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The PIPC Blog

PIPC Weekly Update: August 28, 2023

8/28/2023

 
In this week's edition...
 
— PIPC Submits Comments on ICER Assessment of MLD Treatments. Click here to read the letter.
— PIPC Submits Comments on CMS Proposed Guidance for Coverage with Evidence Development. Click here to read the article.
— Takeaways from AcademyHealth’s Organizational Briefing with PCORI Executive Director Nakela Cook. Click here to read the blog.
— ICHOM Seeks Input on Patient Charter. See details below.
— Emerging Threats in States for Use of Discriminatory Metrics. See details below.
— What Happens in Countries Using QALYs and Cost-Based Thresholds? See details below.
— ICER's QALY-Based Study Topics. See details below.
— Upcoming Events and Webinars. See details below.
— AHRQ Effective Program Updates. See details below.
— Job Openings. See details below.
What We're Reading
 
1. PIPC Submits Comments on ICER Assessment of MLD Treatments. In a letter to the Institute for Clinical and Economic Review (ICER), PIPC submitted comments on ICER's assessment of treatments for Metachromatic Leukodystrophy (MLD). The letter criticizes ICER for its use of the discriminatory quality-adjusted-life-years (QALY) metric, as well as for continuing to conduct premature assessments. In addition to reconsidering the use of QALYs, PIPC also urges ICER to reconsider several of its modeling choices given the severity of and population impacted by this disease. Click here to read the letter.
 
2. PIPC Submits Comments on CMS Proposed Guidance for Coverage with Evidence Development. In a comment letter to the Centers for Medicare and Medicaid Services (CMS), the Partnership to Improve Patient Care (PIPC) offered feedback on CMS's Proposed Guidance Document for Coverage with Evidence Development (CED). The letter stresses that PIPC shares CMS's concerns that a framework is needed for more predictable and transparent evidence development. To that end, Our comments focus on the following concerns and recommendations:

  • CED guidance should promote early and consistent engagement of patients and people with disabilities.
  • Patient safeguards should promote health equity, not restrict access to care.
  • CED should focus on real world data collection.
  • CMS should establish standards for meeting evidence generation requirements.
  • CED should clearly acknowledge and abide by the laws barring use of QALYs and similar measures.
 
Click here to read the article.
 
3. Takeaways from AcademyHealth’s Organizational Briefing with PCORI Executive Director Nakela Cook. AcademyHealth recently hosted a discussion with PCORI Executive Director Nakela Cook on PCORI's priorities going forward and how researchers can take advantage of PCORI resources. “The discussion during the organizational briefing centered on how researchers can leverage PCORI resources to promote evidence generation, dissemination, and application...Dr. Cook’s remarks helped attendees understand how they can use PCORI tools to make evidence accessible to patients, providers, and other stakeholders and improve decision-making." Click here to read the blog.
 
4. ICHOM Seeks Input on Patient Charter. The International Consortium for Health Outcomes Measurement (ICHOM) is a non-profit organization working to define the health outcomes that matter most to patients and is currently seeking input from patients and people with disabilities about its Patient Charter. Jennifer Bright recently joined the ICHOM team as its President. The ICHOM Patient Charter "articulates ICHOM's commitments to the patient community and the rights and empowerment actions that patient representatives are entitled to when co-leading research and other initiatives with ICHOM. It will serve as a framework for fair partnerships to ensure the expertise of patient representatives is acknowledged and integrated at all stages of ICHOM initiatives, and is a step in our journey towards being a stronger ally for the patient community going forward.” To find out more about the Patient Charter, click here. To participate in the survey please click here.
 
Emerging Threats in States for Use of Discriminatory Metrics
 
Several states are considering policies that would reference entities such as the Institute for Clinical and Economic Review (ICER), which calls the discriminatory quality-adjusted life year (QALY) the “gold standard” for value assessment, and others are considering policies to import QALY-based coverage and reimbursement decisions from other countries that restrict access to care. We encourage you to keep track of all state-based threats using this new website tracking state activities. Key issues are highlighted below.

  • Click here to learn more about the potential for Prescription Drug Affordability Boards to discriminate by incorporating the use of QALYS.
  • Click here to view the Value Our Health state template legislation that would protect people with disabilities and chronic conditions from the use of QALYs and similar metrics developed by third parties such as ICER in decisions related to reimbursement and coverage, as well as ensure their engagement in decision-making. 
  • Click here to view a one pager about the flaws in ICER’s methodology. 
  • Click here to view information from experts on the downside of referencing foreign countries. 
  • Click here to learn about statutory protections against use of QALYs. 
 
Colorado
Colorado passed legislation in 2021 creating a Prescription Drug Affordability Review Board. The legislation included language stating that the Upper Payment Limit for selected drugs "shall not consider research or methods that employ a dollars-per-quality adjusted life year, or similar measure, that discounts the value of a life because of an individual's disability or age.” Nevertheless, the board’s rule governing affordability reviews specifically allows for use of the quality-adjusted life year measure, stating, "The Board may identify if the literature uses a quality-adjusted life-year analysis or a similar measure that discounts the value of a life because of an individual’s disability or age. The Board may use information that uses a quality-adjusted life year analysis to evaluate relative financial effects, but will not use quality adjusted life year analysis to determine an upper payment limit or other appropriate costs of a prescription drug. If quality-adjusted life year analysis is used during affordability review, the Board will acknowledge any health equity impacts to priority populations.” 
 
Colorado has now selected the following five drugs to be reviewed for a possible Upper Payment Limit: Enbrel (rheumatoid arthritis), Genvoya (HIV), Cosentyx (psoriasis, psoriatic arthritis), Stelara (ulcerative colitis), Trikafta (cystic fibrosis). The “estimated cost effectiveness” of the drug is allowed for consideration. View the website for more information.
 
Similar to the Massachusetts Health Policy Commission, Colorado has contracted with the Program on Regulation, Therapeutics, and Law (PORTAL), which also has a subcontract with ICER in Massachusetts for its work there. PORTAL supports the use of QALYs, as expressed in a JAMA commentary titled, "Congress’ Misguided Plan to Ban QALYs.” Presentations (including from PORTAL) related to cost effectiveness analyses to the Colorado Board have referenced the use of a cost-per-QALY or the equal value of life-year gained (evLYG) in estimating cost effectiveness of treatments. PORTAL and others have encouraged use of QALYs and evLYG calculations, which have been widely critiqued for failing to account for quality-of-life improvements and for being calculated using the QALY’s flawed health utilities. Several commenters raised concerns about the Board’s potential use of cost effectiveness analyses:

  • Arthritis Foundation: "However, data inputs used to calculate QALYs do not holistically reflect patient experiences, preferences, goals and benefit-risk tolerance.”
  • NORD: "Complexities associated with rare disease therapies and the available data to determine their cost-effectiveness create unique challenges for determining fair prices for these products.”
  • Rare disease orgs: "We are writing out of concern that some decisions made by the Prescription Drug Affordability Board (PDAB) could have a severely detrimental effect on families struggling with rare and severe diseases, making it more difficult for them to have access to the therapies they need and slowing the critical research that offers them the promise of a better life."
  • U.S. Hereditary Angioedema Association: "In our experience, efforts by payers to assess value and cost for the HAE community rarely consider the disability, death, pain, and fear associated with the condition."
 
The Colorado Board will meet on September 15 at 12pm EST. Click here to register. 
 
Pennsylvania
In the last legislative session, the legislature introduced, HB 1722, a bill creating a Prescription Drug Affordability Board that would not bar reference to QALYs and would explicitly authorize the Board to contract with a third party that could include ICER. The bill has not been reintroduced in 2023. The Pennsylvania legislature held an informational meeting on Prescription Drug Boards in the House Health Committee on April 12 at 10am. Click here to learn more about Prescription Drug Affordability Boards and the implications of discriminatory measures of cost effectiveness. Click here to learn more about the committee chair, Rep. Dan Frankel. 
 
Massachusetts
An Act Advancing Health Care Research and Decision-Making Centered on Patients and People with disabilities, SD. 2117 and HD. 3356 has been introduced in both the House and Senate. This bill includes important patient protections including a ban on the discriminatory Quality-Adjusted Life Year (QALY).
 
Oregon
The Oregon legislature held a hearing on March 27, 2023 on SB 492, legislation that would address the use of biased measures of quality of life, such as quality-adjusted life years or QALYs. PIPC Chairman Tony Coelho submitted testimony stating, "This legislation reflects decades of work to advance disability rights and to end the use of discriminatory measures of the effectiveness of health care that too often drive barriers to care for people with disabilities. In the past this may have been considered just a disability issue, but today we recognize the implications of these biased algorithms for health equity more broadly.” Click here to view testimony from PIPC Chairman Tony Coelho. Click here to view testimony submitted by the Caring Ambassadors Program. Click here to view the list of organizations in Oregon supporting the bill. 
 
On October 6, 2022, the Oregon Health Evidence Review Commission (HERC) discussed a proposed plan for using QALYs. The meeting followed CMS approval of Oregon’s waiver application, which does not bar the use of QALYs in the interim. Click here to read comments submitted by PIPC along with 62 other groups asking CMS to reject the waiver. Click here to view the CMS-approved waiver. At the HERC meeting, the Oregon Health Authority expressed its intent to continue using a prioritized list, shifting it from use under a waiver to use as part of the State Plan Amendment after the waiver expires in 2027. The HERC decided to accept comments on their use of QALYs but has not made a decision as to whether they will adjust their methodology. Click here to view the letter from almost 50 advocacy groups asking the HERC to stop using QALYs. Click here to view testimony from PIPC Chairman Coelho to the Oregon HERC expressing his support for the Americans with Disabilities Act. Click here to view the options that continue to be under consideration by the HERC to continue using QALYs. Click here to view all of the comments shared with PIPC.

International News: What Happens in Countries Using QALYs and Cost-Based Thresholds?
 
Other countries are often referenced as examples of how the use of QALYs or similar cost-based thresholds impact access to care.

  • Australia: MS patients in Australia face limited choices with respect to effective treatments covered, and some are forced to raise money for treatment overseas.
 
  • U.K: The family of a patient with MS has had to turn to crowdfunding for treatment that is not funded through the NHS. 

ICER's QALY-Based Study Topics
 
The Institute for Clinical Economic Review (ICER) conducts cost effectiveness studies for insurers using the cost-per-QALY methodology. ICER provides guidance on its website for patients and patient advocates to provide direct input related to their experiences with the disease. Click here to provide patient input. Click here to view the topics and deadlines.

  • Paroxysmal Nocturnal Hemoglobinuria: Draft Scoping Document Available. Comments due August 14, 2023.
 
  • Schizophrenia: Draft Scoping Document available. Comments due on July 26, 2023.
 
  • Metachromatic Leukodystrophy: Draft Evidence Report now available.
 
  • Pulmonary Arterial Hypertension: Draft Scoping Document available. Open for comments until June 5, 2023.
 
  • Sickle Cell Disease: Evidence Report Available. California Technology Assessment Forum (CTAF) to meet on July 27, 2023, to review.
 
  • Non-Alcoholic Steatohepatitis: Final Evidence Report now available.
 
Upcoming Events and Webinars

PCORI Board of Governors Meeting
September 11, 2023
Click here to view.
 
2023 PCORI Annual Meeting
October 4-5, 2023
Click here to view.

Medical Journal Articles

Comparative Effectiveness of Treatments for Rheumatoid Arthritis in Clinical Practice: A Systematic Review. Click here to read the article.
 
QALYs: The Math Doesn’t Work. Click here to read the article.
 
The Implementation of Value-Based Frameworks, Clinical Care Pathways, and Alternative Payment Models for Cancer Care in the United States. Click here to view.
 
Perspectives on Patient-Reported Outcome Data After Treatment Discontinuation in Cancer Clinical Trials. Click here to view.
 
The Implementation of Value-Based Frameworks, Clinical Care Pathways, and Alternative Payment Models for Cancer Care in the United States. Click here to view.
 
Federal Data for Conducting Patient-Centered Outcomes Research on Economic Outcomes. Click here to view.
 
Patient-Reported Outcomes for People with Diabetes: What and How to Measure? A Narrative Review. Click here to view.
 
Patient Engagement in Research; Benefits, Challenges, Importance, and Implications. Click here to view.
 
The Opportunity for Greater Patient and Public Involvement and Engagement in Drug Development and Regulation. Click here to view.

AHRQ Effective Program Updates

Technical Brief: Measuring Healthcare Organization Characteristics in Cancer Care Delivery Research. Click here to view.
 
Systematic Review: Postpartum Care up to 1 Year After Pregnancy: A Systematic Review and Meta-analysis. Click here to view.
 
Draft Report: Impact of Healthcare Algorithms on Racial and Ethnic Disparities in Health and Healthcare. Click here to view.
 
Systematic Review: Partian Breast Irradiation for Breast Cancer. Click here to view.
 
Systematic Review: Use of Telehealth During the COVID-19 Era. Click here to view.
 
Research Report: Analysis of Requirements for Coverage with Evidence Development (CED) - Topic Refinement. Click here to view.
 
Technical Brief: Infection Prevention and Control for the Emergency Medical Services and 911 Workforce. Click here to view.
 
Systematic Review: Management of Infantile Epilepsies. Click here to view.

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