Cancer, the second leading cause of death in the United States,1 has a profound effect on society in terms of both human suffering and economic impact. An aging population will only increase the burden of cancer in the coming decade. Although science has advanced the care of cancer patients through molecular diagnostics, epigenetics, and novel personalized treatments, elimination of this disease is a reality for some but not all Americans living today. It is imperative that health care providers, policymakers, and the public examine the quality of care provided to the ever-increasing number of individuals at risk for, living with, and surviving cancer.
Since its creation in 1970, the Institute of Medicine (IOM) of the National Academy of Sciences has demonstrated its commitment to enhancing health and improving the quality of health care. For example, in 1995, the IOM created the National Round Table on Health Care Quality to assess quality-of-care issues. The resulting workshops and commissioned articles culminated in an important consensus statement, published in 1998, in which the Round Table asserted that health care quality can be defined and measured precisely with a degree of scientific accuracy comparable to that of most measures used in clinical medicine (Donaldson 19982). This statement highlighted widespread problems associated with the under use, overuse, or misuse of health care and called for major revisions in health care delivery, clinician education and training, and quality-improvement efforts.2 Subsequently, the IOM initiated the Quality of Health Care in America project, which led to the publication of the 2000 landmark report To Err is Human: Building a Safer Health System3 and the 2001 report Crossing the Quality Chasm.4
In parallel, Dr. Richard Klausner, then director of the National Cancer Institute (NCI), approached the leadership of the IOM and the National Academy of Sciences in late 1996 with a proposal to create a board with broad membership to address the organization and delivery of cancer care. The National Cancer Policy Board was thus established. Early in its deliberations, the board set out to articulate an ideal cancer care system from the patient's perspective. The board then compared this ideal state with the state of cancer care delivery at that time and, in doing so, identified a wide gulf between the ideal and the reality (Hewitt and Simone, 19995) of patients' experience with cancer care.
Accordingly, the board developed 10 recommendations for optimizing the delivery of cancer care for all Americans. These recommendations, which are encapsulated in the seminal report Ensuring Quality Cancer Care,5 are organized around 3 central questions (Hewitt and Simone, 19995):
- 1)What problems are evident in the quality of cancer care and what steps can be taken to improve care?
- 2)How can we improve what we know about the quality of cancer care?
- 3)What steps can be taken to overcome barriers of access to quality cancer care?
Thus, as we enter the second decade of the 21st century, it seems appropriate to examine the 10 recommendations of Ensuring Quality Cancer Care with respect to the current state of cancer care delivery. This review examines each recommendation and describes the progress that has been made and what further work needs to be accomplished.
What Problems Are Evident in the Quality of Cancer Care and What Steps Can Be Taken to Improve Care?
In the report, the IOM described a substantial gap in health care delivery, whereby the survival and quality of life of many patients with cancer was compromised when they did not receive evidence-based care. Recommendations 1 through 5 of this report describe optimal cancer care, which, when fully implemented, would narrow this gap.
Ensure that patients undergoing procedures that are technically difficult to perform and have been associated with higher mortality in lower volume settings receive care at facilities with extensive experience.
The relation between volume and favorable outcomes in cancer care, and in cancer surgery in particular, has been established across multiple oncologic diagnoses.6-8 Research in this area, together with the 1999 IOM report, has induced efforts to concentrate complex cancer care at high-volume programs. Although the success of these efforts has varied, evidence suggests that declining mortality rates for selected complex cancer operations has been achieved by redirecting certain patients to high-volume centers.9 A more dramatic, long-term shift may be achieved by increasing the capacity of and access to higher volume, higher performing cancer facilities. Currently, high-volume centers are under resourced to care for as much as half of the complex cancer cases.9
In the interim, contingency plans, such as directing patients to high-quality, lower volume providers, are needed. Throughout the nation, some lower volume hospitals and providers are performing complex care at a high level. Several quality-assessment programs aim to increase performance transparency and assist referring physicians, patients, and payors to identify high-quality providers: the American College of Surgeons National Surgical Quality Improvement Program, the American Board of Medical Specialties Maintenance of Certification Evaluation of Performance in Practice, the Joint Commission Ongoing Professional Practice Evaluation, and payor-driven pay-for-performance initiatives. These programs have initiated low-cost pathways for practitioners at lower volume hospitals to attain, verify, and maintain competence in these areas. Continued development of these programs will support provider and hospital benchmark certifications in complex cancer care. This, in turn, may guide patients with complex cancer issues to competent programs regardless of the program size.
Use systematically developed guidelines based on the best available evidence for prevention, diagnosis, treatment, and palliative care.
Despite recent trends toward patient-driven, personalized cancer care delivery, most cancer care is structured around accepted practice algorithms that are disease-specific and stage-specific. More than 1000 clinician experts, led by the National Comprehensive Cancer Network (NCCN), collaborated to develop evidence-based guidelines for more than 135 diseases or processes of cancer care. These guidelines have been adopted nationally10 and have been incorporated into a drug compendium that is used by the Centers for Medicare and Medicare Services (CMS) and other payors for reimbursement purposes.
Guidelines exist for cancer screening, diagnosis, and palliative care, thus spanning the entire cancer care cycle. The American Society of Clinical Oncology (ASCO) has incorporated many of these guidelines into its Quality Oncology Practice Initiative,11 which CMS adopted as a component of its Physician Quality Reporting System.12 Through this program, CMS awards incentive payments for eligible physicians who report on adherence to evidence-based guidelines for services furnished to Medicare beneficiaries.
Despite this progress, investigators have identified variations in adherence for selected providers and diseases and within individual institutions (including NCI-designated comprehensive cancer centers).13, 14 Underlying these variations are 4 important factors. First, physician adoption and reporting of systematically developed guidelines are voluntary. Second, the precise relation between the use of evidence-based guidelines and long-term outcomes has not been established. Because the guidelines are process-oriented, the relation to intermediate outcomes is more readily ascertained. With longer time frames, other influences, such as coexistent medical conditions, may become the primary drivers of outcomes. Additional research is needed in this area. Third, physiologic factors resulting from prior cancer treatment and comorbidities can affect adherence. Finally, patient preference sometimes prevents guideline-based treatment.
Since 1999, systematic development, adoption, and support for evidence-based guidelines in oncology practices have increased significantly. Continued adoption of electronic health records (EHRs) by individual practices will enable assessing and reporting guideline adherence without time-intensive and costly chart abstraction. Also, in the coming years, stronger mandates for systems of accountability, such as the mandatory reporting outlined in the Patient Protection and Affordable Care Act of 2010 (ACA) for selected cancer centers,15 are needed to ensure uniform adherence to evidence-based guidelines for cancer care.
Measure and monitor the quality of care using a core set of quality measures.
In its third recommendation, the IOM advocated the creation of a core set of quality measures for cancer that would effectively define the output of clinical programs. This standardized reporting process would provide benchmarks to increase transparency and identify key elements of quality outcomes. The universal core measure set described by the IOM has not been defined.
Over the past decade, organizations, including ASCO and NCCN, have collaborated to develop cancer care measures, and the National Quality Forum has endorsed more than 150 cancer-related measures for use in public reporting.16 These measures are largely process-oriented and fail to assess the entire care cycle. An ideal core measure set would include simplified cancer outcomes metrics that are stratified by stage or extent of disease and that include survival, 2 or 3 key quality-of-life indicators, treatment assessment, and costs of care. These measures are described below and are summarized in Table 1.
|Outcome Variable||Head and Neck Cancer||Breast Cancer||Esophageal Cancer||Gynecologic Cancer||Sarcoma||Lung Cancer||Colon and Rectal Cancer||Prostate Cancer|
|Patient Survival||Survival rates at 1 y and 2 y||DFS rates at 5 y and 10 y||Survival rate at 2 y||Survival rates at 2 y and 5 y||Survival rates at 2 y and 5 y||Survival rates at 1 and 2 y||Survival rates at 2 y and 5 y||Survival rates at 5 y and 10 y|
|Patient-Defined Quality of Life||Swallowing||Satisfaction with cosmetic appearance||Swallowing||Bladder and bowel function||Amputation rate||Pulmonary function||Bladder and bowel function||Bladder and bowel function|
|Speaking||Hormonal health||Weight||Limb function||Stoma rate||Sexual function|
|Long-Term Complications of Care||Second primary cancers|
|Other treatment-related complications|
|Treatment Assessment||Adherence to treatment guidelines|
|Time to complete treatment|
|Short-term complications of care|
|Costs of Care||Initial treatment|
All patients with cancer want to know their prognosis, particularly their chance of cure and long-term survival. The Surveillance, Epidemiology, and End Results Program collects and reports US cancer statistics, such as incidence rates and survival.17 National registries represent the best survival data available, but the data are not independently verified; and, because the program lacks a central pathology review, there is no consistency in pathology diagnosis.18
Patient-Defined Quality of Life.
In addition to survival, patients are concerned about the immediate and long-term consequences of their disease and treatment. Providers use several surveys to assess key indicators of quality of life for cancer patients. However, these tools commonly are used at the provider's discretion (often as a component of a research trial) and do not always evaluate essential outcomes after treatment.
Hundreds of tools exist to evaluate provider adherence to established standards of preventive, diagnostic, and therapeutic care. However, these tools often are limited in scope and apply to brief segments of care. Integrated care should be more rapid and efficient than fragmented care. Thus, process measures for cancer should emphasize diagnostic and staging accuracy, multidisciplinary treatment planning, and post-therapy management.
Also important is measuring treatment cycle time. Some oncologists associate shorter treatment cycles times with better long-term outcomes for certain cancers.19 More study in this area is needed to establish the precise relation between treatment cycle time and long-term outcomes.
Costs of Care.
Currently, as the US economy buckles under rising health care costs, there is increasing recognition that health care costs must be compared across providers to identify cost inefficiencies and to quantify cost increases associated with comorbidities, delayed diagnoses, and adverse events. It is unclear, however, whether costs may be used as an overall indicator of quality. Current reimbursement models use costs as a marker for quality, which is appropriate for hospital-acquired conditions. However, costs are a poor marker of quality for patients with late-stage diagnoses and complex comorbidities, which require more intensive treatment.
Even getting at cost data is problematic, because there is no uniform costing methodology across providers to facilitate cost comparisons. Thus, a standardized methodology and reporting structure is needed to benchmark health care costs across providers throughout the cycle of care and to identify situations in which health care costs may serve as a marker of quality.
To define and influence desired outcomes, health care quality measures must be standardized, reproducible, and widely available. Furthermore, these measures must span the entire treatment cycle (prevention, intervention, and survivorship) and must quantify dimensions of health care delivery that are meaningful to a variety of audiences. The resulting meaningful measures will support comparative benchmarking of current and long-term performance.
Ensure the following elements of quality care for each individual with cancer: 1) that recommendations about initial cancer management, which are critical in determining long-term outcome, are made by experienced professionals; 2) an agreed-upon care plan that outlines goals of care; 3) access to the full complement of resources necessary to implement the care plan; 4) access to high-quality clinical trials; 5) policies to ensure full disclosure of information about appropriate treatment options; 6) a mechanism to coordinate services; and 7) psychosocial support services and compassionate care.
The IOM enumerated previous definitions of quality care with its fourth recommendation, which advocated care coordination, equitable access, informed decision making, and supportive care.
Research suggests that outcomes are improved when patients receive cancer care from a highly functioning, multidisciplinary care team when treatment is guided by a written plan of care.20, 21 Despite this recognition, health care remains fragmented, and patients or their caregivers bear the burden of transitioning between providers.
In a 2011 report, the IOM attributed poor care coordination to systemic issues in the US healthcare system, including lack of provider accountability for delivering patient-centered care and inadequate financial resources to incentivize providers to deliver patient-centered care.21 To date, there have been no successful national strategies to improve care coordination for cancer patients. Universal adoption of EHRs has been recommended to improve care coordination. This is a key requirement for “meaningful use” incentives outlined in the Health Information Technology for Economic and Clinical Health Act provision of the American Recovery and Reinvestment Act of 2009 (ARRA). The ACA also provides for shared savings to providers that deliver coordinated care through accountable care organizations. The impact of these provisions has not been realized.
Equitable access to care.
The 2010 National Healthcare Disparities Report from the Agency for Healthcare Research and Quality (AHRQ) reported continued access issues for minorities, individuals of low socioeconomic status, and residents in certain geographic areas. That report cited lack of insurance as an ongoing barrier to equitable access to cancer care, particularly for preventive care.22 Even insured patients experience delays in care because of primary care referrals and coverage preauthorizations. Patient-specific psychological and socioeconomic hurdles further limit access to coordinated oncology care.23 Individuals with fewer resources tend to seek care based on geographic proximity and accessibility, often at the expense of quality.24 Thus, although the ACA seeks to redress insurance barriers to equitable access, effort is needed to eliminate the geographic, financial, and social barriers that prevent patients from seeking comprehensive cancer care.
Patient access to high-quality clinical trials is also an issue. Historically, lack of coverage for clinical trials created financial barriers to patient participation in novel and potentially beneficial interventions. This situation has improved since Medicare implemented coverage for standard costs of clinical trials in 2000 and since many states have mandated coverage of “routine care” costs for clinical trials participants.25 Investigators suggest that other barriers to participation exist, including a lack of general knowledge about clinical trials, socioeconomic status, and trial design.26, 27 Hospital-based patient navigation programs have improved enrollment and retention rates in clinical trials, suggesting this as a means for improving access.21
Informed decision making.
Patient education at the onset of treatment planning is associated with better outcomes.21 Many patients do not feel adequately informed of their treatment options and the associated prognoses,21 whereas other patients cope with information overload. Patient-focused educational materials from reputable resources, such as the American Cancer Society, NCI, ASCO, and patient advocacy groups, may be used by clinicians to better educate patients regarding appropriate treatment options.
Several studies have documented improvements in survival and multiple indicators of well being after psychosocial support interventions.28, 29 Many providers lack the resources and, in some cases, the skills to provide adequate psychosocial services to cancer patients. Where these services are offered, they are either denied for reimbursement by insurers or reimbursed at very low rates, making these services an absorbed cost for hospitals. Some experts recommend incorporating psychosocial support into oncology provider education and certification programs to improve psychosocial support for cancer patients.21
Supportive care, together with care coordination, equitable access, and informed decision making, represents ideal cancer care from the patient's perspective.5 Additional efforts, as described above, are needed to ensure that these services are made available to all cancer patients.
Ensure quality of care at the end of life, in particular, the management of cancer-related pain and timely referral to palliative and hospice care.
Early referral to palliative care significantly decreases symptom burden and also may increase survival among patients with advanced lung cancer.30 Although patients with advanced cancer are diagnosed a median of 200 to 250 days before death, patients are referred to the palliative care team approximately 45 days before death.31 This delay in referral, which compromises end-of-life quality for cancer patients, may relate to the misconception that palliative care reduces hope. Another barrier to early palliative care referral is the perception by oncologists that such care must occur sequentially rather than concurrently with cancer treatment. In addition, although most cancer centers in the United States have inpatient consult teams, less than half have outpatient clinics, which provide early access to symptom control and advance care planning. Even fewer have dedicated acute palliative care units (Fig. 1).32 Cancer centers that offer these services often are under resourced to care for the high volumes of patients receiving treatment at their institutions.
For cancer patients who have a life expectancy of ≤6 months, hospice programs deliver excellent end-of-life care. However, it is important that patients receive optimal therapy for their physical and emotional distress before their referral to hospice. In addition, providers must have appropriate discussions with patients and their families regarding the transition from cancer treatment to comfort care.
Several strategies have been developed to improve end-of-life care. Conceptual models are under development to help referring physicians, nurses, patients, and their families better understand the role of palliative care.33 Several studies also have demonstrated improved quality of life and, in some cases, better survival for patients who received nurse-led palliative care.21 Some insurers have addressed end-of-life care shortages by offering palliative care and hospice services directly to patients, leading to higher use of hospice services and dramatic reductions in inpatient days and intensive care unit admissions.34 Another approach is discussing advance care during treatment planning.35 Because of these interventions and health reform-generated programs, supportive and psychosocial services may be better integrated into our delivery system.
How Can We Improve What We Know About the Quality of Cancer Care?
The IOM attributed the gaps in the quality of cancer care in part to the lack of clinical trials to evaluate the aspects of cancer care delivery. Recommendations 6 through 8 of this report outline how such research may be supported.
Federal and private research sponsors such as the National Cancer Institute, the Agency for Health Care Policy and Research, and various health plans should invest in clinical trials to address questions about cancer care management.
Currently, there are no adequate studies to identify why established therapies are not offered to some patients, and there is no mechanism for data collection to support this. National tumor registries, other repositories, and health plans do not collect data to address these questions. However, prospective data collection on newly diagnosed cancer cases with appropriate endpoints should assist investigators in identifying these issues.
With its sixth recommendation, the IOM suggested that clinical trials may be 1 setting in which this type of prospective data collection could occur. However, in their current form, clinical trials do not identify issues of cancer care management, because they are conducted in controlled settings with prescreened populations. A few studies have successfully incorporated a health services research approach into clinical trial design.36, 37 However, cancer care management is still under represented in clinical trials as a whole.
Investigators have identified informed consent as a potential barrier to randomized controlled studies of care management.38 For patients with advanced disease, poor health drives high attrition rates from clinical trials. Alternative approaches, such as using telemedicine to communicate with study participants, may improve patient retention in such studies.39 By adapting clinical trials for health services research, the efficacy of health care technologies and interventions may be evaluated in clinical settings. Alternatively, carefully designed observational studies may be used to answer clinical questions that cannot be addressed with a randomized controlled trial.40
A cancer data system is needed that can provide quality benchmarks for use by systems of care (such as hospitals, provider groups, and managed care systems).
Quality benchmarking requires the existence of measures with standardized definitions, processes, and systems for data collection and with standardized reporting formats. Despite concerted efforts in this arena, minimal progress has been made since the IOM report was first published.
Large health care systems in certain geographic areas have implemented EHRs that capture relevant data fields. However, these systems focus on primary care.41 Oncology-specific data elements that capture current disease status, functional status, and adherence to national treatment standards are not standard in such systems,42 although vendors are beginning to market oncology-specific EHRs.43, 44 For most providers, this reporting depends on time-intensive and resource-intensive abstraction of medical charts in the absence of EHR adoption by individual practices.
To date, it has not been economically feasible to develop a scalable, cancer-specific data system that integrates the increasingly sophisticated, tumor-specific biology with more general clinical aspects. Stronger mandates, such as those outlined in the ACA for selected cancer centers, are needed to advance the development of this cancer-specific data system.
Public and private sponsors of cancer care research should support national studies of recently diagnosed individuals with cancer, using information sources with sufficient detail to assess patterns of cancer care and factors associated with the receipt of good care. Research sponsors should also support training for cancer care providers interested in health services research.
In recent decades, there has been significant progress in altering the progression of several malignancies through screening, appropriate local therapies, and incorporation of systemic therapies to reduce the risk of recurrence and death. However, these advances are not universally offered to appropriate candidates for these approaches, and little is known about why this occurs.
The American Recovery and Reinvestment Act of 2009, which directed $1.1 billion to comparative effectiveness research (CER), accelerated activity in this area.45 In June 2011, the Government Accountability Office reported that the funds had been assigned to new CER programs.46 To guide funding agencies in the use of ARRA-generated monies, the IOM prepared a report outlining national CER priorities. Cancer was addressed in 6 primary CER topics.47, 48
This activity reignited interest in CER throughout the cancer community. The National Institutes of Health directed funding to previously approved, but unfunded CER, Challenge Grants and Grand Opportunity award programs, and other ongoing programs as administrative supplements. The NCI and AHRQ awarded more than 80 grants to CER studies evaluating cancer prevention, screening, and treatment. The NCI also funded network programs designed to organize smaller programs into national programs of cancer control by merging clinical research and community-based programs. Funding was directed to link the Surveillance, Epidemiology, and End Results national database with other databases to enumerate cancer outcome issues specific to Medicare patients.49 Furthermore, the Secretary of Health and Human Services directed funding to improve clinical registries and data networks and recently announced the creation of a Comparative Effectiveness Research Inventory to merge CER databases.50
This first round of major funding of CER for cancer care represents the first major national funding initiative that corresponds to the IOM's recommendation. The impact of this funding has yet to be realized. It is unclear whether this funding effort will continue in the current legislative and economic climate. However, the Patient-Centered Outcomes Research Institute created by the ACA has been charged with directing and funding ongoing CER. There is little evidence that health plans have made similar investments in this type of research.
To address the shortage of investigators trained in health services research, the NCI issued 8 career development awards aimed at training investigators in CER. Training more investigators in CER, identifying which outcomes are important to patients, and determining how to build better patient/provider partnerships will set the future course for CER in cancer care.
What Steps Can Be Taken to Overcome Barriers of Access to Quality Cancer Care?
Although advances in medical science have improved short-term and long-term outcomes for insured cancer patients, certain populations with cancer have not experienced similar progress. Recommendations 9 and 10 of this report examine the barriers these individuals face in accessing quality cancer care.
Services for the un- and underinsured should be enhanced to ensure entry to, and equitable treatment within, the cancer care system.
Access and coverage issues for the uninsured and underinsured have worsened since the publication of this recommendation. The uninsured population stresses the health care system, and the rising costs of cancer care coupled with access issues magnify the problem. The estimated 2010 cancer care expenditures were $125 billion, and it is projected that these costs will to rise to $207 billion in 2020.51 Beyond the financial implications for patients and their families, lack of insurance is associated with poorer outcomes and lower survival rates.52
The 2009 and 2010 AHRQ National Healthcare Disparities Reports cited ongoing disparities in access to care. Those reports indicated that racial and ethnic minorities and individuals with lower incomes and education levels had disproportionate uninsured rates. The reports also identified poorer quality of care, including lower rates of screening for breast cancer and colon cancer, and increased barriers to care, leading to advanced-stage breast and colon cancer diagnoses for minority populations compared with non-Hispanic whites.22, 53
Several agencies have attempted to address access issues through the development of programs, such as the National Breast and Cervical Cancer Early Detection Program. These programs provide funding to states for the screening for and early detection of cancer in underserved populations. Several states, such as Massachusetts, have implemented insurance reforms with reductions in rates of uninsured. The federal prescription drug program, Medicare Part D, was enacted in 2006 to subsidize the costs of prescription drugs for Medicare beneficiaries. That program is particularly important for cancer patients, because the cost of pharmaceutical therapies will continue to rise as treatment options become more advanced. In 2010, legislators attempted to broaden the scope of coverage through the ACA. If the ACA survives the current legal and legislative challenges, then its access provisions may improve coverage in several years.
Studies are needed to find out why specific segments of the population (eg, members of certain racial or ethnic groups, older patients) do not receive appropriate cancer care. These studies should measure provider and individual knowledge, attitudes, and beliefs, as well as other potential barriers to access to care.
Since this recommendation was published, studies have examined racial, cultural, age-related, and sex-related disparities to identify why, when, and how patients seek care. One study indicated that providers are inadequately prepared to address and communicate the complexities of cancer care to diverse patient populations.54 Despite compelling data describing the nature and impact of disparities in cancer care, more than 10 years after the IOM report, there has been limited progress.
Several programs established through the NCI's Center to Reduce Cancer Health Disparities are in place to address these issues. For example, the Comprehensive Partnerships to Reduce Cancer Health Disparities program is designed to increase the participation of institutions targeting communities with cancer health disparities in cancer research and research training. The initiative also aims to increase the involvement and effectiveness of NCI-designated cancer centers in developing effective research, education, and outreach programs to encourage diversity among competitive researchers and to reduce cancer health disparities.55 In addition, the AHRQ Health Care Innovations Exchange program was launched in 2008 to accelerate health care delivery improvements and to reduce nationwide health care disparities through early adoption of evidence-based innovations.56
Important progress has been made in understanding the factors that contribute to health disparities. Significant work is now needed to develop and implement interventions for those population segments that do not receive appropriate cancer care.57
In conclusion, the 1999 IOM report presented a well researched and timely description of the state of US cancer care delivery. Its 10 recommendations described what constitutes quality cancer care, how we can improve our knowledge of quality cancer care, and how to overcome the barriers of access to quality cancer care. The ferment created by the report reignited interest in patient safety, preventing medical errors, and improving the overall quality of care, leading to significant health care improvements through the efforts of the health care industry and the government. Much of the progress has been stimulated and funded by 2 recent pieces of legislation: the ARRA and the ACA.
It is clear that, as we enter the second decade of the 21st century, some cancer patients are not receiving ideal care despite these efforts. Progress-to-date, current gaps, and potential management strategies are summarized in Table 2. The greatest challenges center on how to define and implement nationwide solutions, especially universal transparent metrics, access to care, and end-of-life care. More work is needed, especially in the areas of cancer care access and treatment of minority populations, to ensure that all Americans have access to the finest quality care throughout the cycle of care. Increased awareness of the current deficiencies of our cancer care delivery system and action by providers and policy experts should further accelerate improvement.
|Recommendation 1: Ensure that patients undergoing procedures that are technically difficult to perform and have been associated with higher mortality in lower volume settings receive care at facilities with extensive experience|
|Progress to date|
|•Declining mortality rates for selected complex cancer operations have been achieved by redirecting certain patients to high-volume cancer centers|
|•The capacity at high-volume centers is insufficient to provide care for all complex cancer cases|
|•Increase capacity for complex cancer cases at high-volume centers|
|•Develop contingency plans to direct patients with complex cancers to high-quality, lower volume providers|
|Recommendation 2: Use systematically developed guidelines based on the best available evidence for prevention, diagnosis, treatment, and palliative care|
|Progress to date|
|•The NCCN worked with clinical experts to develop guidelines for more than 135 cancer diseases or processes of care|
|•Physician adoption and reporting of adherence to these guidelines is voluntary|
|•EHR adoption by individual practices should facilitate cost-effective and timely reporting of guideline adherence|
|•Stronger mandates for systems of accountability are needed to ensure uniform adherence to evidence-based guidelines for cancer care|
|Recommendation 3: Measure and monitor the quality of care using a core set of quality measures|
|Progress to date|
|•Cancer care measures have been developed and endorsed for use in quality reporting|
|•These measures are largely process-oriented|
|•There is no nationally mandated program to which providers report data for core measures for cancer|
|•Implement a core measure set for cancer with simplified outcomes metrics that are stratified by stage or extent of disease and include survival, 2 or 3 key quality-of-life indicators, treatment assessment, and costs of care|
|Recommendation 4: Ensure the following elements of quality care for each individual with cancer|
|That recommendations about initial cancer management, which are critical in determining long-term outcome, are made by experienced professionals|
|An agreed-upon care plan that outlines goals of care|
|Access to the full complement of resources necessary to implement the care plan|
|Access to high-quality clinical trials|
|Policies to ensure full disclosure of information about appropriate treatment options|
|A mechanism to coordinate services|
|Psychosocial support services and compassionate care|
|Progress to date|
|•Multidisciplinary care planning is used by many clinicians to provide coordinated care to cancer patients|
|•Medicare and several states cover standard or routine costs of clinical trials, which has improved cancer patients' access to clinical trials|
|•Patient-focused educational materials are available to clinicians when discussing appropriate treatment options with patients|
|•Continuing geographic, financial, and social barriers prevent patients from seeking and receiving multidisciplinary care planning and comprehensive cancer care|
|•Many cancer patients receive inadequate psychosocial support|
|•Universal adoption of EHRs by individual practices should improve care coordination|
|•Implement programs to ensure provider accountability for delivering patient-centered care and incentivize providers to deliver patient-centered care|
|•Incorporate psychosocial support into oncology provider education and certification programs to improve psychosocial support for cancer patients|
|Recommendation 5: Ensure quality of care at the end of life, in particular, the management of cancer-related pain and timely referral to palliative and hospice care|
|Progress to date|
|•Screening tools are available to monitor the frequency and severity of patients' symptoms to guide patients to supportive and palliative care services|
|•Most cancer centers in the United States have inpatient consult teams|
|•Patients with advanced cancer often are referred to palliative care late in their course, which compromises quality of life for these patients|
|•Incorporate advance care planning into oncology provider education and certification programs to improve advance care planning for cancer patients|
|•Consider nurse-led and insurer-led palliative care initiatives to increase palliative care access for patients|
|Recommendation 6: Federal and private research sponsors such as the National Cancer Institute, the Agency for Health Care Policy and Research, and various health plans should invest in clinical trials to address questions about cancer care management|
|Progress to date|
|•This recommendation has not been implemented because of the current nature of clinical trials|
|•Cancer care management is addressed in Recommendation 8|
|•Adapt clinical trials for health services research|
|•Carefully design observational studies to answer clinical questions that cannot be addressed with a randomized controlled trial|
|Recommendation 7: A cancer data system is needed that can provide quality benchmarks for use by systems of care (such as hospitals, provider groups, and managed care systems)|
|Progress to date|
|•Some large health care systems have implemented EHRs that capture data fields relevant to cancer care|
|•There is no standardized system for all cancer care providers to report on quality benchmarks|
|•Stronger mandates for cancer-specific data systems are needed to ensure that EHRs capture oncology-specific data elements, such as disease status, functional status, and adherence to national treatment standards|
|Recommendation 8: Public and private sponsors of cancer care research should support national studies of recently diagnosed individuals with cancer, using information sources with sufficient detail to assess patterns of cancer care and factors associated with the receipt of good care; research sponsors should also support training for cancer care providers interested in health services research|
|Progress to date|
|•The ARRA, which directed $1.1 billion to CER, has accelerated CER activity|
|•CER for cancer is just beginning|
|•There is a shortage of investigators trained in health services research|
|•Continue funding in CER for cancer and health services research training|
|Recommendation 9: Services for the un- and underinsured should be enhanced to ensure entry to, and equitable treatment within, the cancer care system|
|Progress to date|
|•Programs are directing funds to screening for and early detection of cancer in underserved populations|
|•The ACA introduced new programs to improve access for many uninsured individuals|
|•The uninsured population continues to grow despite ongoing health care legislation|
|•Uninsured status is associated with poorer outcomes and lower survival rates|
|•Additional state and federal programs are needed to improve access to cancer prevention and treatment services for the uninsured|
|Recommendation 10: Studies are needed to find out why specific segments of the population (eg, members of certain racial or ethnic groups, older patients) do not receive appropriate cancer care|
|Progress to date|
|•Programs have been introduced to increase the involvement of NCI-designated cancer centers in developing research, education, and outreach programs to reduce cancer health disparities|
|•There are ongoing disparities, including later stage diagnoses and poorer outcomes for minorities with cancer|
|•Progress has been made in understanding the factors that contribute to health disparities, but this focus should be shifted to developing and implementing interventions to reduce these disparities|