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将报销与先进治疗药物产品和其他高成本创新药物的患者获益相挂钩:欧洲基于结果的协议的政策建议。

Linking Reimbursement to Patient Benefits for Advanced Therapy Medicinal Products and Other High-Cost Innovations: Policy Recommendations for Outcomes-Based Agreements in Europe.

机构信息

Science Policy and Research Program, National Institute for Health and Care Excellence (NICE), United Kingdom.

Science Policy and Research Program, National Institute for Health and Care Excellence (NICE), United Kingdom.

出版信息

Value Health. 2024 Nov;27(11):1497-1506. doi: 10.1016/j.jval.2024.07.007. Epub 2024 Jul 31.

DOI:10.1016/j.jval.2024.07.007
PMID:39094693
Abstract

OBJECTIVES

Health technology assessment (HTA) of advanced therapy medicinal products (ATMPs), such as high-cost and one-time cell and gene therapies, is particularly challenging. Outcomes-based agreements (OBAs) are a potential solution to mitigate the risks while providing access to patients but are not widely used across Europe. This study aimed to develop policy recommendations to support the acceptability and implementation of OBAs in Europe.

METHODS

A policy sandbox approach was used to engage with stakeholders and explore how HTA organizations can support reimbursement decisions regarding OBAs for ATMPs. A panel of 38 experts from across the European region was convened in 2 workshops, representing payers, HTA organizations, patients, registries, and an industry trade body.

RESULTS

Policy recommendations were developed to support the appropriate consideration of OBAs for reimbursing highly uncertain technologies, such as ATMPs. If a positive HTA recommendation cannot be made at the proposed price, then a simple price discount reflecting the uncertainty is preferred over complex solutions such as OBAs. If an OBA is pursued, it should be designed collaboratively with all stakeholders to understand data collection feasibility and minimize burden to patients and providers. Payers are encouraged to approach OBAs as a tool for informed decision making, including a readiness to make negative reimbursement decisions based on unfavorable evidence.

CONCLUSIONS

The study presents a policy framework for using OBAs in reimbursement decisions. OBAs must be carefully designed, focusing on appropriateness and the burden of implementation. The relevant authorities should be committed to making decisions in light of the resulting evidence.

摘要

目的

对高级治疗药物产品(ATMP)进行卫生技术评估(HTA),例如高成本、一次性细胞和基因治疗,极具挑战性。基于结果的协议(OBA)是降低风险的一种潜在解决方案,同时也为患者提供了获得药物的机会,但在整个欧洲并未广泛使用。本研究旨在制定政策建议,以支持欧洲接受和实施 OBA。

方法

采用政策沙盒方法,与利益相关者进行接触,探讨 HTA 组织如何支持针对 ATMP 的 OBA 做出报销决策。召集了来自欧洲各地的 38 名专家参加了 2 次研讨会,他们代表了支付方、HTA 组织、患者、登记处和行业贸易机构。

结果

制定了政策建议,以支持适当考虑 OBA 来报销高度不确定的技术,如 ATMP。如果不能按照提议的价格做出积极的 HTA 推荐,那么最好采用简单的价格折扣来反映不确定性,而不是采用 OBA 等复杂解决方案。如果选择使用 OBA,则应与所有利益相关者共同设计,以了解数据收集的可行性并最大限度地减少对患者和提供者的负担。鼓励支付方将 OBA 视为知情决策的工具,包括根据不利证据做出负面报销决策的准备。

结论

本研究提出了在报销决策中使用 OBA 的政策框架。OBA 必须精心设计,注重适当性和实施负担。相关当局应根据由此产生的证据做出决策。

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