Availability and financing of CAR-T cell therapies: A cross-country comparative analysis

IF 3.6 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health Policy Pub Date : 2024-09-12 DOI:10.1016/j.healthpol.2024.105153
Yulia Litvinova , Sherry Merkur , Sara Allin , Ester Angulo-Pueyo , Daiga Behmane , Enrique Bernal-Delgado , Miriam Dalmas , Antonio De Belvis , Nigel Edwards , Francisco Estupiñán-Romero , Peter Gaal , Sophie Gerkens , Margaret Jamieson , Alisha Morsella , Dario Picecchi , Hilde Røshol , Ingrid Sperre Saunes , Terry Sullivan , Balázs Szécsényi-Nagy , Inneke Van De Vijver , Dimitra Panteli
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Abstract

Chimeric antigen receptor T-cell therapies (CAR-T therapies) are a type of advanced therapy medicinal product (ATMP) that belong to a new generation of personalised cancer immunotherapies. This paper compares the approval, availability and financing of CAR-T cell therapies in ten countries. It also examines the implementation of this type of ATMP within the health care system, describing the organizational elements of CAR-T therapy delivery and the challenges of ensuring equitable access to all those in need, taking a more systems-oriented view. It finds that the availability of CAR-T therapies varies across countries, reflecting the heterogeneity in the organization and financing of specialised care, particularly oncology care. Countries have been cautious in designing reimbursement models for CAR-T cell therapies, establishing limited managed entry arrangements under public payers, either based on outcomes or as an evidence development scheme to allow for the study of real-world therapeutic efficacy. The delivery model of CAR-T therapies is concentrated around existing experienced cancer centres and highlights the need for high networking and referral capacity. Some countries have transparent and systematic eligibility criteria to help ensure more equitable access to therapies. Overall, as with other pharmaceuticals, there is limited transparency in pricing, eligibility criteria and budgeting decisions in this therapeutic area.

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CAR-T 细胞疗法的可用性和融资:跨国比较分析
嵌合抗原受体 T 细胞疗法(CAR-T疗法)是一种高级治疗药物产品(ATMP),属于新一代个性化癌症免疫疗法。本文比较了十个国家对 CAR-T 细胞疗法的批准、供应和融资情况。本文还从更注重系统性的角度出发,探讨了这类 ATMP 在医疗保健系统中的实施情况,描述了 CAR-T 疗法的组织要素,以及确保所有有需要的人都能公平获得治疗所面临的挑战。报告发现,CAR-T疗法在不同国家的可用性各不相同,这反映了专科医疗,特别是肿瘤医疗的组织和融资方面的差异。各国在设计CAR-T细胞疗法的报销模式时一直很谨慎,在公共支付机构下建立了有限的有管理的准入安排,或以疗效为基础,或作为证据开发计划,以便对真实世界的疗效进行研究。CAR-T 疗法的提供模式主要集中在现有的经验丰富的癌症中心,这就凸显了高度联网和转诊能力的必要性。一些国家制定了透明、系统的资格标准,以帮助确保更公平地获得治疗。总体而言,与其他药品一样,该治疗领域的定价、资格标准和预算决策透明度有限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health Policy
Health Policy 医学-卫生保健
CiteScore
6.40
自引率
6.10%
发文量
157
审稿时长
3-8 weeks
期刊介绍: Health Policy is intended to be a vehicle for the exploration and discussion of health policy and health system issues and is aimed in particular at enhancing communication between health policy and system researchers, legislators, decision-makers and professionals concerned with developing, implementing, and analysing health policy, health systems and health care reforms, primarily in high-income countries outside the U.S.A.
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