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Aligning Incentives: Quality of Care Initiatives and Precision Medicine

Keren Freydman, 2018 PharmD Candidate and Michael R. Page, PharmD, RPh
Current shifts in healthcare delivery and reimbursement models reflect the changing needs of a healthcare field that is rapidly advancing as novel technologies become available. Especially in oncology, the growth of precision medicine is transforming not only the way physicians provide care to their patients, but also the framework for how they are reimbursed. However, the increasing costs of medical treatments and devices combined and the lack of consistent regulation and reimbursement are issues all stakeholders face. These government and managed care initiatives, discussed in this article, are designed to align stakeholder incentives to help improve the quality of care and translate technological advances into improved patient outcomes and decreased healthcare costs. 
Government Initiatives (CMS)

The Medicare Access and CHIP Reauthorization Act (MACRA), passed in 2015, established the Quality Payment Program (QPP) as a replacement for the sustainable growth rate formula, with the goal of enabling physicians to provide higher quality care while reducing costs. The QPP consists of 2 methods of aligning incentives: the Merit-based Incentive Payment System (MIPS) and Advanced Alternative Payment Models (APMs).

Under MIPS, Medicare payments are determined by 4 interrelated performance categories: quality, clinical practice improvement activities, use of certified electronic health record technology, and resource use.1 Of these performance categories, improvement activities consists of activities that fall into 9 subcategories, including population management, care coordination, and achieving health equity, among others (Table 11).1 Improvement activities that are performed for 90 consecutive days are reported to Medicare for certification and scoring.1 The goal of the APM program, which is the second track under QPP, is to help physicians overcome reimbursement barriers in the current payment system.2 According to a 2015 guide to physician-focused APMs published by the American Medical Association, “APMs are needed that support the delivery of higher-quality care for patients, at lower costs for purchasers, in ways that are financially feasible for physician practices.”2 Physicians who participate in qualified APMs that meet certain thresholds are awarded a 5% annual lump sum payment and are exempted from MIPS.3 Participation in other APMs may help physicians improve MIPS scores.3 Physicians can choose from a variety of APM models to best address the specific barriers and opportunities their practice faces. Each model provides a framework that can be applied to practices of various sizes and specialties to help clinicians improve care, reduce costs, and qualify for incentive payments through MACRA (Table 22).

In the realm of oncology, general improvement opportunities may include more accurate diagnosis and staging, as well as methods to standardize use of treatments. Quality improvement activities may also focus on reducing the incidence of neoplastic symptoms and adverse events, such as nausea, vomiting, and pain, or in reducing complications, especially those that require hospital admissions. Other opportunities for improving quality of care may include optimizing the appropriate selection of patients for imaging studies.3 Successful APMs give providers flexibility in the services they provide, ensure adequate and predictable payments, and hold physicians accountable only for the costs and quality measures that are within their control.2

The Oncology Care Model (OCM) is another government initiative designed to bring about “better care, smarter spending, and healthier people.”4 The goal of this payment and delivery model is to align financial incentives to provide higher-quality, highly coordinated oncology care while minimizing costs. The OCM is currently being implemented for beneficiaries of Medicare and 17 participating commercial payers who have the flexibility to design unique payment incentives for their beneficiaries.4 A foundational aspect of this model is the use of current medical knowledge and shared decision making between physicians and patients to determine the best course of treatment that addresses each patient’s unique complex care needs.4

Under the OCM, physicians participate in arrangements that are based on episode payment models and include a 2-part payment system that incentivizes coordinated quality care.4 The first type of reimbursement is the monthly enhanced oncology services payment, which provide $160 per beneficiary per month for the duration of the episode of treatment. The second type of reimbursement is a performance-based payment that is given if oncology practices lower their total cost of care while improving quality during the treatment episode.

Other Quality Initiatives

The National Committee for Quality Assurance (NCQA) is a nonprofit organization whose general goal is to improve health care quality. NCQA collaborates with policymakers, large employers, physicians, patients, and health plans to identify key issues, decide how to promote improvement, and determine how to best measure outcomes.5 Over the past 5 years, NCQA’s yearly statistics have shown continuous improvement in the healthcare delivery system with regard to improved protocols, more efficient practices, and more engaged patients. Overall, these improvements have resulted in reduced morbidity, mortality, and costs.5

The standards and performance measures developed by the NCQA are applicable to a wide range of health care organizations and are used by consumers, media, and health plans to assess quality.5 NCQA quality improvement practices generally follow a framework of measuring, analyzing, improving, and then repeating the process. Organizations accredited by the NCQA must meet rigorous standards and report their performance yearly. Accredited health plans must adhere to over 60 standards and report their performance in over 40 areas to maintain accreditation. Currently, accredited plans cover 70.5% of Americans enrolled in health plans.5

Unlike NCQA standards, some initiatives in performance improvement are specific to certain disease state areas. For instance, the Institute for Quality (iQ) initiative was developed by the American Society of Clinical Oncology (ASCO) to “promote quality, value, and accountability in cancer care.” Several programs have been developed by the Institute for Quality to realize this goal, including the quality oncology practice initiative (QOPI).6 The QOPI is a quality assessment program that provides oncologists with standards of practice, a library of quality metrics, and tools to assess care and improve quality. Practices that participate in QOPI can compare themselves to national benchmarks, keep up-to-date with national practice guidelines, and access over 180 quality measures that have been developed by experts in oncology and organized into modules and pathways to assess the team-based care provided to outpatients. QOPI-certified practices are better prepared to meet the requirements of new payment models and reporting standards established by the government and payers.7,8

The QOPI certification program (QCP) provides a 3-year certification for outpatient oncology practices that apply and continually meet rigorous standards and target measures. Attaining QCP certification demonstrates that a practice is committed to continuous quality improvement and has validated processes for providing high quality care.7 The iQ also provides a quality training program that prepares oncology teams to design and implement quality improvement activities while balancing the priorities of running a practice. The program includes 5 focused days of learning via seminars, case examples, small group exercises, and access to faculty and coaches, followed by 6 months of as-needed remote coaching sessions.9

CancerLinQ, a subsidiary of ASCO, is an additional resource that collects real-world cancer data and uses big data analytics technology to provide treatment decision support and assist clinicians in providing personalized care.10 The iQ also provides access to clinical practice guidelines, provisional clinical opinions, and guideline endorsements to aid clinicians in providing high quality care.11

Value of Precision Oncology

A poster based on a retrospective analysis presented at the 2014 ASCO Quality Care Symposium offered proof that genomic targeted therapy was comparable in cost to standard therapies, but reduced the incidence and costs related to morbidities and complications.12 Genomic targeted therapy is enabled, in part, by companion diagnostics, which are used to inform the risk-benefit ratio of including certain drugs in a patient’s treatment plan. These tests can identify the presence or absence of specific mutations or biomarkers to predict a patient’s response to a targeted therapy. Having access to this information enables clinicians to select the most effective drug for the patient who is most likely to benefit from it, thereby reducing the toxicities and costs associated with trial-and-error prescribing.13

Currently, companion diagnostics account for less than 1% of total healthcare expenditures and make up only a small share of spending on in vitro diagnostics. However, their potential impact on improving patient outcomes and reducing inefficient use of healthcare spending is substantial.13 According to the results of a 2016 study, the use of a KRAS companion diagnostic test to select patients with metastatic colorectal cancer for treatment with epidermal growth factor receptor (EGFR) inhibitors, such as cetuximab or panitumumab, resulted in equivalent clinical outcomes and savings that ranged from $7500 to $12,400 per patient.13 Based on an estimate of 50,000 patients with metastatic colorectal cancer per year in the United States, the cost savings observed in this study could translate into over $400 million in savings per year from the regular use of KRAS testing. A poster presented at the ASCO 2009 Gastrointestinal Cancers Symposium estimated these savings to be as much as $740 million. Variation in these estimates is likely due to the inclusion of costs incurred from laboratory tests, clinical visits, and palliative care and differences in the length of treatment and costs of the drugs at the time each study was conducted. Despite the wide range in estimates, both studies found that regular KRAS testing would result in substantial cost savings.14

Another test used to direct precision oncology is Oncotype DX, a breast cancer assay that has been used to calculate the recurrence score (RS) in specific subsets of women diagnosed with stage I to III disease, although recent data have been released that show the safety and efficacy of this test in a broader range of patients.15 Oncotype DX has been found to be reasonable and necessary to contribute to breast cancer diagnosis and major treatment decisions for patients with estrogen receptor-positive disease and 0 to 3 postive nodes.15 Based on predictions, the Oncotype DX breast cancer assay could increase quality-adjusted survival by 8.6 years and reduce overall costs by $202,828.15

The Oncotype DX test predicts recurrence risk in node-negative, estrogen receptor-positive patients with early stage breast cancer more accurately than the current standard of care. In this way, Oncotype DX is especially useful for identifying low-risk patients and determining the need for chemotherapy, as defined by the NCCN guidelines.15 A study on the utility of the assay found that Oncotype DX was a cost-saving intervention in over two-thirds of probabilistic simulations. Therapy guided by Oncotype DX was associated with a net cost savings of about $2256 compared with treatment with tamoxifen and chemotherapy, with an incremental cost-effectiveness ratio of $1944 per life year saved compared with tamoxifen alone.15

Copyright AJMC 2006-2017 Clinical Care Targeted Communications Group, LLC. All Rights Reserved.
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