An overview of health technology assessments of gene therapies with the focus on cost-effectiveness models.

Q2 Medicine Journal of market access & health policy Pub Date : 2021-11-13 eCollection Date: 2021-01-01 DOI:10.1080/20016689.2021.2002006
Michał Pochopień, Ewelina Paterak, Emilie Clay, Justyna Janik, Samuel Aballea, Małgorzata Biernikiewicz, Mondher Toumi
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引用次数: 6

Abstract

Background: Gene therapies can treat, prevent, or cure a disease by changing the expression of a person's genes. They are an innovative strategy for treating genetic disorders; however, they are still emerging on the market access and in the healthcare system. Health technology assessment (HTA) agencies have not yet elaborated any standardised approach for assessing gene therapies; therefore, significant differences can be seen during HTAs carried out in various countries. In this review, we focused on submitted economic models of gene therapies approved for use by the US FDA and EMA with the aim to provide a comprehensive summary of how selected HTA bodies assessed the cost-effectiveness of gene therapies. An additional objective was to examine and discuss differences in the methods used in economic models across countries and drugs.

Methods: We identified economic models of gene therapies from six countries (NICE, IQWiG, SMC, HAS, CADTH, ICER) and focused on nine agents (Glybera, Imlygic, Strimvelis, Yescarta, Kymriah, Luxturna, Zynteglo, Zolgensma, Tecartus). Details of cost-utility evaluations and budget impact models were reviewed and extracted.

Results: Overall, 983 publications were identified, and 17 studies were included for the analysis. Reviewed evaluations of gene therapies differed in terms of the study perspective, discounting, extrapolation of outcomes based on limited and immature data, time horizon, and adequate estimation of benefits in terms of quality-adjusted life-years. Methods of economic evaluations were in line with the current recommendations; however, long-term follow-up studies are still missing.

Conclusions: Discrepancies in an economic evaluation of gene therapies between different HTA bodies are rooted in a lack of general assessment frameworks specific to gene therapies. Although challenges were resolved by adjustments to the currently used value assessment framework, new methodological approaches would be useful. In addition, to improve the methods and quality of an evaluation, further research would be valuable.

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基因疗法的卫生技术评估概述,重点是成本效益模型。
背景:基因疗法可以通过改变一个人的基因表达来治疗、预防或治愈疾病。它们是治疗遗传疾病的创新策略;然而,它们仍在市场准入和医疗体系中出现。卫生技术评估(HTA)机构尚未制定任何评估基因疗法的标准化方法;因此,在不同国家进行的HTA中可以看到显著的差异。在这篇综述中,我们重点介绍了美国食品药品监督管理局和欧洲药品管理局批准使用的基因疗法的经济模型,目的是全面总结选定的HTA机构如何评估基因疗法的成本效益。另一个目的是研究和讨论各国和不同药物在经济模型中使用的方法的差异。方法:我们确定了来自六个国家(NICE、IQWiG、SMC、HAS、CADTH、ICER)的基因治疗的经济模型,并重点研究了九种药物(Glybera、Imlygic、Strimvelis、Yescarta、Kymriah、Luxturna、Zynteglo、Zolgensma、Tecartus)。审查并摘录了成本效用评估和预算影响模型的细节。结果:总共确定了983篇出版物,并纳入了17项研究进行分析。基因疗法的回顾性评估在研究视角、贴现、基于有限和不成熟数据的结果推断、时间范围以及对质量调整生命年的益处的充分估计方面存在差异。经济评价方法符合目前的建议;然而,长期的后续研究仍然缺失。结论:不同HTA机构对基因治疗的经济评估存在差异,其根源在于缺乏针对基因治疗的通用评估框架。尽管通过调整目前使用的价值评估框架解决了挑战,但新的方法论方法将是有用的。此外,为了改进评估的方法和质量,进一步的研究将是有价值的。
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审稿时长
14 weeks
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