医学
临床试验
食品药品监督管理局
背景(考古学)
临床终点
药物开发
肿瘤科
内科学
重症监护医学
医学物理学
药品
药理学
生物
古生物学
作者
Sundeep Agrawal,Shaily Arora,Laleh Amiri‐Kordestani,R. Angelo de Claro,Lola A. Fashoyin-Aje,Nicole Gormley,Tamy Kim,Steven J. Lemery,Gautam U. Mehta,Emma C. Scott,Harpreet Singh,Shenghui Tang,Marc R. Theoret,Richard Pazdur,Paul G. Kluetz,Julia A. Beaver
出处
期刊:JAMA Oncology
[American Medical Association]
日期:2022-12-29
卷期号:9 (2): 266-266
被引量:35
标识
DOI:10.1001/jamaoncol.2022.5985
摘要
Single-arm trials have allowed for transformative therapies to be made available to patients expeditiously. However, using single-arm trials to support drug approval presents several challenges that must be carefully considered.Between January 1, 2002, and December 31, 2021, the US Food and Drug Administration granted 176 new malignant hematology and oncology indications based on single-arm trials, including 116 accelerated approvals (AAs) and 60 traditional approvals. Overall, 87 approvals (49%) were for new molecular entities or original biologics and 89 (51%) were supplemental indications. Response rate (RR) was the most common end point used to support approval in these single-arm trials (173 of 176 [98%]). Of the 116 AAs based on single-arm trials, 45 (38%) fulfilled their postmarketing requirement to verify clinical benefit, 61 (52%) are pending verification of benefit, and 10 (9%) were withdrawn from the market as of December 31, 2021. Most (56 of 61 [92%]) AAs based on single-arm trials pending verification of benefit occurred during the previous 5 years and have ongoing confirmatory trials as of December 2021.Single-arm trials have been a common development strategy to support regulatory approval as early-stage expansion cohorts with promising durable RRs have become more prevalent. In the appropriate context, single-arm trials using durable RRs can allow patients expedited access to novel therapies and will continue to serve a role in advancing drug development in oncology. However, single-arm trials have a smaller noncomparative safety data set, inability to use time-to-event end points, and other limitations that require careful consideration within the context of the disease and available therapies. The randomized clinical trial remains the preferred approach in clinical investigation.
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