li>
<li>Bladder tissues and iliac arteries were processed for pharmacological studies, and for immunohistochemical and histological examination.</li>
</ul></div></div>
<div class="section" id="bju11746-sec-1004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11746-list-0004" class="bullet">
<li>Iliac arteries from AI, AI-ML and AI-MH rats displayed neo-intimal formation and luminal occlusion.</li>
<li>In the AI group, the micturition interval was significantly shorter, and bladder capacity and voided volume were lower than in the controls. Contractile responses of bladder strips to KCl, electrical field stimulation and carbachol were significantly lower after AI than in the controls.</li>
<li>The AI bladders were found to have a significantly increased collagen ratio, oxidative stress and inducible nitric oxide synthase (NOS) expression, and decreased constitutive NOS expression compared with the controls.</li>
<li>In the AI-ML and AI-MH groups, neo-intimal formation was not prevented, but there were beneficial effects on bladder function and morphology. In the AI-ML group, the beneficial effects failed to reach statistical significance.</li>
<li>In the AI-MH group, melatonin significantly improved oxidative stress and NOS expression, and there were significant improvements in all the functional and morphological variables compared with the AI group.</li>
</ul></div></div>
<div class="section" id="bju11746-sec-1005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11746-list-0005" class="bullet">
<li>Arterial occlusive disease may lead to chronic bladder ischaemia and bladder hyperactivity associated with oxidative stress.</li>
<li>In the model used, chronic treatment with melatonin protected bladder function and morphology, probably through its free radical scavenging and antioxidative properties.</li>
<li>Melatonin may prevent oxidative damage and improve ischaemia-related bladder dysfunction.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

There are many studies showing melatonin's potent endogenous free radical scavenging and antioxidative properties, which protect against oxidative insult, but there is no information about the effect of chronic treatment with melatonin on oxidative-stress-related bladder dysfunction caused by chronic ischaemia.
The model used in this study shows that functional and morphological changes caused by chronic bladder ischaemia and oxidative stress were protected by chronic treatment with melatonin, resulting in improvement of bladder hyperactivity.


 Objective

To investigate the potential therapeutic benefit of melatonin for chronic ischaemia-related bladder dysfunction.



Materials and Methods

Adult male Sprague–Dawley rats were divided into control, arterial injury (AI), AI with low-dose melatonin treatment (AI-ML) and AI with high-dose melatonin treatment (AI-MH) groups. The AI, AI-ML and AI-MH groups underwent a procedure to induce endothelial injury of the iliac arteries and received a 2% cholesterol diet after AI.
The rats in the AI-ML and AI-MH groups were treated with melatonin 2.5 or 20 mg/kg/day orally for 8 weeks after AI. The control group received a regular diet. After 8 weeks, urodynamic investigations were performed.
Bladder tissues and iliac arteries were processed for pharmacological studies, and for immunohistochemical and histological examination.



Results

Iliac arteries from AI, AI-ML and AI-MH rats displayed neo-intimal formation and luminal occlusion.
In the AI group, the micturition interval was significantly shorter, and bladder capacity and voided volume were lower than in the controls. Contractile responses of bladder strips to KCl, electrical field stimulation and carbachol were significantly lower after AI than in the controls.
The AI bladders were found to have a significantly increased collagen ratio, oxidative stress and inducible nitric oxide synthase (NOS) expression, and decreased constitutive NOS expression compared with the controls.
In the AI-ML and AI-MH groups, neo-intimal formation was not prevented, but there were beneficial effects on bladder function and morphology. In the AI-ML group, the beneficial effects failed to reach statistical significance.
In the AI-MH group, melatonin significantly improved oxidative stress and NOS expression, and there were significant improvements in all the functional and morphological variables compared with the AI group.



Conclusions

Arterial occlusive disease may lead to chronic bladder ischaemia and bladder hyperactivity associated with oxidative stress.
In the model used, chronic treatment with melatonin protected bladder function and morphology, probably through its free radical scavenging and antioxidative properties.
Melatonin may prevent oxidative damage and improve ischaemia-related bladder dysfunction.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11713.x" xmlns="http://purl.org/rss/1.0/"><title>Internet-based treatment of stress urinary incontinence: a randomised controlled study with focus on pelvic floor muscle training</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11713.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Internet-based treatment of stress urinary incontinence: a randomised controlled study with focus on pelvic floor muscle training</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Malin Sjöström, Göran Umefjord, Hans Stenlund, Per Carlbring, Gerhard Andersson, Eva Samuelsson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T11:59:02.522072-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11713.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11713.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11713.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Functional Urology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11713-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11713-list-0001" class="bullet">
<li>Stress urinary incontinence (SUI) affects 10‒35% of women, and it is sometimes very distressful. Pelvic floor exercises are the first line of treatment, but access barriers or embarrassment may prevent women from seeking help. There is a need for new, simple, and effective ways to deliver treatment.</li>
<li>Management of SUI without face-to-face contact is possible, and Internet-based treatment is a new, promising treatment alternative.</li>
</ul></div></div>
<div class="section" id="bju11713-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11713-list-0002" class="bullet">
<li>To compare two treatment programmes for stress urinary incontinence (SUI) without face-to-face contact: one Internet-based and one sent by post.</li>
</ul></div></div> <div class="section" id="bju11713-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11713-list-0003" class="bullet">
<li>Randomised, controlled trial conducted in Sweden 2009–2011. Computer-generated block-randomisation, allocation by independent administrator. No ‘blinding’.</li>
<li>The study included 250 community-dwelling women aged 18–70 years, with SUI ≥1 time/week. Consecutive online recruitment.</li>
<li>The women had 3 months of either; (i) An Internet-based treatment programme (124 women), including e-mail support and cognitive behavioural therapy assignments or (ii) A treatment programme sent by post (126). Both programmes focused mainly on pelvic floor muscle training.</li>
<li>Primary outcomes: symptom-score (International Consultation on Incontinence Questionnaire Short Form, ICIQ-UI SF) and condition-specific quality of life (ICIQ-Lower Urinary Tract Symptoms Quality of Life, ICIQ-LUTSQoL). Secondary outcomes: (i) Patient Global Impression of Improvement, (ii) Incontinence aids, (iii) Patient satisfaction, (iv) Health-specific QoL (EQ5D-Visual Analogue Scale), and (v) Incontinence episode frequency. Follow-up after 4 months via self-assessed postal questionnaires.</li>
</ul></div></div>
<div class="section" id="bju11713-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11713-list-0004" class="bullet">
<li>In all, 12% (30 women) were lost to follow-up. Intention-to-treat analysis showed highly significant improvements (<em>P</em> &lt; 0.001) with large effect sizes (&gt;0.8) with both interventions, but there were no significant differences between groups in primary outcomes. The mean (<span class="smallCaps">sd</span>) changes in symptom-score were: Internet 3.4 (3.4), Postal 2.9 (3.1) (<em>P</em> = 0.27). The mean (<span class="smallCaps">sd</span>) changes in condition-specific QoL were: Internet 4.8 (6.1), Postal 4.6 (6.7) (<em>P</em> = 0.52).</li>
<li>Compared with the postal-group, more participants in the Internet-group perceived they were much or very much improved (40.9% (43/105) vs 26.5% (30/113), <em>P</em> = 0.01), reported reduced usage of incontinence aids (59.5% (47/79) vs 41.4% (34/82), <em>P</em> = 0.02) and were satisfied with the treatment programme (84.8% (89/105) vs 62.9% (71/113), <em>P</em> &lt; 0.001).</li>
<li>Health-specific QoL improved in the Internet-group (mean change 3.7 (10.9), <em>P</em> = 0.001), but not in the postal-group (1.9 (13.0), <em>P</em> = 0.13).</li>
<li>Overall, 69.8% (120/172) of participants reported complete lack of leakage or reduced number of leakage episodes by &gt;50%.</li>
</ul></div></div>
<div class="section" id="bju11713-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11713-list-0005" class="bullet">
<li>Concerning primary outcomes, treatment effects were similar between groups whereas for secondary outcomes the Internet-based treatment was more effective.</li>
<li>Internet-based treatment for SUI is a new, promising treatment alternative.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Stress urinary incontinence (SUI) affects 10‒35% of women, and it is sometimes very distressful. Pelvic floor exercises are the first line of treatment, but access barriers or embarrassment may prevent women from seeking help. There is a need for new, simple, and effective ways to deliver treatment.
Management of SUI without face-to-face contact is possible, and Internet-based treatment is a new, promising treatment alternative.


 Objective

To compare two treatment programmes for stress urinary incontinence (SUI) without face-to-face contact: one Internet-based and one sent by post.

 
Patients and Methods

Randomised, controlled trial conducted in Sweden 2009–2011. Computer-generated block-randomisation, allocation by independent administrator. No ‘blinding’.
The study included 250 community-dwelling women aged 18–70 years, with SUI ≥1 time/week. Consecutive online recruitment.
The women had 3 months of either; (i) An Internet-based treatment programme (124 women), including e-mail support and cognitive behavioural therapy assignments or (ii) A treatment programme sent by post (126). Both programmes focused mainly on pelvic floor muscle training.
Primary outcomes: symptom-score (International Consultation on Incontinence Questionnaire Short Form, ICIQ-UI SF) and condition-specific quality of life (ICIQ-Lower Urinary Tract Symptoms Quality of Life, ICIQ-LUTSQoL). Secondary outcomes: (i) Patient Global Impression of Improvement, (ii) Incontinence aids, (iii) Patient satisfaction, (iv) Health-specific QoL (EQ5D-Visual Analogue Scale), and (v) Incontinence episode frequency. Follow-up after 4 months via self-assessed postal questionnaires.



Results

In all, 12% (30 women) were lost to follow-up. Intention-to-treat analysis showed highly significant improvements (P &lt; 0.001) with large effect sizes (&gt;0.8) with both interventions, but there were no significant differences between groups in primary outcomes. The mean (sd) changes in symptom-score were: Internet 3.4 (3.4), Postal 2.9 (3.1) (P = 0.27). The mean (sd) changes in condition-specific QoL were: Internet 4.8 (6.1), Postal 4.6 (6.7) (P = 0.52).
Compared with the postal-group, more participants in the Internet-group perceived they were much or very much improved (40.9% (43/105) vs 26.5% (30/113), P = 0.01), reported reduced usage of incontinence aids (59.5% (47/79) vs 41.4% (34/82), P = 0.02) and were satisfied with the treatment programme (84.8% (89/105) vs 62.9% (71/113), P &lt; 0.001).
Health-specific QoL improved in the Internet-group (mean change 3.7 (10.9), P = 0.001), but not in the postal-group (1.9 (13.0), P = 0.13).
Overall, 69.8% (120/172) of participants reported complete lack of leakage or reduced number of leakage episodes by &gt;50%.



Conclusions

Concerning primary outcomes, treatment effects were similar between groups whereas for secondary outcomes the Internet-based treatment was more effective.
Internet-based treatment for SUI is a new, promising treatment alternative.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11666.x" xmlns="http://purl.org/rss/1.0/"><title>Chromosomal instability and bladder cancer: the UroVysionTM test in the UroScreen study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11666.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Chromosomal instability and bladder cancer: the UroVysionTM test in the UroScreen study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nadine Bonberg, Dirk Taeger, Katarzyna Gawrych, Georg Johnen, Séverine Banek, Christian Schwentner, Karl-Dietrich Sievert, Harald Wellhäußer, Matthias Kluckert, Gabriele Leng, Michael Nasterlack, Arnulf Stenzl, Thomas Behrens, Thomas Brüning, Beate Pesch, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T11:58:59.997275-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11666.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11666.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11666.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11666-sec-0014" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11666-list-0001" class="bullet">
<li>UroVysion™ is a multicolour fluorescence <em>in situ</em> hybridisation assay that detects DNA gain at chromosomes 3, 7 and 17 and loss at the 9p21 locus in exfoliated urothelial cells. This cell-based test is time-consuming and costly compared with voided urine cytology or other molecular markers for the early detection of bladder cancer.</li>
<li>We determined copy number changes at chromosomes 3, 7 and 17 and at the 9p21 locus with UroVysion in a prospective screening study among chemical workers. Strong correlations between DNA gains yield a similar performance in detecting bladder cancer with just one of the probes for chromosomes 3, 7 or 17 instead of all, supporting the development of a simpler and cheaper assay.</li>
</ul></div></div>
<div class="section" id="bju11666-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11666-list-0002" class="bullet">
<li>To explore changes at chromosomes 3, 7, 17 and 9p21 in order to assess associations with bladder cancer for possible improvements of the UroVysion™ assay regarding screening.</li>
</ul></div></div>
<div class="section" id="bju11666-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Subjects and Methods</h4><div class="para"><ul id="bju11666-list-0003" class="bullet">
<li>In all, 1609 men took part in the prospective study UroScreen. Annual screening for bladder cancer was offered to male chemical workers with former exposure to aromatic amines as a voluntary surveillance programme between 2003 and 2010.</li>
<li>In all, 191 434 cells in 6517 UroVysion tests were analysed for copy number variations (CNV) at chromosome 3, 7, 17 (gains) and 9p21 (deletions) in 1595 men.</li>
<li>We assessed CNVs at single or multiple loci using polysomy indices (PIs, called multiple PI and PI 3, PI 7 and PI 17).</li>
<li>We calculated Spearman's rank correlation coefficients (r<sub>s</sub>) between these PIs and receiver operating characteristic (ROC) curves with areas under the curves (AUCs). We applied Cox regression to estimate hazard ratios (HRs) to assess the risk of developing bladder cancer.</li>
</ul></div></div>
<div class="section" id="bju11666-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11666-list-0004" class="bullet">
<li>Nine out of 21 bladder tumours detected in 20 participants (‘cases’) had a positive UroVysion test, including seven high-grade carcinomas and seven overlapping results with a positive cytology. Four cases with negative test results did not attend screening annually.</li>
<li>No case was found because of a complete loss of 9p21 in at least 12 cells.</li>
<li>There were strong correlations between pairwise combinations of gains at chromosome 3, 7 or 17, ranging between r<sub>s</sub> = 0.98 and r<sub>s</sub> = 0.99 in cases and between r<sub>s</sub> = 0.84 and r<sub>s</sub> = 0.88 in non-cases (<em>P</em> &lt; 0.001). Associations were less pronounced with CNVs at 9p21 among cases and were lacking in non-cases.</li>
<li>Estimates of the relative risk of DNA gain for developing a bladder tumour assessed with PIs (threshold 10% of cells) were 47.7 (95% confidence interval [CI] 18.3–124.1) for the multiple PI, 44.5 (95%CI 16.5–119.9) for PI 3, 34.7 (95%CI 13.1–92.1) for PI 7 and 52.4 (95%CI 20.7–132.6) for PI 17, as well as 7.9 (95%CI 3.0–20.6) for a complete loss of 9p21 (threshold 2.5% of cells), respectively.</li>
<li>ROC analyses showed similar AUCs for multiple PI compared with PIs of single chromosomes 3, 7 and 17 (all AUCs between 0.79 and 0.80) and a lower AUC for a homozygous loss of 9p21 (AUC 0.72).</li>
</ul></div></div>
<div class="section" id="bju11666-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11666-list-0005" class="bullet">
<li>The UroVysion assay showed a reasonable performance in detecting bladder cancer in the present study population and shared positive test results with cytology, which is much cheaper.</li>
<li>A simpler, faster and cheaper version of the UroVysion assay might rely on the very strong correlations between gains at chromosomes 3, 7 and 17, resulting in a similar performance in detecting bladder cancer with single-probe PIs compared with the full set of these probes.</li>
<li>Loss of 9p21 was less predictive for developing bladder cancer in UroScreen.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

UroVysion™ is a multicolour fluorescence in situ hybridisation assay that detects DNA gain at chromosomes 3, 7 and 17 and loss at the 9p21 locus in exfoliated urothelial cells. This cell-based test is time-consuming and costly compared with voided urine cytology or other molecular markers for the early detection of bladder cancer.
We determined copy number changes at chromosomes 3, 7 and 17 and at the 9p21 locus with UroVysion in a prospective screening study among chemical workers. Strong correlations between DNA gains yield a similar performance in detecting bladder cancer with just one of the probes for chromosomes 3, 7 or 17 instead of all, supporting the development of a simpler and cheaper assay.


 Objective

To explore changes at chromosomes 3, 7, 17 and 9p21 in order to assess associations with bladder cancer for possible improvements of the UroVysion™ assay regarding screening.



Subjects and Methods

In all, 1609 men took part in the prospective study UroScreen. Annual screening for bladder cancer was offered to male chemical workers with former exposure to aromatic amines as a voluntary surveillance programme between 2003 and 2010.
In all, 191 434 cells in 6517 UroVysion tests were analysed for copy number variations (CNV) at chromosome 3, 7, 17 (gains) and 9p21 (deletions) in 1595 men.
We assessed CNVs at single or multiple loci using polysomy indices (PIs, called multiple PI and PI 3, PI 7 and PI 17).
We calculated Spearman's rank correlation coefficients (rs) between these PIs and receiver operating characteristic (ROC) curves with areas under the curves (AUCs). We applied Cox regression to estimate hazard ratios (HRs) to assess the risk of developing bladder cancer.



Results

Nine out of 21 bladder tumours detected in 20 participants (‘cases’) had a positive UroVysion test, including seven high-grade carcinomas and seven overlapping results with a positive cytology. Four cases with negative test results did not attend screening annually.
No case was found because of a complete loss of 9p21 in at least 12 cells.
There were strong correlations between pairwise combinations of gains at chromosome 3, 7 or 17, ranging between rs = 0.98 and rs = 0.99 in cases and between rs = 0.84 and rs = 0.88 in non-cases (P &lt; 0.001). Associations were less pronounced with CNVs at 9p21 among cases and were lacking in non-cases.
Estimates of the relative risk of DNA gain for developing a bladder tumour assessed with PIs (threshold 10% of cells) were 47.7 (95% confidence interval [CI] 18.3–124.1) for the multiple PI, 44.5 (95%CI 16.5–119.9) for PI 3, 34.7 (95%CI 13.1–92.1) for PI 7 and 52.4 (95%CI 20.7–132.6) for PI 17, as well as 7.9 (95%CI 3.0–20.6) for a complete loss of 9p21 (threshold 2.5% of cells), respectively.
ROC analyses showed similar AUCs for multiple PI compared with PIs of single chromosomes 3, 7 and 17 (all AUCs between 0.79 and 0.80) and a lower AUC for a homozygous loss of 9p21 (AUC 0.72).



Conclusions

The UroVysion assay showed a reasonable performance in detecting bladder cancer in the present study population and shared positive test results with cytology, which is much cheaper.
A simpler, faster and cheaper version of the UroVysion assay might rely on the very strong correlations between gains at chromosomes 3, 7 and 17, resulting in a similar performance in detecting bladder cancer with single-probe PIs compared with the full set of these probes.
Loss of 9p21 was less predictive for developing bladder cancer in UroScreen.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11602.x" xmlns="http://purl.org/rss/1.0/"><title>Differing risk of cancer death among patients with lymph node metastasis after radical prostatectomy and pelvic lymph node dissection: identification of risk categories according to number of positive nodes and Gleason score</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11602.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Differing risk of cancer death among patients with lymph node metastasis after radical prostatectomy and pelvic lymph node dissection: identification of risk categories according to number of positive nodes and Gleason score</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Riccardo Schiavina, Marco Borghesi, Eugenio Brunocilla, Fabio Manferrari, Michelangelo Fiorentino, Valerio Vagnoni, Alessandro Baccos, Cristian Vincenzo Pultrone, Giovanni Christian Rocca, Simona Rizzi, Giuseppe Martorana</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-17T11:47:51.282744-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11602.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11602.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11602.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11602-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11602-list-1001" class="bullet">
<li>Lymph node (LN) status is one of the most important prognostic variables in patients undergoing radical prostatectomy, but not all patients with node-positive PCa are at the same risk of recurrence and cancer-specific death.</li>
<li>In this study we evaluated the role of pathological variables in stratifying the risk of cancer death in patients with prostate cancer. Patients with 1–3 positive LNs and Gleason score (GS) ≤7 experienced better CSS and OS than those with &gt;3 metastatic LNs and/or GS &gt;7. This evidence could allow urologists to better predict oncological outcomes of patients and select more appropriate therapeutic management.</li>
</ul></div></div>
<div class="section" id="bju11602-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11602-list-0001" class="bullet">
<li>To evaluate the outcomes in patients with node-positive prostate cancer (PCa) after radical prostatectomy (RP) and pelvic lymph node dissection (PLND) according to the number of positive lymph nodes (LNs).</li>
<li>To identify different risk groups among patients with node-positive PCa.</li>
</ul></div></div>
<div class="section" id="bju11602-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11602-list-0002" class="bullet">
<li>We evaluated 98 consecutive patients with pN1M0 PCa who underwent RP between November 1995 and May 2011.</li>
<li>Kaplan–Meier and Cox proportional univariable and multivariable regression models were used to analyse the survival rates.</li>
<li>Patients were divided into two groups according to number of positive LNs using the most informative positive LN theshold for predicting survival, then into three different risk groups according to number of positive LNs and pathological Gleason score (GS).</li>
</ul></div></div>
<div class="section" id="bju11602-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11602-list-0003" class="bullet">
<li>Mean (range) follow-up was 68.4 (10–192) months.</li>
<li>Patients with 1–3 positive LNs (<em>n</em> = 75; 76.5%) had significantly better cancer-specific survival (CSS) and overall survival (OS) compared with those with &gt;3 positive nodes (<em>n</em> = 23; 23.4%; <em>P</em> &lt; 0.01).</li>
<li>Patients with 1–3 positive LNs and pathological GS ≤7 (Group 1) had significantly better CSS than those with &gt;3 positive LNs or GS 8–10 (Group 2 [<em>P</em> = 0.015]). Group 2 patients, moreover, had significantly better CSS (<em>P</em> = 0.019) and OS (<em>P</em> = 0.021) than those with &gt;3 positive LNs and GS 8–10 (Group 3).</li>
</ul></div></div>
<div class="section" id="bju11602-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11602-list-0004" class="bullet">
<li>Patients with 1–3 positive LNs have higher CSS and OS rates than those with &gt;3 metastatic LNs.</li>
<li>Taking into account the pathological GS, as well as the number of positive nodes, three risk group categories with considerable differences in terms of survival can be found. Patients with LN-positive PCa should be stratified into different groups according to these two measures, to obtain a better prediction of oncological outcomes.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Lymph node (LN) status is one of the most important prognostic variables in patients undergoing radical prostatectomy, but not all patients with node-positive PCa are at the same risk of recurrence and cancer-specific death.
In this study we evaluated the role of pathological variables in stratifying the risk of cancer death in patients with prostate cancer. Patients with 1–3 positive LNs and Gleason score (GS) ≤7 experienced better CSS and OS than those with &gt;3 metastatic LNs and/or GS &gt;7. This evidence could allow urologists to better predict oncological outcomes of patients and select more appropriate therapeutic management.


 Objectives

To evaluate the outcomes in patients with node-positive prostate cancer (PCa) after radical prostatectomy (RP) and pelvic lymph node dissection (PLND) according to the number of positive lymph nodes (LNs).
To identify different risk groups among patients with node-positive PCa.



Patients and Methods

We evaluated 98 consecutive patients with pN1M0 PCa who underwent RP between November 1995 and May 2011.
Kaplan–Meier and Cox proportional univariable and multivariable regression models were used to analyse the survival rates.
Patients were divided into two groups according to number of positive LNs using the most informative positive LN theshold for predicting survival, then into three different risk groups according to number of positive LNs and pathological Gleason score (GS).



Results

Mean (range) follow-up was 68.4 (10–192) months.
Patients with 1–3 positive LNs (n = 75; 76.5%) had significantly better cancer-specific survival (CSS) and overall survival (OS) compared with those with &gt;3 positive nodes (n = 23; 23.4%; P &lt; 0.01).
Patients with 1–3 positive LNs and pathological GS ≤7 (Group 1) had significantly better CSS than those with &gt;3 positive LNs or GS 8–10 (Group 2 [P = 0.015]). Group 2 patients, moreover, had significantly better CSS (P = 0.019) and OS (P = 0.021) than those with &gt;3 positive LNs and GS 8–10 (Group 3).



Conclusions

Patients with 1–3 positive LNs have higher CSS and OS rates than those with &gt;3 metastatic LNs.
Taking into account the pathological GS, as well as the number of positive nodes, three risk group categories with considerable differences in terms of survival can be found. Patients with LN-positive PCa should be stratified into different groups according to these two measures, to obtain a better prediction of oncological outcomes.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11664.x" xmlns="http://purl.org/rss/1.0/"><title>Positive surgical margins and their locations in specimens are adverse prognosis features after radical cystectomy in non-metastatic carcinoma invading bladder muscle: results from a nationwide case–control study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11664.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Positive surgical margins and their locations in specimens are adverse prognosis features after radical cystectomy in non-metastatic carcinoma invading bladder muscle: results from a nationwide case–control study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yann Neuzillet, Michel Soulie, Stéphane Larre, Morgan Roupret, Guillaume Defortescu, Thibaut Murez, Géraldine Pignot, Aurélien Descazeaud, Jean-Jacques Patard, Pierre Bigot, Laurent Salomon, Pierre Colin, Jérôme Rigaud, Cyrille Bastide, Xavier Durand, Antoine Valeri, François Kleinclauss, Franck Bruyere, Christian Pfister, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-17T11:45:33.466258-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11664.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11664.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11664.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11664-sec-1001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11664-list-0001" class="bullet">
<li>Positive surgical margin (PSM) frequency after radical cystectomy has been estimated to be 4–15%. Studies that have not distinguished between the different sites of PSM have failed to show that they are an independent prognostic factor for disease-free survival. Only perivesical soft tissue PSMs have been associated with an increased risk of cancer recurrence and cancer-specific death.</li>
<li>This is the first comprehensive published analysis of PSMs occurring during radical cystectomy for pTx pN0 M0 bladder cancer according to their location, comparing their cancer-specific survival (CSS) and other outcomes with those of a control group paired according to TNM status, age, sex and urinary diversion method. Local recurrence-free survival rates were found to be lower in patients with both soft tissue and urethral PSMs. Moreover, soft-tissue PSMs were associated with lower metastatic recurrence-free and CSS rates.</li>
</ul></div></div>
<div class="section" id="bju11664-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11664-list-0002" class="bullet">
<li>To compare the prognoses associated with positive surgical margins (PSMs) according to their urethral, ureteric and/or soft tissue locations in patients with pN0 M0 bladder cancer who have not undergone neoadjuvant chemotherapy.</li>
</ul></div></div>
<div class="section" id="bju11664-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11664-list-0003" class="bullet">
<li>A retrospective, case–control study was conducted between 1991 and 2011 using data from 17 academic centres in France.</li>
<li>A total of 154 patients (cases) with PSMs met the eligibility criteria and were matched according to centre, pT stage, gender, age and urinary diversion method with a population-based sample of 154 patients (controls) from 3651 patients who had undergone cystectomies.</li>
<li>The median follow-up period was 23.9 months.</li>
<li>Multivariable Cox regression analysis was used to test the effects of PSMs on local recurrence (LR)-free survival, metastatic recurrence (MR)-free survival and cancer-specific survival (CSS).</li>
</ul></div></div>
<div class="section" id="bju11664-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11664-list-0004" class="bullet">
<li>The 5-year LR-free survival and CSS rates of patients with urethral and soft tissue PSMs were lower than those in the control group.</li>
<li>A significant decrease in CSS was associated with soft tissue PSMs (<em>P =</em> 0.003, odds ratio = 0.425, 95% confidence interval 0.283–0.647). The prognosis was not affected in cases of ureteric PSMs.</li>
</ul></div></div>
<div class="section" id="bju11664-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11664-list-0005" class="bullet">
<li>Soft tissue PSMs were associated with poor CSS rates in patients with pN0 M0 bladder cancer.</li>
<li>A correlation between urethrectomy and a reduction of the risk of LR in a urethral PSM setting was observed.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Positive surgical margin (PSM) frequency after radical cystectomy has been estimated to be 4–15%. Studies that have not distinguished between the different sites of PSM have failed to show that they are an independent prognostic factor for disease-free survival. Only perivesical soft tissue PSMs have been associated with an increased risk of cancer recurrence and cancer-specific death.
This is the first comprehensive published analysis of PSMs occurring during radical cystectomy for pTx pN0 M0 bladder cancer according to their location, comparing their cancer-specific survival (CSS) and other outcomes with those of a control group paired according to TNM status, age, sex and urinary diversion method. Local recurrence-free survival rates were found to be lower in patients with both soft tissue and urethral PSMs. Moreover, soft-tissue PSMs were associated with lower metastatic recurrence-free and CSS rates.


 Objective

To compare the prognoses associated with positive surgical margins (PSMs) according to their urethral, ureteric and/or soft tissue locations in patients with pN0 M0 bladder cancer who have not undergone neoadjuvant chemotherapy.



Patients and Methods

A retrospective, case–control study was conducted between 1991 and 2011 using data from 17 academic centres in France.
A total of 154 patients (cases) with PSMs met the eligibility criteria and were matched according to centre, pT stage, gender, age and urinary diversion method with a population-based sample of 154 patients (controls) from 3651 patients who had undergone cystectomies.
The median follow-up period was 23.9 months.
Multivariable Cox regression analysis was used to test the effects of PSMs on local recurrence (LR)-free survival, metastatic recurrence (MR)-free survival and cancer-specific survival (CSS).



Results

The 5-year LR-free survival and CSS rates of patients with urethral and soft tissue PSMs were lower than those in the control group.
A significant decrease in CSS was associated with soft tissue PSMs (P = 0.003, odds ratio = 0.425, 95% confidence interval 0.283–0.647). The prognosis was not affected in cases of ureteric PSMs.



Conclusions

Soft tissue PSMs were associated with poor CSS rates in patients with pN0 M0 bladder cancer.
A correlation between urethrectomy and a reduction of the risk of LR in a urethral PSM setting was observed.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11650.x" xmlns="http://purl.org/rss/1.0/"><title>Laparoscopic pelvic lymph node dissection system based on preoperative primary tumour stage (T stage) by computed tomography in urothelial bladder cancer: results of a single-institution prospective study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11650.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Laparoscopic pelvic lymph node dissection system based on preoperative primary tumour stage (T stage) by computed tomography in urothelial bladder cancer: results of a single-institution prospective study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jun-Bin Yuan, Xiong-Bing Zu, Jian-Guang Miao, Jun Wang, Min-Feng Chen, Lin Qi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T21:07:40.816506-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11650.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11650.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11650.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Robotics and Laparoscopy</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11650-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11650-list-1001" class="bullet">
<li>Bladder cancer (BC) is a public health problem throughout the world, and now radical cystectomy (RC) has been introduced as a standard treatment for BC invading muscle and some BCs not invading muscle. Pelvic lymph node dissection (PLND) is considered an integral part of RC for its prognostic and therapeutic significance, but the extent of the PLND has not been precisely defined.</li>
<li>Computed tomography is considered one of the most preferable methods to assess the BC stage preoperatively because of its high sensitivity and specificity. However, there are few articles referring to CT as an aid in deciding the extent of lymphadenectomy during RC.</li>
<li>In the present study, we prospectively studied the clinical value of preoperative CT staging of primary tumours in deciding the extent of PLND during laparoscopic RC in the management of BC. The preliminary findings suggested that all patients with higher preoperative CT stage should be given super-extended PLND during RC. For those with lower CT stage, careful and thorough clearance of all lymphatic and adipose tissues within the true pelvis could be more helpful than super-extended PLND.</li>
</ul></div></div>
<div class="section" id="bju11650-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11650-list-0001" class="bullet">
<li>To study prospectively the clinical value of preoperative spiral computed tomography (CT) staging of primary tumours in deciding the extent of pelvic lymph node dissection (PLND) during laparoscopic radical cystectomy (RC) in the management of bladder cancer (BC).</li>
</ul></div></div>
<div class="section" id="bju11650-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11650-list-0002" class="bullet">
<li>Between January 2010 and December 2011, a total of 63 patients with urothelial BC received laparoscopic RC, super-extended PLND and ileac conduit.</li>
<li>The super-extended PLND removed all lymphatic tissues in the boundaries at the level of the inferior mesenteric origin from the aorta (cephalad), the pelvic floor (distally), the genitofemoral nerve (laterally) and the sacral promontory (posteriorly).</li>
<li>All of the operations were performed by one experienced surgeon, and all harvested lymph nodes were submitted separately.</li>
<li>CT was used to evaluate the preoperative CT stage (CTx) of each primary bladder tumour.</li>
</ul></div></div>
<div class="section" id="bju11650-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11650-list-0003" class="bullet">
<li>All patients were divided into five categories according to their CTx stages: three at CT1, seven at CT2a, 38 at CT2b, seven at CT3b, and eight at CT4a.</li>
<li>All 63 procedures were completed successfully without any conversion to open surgery. The mean estimated blood loss was 450 mL, and 14 patients (22.2%) had postoperative lymphatic leakage.</li>
<li>Each case was pathologically confirmed as transitional cell carcinoma with negative margins at the urethral and ureteric stumps.</li>
<li>None of the patients with a low CTx stage (CT1–CT2a) had positive lymph nodes above the level of the common iliac artery bifurcation.</li>
<li>There was no jump lymph node metastasis, and no positive lymph node was detected above the level of aortic bifurcation in all cases.</li>
</ul></div></div>
<div class="section" id="bju11650-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><ul id="bju11650-list-0004" class="bullet">
<li>Based on the preoperative CT staging, urological surgeons can determine the boundaries of PLND to reduce intraoperative injury and postoperative complications in patients with BC, especially those at the lower CTx stages (CT1 and CT2a).</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Bladder cancer (BC) is a public health problem throughout the world, and now radical cystectomy (RC) has been introduced as a standard treatment for BC invading muscle and some BCs not invading muscle. Pelvic lymph node dissection (PLND) is considered an integral part of RC for its prognostic and therapeutic significance, but the extent of the PLND has not been precisely defined.
Computed tomography is considered one of the most preferable methods to assess the BC stage preoperatively because of its high sensitivity and specificity. However, there are few articles referring to CT as an aid in deciding the extent of lymphadenectomy during RC.
In the present study, we prospectively studied the clinical value of preoperative CT staging of primary tumours in deciding the extent of PLND during laparoscopic RC in the management of BC. The preliminary findings suggested that all patients with higher preoperative CT stage should be given super-extended PLND during RC. For those with lower CT stage, careful and thorough clearance of all lymphatic and adipose tissues within the true pelvis could be more helpful than super-extended PLND.


 Objective

To study prospectively the clinical value of preoperative spiral computed tomography (CT) staging of primary tumours in deciding the extent of pelvic lymph node dissection (PLND) during laparoscopic radical cystectomy (RC) in the management of bladder cancer (BC).



Patients and Methods

Between January 2010 and December 2011, a total of 63 patients with urothelial BC received laparoscopic RC, super-extended PLND and ileac conduit.
The super-extended PLND removed all lymphatic tissues in the boundaries at the level of the inferior mesenteric origin from the aorta (cephalad), the pelvic floor (distally), the genitofemoral nerve (laterally) and the sacral promontory (posteriorly).
All of the operations were performed by one experienced surgeon, and all harvested lymph nodes were submitted separately.
CT was used to evaluate the preoperative CT stage (CTx) of each primary bladder tumour.



Results

All patients were divided into five categories according to their CTx stages: three at CT1, seven at CT2a, 38 at CT2b, seven at CT3b, and eight at CT4a.
All 63 procedures were completed successfully without any conversion to open surgery. The mean estimated blood loss was 450 mL, and 14 patients (22.2%) had postoperative lymphatic leakage.
Each case was pathologically confirmed as transitional cell carcinoma with negative margins at the urethral and ureteric stumps.
None of the patients with a low CTx stage (CT1–CT2a) had positive lymph nodes above the level of the common iliac artery bifurcation.
There was no jump lymph node metastasis, and no positive lymph node was detected above the level of aortic bifurcation in all cases.



Conclusion

Based on the preoperative CT staging, urological surgeons can determine the boundaries of PLND to reduce intraoperative injury and postoperative complications in patients with BC, especially those at the lower CTx stages (CT1 and CT2a).


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11661.x" xmlns="http://purl.org/rss/1.0/"><title>Do differences in clinical symptoms and referral patterns contribute to the gender gap in bladder cancer?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11661.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Do differences in clinical symptoms and referral patterns contribute to the gender gap in bladder cancer?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Armin Henning, Marlies Wehrberger, Stephan Madersbacher, Armin Pycha, Thomas Martini, Evi Comploj, Klaus Jeschke, Christian Tripolt, Michael Rauchenwald</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-15T08:01:56.77174-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11661.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11661.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11661.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11661-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11661-list-0001" class="bullet">
<li>Urothelial carcinoma of the bladder (UCB) is more prevalent in men than women; however, in women the tumour stage is generally more advanced at the time of the diagnosis and the prognosis is worse. Possible explanations include anatomical, genetic and socio-economic factors.</li>
<li>The study shows that clinical symptoms before the first-time diagnosis of UCB did not differ between the sexes, while primary care and referral patterns did. Women were more likely to receive symptomatic treatment or therapies for alleged UTIs without further investigation or referral to urological evaluation. The study highlights the fact that there may be a diagnostic delay in women which could contribute to the gender-dependent disparities in stage distribution and prognosis of UCB.</li>
</ul></div></div>
<div class="section" id="bju11661-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11661-list-0002" class="bullet">
<li>To evaluate gender-dependent disparities regarding clinical symptoms, referral patterns or treatments before diagnosis of urothelial carcinoma of the bladder (UCB).</li>
</ul></div></div> <div class="section" id="bju11661-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11661-list-0003" class="bullet">
<li>A consecutive series of patients with newly diagnosed UCB completed a questionnaire at the time of admission for elective transurethral resection of a bladder tumour (TURBT).</li> <li>The questionnaire surveyed the presence of haematuria, dysuria, urgency and bladder pain as well as the number of consultations and treatments before urological evaluation.</li> <li>Tumour characteristics, clinical symptoms, treatments and referrals were compared between men and women in the patient series.</li>
</ul></div></div>
<div class="section" id="bju11661-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11661-list-0004" class="bullet">
<li>In men (<em>n</em> = 130) the distribution of tumour stages was pTa 62.3%, pT1 23.1% and pT ≥ 2 12.3%. The respective percentages in women (<em>n</em> = <em>38</em>) were pTa 57.9%, pT1 23.7% and pT ≥ 2 18.4% (<em>P</em> &gt; 0.05).</li> <li>The prevalence of clinical symptoms in men vs women was as follows: gross haematuria 65 vs 68%, dysuria 32 vs 44%, urgency 61 vs 47%, and nocturia 57 vs 66%, respectively (<em>P</em> &gt; 0.05).</li> <li>A total of 78% of men vs 55% of women directly consulted a urologist (<em>P</em> &lt; 0.05).</li> <li>Symptomatic treatment for voiding disorders/pain was given without further evaluation to 19% of men vs 47% of women 1 year before the diagnosis of UCB (<em>P</em> &lt; 0.05).</li> <li>A total of 3.8% of men vs 15.8% of women received three or more treatments for urinary tract infections (UTIs) within the same time period (<em>P</em> &lt; 0.05).</li>
</ul></div></div> <div class="section" id="bju11661-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11661-list-0005" class="bullet">
<li>In the present study there were no gender-related differences in clinical symptoms of UCB, but women were more likely to be treated for voiding complaints or alleged UTIs without further evaluation or referral to urology than men.</li>
<li>Gender-dependent disparities in referral patterns exist and might delay definitive diagnosis of UCB in women.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Urothelial carcinoma of the bladder (UCB) is more prevalent in men than women; however, in women the tumour stage is generally more advanced at the time of the diagnosis and the prognosis is worse. Possible explanations include anatomical, genetic and socio-economic factors.
The study shows that clinical symptoms before the first-time diagnosis of UCB did not differ between the sexes, while primary care and referral patterns did. Women were more likely to receive symptomatic treatment or therapies for alleged UTIs without further investigation or referral to urological evaluation. The study highlights the fact that there may be a diagnostic delay in women which could contribute to the gender-dependent disparities in stage distribution and prognosis of UCB.


 Objective

To evaluate gender-dependent disparities regarding clinical symptoms, referral patterns or treatments before diagnosis of urothelial carcinoma of the bladder (UCB).

 
Patients and Methods

A consecutive series of patients with newly diagnosed UCB completed a questionnaire at the time of admission for elective transurethral resection of a bladder tumour (TURBT). The questionnaire surveyed the presence of haematuria, dysuria, urgency and bladder pain as well as the number of consultations and treatments before urological evaluation. Tumour characteristics, clinical symptoms, treatments and referrals were compared between men and women in the patient series.



Results

In men (n = 130) the distribution of tumour stages was pTa 62.3%, pT1 23.1% and pT ≥ 2 12.3%. The respective percentages in women (n = 38) were pTa 57.9%, pT1 23.7% and pT ≥ 2 18.4% (P &gt; 0.05). The prevalence of clinical symptoms in men vs women was as follows: gross haematuria 65 vs 68%, dysuria 32 vs 44%, urgency 61 vs 47%, and nocturia 57 vs 66%, respectively (P &gt; 0.05). A total of 78% of men vs 55% of women directly consulted a urologist (P &lt; 0.05). Symptomatic treatment for voiding disorders/pain was given without further evaluation to 19% of men vs 47% of women 1 year before the diagnosis of UCB (P &lt; 0.05). A total of 3.8% of men vs 15.8% of women received three or more treatments for urinary tract infections (UTIs) within the same time period (P &lt; 0.05).

 
Conclusions

In the present study there were no gender-related differences in clinical symptoms of UCB, but women were more likely to be treated for voiding complaints or alleged UTIs without further evaluation or referral to urology than men.
Gender-dependent disparities in referral patterns exist and might delay definitive diagnosis of UCB in women.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11648.x" xmlns="http://purl.org/rss/1.0/"><title>Clinical implications of family history of prostate cancer and genetic risk single nucleotide polymorphism (SNP) profiles in an active surveillance cohort</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11648.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clinical implications of family history of prostate cancer and genetic risk single nucleotide polymorphism (SNP) profiles in an active surveillance cohort</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chee L. Goh, Edward J. Saunders, Daniel A. Leongamornlert, Malgorzata Tymrakiewicz, Karen Thomas, Elizabeth D. Selvadurai, Ruth Woode-Amissah, Tokhir Dadaev, Nadiya Mahmud, Elena Castro, David Olmos, Michelle Guy, Koveela Govindasami, Lynne T. O'Brien, Amanda L. Hall, Rosemary A. Wilkinson, Emma J. Sawyer, Ali Amin Al Olama, Douglas F. Easton, Zsofia Kote-Jarai, Chris C. Parker, Rosalind A. Eeles</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-15T08:01:53.641894-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11648.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11648.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11648.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Translational Science</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11648-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11648-list-1001" class="bullet">
<li>Family history (FH) is a major risk factor for the development of prostate cancer. The search for genetic variants has led to genome-wide association studies (GWAS), which have so far reported 47 susceptibility loci that predispose men to prostate cancer. However, the use of genetics or FH status in predicting clinical outcomes after prostate cancer diagnosis remains uncertain. Guidelines currently exist for clinicians and patients summarising evidence relating to the best outcomes of different prostate cancer treatment methods. Genetics and FH could potentially add to this stratification.</li>
<li>Our study aimed to ascertain the potential prognostic roles of FH or genetic risk scores in patients managed by active surveillance.</li>
</ul></div></div>
<div class="section" id="bju11648-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><ul id="bju11648-list-0001" class="bullet">
<li>To explore the potential prognostic role of family history (FH) of prostate cancer and prostate cancer risk single nucleotide polymorphisms (SNPs) in patients undergoing active surveillance (AS) for prostate cancer.</li>
<li>This is the first study to date, which has investigated the potential prognostic role of SNP profiles in an AS cohort</li>
</ul></div></div>
<div class="section" id="bju11648-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11648-list-0002" class="bullet">
<li>FH data were collected from patients in the Royal Marsden Hospital AS study.</li>
<li>In all, 39 prostate cancer-risk SNPs identified from published genome wide association studies (GWAS) were genotyped using the Sequenom Platform and TaqMan™ assays from available DNA.</li>
<li>The cumulative genetic-risk scores for each patient were then calculated using the weighted effect estimated from previous GWAS (log-additive model).</li>
<li>FH status and the genetic-risk scores were assessed against adverse outcomes in AS, time to treatment and adverse histology on repeat biopsy, using univariable and multivariable Cox regression models to address time to treatment; and binary logistic regression to address biopsy upgrade.</li>
</ul></div></div>
<div class="section" id="bju11648-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11648-list-0003" class="bullet">
<li>Of 471 patients, 55 (13.6%) had adverse histology on repeat biopsies and 145 (30.8%) had deferred treatment.</li>
<li>On univariate analysis, there was no significant relationship between FH of prostate cancer in any degree of relation, and adverse histology or time to treatment.</li>
<li>For risk score analyses, 386 patients' DNA was studied; and there was also no relationship found between the calculated genetic risk scores and adverse histology or time to treatment (<em>P</em> = 0.573 and <em>P</em> = 0.965, respectively).</li>
<li>The retrospective study design and the few events were the main limitation of the study.</li>
</ul></div></div>
<div class="section" id="bju11648-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11648-list-0004" class="bullet">
<li>There is currently insufficient data to support the use of FH status or prostate cancer SNP profile risk scores as prognostic factors in AS and these should not be used to influence management decisions.</li>
<li>As more genetic variants are discovered this may change and should be reassessed in multicentre AS cohorts.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

Family history (FH) is a major risk factor for the development of prostate cancer. The search for genetic variants has led to genome-wide association studies (GWAS), which have so far reported 47 susceptibility loci that predispose men to prostate cancer. However, the use of genetics or FH status in predicting clinical outcomes after prostate cancer diagnosis remains uncertain. Guidelines currently exist for clinicians and patients summarising evidence relating to the best outcomes of different prostate cancer treatment methods. Genetics and FH could potentially add to this stratification.
Our study aimed to ascertain the potential prognostic roles of FH or genetic risk scores in patients managed by active surveillance.


 Objectives

To explore the potential prognostic role of family history (FH) of prostate cancer and prostate cancer risk single nucleotide polymorphisms (SNPs) in patients undergoing active surveillance (AS) for prostate cancer.
This is the first study to date, which has investigated the potential prognostic role of SNP profiles in an AS cohort



Patients and Methods

FH data were collected from patients in the Royal Marsden Hospital AS study.
In all, 39 prostate cancer-risk SNPs identified from published genome wide association studies (GWAS) were genotyped using the Sequenom Platform and TaqMan™ assays from available DNA.
The cumulative genetic-risk scores for each patient were then calculated using the weighted effect estimated from previous GWAS (log-additive model).
FH status and the genetic-risk scores were assessed against adverse outcomes in AS, time to treatment and adverse histology on repeat biopsy, using univariable and multivariable Cox regression models to address time to treatment; and binary logistic regression to address biopsy upgrade.



Results

Of 471 patients, 55 (13.6%) had adverse histology on repeat biopsies and 145 (30.8%) had deferred treatment.
On univariate analysis, there was no significant relationship between FH of prostate cancer in any degree of relation, and adverse histology or time to treatment.
For risk score analyses, 386 patients' DNA was studied; and there was also no relationship found between the calculated genetic risk scores and adverse histology or time to treatment (P = 0.573 and P = 0.965, respectively).
The retrospective study design and the few events were the main limitation of the study.



Conclusions

There is currently insufficient data to support the use of FH status or prostate cancer SNP profile risk scores as prognostic factors in AS and these should not be used to influence management decisions.
As more genetic variants are discovered this may change and should be reassessed in multicentre AS cohorts.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11651.x" xmlns="http://purl.org/rss/1.0/"><title>Changes in serum prostate-specific antigen levels and the identification of prostate cancer in a large managed care population</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11651.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Changes in serum prostate-specific antigen levels and the identification of prostate cancer in a large managed care population</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lauren P. Wallner, Stanley K. Frencher, Jin-Wen Y. Hsu, Chun R. Chao, Michael B. Nichol, Ronald K. Loo, Steven J. Jacobsen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-15T07:54:09.056866-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11651.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11651.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11651.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Urological Oncology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11651-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11651-list-1001" class="bullet">
<li>The use of a single, elevated PSA level to screen for prostate cancer is controversial given its reported low specificity and the questionable benefits of PSA screening on prostate cancer mortality. Current guidelines in the USA recommend against screening using a single PSA measurement. Previous studies suggest that using changes in PSA level over time, or PSA velocity, may improve the detection of prostate cancer and/or aggressive disease; however, this is also controversial as other studies suggest PSA velocity does not improve detection and may further contribute to the overdetection of indolent prostate cancer.</li>
<li>Given the questions that remain regarding the use of the rate of change in PSA as a screening tool for prostate cancer because of previous conflicting studies, which to date have included small, highly selected populations, this study adds to the existing knowledge by assessing this question in general practice settings among a large, diverse population.</li>
</ul></div></div>
<div class="section" id="bju11651-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11651-list-0001" class="bullet">
<li>To determine whether the rate of change in total serum prostate-specific antigen (PSA) levels accurately detects prostate cancer and to evaluate whether it adds any predictive value to a single measurement of serum PSA alone, in general practice settings.</li>
</ul></div></div>
<div class="section" id="bju11651-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Materials and Methods</h4><div class="para"><ul id="bju11651-list-0002" class="bullet">
<li>A retrospective cohort of 219 388 community-dwelling men, aged ≥45 years, enrolled in the Kaiser Permanente Southern California health plan, with no history of prostate cancer and at least three PSA measurements, were followed from 1 January 1998 to 31 December 2007, for the development of biopsy-confirmed prostate cancer.</li>
<li>Annual percent changes in total serum PSA levels were estimated using linear mixed models.</li>
<li>The accuracy of prostate cancer prediction was assessed for prostate cancer overall and for aggressive disease (Gleason score ≥7) and compared with that of a single measure of PSA level using area under the receiver-operating characteristic curves (AUCs).</li>
</ul></div></div>
<div class="section" id="bju11651-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11651-list-0003" class="bullet">
<li>The men in this cohort experienced a mean change of 2.9% in PSA levels per year and the rate of change in PSA increased modestly with age (<em>P</em> ≤ 0.001).</li>
<li>Annual percent changes in PSA accurately predicted the presence of prostate cancer (AUC = 0.963) and aggressive disease (AUC = 0.955) and had more predictive accuracy for aggressive disease than did a single measurement of PSA alone (AUC = 0.727).</li>
</ul></div></div>
<div class="section" id="bju11651-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><ul id="bju11651-list-0004" class="bullet">
<li>Longitudinal measures of PSA improve the accuracy of aggressive prostate cancer detection when compared with a single measurement of PSA alone.</li>
<li>Findings from this study provide insight into the usefulness of PSA velocity as a detection marker for aggressive prostate cancer.</li>
</ul></div></div>
]]></content:encoded><description>

What's known on the subject? and What does the study add?

The use of a single, elevated PSA level to screen for prostate cancer is controversial given its reported low specificity and the questionable benefits of PSA screening on prostate cancer mortality. Current guidelines in the USA recommend against screening using a single PSA measurement. Previous studies suggest that using changes in PSA level over time, or PSA velocity, may improve the detection of prostate cancer and/or aggressive disease; however, this is also controversial as other studies suggest PSA velocity does not improve detection and may further contribute to the overdetection of indolent prostate cancer.
Given the questions that remain regarding the use of the rate of change in PSA as a screening tool for prostate cancer because of previous conflicting studies, which to date have included small, highly selected populations, this study adds to the existing knowledge by assessing this question in general practice settings among a large, diverse population.


 Objective

To determine whether the rate of change in total serum prostate-specific antigen (PSA) levels accurately detects prostate cancer and to evaluate whether it adds any predictive value to a single measurement of serum PSA alone, in general practice settings.



Materials and Methods

A retrospective cohort of 219 388 community-dwelling men, aged ≥45 years, enrolled in the Kaiser Permanente Southern California health plan, with no history of prostate cancer and at least three PSA measurements, were followed from 1 January 1998 to 31 December 2007, for the development of biopsy-confirmed prostate cancer.
Annual percent changes in total serum PSA levels were estimated using linear mixed models.
The accuracy of prostate cancer prediction was assessed for prostate cancer overall and for aggressive disease (Gleason score ≥7) and compared with that of a single measure of PSA level using area under the receiver-operating characteristic curves (AUCs).



Results

The men in this cohort experienced a mean change of 2.9% in PSA levels per year and the rate of change in PSA increased modestly with age (P ≤ 0.001).
Annual percent changes in PSA accurately predicted the presence of prostate cancer (AUC = 0.963) and aggressive disease (AUC = 0.955) and had more predictive accuracy for aggressive disease than did a single measurement of PSA alone (AUC = 0.727).



Conclusions

Longitudinal measures of PSA improve the accuracy of aggressive prostate cancer detection when compared with a single measurement of PSA alone.
Findings from this study provide insight into the usefulness of PSA velocity as a detection marker for aggressive prostate cancer.


</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11745.x" xmlns="http://purl.org/rss/1.0/"><title>Risk factors for different phenotypes of hypospadias: results from a Dutch case–control study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11745.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Risk factors for different phenotypes of hypospadias: results from a Dutch case–control study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Iris A.L.M. Rooij, Loes F.M. Zanden, Marijn M. Brouwers, Nine V.A.M. Knoers, Wout F.J. Feitz, Nel Roeleveld</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-10T08:22:52.532215-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1464-410X.2012.11745.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1464-410X.2012.11745.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1464-410X.2012.11745.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Paediatrics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="bju11745-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>What's known on the subject? and What does the study add?</h4><div class="para"><ul id="bju11745-list-0001" class="bullet">
<li>The various phenotypes of hypospadias may result from disturbances of dissimilar embryonic processes in different time windows, suggesting aetiological heterogeneity; however, only a few studies have investigated the risk factors for the different hypospadias phenotypes.</li>
<li>The study confirmed that genetic predisposition possibly plays a role in anterior and middle hypospadias, as shown by the large effect estimates for familial occurrence of these forms of hypospadias. By contrast, the posterior phenotype was more often associated with pregnancy-related factors, such as primiparity, preterm delivery, and being small for gestational age. New findings were that hormone-containing contraceptive use after conception increased the risk of middle and posterior hypospadias, while multiple pregnancies were associated with the posterior form in particular.</li>
</ul></div></div>
<div class="section" id="bju11745-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><ul id="bju11745-list-0002" class="bullet">
<li>To identify specific risk factors for different phenotypes of hypospadias that may arise as a result of dissimilar embryonic processes in different time windows.</li>
</ul></div></div>
<div class="section" id="bju11745-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Patients and Methods</h4><div class="para"><ul id="bju11745-list-0003" class="bullet">
<li>A total of 405 hypospadias cases and 627 male controls were included in a Dutch case–control study.</li>
<li>Medical records of cases were reviewed to determine the anatomical location of the urethral opening, while demographic, lifestyle and pregnancy-related risk factor data were obtained from self-administered questionnaires.</li>
<li>Multivariable and multinomial logistic regression analyses were used to calculate effect estimates for the group containing all cases of hypospadias and for the different hypospadias phenotypes.</li>
</ul></div></div>
<div class="section" id="bju11745-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><ul id="bju11745-list-0004" class="bullet">
<li>Cases were subdivided into anterior (glandular and coronal; 59%), middle (penile; 29%) and posterior (penoscrotal, scrotal and perineal; 12%) hypospadias.</li>
<li>Being a twin/triplet, primiparity, preterm delivery, and being small for gestational age were associated with hypospadias, particularly in posterior cases.</li>
<li>Family history of hypospadias increased the risk of hypospadias, an effect that seemed to be more predominant in anterior and middle forms.</li>
<li