See editorial on pages 2602-4, this issue.
Treatment of nonmuscle invading bladder cancer: Do physicians in the United States practice evidence based medicine?†
The use and economic implications of intravesical chemotherapy after transurethral resection of bladder tumors
Article first published online: 19 MAY 2009
Copyright © 2009 American Cancer Society
Volume 115, Issue 12, pages 2660–2670, 15 June 2009
How to Cite
Madeb, R., Golijanin, D., Noyes, K., Fisher, S., Stephenson, J. J., Long, S. R., Knopf, J., Lyman, G. H. and Messing, E. M. (2009), Treatment of nonmuscle invading bladder cancer: Do physicians in the United States practice evidence based medicine?. Cancer, 115: 2660–2670. doi: 10.1002/cncr.24311
Fax: (716) 442-8350
- Issue published online: 4 JUN 2009
- Article first published online: 19 MAY 2009
- Manuscript Accepted: 25 MAR 2008
- Manuscript Revised: 21 MAR 2008
- Manuscript Received: 21 DEC 2007
- National Institute of Aging. Grant Number: K01 AG 20,980
- Empire State Grant
- Ashley Family Foundation
- intravesical therapy;
- bladder cancer;
- evidence based medicine;
- transurethral resection of bladder tumor
Phase 3 clinical trials performed primarily outside the US demonstrate that intravesical instillation of chemotherapy immediately after transurethral resection of the bladder (TURB) decreases cancer recurrence rates. The authors sought to determine whether US urologists have adopted this practice, and its potential effect on costs of bladder cancer (BC) care.
By using 1997-2004 MEDSTAT claims data, the authors identified patients with newly diagnosed BC who underwent cystoscopic biopsy or TURB, and those who received intravesical chemotherapy within 1 day after TURB. Economic consequences of this treatment compared with TURB alone were modeled using published efficacy estimates and Medicare reimbursements. The authors used a time horizon of 3 years and assumed that this treatment was given for all newly diagnosed low-risk BC patients.
Between 1997 and 2004, the authors identified 16,748 patients with newly diagnosed BC, of whom 14,677 underwent cystoscopic biopsy or TURB. Of these, only 49 (0.33%) received same-day intravesical instillation of chemotherapy. From 1997 through 2004, there has been little change in the use of this treatment. The authors estimated a 3-year savings of $538 to $690 (10% to 12%) per patient treated with TURB and immediate intravesical chemotherapy compared with TURB alone, reflecting a yearly national savings of $19.8 to $24.8 million.
Instillation of intravesical chemotherapy immediately after TURB has not been embraced in the US. Adopting this policy would significantly lower the cost of BC care. Cancer 2009. © 2009 American Cancer Society.
Bladder cancer is the 4th most commonly diagnosed cancer in men and the 8th in women in the US. An estimated 61,420 new cases will be diagnosed in 2007, and 13,060 patients will die of this disease.1
Seventy-five percent of newly diagnosed bladder cancers are nonmuscle invasive (NMI).2, 3 These cancers often recur after seemingly complete transurethral resection of the bladder (TURB) because of new tumor development in other regions of the urothelium, tumor cell implantation resulting from spontaneous perturbations or those induced by instrumentation, and/or incomplete resection of the original malignancy.4, 5
Although recurring well and moderately differentiated NMI bladder cancer rarely progresses to a life-threatening condition, repeated TURBs and courses of intravesical instillations of immuno- and chemotherapeutic agents cause considerable inconvenience, expense, and morbidity. A single instillation of chemotherapy immediately after TURB has been proposed as a means of reducing recurrence by decreasing procedure-facilitated tumor implantation and eradicating field effect or persistent (incompletely resected or unrecognized) tumors.5-7 For over a decade, several prospective randomized-controlled clinical trials have shown that this treatment is safe and decreases recurrences by 17% to 44% compared with controls8-10 (Table 1), particularly for patients with newly diagnosed bladder cancers.5-7,11-13 Agents used include mitomycin C, doxorubicin, and thiotepa (all available in the US), as well as epirubicin and Epodil (neither available in the US).
|Reference||Agent (dose)/ Control||No. of Patients||Type of Patient||Stage||Interval of Follow-up||Recurrence Rate Outcome (Study Arm vs Control)|
|Burnand6 1976||Thiotepa (90 mg/100 cc)/observation||51||Unknown||Ta and T1||Recurrences at 2-5–y follow-up||57.9% vs 96.8% (P < .005)|
|Zincke35 1983||Thiotepa (60 mg/60 mL H2O) vs doxir (50 mg/60mL H2O) vs H2O (3-arm study)||45||21% new||Ta, T1, Tis||Recurrence rate at 3-4 mo||Thiotepa||Doxir||H2O|
|MRC 1985||Thiotepa (30 mg/50 mL)/observation||256||100% new||Ta and T1||Recurrence rate at 2 y||35.4% vs 41.3% (P = .7)|
|MRC 1994||Follow-up of above study at 8.75 y showed no difference of time to primary recurrence, recurrence rate, or failure-free interval|
|Oosterlinck7 1993||Epirubicin (80 mg in 50 ccNS)/50 cc of H2O||399||80% new||Ta and T1||Recurrence rate per year||New: 15% vs 31% (P < .0001)|
|20% recurrent||Recurrent: 26% vs 35% (P = .38)|
|Overall||Overall: 17 vs 32% (P < .0001)|
|Tolley10 1996||Mitomycin C (40 mg/40 ccH2O)/observation||306||100% new||Ta and T1||Recurrence rate at 2 years||42% vs 55% (P = .01)|
|Ali-el-Dein8 1997||Epirubicin (50 mg/50 mL NS)/observation||109||55% new||Ta and T1||Recurrence rate at mean of 2.5 y||24% vs 52% (P < .002)|
|Solsona5 1999||Mitomycin C (30 mg/50 mL of NS)/observation||121||90% new||Ta and T1||Recurrence rate at 1 y||22% vs 59% (P < .005)|
|Rajala15 1999||Epirubicin (100 mg) vs INF-α2b (50-M units) vs observation (3-arm study)||200||100% new||Ta and T1||Recurrence rate at 2 y||Epirubicin||INF-α||Observation|
|Overall||32%||62%||60% (P < .05)|
In view of this evidence, we set out to determine whether US urologists have adopted this practice and to ascertain whether implementing post-TURB intravesical instillation therapy would be cost-saving.
MATERIALS AND METHODS
The study was based on the analysis of individual medical claims provided by MEDSTAT (www.MEDSTAT.com), a healthcare information company currently following over 7 million covered lives, which provides benchmark databases and research services for managing costs and quality of healthcare in the US. We used MEDSTAT's Commercial Claims and Encounters (CCAE) and Medicare Supplemental Coverage claims databases, which have been validated and used for oncological and nononcological research studies.8-10 These databases are generally representative of the US population in terms of sex (49% male). The mean ages of the CCAE and Medicare populations were 34 and 74 years, respectively. This compares with a mean age of 72 years for all Medicare beneficiaries and 75 years if only those 65 years and older are included. A higher percentage of individuals included in MEDSTAT databases reside in the Southern US (50%) than the general population, whereas 36% of Medicare beneficiaries live in the Southern US.14
Study Sample and Drug Use
By using 1997-2004 MEDSTAT claims, we identified bladder cancer patients based on the International Classification of Diseases–Ninth Revision (ICD-9) code of 188.9. We chose 1997 because it was the first calendar year after a positive large randomized clinical trial using an agent readily available in the US was reported in the American literature.11,13,15 Several studies have examined the accuracy of ICD-9 coding for various conditions compared with medical records and physician assessment, and demonstrated significant sensitivity and specificity in identifying patients with index conditions (diabetes, chronic kidney disease, breast cancer, cerebral vascular accident, and stroke).16-18 Figure 1 presents the algorithm used to identify newly diagnosed patients with bladder cancer who received same-day post-TURB intravesical chemotherapy. We then identified patients who underwent cystoscopy with biopsy or TURB for any size bladder tumor (using Current Procedure Terminology [CPT] codes 52,204, 52,224, 52,234, 52,235, and 52,240). From these, using prescription drug claims and National Drug Code and CPT codes, we selected patients who received an intravesical instillation of a chemotherapeutic agent (mitomycin C, doxorubicin, or interferon alpha) on the day of, or the day after TURB. Administration of immediate intravesical therapy post-TURB is billed as an outpatient/ambulatory procedure (CPT 51,720) rather than a prescription drug, because it can only be administered by qualified medical personnel. Use of administrative claims data for evaluation of patterns of healthcare use is quite common and has been validated.8-10 Moreover, because errors in billing would lead to problems with payments, the quality of billing data is generally high.19
Cost and Utilization
On the basis of prospective, randomized studies reported in the English language literature, we identified standard care and likely outcomes for patients with newly diagnosed NMI bladder cancer after initial TURB with 0, 1, 2, or 3 episodes of recurrence over a 3-year period.20-29 To assign cost values to the typical utilization associated with each of the recurrence patterns, with and without immediate post-TURB intravesical instillation of chemotherapeutic agents, we used Medicare reimbursement fees for the related procedures and medications (Table 2). We assumed that all predicted recurrences would be recognized at the first (3 month) cystoscopy after the most recent TURB. In 1 analysis, we assumed intravesical bacillus Calmette-Guérin (BCG) would be used after the initial recurrence, whereas in the second we assumed mitomycin C would be.
|BCG and INF instillation||1055|
|TURB with intravesical instillation||1856|
|Medication cost (mitomycin C)||260|
The results for each analysis are presented as an average cost per patient for a 3-year period. For the group not receiving immediate post-TURB instillation therapy, we assumed that 60% would not have a recurrence during this period.26 For the first analysis, the initial recurrence would be treated with induction (and maintenance, if successful) BCG, and BCG + alpha-interferon would be used after the second recurrence. For the group receiving same-day intravesical instillation therapy, we assumed that recurrences would be reduced by 25% and that initial and second recurrences would be treated with induction and maintenance BCG and BCG + alpha-interferon, respectively, with the same the efficacy as for those not receiving same-day intravesical instillation therapy who recurred.
In the second analysis, we assumed that 6 instillations of mitomycin C would be given for the initial recurrence, and those experiencing a second recurrence would receive induction (and maintenance, if successful) BCG, whereas those with a second recurrence would receive BCG + alpha-interferon. The efficacy of these agents was assumed to be the same as in our first analysis. The same assumption was made for the efficacy of immediate post-TURB intravesical therapy as in the first analysis: a 25% reduction in first recurrences. The 3-year time horizon was chosen, because the overwhelming majority of bladder cancer recurrences occur within this period.26 In addition, the American Urological Association (AUA) protocol is set for intense follow-up for 3 years after the initial TURB to detect recurrence and then switches to a less intense regimen. Furthermore, we believe that the majority of patients do not undergo more than 3 resections of bladder cancer and therefore have spread it over a 3-year period, which would typically be seen in patients with low-risk disease. We assumed that prior use of intravesical chemotherapy after TURB would have no effect on the progression of subsequently diagnosed muscle-invasive bladder cancer. We did not apply discounting in this study, because we did not anticipate a dramatic effect over a 3-year period.
Because same-day intravesical instillation therapy is not recommended for high-grade or muscle-invading cancers, carcinoma in situ (TIS), or predominantly nonurothelial cancers, we assumed that no patients in our analysis had these cancers. To be very conservative in terms of predicting cost savings and effectiveness, we assumed no patient would progress to high grade, carcinoma in situ (TIS), or stage T2 + disease during the period of follow-up (because progression to any of these stages/grades mandates more complex and expensive therapies).
Because there is wide variation in the reported efficacy of intravesical instillation therapy, we conducted a threshold analysis to estimate the minimal effectiveness of this treatment required to balance the added cost of medication and care compared with the standard TURB. To perform the threshold analysis, we expressed the average cost of a patient treated with mitomycin C for the first occurrence as a function of risk reduction, compared the average cost of a patient treated with BCG for the first occurrence of bladder cancer to the average cost of a patient treated with mitomycin C, and solved this equation for risk reduction. This value represented the minimal treatment effect needed for the 2 options to be considered equal in terms of cost.
Use of an Intravesical Chemotherapeutic Agent After TURB
By using the CCAE and Medicare databases from 1997 to 2004, we identified 16,748 patients whose claims listed bladder cancer as their primary or secondary diagnosis. From 1997 through 2004, 444,740 patients were estimated from Surveillance, Epidemiology, and End Results data to develop bladder cancer,30 and thus 4% of all newly diagnosed bladder cancers were captured by these databases. A total of 14,677 (87.6%) subsequently underwent cystoscopy with biopsy or TURB of their bladder cancer (Table 3). Of these, only 49 (0.33%) received same- or following-day instillation therapy after their surgical procedure (Table 3). Most of these patients received mitomycin C (48 of the 49; 98%), whereas 1 patient (2%) received interferon alpha-2B. No patient received doxorubicin or thiotepa. When analyzing data from between 1997 and 2004, we detected no statistically significant changes in the annual rates of new diagnosis or treatment of bladder cancer, or the use of same-day intravesical therapy after TURB in this cohort (Table 3).
|Total No. of intravesical instillations post-TURB||1||7||5||3||9||9||9||6||49|
|% of instillations/y||0.093||0.420||0.353||0.251||0.288||0.413||0.39||0.336||0.333|
Economic Benefits of Instilling Intravesical Chemotherapy Immediately After TURB
For the base case analysis, we assumed that the treatment was given for all newly diagnosed low-risk patients (grades 1 and 2 and stages Ta andT1). By evaluating the literature, we estimated that bladder cancer patients without recurrence for >3 years will receive 10 surveillance cystoscopies (Fig. 2). Based largely on AUA guidelines and the results of randomized clinical trials,20-26,28,29,31 patients who had recurrences underwent further resections and 6 weekly instillations of BCG with 3 maintenance instillations of BCG every 6 months for 3 years. Of those starting this course, we assumed that 25% would recur and undergo another TURB followed by instillations with BCG and alpha-interferon. Of these patients, we assumed that 60% would recur. Treatment after a second or third recurrence in this brief a time is not standardized20-26,28,29,31; to be extremely conservative, we assumed patients would subsequently not recur and be observed closely (ie, frequent cystoscopies) (Fig. 2). The second model used mitomycin C for the first recurrence, assuming 50% would recur during the period of follow-up.20,22-25,27,31-34 The second recurrence was treated with induction BCG and maintenance therapy if successful, and BCG + alpha-interferon was used for the third recurrence. The anticipated efficacy of BCG and BCG + alpha-interferon was assumed to be the same as in the first analysis. As with model 1, we assumed patients experiencing a third recurrence would not recur subsequently, and be managed by frequent monitoring. Because the literature is equivocal regarding advantages of post-TURB single-instillation intravesical therapy in patients with recurrent bladder cancers,7, 29 we did not presume that patients with recurrences would receive this treatment.11, 35
With the utilization rates and outcomes discussed, we estimated that without same-day therapy and assuming BCG was administered at first recurrence (model 1) it would cost on average $5760 to treat 1 patient with low-risk NMI bladder cancer for 3 years (Table 4). If all patients receive same-day post-TURB intravesical chemotherapy (we assumed mitomycin C would be used), the average per patient cost of 3 years of care is reduced to $5070, a cost savings of $689 (12%) per patient for treatment with same-day intravesical chemotherapy compared with TURB alone. Nationally, this represents annual savings of $24.8 million (60% of newly diagnosed bladder cancer per year1, 36). A similar analysis was done with patients receiving mitomycin C on initial recurrence, BCG for the second recurrence, and BCG and alpha-interferon for the third. This would save $538 per patient and save $19.8 million nationally (Fig. 2, Table 4). Even if patients who failed the first BCG induction course were treated with a repeat course of BCG rather than BCG + alpha-interferon, the savings for immediate post-TURB intravesical instillation therapy would still be substantial: $21.2 million if BCG was used for the first recurrence, and $19.8 million if mitomycin C was used (data not shown).
|No Recurrence||One Recurrence||Two Recurrences||Three Recurrences|
|Model 1: Patients Treated With BCG for First Recurrence|
|% of Patients, without intravesical instillation||60%||30%||4%||6%|
|Decrease in Recurrence by 25%|
|% of patients treated with intravesical instillation||70%||22.5%||3%||4.5%|
|Average+$260 for instillation mitomycin||5070|
|Model 2: Patients Treated With Mitomycin C for First Recurrence|
|% of patients, without intravesical instillation||60%||20%||15%||5%|
|Costs, $||1,176,420||1,102, 168||1,947,687||927,981|
|Decrease in Recurrence by 25%|
|% of patients treated with intravesical instillation||70%||15%||11.25%||3.75%|
|Average+$260 for instillation mitomycin||4616|
Our threshold analysis demonstrated that the addition of single-dose intravesical therapy after TURB must decrease recurrence by at least 7% (for the BCG assumption) to 10% (for mitomycin C) to cover the additional cost of services and medication.
Despite compelling evidence regarding the effectiveness of same-day intravesical therapy, between 1997 and 2004, only 0.33% of eligible US patients received this treatment. We demonstrated that in addition to reducing the rate of bladder cancer recurrences, same-day intravesical therapy could also save $538 to $689 of medical expenses per patient, or over $15 to nearly $25 million a year nationally.
The rationale behind single immediate instillation intravesical chemotherapy is that by reducing the rate of implantation, the likelihood of disease recurrence will decrease, as will the need for repeat TURBs and for longer courses of intravesical therapy. Table 1 reviews the results of randomized prospective trials of same-day intravesical instillation chemotherapy after TURB. This treatment has been shown to reduce recurrences by 17% to 44% compared with controls. A recent meta-analysis has confirmed that this treatment has decreased the risk of recurrence by 39% in patients with stage Ta and T1 bladder cancer.37
The purpose of the analysis was to provide a conservative estimate of the economic benefit associated with using intravesical chemotherapy after TURB in the US. Because differences between countries in terms of healthcare systems (eg, financing and organization) could have a substantial impact on the types of services patients receive, it is necessary to focus on a specific healthcare system. We chose the US healthcare system, and specifically the health insurer's perspective, to evaluate the impact of this treatment on the overall cost of bladder cancer care. Similarly, we used Medicare reimbursement rates as a more conservative, lower-bound estimate of the potential savings associated with the use of this intervention among both Medicare and privately insured patients. Another reason for using Medicare rates is that the average age of bladder cancer patients at the time of diagnosis is >70 years.2
Several assumptions were made to identify our sample population. The first was that the 3-year recurrence rate of newly resected NMI bladder cancer is 40%. This has been shown in a variety of follow-up studies of NMI bladder cancer as well as in placebo arms of randomized trials using BCG.20-26,28,29,31 Thus, in building our model we assumed that 40% of patients with newly diagnosed and completely resected low-risk bladder cancer will have recurrence during the 3-year follow-up period. We also assumed that there was no stage progression to muscularis propria invading disease. This was an extremely conservative estimate, because in published series, stage progression has been reported to occur in 1% to 20% of patients with low-risk NMI cancer. The cost of managing invasive bladder cancer is far greater than for NMI disease, and so failure to consider stage progression biased our cost projections against immediate post-TURB instillation therapy. At the time this study was carried out, the AUA had not established immediate intravesical therapy as the standard of care but did recommend it as a therapeutic option,38 whereas the European Association of Urology had included it as the standard of care for superficial bladder cancer.39 The recently revised AUA guidelines have now included it as an “option” (the weakest grade of guideline with the greatest flexibility in application) for care, although not as a “standard” or “recommendation”.28
The next part of the model dealt with the treatment of patients with recurrences. Largely based on professional guidelines by the AUA and the results of randomized clinical trials,20-26,28,29,31 such patients underwent 6 weekly instillations of BCG with 3 maintenance instillations of BCG every 6 months for 3 years (although other forms of intravesical therapy could be used). Again based on published reports,20-26,28,29,31 we assumed that 25% of those receiving this course would recur and undergo further instillations with BCG and alpha-interferon. Of those patients, we assumed that 60% would recur again.36, 40 At this point, the decision would be influenced by the patient's comorbidities and wishes and nonstandard treatment by the treating physician; to be very conservative, we projected that there would not be further recurrences, and that only frequent cystoscopic monitoring would take place. This again reduced costs compared with the more aggressive therapies that would often be selected (eg, cystectomy). Similarly, we modeled the cost if for the first recurrence 6 intravesical instillations of mitomycin C were used with an assumption that 50% receiving this treatment would recur.24, 41 Subsequent recurrences were treated with BCG or BCG + alpha-interferon. For both of these models, we estimated that were they to occur, all recurrences took place immediately after the index or subsequent TURB. Although this is an oversimplification, the majority of recurrences take place within 3 to 6 months of the index TURB and over 70% occur within 1 year.28 Because most published trials and series end at the time of the initial recurrence, few data are available about the times of second and third recurrences. With longer intervals between recurrences, expenses would have changed little, as long as recurrences were treated as they were in the models. In addition, because recurrences took place at the first cystoscopic evaluation after TURB, it is likely that standard intravesical therapy would have been recommended (because of the frequent recurrences), rather than simple continuation of observational management. By using the above assumptions, we formulated models for the treatment of a patient with newly diagnosed NMI bladder cancer.
Although cystectomy is sometimes performed for patients who recur after BCG treatments, this is almost exclusively reserved for patients with high-grade disease. It is likely that very few (if any) patients would undergo it within the first 3 years of being diagnosed with low-grade, NMI bladder cancer.28 Furthermore, we are unaware of any data addressing the circumstance (the proportion of patients with low-risk newly diagnosed bladder cancer who are treated with BCG, recur after that treatment, and immediately go on to cystectomy) to guide our model. Both because such a circumstance is very rare and generally would occur beyond the time horizon of this study, it is not included in our model. Moreover, to be conservative, we assumed no grade (to high grade) or stage progression (to stage T2) would occur. These occur rarely in the population being considered.28 If either occurred, cystectomy would be more likely. The huge cost associated with this procedure, which would be far more likely to occur in the observed arm, would further bias the results of the study in favor of immediate post-TURB intravesical therapy. Lastly, we took a conservative estimate of 25% for the reduction in recurrence rate after immediate post-TURB intravesical instillation.37
As with all studies using healthcare databases, several factors should be considered when interpreting our findings. First, although the sample was drawn from more than 7 million lives, it may not be representative of the general population. There are regional biases in medical and urologic care,37, 42 and it is possible that the geographic imbalance in our data may misrepresent what is occurring in the US as a whole. However, given the only modest imbalance in geographic distribution, and the verified utilization of this database for other medical and oncologic conditions, this likely provides a relatively small bias, not explaining our results. Furthermore, although the databases allowed for the analysis of a large sample of patients across the US, only patients with commercial health coverage or private Medicare supplemental coverage were analyzed. Finally, these findings are based on retrospective analyses of claims data, and reliance on this data has limitations. For example, patients may receive treatment that is not submitted to their health plan for reimbursement, and thus is not included in claims data, and a small proportion of claims may be subject to coding errors. However, we believe our methodology to determine how often immediate post-TURB instillation therapy is used is reliable, because it is administered by qualified medical personnel (and thus has a CPT code). Moreover, because errors in billing that lead to problems in payments rarely go uncorrected, billing data are usually highly reliable.19
Because we used Medicare reimbursement rates (which are usually lower than the rates reimbursed by private health plans) to estimate the cost of interventions, our estimates represent the lower bound of possible savings. However, the effectiveness of the same-day intravesical instillation chemotherapy may also vary depending on patient risk factors and medical histories. We demonstrated that as long as the intervention is at least 7% to 10% more effective than the TURB alone, post-TURB single intravesical instillation chemotherapy provides economic savings.
Why is the treatment performed so rarely? One reason is that although it is considered safe and well tolerated,5-7,11-13 there obviously are some patients with suspected bladder perforation or post-TURB hematuria who should not receive it. Another reason is a technical matter involving dispensing and administering chemotherapy. Many American centers require chemotherapy nurses and ancillary staff to handle and instill these agents, preventing most operating or recovery room nurses from administering them. Currently, some urologists resort to instilling and overseeing the dispensing and handling themselves. The inconvenience of ordering, instilling, and waiting for the chemotherapy to dwell for 1-2 hours is, for a busy practitioner, clearly a deterrent to its use. Another barrier to its acceptance is the economic burden placed on the hospital. Currently, the additional expense of using intravesical chemotherapy in a hospital-based setting (eg, operating room) is borne by the hospital without reimbursement for longer recovery room time, increased monitoring by specially trained nursing staff, and the expenses of disposing of the chemotherapeutic agent.
Another possible reason for not performing this treatment may be the way new scientific data are transmitted to and incorporated into practice by physicians. Although numerous clinical trials have shown its effectiveness, these data have not been widely accepted by US urologists. Whether this is because they are unaware of the published data or because these trials have largely been performed outside the US without the participation of American centers is unclear. American urologists may be resistant to embracing this approach without validation by a large American study. The recent revision of AUA guidelines may have an influence on altering this practice, but this will not be ascertainable for several years.
Despite generalized acceptance of same-day intravesical instillation chemotherapy after TURB by urologists outside the US, this policy has not been embraced by American urologists. Reasons for this are unclear. Regardless of the reasons, we have shown that assuming conservative parameters for efficacy, adopting this policy would considerably lower the cost of caring for bladder cancer in the US.
Conflict of Interest Disclosures
Katia Noyes was supported in part by grant K01 AG 20,980 from the National Institute of Aging.
Ralph Madeb was supported in part by an Empire State Grant.
This work was also supported by the Ashley Family Foundation.
- 3Urothelial tumors of the urinary tract. In: WalshPC, RetikAB, VaughanED, eds. Campbell's Urology. 8th ed. Philadelphia, PA: WB Saunders; 2002: 2732-2784..
- 7A prospective European Organization for Research and Treatment of Cancer Genitourinary Group randomized trial comparing transurethral resection followed by a single intravesical instillation of epirubicin or water in single stage Ta, T1 papillary carcinoma of the bladder. J Urol. 1993; 149: 749-752., , , , , .
- 14Medicare Current Beneficiary Survey. Baltimore, MD: Center for Medicare and Medicaid Services; 2000.
- 19Risk Adjustment for Measuring Health Care Outcomes. 3rd ed. Chicago, IL: Health Administration Press; 2003.
- 30American Cancer Society. Statistics of Cancer Incidence 1997-2006. Available at: http://www.cancer.org/docroot/STT/stt_0_2004.asp?sitearea=STT&level=1 Accessed March 2009.