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美国晚期非小细胞肺癌靶向治疗和免疫治疗的成本效益分析:系统评价。

Cost-effectiveness analyses of targeted therapy and immunotherapy for advanced non-small cell lung cancer in the United States: a systematic review.

机构信息

School of Pharmacy, Bouvé College of Health Sciences, Northeastern University, Boston, MA, United States.

College of Pharmacy, The Catholic University of Korea, Bucheon, South Korea.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2021 Jun;21(3):381-393. doi: 10.1080/14737167.2021.1886928. Epub 2021 Feb 22.

DOI:10.1080/14737167.2021.1886928
PMID:33554675
Abstract

: Mutation-targeting and immuno-oncology drugs are revolutionizing the treatment of advanced non-small cell lung cancer (NSCLC). Cost-effectiveness analyses (CEA) of these drugs have been conducted using various analytical methods and cost-effectiveness thresholds. This systematic review provides a comprehensive summary of the available evidence.: PubMed, Embase, and Cochrane Library were used to select for CEA of targeted therapies for NSCLC in the United States published between 2008 and 2020. Among the 28 included studies, a majority were published from 2017 to 2020 ( = 18) and more than half targeted non-squamous NSCLC ( = 15). The most frequently evaluated therapy was pembrolizumab ( = 11), followed by bevacizumab ( = 8) and erlotinib ( = 4). After 2009, all included studies applied $100,000 or more thresholds. Thresholds of studies supported by industry (median = $150,000) were more distributed than those of studies supported by nonprofits (median = $100,000).: Medications of interest have changed and are individualized to particular mutations. The cost-effectiveness thresholds varied among sponsors but generally trended to increase over time. This review provides an overview of the available cost-effectiveness findings for stakeholders and contributes to evidence-based practice.

摘要

:突变靶向和免疫肿瘤药物正在彻底改变晚期非小细胞肺癌(NSCLC)的治疗方法。这些药物的成本效益分析(CEA)已经使用了各种分析方法和成本效益阈值进行了研究。本系统评价提供了对 2008 年至 2020 年在美国发表的 NSCLC 靶向治疗药物的现有证据的全面总结。在 28 项纳入的研究中,大多数发表于 2017 年至 2020 年(= 18 项),超过一半的研究针对非鳞状 NSCLC(= 15 项)。评估最多的治疗药物是 pembrolizumab(= 11 项),其次是 bevacizumab(= 8 项)和 erlotinib(= 4 项)。2009 年之后,所有纳入的研究都应用了 10 万美元或更高的阈值。与非盈利性研究(中位数= 10 万美元)相比,行业支持研究的阈值(中位数= 15 万美元)分布更为广泛。:研究药物已经发生变化,并针对特定的突变进行了个体化治疗。赞助商之间的成本效益阈值存在差异,但总体上随着时间的推移呈上升趋势。本综述为利益相关者提供了现有成本效益发现的概述,并为循证实践做出了贡献。

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