{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T22:21:28Z","timestamp":1790029288318,"version":"4.0.1"},"reference-count":37,"publisher":"American Medical Association (AMA)","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi251167-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Price reductions for originator biologics with biosimilar competitors have been modest in the US. This may be due to the US reimbursement model, where clinicians or their employing medical institution receive payment based on the percentage of the cost billed, incentivizing the highest-cost product. Currently, US policymakers are debating changing this policy. However, a clear understanding of price reductions achieved by the current system is needed to inform future reform efforts.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To assess the associations of biosimilar entry with the prices of originator biologics under Medicare Part B reimbursement.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This cohort study used bayesian structural time series models to analyze Medicare Part B Drug average sales price (ASP) data from quarter 1 of 2005 to quarter 1 of 2025, including 7 biologics with biosimilars available for at least 3 years (bevacizumab, epoetin, filgrastim, infliximab, pegfilgrastim, rituximab, and trastuzumab).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-7\">\n                    <jats:title>Exposure<\/jats:title>\n                    <jats:p>Biosimilar entry.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Relative differences in observed ASPs for originators and biosimilars vs the bayesian structural time series\u2013estimated counterfactual ASPs for originators had biosimilars not entered the market.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Analysis included 7 originator biologics that entered the market between 1989 and 2024. The number of biosimilars marketed during the study period ranged between 1 and 6 for originator biologics studied. Biosimilar entry was associated with changes in the ASP of the originator biologic of \u22127.4% (95% prediction interval, \u201310.5% to \u22124.3%) at 1 year, \u221231.7% (95% prediction interval, \u201341.6% to \u221221.9%) at 3 years, and \u221243.1% (95% prediction interval, \u201361.3% to \u221224.8%) at 5 years. Savings varied by drug, with the largest price reductions observed with pegfilgrastim and infliximab, with 5-year price reductions of \u221282.0% (95% prediction interval, \u201395.2% to \u221254.0%) for pegfilgrastim and \u221262.3% (95% prediction interval, \u201373.4% to \u221245.2%) for infliximab. Biosimilar prices were generally lower than the originator biologics at all postentry periods and decreased over time.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251167-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this cohort study, counterfactual analysis found that price reductions from biosimilar entry were more substantial than suggested by simpler pre-post comparisons. However, these savings remained less than those achieved by small-molecule generics, highlighting the need for policy reforms to enhance market competition and realize greater savings.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2025.42937","type":"journal-article","created":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T16:00:16Z","timestamp":1762876816000},"page":"e2542937","source":"Crossref","is-referenced-by-count":9,"title":["Biologic Drug Prices in Medicare Part B After Entry of Biosimilars to the Market"],"prefix":"10.1001","volume":"8","author":[{"given":"Abdullah","family":"Abdelaziz","sequence":"first","affiliation":[{"name":"Department of Pharmacy Systems, Outcomes and Policy, College of Pharmacy, University of Illinois Chicago, Chicago"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aaron N.","family":"Winn","sequence":"additional","affiliation":[{"name":"Department of Pharmacy Systems, Outcomes and Policy, College of Pharmacy, University of Illinois Chicago, Chicago"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stacie B.","family":"Dusetzina","sequence":"additional","affiliation":[{"name":"Department of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee"},{"name":"Vanderbilt Ingram Cancer Center, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aaron P.","family":"Mitchell","sequence":"additional","affiliation":[{"name":"Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10","published-online":{"date-parts":[[2025,11,11]]},"reference":[{"issue":"8","key":"zoi251167r1","first-page":"469","article-title":"The economics of biosimilars.","volume":"6","author":"Blackstone","year":"2013","journal-title":"Am Health Drug Benefits"},{"issue":"4","key":"zoi251167r3","first-page":"3","article-title":"Biosimilar cost savings in the united states: initial experience and future potential.","volume":"7","author":"Mulcahy","year":"2018","journal-title":"Rand Health Q"},{"issue":"12","key":"zoi251167r5","doi-asserted-by":"publisher","DOI":"10.1001\/jamanetworkopen.2022.44670","article-title":"Comparison of uptake and prices of biosimilars in the US, Germany, and Switzerland.","volume":"5","author":"Carl","year":"2022","journal-title":"JAMA Netw Open"},{"issue":"11","key":"zoi251167r7","doi-asserted-by":"publisher","DOI":"10.1001\/jamanetworkopen.2021.33451","article-title":"Association of generic competition with price decreases in physician-administered drugs and estimated price decreases for biosimilar competition.","volume":"4","author":"Dickson","year":"2021","journal-title":"JAMA Netw Open"},{"issue":"4","key":"zoi251167r8","doi-asserted-by":"publisher","first-page":"481","DOI":"10.1016\/j.jval.2019.12.007","article-title":"Biosimilar uptake in Medicare Part B varied across hospital outpatient departments and physician practices: the case of filgrastim.","volume":"23","author":"Socal","year":"2020","journal-title":"Value Health"},{"issue":"6","key":"zoi251167r9","doi-asserted-by":"publisher","first-page":"893","DOI":"10.1001\/jamaoncol.2018.6196","article-title":"Association between reimbursement incentives and physician practice in oncology: a systematic review.","volume":"5","author":"Mitchell","year":"2019","journal-title":"JAMA Oncol"},{"issue":"12","key":"zoi251167r10","doi-asserted-by":"publisher","DOI":"10.1001\/jamahealthforum.2023.4335","article-title":"Biosimilar uptake in Medicare Advantage vs traditional Medicare.","volume":"4","author":"Kozlowski","year":"2023","journal-title":"JAMA Health Forum"},{"issue":"1","key":"zoi251167r11","doi-asserted-by":"publisher","first-page":"15","DOI":"10.18553\/jmcp.2024.30.1.15","article-title":"Filgrastim and infliximab biosimilar uptake in Medicare Advantage compared with traditional Medicare, 2016-2019.","volume":"30","author":"Liu","year":"2024","journal-title":"J Manag Care Spec Pharm"},{"issue":"20","key":"zoi251167r12","doi-asserted-by":"publisher","first-page":"2245","DOI":"10.1200\/JCO-24-01907","article-title":"Use of low-value cancer treatments in Medicare Advantage versus traditional Medicare.","volume":"43","author":"Jung","year":"2025","journal-title":"J Clin Oncol"},{"issue":"5","key":"zoi251167r13","doi-asserted-by":"publisher","first-page":"632","DOI":"10.1377\/hlthaff.2022.00812","article-title":"The role of financial incentives in biosimilar uptake in Medicare: evidence from the 340B program.","volume":"42","author":"Bond","year":"2023","journal-title":"Health Aff (Millwood)"},{"issue":"5","key":"zoi251167r14","doi-asserted-by":"publisher","first-page":"799","DOI":"10.1007\/s40258-023-00812-w","article-title":"What about offering a financial incentive directly to clinical units to encourage the use of biosimilars? 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