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ARM对首个细胞和基因治疗产品联合临床评估的看法:前行道路上的挑战与机遇

ARM's Perspective on the First Joint Clinical Assessments for ATMPs: Challenges and Opportunities on the Path Ahead.

作者信息

Morgese Paolo, Majors Stephen, Patel Dilip

机构信息

Alliance for Regenerative Medicine (ARM), B-1040 Brussels, Belgium;

Autolus Therapeutics PLC London, London W12 7FP, UK;

出版信息

J Mark Access Health Policy. 2025 Apr 3;13(2):14. doi: 10.3390/jmahp13020014. eCollection 2025 Jun.

Abstract

Advanced Therapy Medicinal Products (ATMPs) are revolutionising modern medicine. By addressing the root cause rather than the symptoms of disease, ATMPs hold the promise of long-lasting benefits or even cures for severe, genetic, and rare diseases-including rare cancers-for patients with few or no viable treatment options. At the same time, the inherent complexities of ATMPs pose challenges to traditional HTA frameworks. Unlike conventional treatments, ATMPs are often one-time therapies with a high magnitude of effect. However, their long-term durability remains uncertain at launch. The Joint Clinical Assessment (JCA), under the EU's Health Technology Assessment (HTA) Regulation, represents a once-in-a-generation opportunity to consolidate the strengths of national HTA processes into a unified framework that accounts for the specificities of ATMPs and streamlines decision-making, cementing Europe's position as a pioneer in innovative HTA approaches. While concerns remain regarding the suitability of current JCA methodologies for ATMPs, the HTA Regulation continues to bring the HTA ecosystem closer together, with numerous benefits already emerging from EU-wide collaboration on JCAs. This article outlines the HTA challenges posed for and by ATMPs, and ARM's perspective on the JCA's implementation. A 'fit for purpose' JCA holds the promise to unlocking these therapies' benefits for individuals across Europe.

摘要

先进治疗医药产品(ATMPs)正在彻底改变现代医学。通过解决疾病的根本原因而非症状,ATMPs有望为患有严重、遗传和罕见疾病(包括罕见癌症)且几乎没有或没有可行治疗选择的患者带来长期益处甚至治愈方法。与此同时,ATMPs固有的复杂性给传统卫生技术评估(HTA)框架带来了挑战。与传统治疗方法不同,ATMPs通常是一次性治疗,效果显著。然而,在推出时其长期耐久性仍不确定。根据欧盟卫生技术评估(HTA)法规进行的联合临床评估(JCA),是一个千载难逢的机会,可将国家HTA流程的优势整合到一个统一框架中,该框架考虑到ATMPs的特殊性并简化决策,巩固欧洲在创新HTA方法方面的先驱地位。尽管人们对当前JCA方法对ATMPs的适用性仍存在担忧,但HTA法规继续使HTA生态系统更加紧密地结合在一起,欧盟范围内关于JCA的合作已经带来了诸多益处。本文概述了ATMPs给HTA带来的挑战以及HTA给ATMPs带来的挑战,以及高级远程医疗协会(ARM)对JCA实施的看法。一个“适用的”JCA有望为欧洲各地的个人释放这些疗法的益处。

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本文引用的文献

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Evolving Evidence-Based Value Assessment of One-Time Therapies: Tisagenlecleucel as a Case Study.
Appl Health Econ Health Policy. 2024 Sep;22(5):749-765. doi: 10.1007/s40258-024-00882-4. Epub 2024 Apr 29.
2
The role of stakeholder involvement in the evolving EU HTA process: .
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3
Cilta-cel or Standard Care in Lenalidomide-Refractory Multiple Myeloma.
N Engl J Med. 2023 Jul 27;389(4):335-347. doi: 10.1056/NEJMoa2303379. Epub 2023 Jun 5.
4
Ide-cel or Standard Regimens in Relapsed and Refractory Multiple Myeloma.
N Engl J Med. 2023 Mar 16;388(11):1002-1014. doi: 10.1056/NEJMoa2213614. Epub 2023 Feb 10.
7
HTA decision-making for drugs for rare diseases: comparison of processes across countries.
Orphanet J Rare Dis. 2022 Jul 8;17(1):258. doi: 10.1186/s13023-022-02397-4.
8
European union regulation of health technology assessment: what is required for it to succeed?
Eur J Health Econ. 2022 Aug;23(6):913-915. doi: 10.1007/s10198-022-01458-6. Epub 2022 Mar 29.
9
The cost of severe haemophilia in Europe: the CHESS study.
Orphanet J Rare Dis. 2017 May 31;12(1):106. doi: 10.1186/s13023-017-0660-y.
10
The correlation between HTA recommendations and reimbursement status of orphan drugs in Europe.
Orphanet J Rare Dis. 2016 Sep 6;11(1):122. doi: 10.1186/s13023-016-0501-4.

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