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在医疗保险药品价格谈判计划中使用真实世界证据:给医疗保险和医疗补助服务中心及制造商的一份清单。

Use of real-world evidence in the Medicare Drug Price Negotiation Program: A checklist for the Centers for Medicare and Medicaid Services and manufacturers.

作者信息

Tunis Sean R, Shafrin Jason, Than Kyi-Sin, Whittington Melanie D, Willke Richard J, Bharmal Murtuza

机构信息

Center for Evaluation of Value and Risk in Health, Tufts Medical Center, Boston, MA 02111, United States.

Rubix Health LLC, Baltimore, MD 21210, United States.

出版信息

Health Aff Sch. 2025 Mar 21;3(3):qxaf030. doi: 10.1093/haschl/qxaf030. eCollection 2025 Mar.

Abstract

Under the Inflation Reduction Act's (IRA's) - Medicare Drug Price Negotiation Program, the Centers for Medicare & Medicaid Services' (CMS's) "maximum fair price" must be informed by evidence on factors such as therapeutic advance of the selected drug compared with its alternative, comparative effectiveness across clinical and patient-reported outcomes, the impact on specific populations, and the ability to address unmet medical needs. This paper describes how real-world evidence could improve CMS decision-making and creates a best practices checklist to help CMS evaluate the quality of any manufacturer-submitted evidence. The checklist was developed in four steps: (i) identification of the IRA requirements for determining the maximum fair price through a review of official guidance from CMS, (ii) assessment of provisions that could be supported by real-world evidence (RWE) in addition to clinical trial evidence, (iii) literature review on existing best-practice guidelines relevant to RWE, and (iv) consolidation of these RWE guidelines into a checklist through a series of web conference discussions among experts. The checklist aims to improve the quality of the information available to CMS during the drug price negotiation process.

摘要

根据《降低通胀法案》(IRA)的医疗保险药品价格谈判计划,医疗保险和医疗补助服务中心(CMS)的“最高公平价格”必须依据相关证据来确定,这些证据涉及所选药物与其替代药物相比的治疗进展、临床和患者报告结果方面的比较有效性、对特定人群的影响以及满足未满足医疗需求的能力等因素。本文描述了真实世界证据如何能改善CMS的决策制定,并创建了一份最佳实践清单,以帮助CMS评估任何制造商提交证据的质量。该清单分四个步骤制定:(i)通过审查CMS的官方指南确定IRA中关于确定最高公平价格的要求;(ii)评估除临床试验证据外可由真实世界证据(RWE)支持的条款;(iii)对与RWE相关的现有最佳实践指南进行文献综述;(iv)通过专家之间的一系列网络会议讨论,将这些RWE指南整合到一份清单中。该清单旨在提高药品价格谈判过程中CMS可获得信息的质量。

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