Potential Impact of the Medicare Prescription Payment Plan for Medicare Part D Beneficiaries With a Cancer Diagnosis
Abstract
PURPOSE To address high out-of-pocket (OOP) medication costs among Medicare Part D beneficiaries, the 2022 Inflation Reduction Act introduced the Medicare Prescription Payment Plan (M3P), a voluntary program that allows beneficiaries to spread OOP costs over the calendar year. We examined M3P's potential impact among beneficiaries with cancer, who frequently incur substantial early-year Part D medication costs. MATERIALS AND METHODS We evaluated a 2022 5% random sample of Medicare beneficiaries with a cancer diagnosis and ≥1 fill for a cancer-indicated Part D medication. We estimated 2025-adjusted annual true OOP spending and median monthly beneficiary OOP payment obligations with and without M3P enrollment. Subgroup analyses were performed by demographics, nonadherence status in 2022, and Part D benefit phase. RESULTS Among 168,480 beneficiaries with cancer, most were diagnosed with breast (47.6%), dermatologic (17.6%), or prostate (13.3%) cancers. Overall, 46.7% were projected to reach catastrophic coverage in 2025, with 32.4% doing so in January. Breast (29.7%), prostate (21.20%), and hematologic (20.0%) cancers were most common among those reaching catastrophic coverage. Overall, 43.0% were nonadherent to cancer-indicated Part D medications, with 31.5% reaching catastrophic coverage in January 2025. M3P reduced beneficiary payment obligation variability, especially among those reaching the catastrophic phase in January (IQR, $1,798 US dollars [USD] no M3P v $118 USD M3P). Of those reaching catastrophic coverage with a cancer-indicated drug (58.6% overall), 89.2% did so in January. CONCLUSION Early-year entry into catastrophic coverage is common among beneficiaries with certain high-cost cancers. M3P may most effectively reduce financial burden when enrollment occurs before January. Targeted outreach from cancer care teams and Part D plans to nonadherent patients and those considering costly therapies could maximize program impact and improve treatment outcomes.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Aryana Sepassi
Department of Pharmacy Practice & Sciences, University of California, San Diego Skaggs School of Pharmacy & Pharmaceutical Sciences, La Jolla, CA
Scott D. Ramsey
A. Mark Fendrick
Department of Internal Medicine, Division of General Medicine, University of Michigan, School of Medicine, Ann Arbor, MI
Nico Gabriel
University of Colorado Skaggs School of Pharmacy, Aurora, Colorado, United States
Jason A. Zell
UC Irvine Health, Chao Family Comprehensive Cancer Center, Orange, CA
Dana B. Mukamel
Department of Medicine, Division of Internal Medicine, iTEQC Research Program, University of California, Irvine, Irvine, CA
Sean D. Sullivan
The Comparative Health Outcomes, Policy, and Economics Institute, University of Washington, School of Pharmacy, Seattle, WA