Development, review, and activation of thoracic oncology investigator-initiated trials

IF 10 1区 医学 Q1 ONCOLOGY
David E. Gerber, Claire R. Wynters, Tanushree Prasad, Ronny K. Schnel, Song Zhang, Thomas E. Stinchcombe, Liza C. Villaruz, Joshua M. Bauml, Wade T. Iams, Tejas Patil, Stephen V. Liu, Leora Horn, John M. Hudak, D. Ross. Camidge
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Abstract

Background: Investigator-initiated trials (IITs) may address important biological and clinical questions that may not be prioritized by pharmaceutical sponsors. However, little is known about the process by which IIT proposals are evaluated and activated. Methods: We performed a retrospective study of IIT concepts submitted through the Academic Thoracic Oncology Medical Investigators Consortium (ATOMIC), which comprises 13 institutions in the U.S. and Canada, from 2014 (consortium inception) to 2024. We compared approved and disapproved concepts using chi-squared tests, Fisher’s exact tests, and Wilcoxon Rank-Sum tests. Results: Among a total of 68 presented IIT concepts, 60 (88%) received consortium approval a median of 30 days (interquartile range [IQR] 31-59 days) after submission. Concepts submitted by junior faculty were more likely to be approved than those from full professors (P=0.003). Of the 60 concepts subsequently submitted to pharmaceutical sponsors, 15 (25%) were approved, 43 (72%) were disapproved, and 2 (3%) remain under review. The median time between concept submission to a sponsor and the sponsor’s decision was 61 days (IQR 31-183 days). Concepts with shorter projected durations were more likely to be approved by the pharmaceutical sponsor (P=0.05). For sponsor-approved IIT concepts, median overall time from initial submission to trial activation was 18 months. Conclusions: Only a small proportion of proposed investigator-initiated cancer clinical trials are successfully activated following a prolonged development process. Given the importance of IITs in addressing real-world, practical questions and the growing professional challenges facing clinical research physician faculty, further attention to IIT development facilitators and barriers is warranted.
胸部肿瘤学研究者发起试验的发展、回顾和激活
背景:研究者发起的试验(iit)可能解决重要的生物学和临床问题,而这些问题可能不是制药申办者优先考虑的。然而,人们对IIT提案被评估和激活的过程知之甚少。方法:我们对2014年(联盟成立)至2024年期间通过学术胸肿瘤学医学研究者联盟(ATOMIC)提交的IIT概念进行了回顾性研究,该联盟由美国和加拿大的13家机构组成。我们使用卡方检验、Fisher精确检验和Wilcoxon秩和检验来比较认可和不认可的概念。结果:在提交的68个IIT概念中,60个(88%)在提交后中位数为30天(四分位间距[IQR] 31-59天)获得了联合体批准。初级教师提交的概念比正教授提交的概念更容易被批准(P=0.003)。在随后提交给制药申办者的60个概念中,15个(25%)被批准,43个(72%)不被批准,2个(3%)仍在审查中。从概念提交给发起人到发起人做出决定的中间时间是61天(IQR 31-183天)。计划持续时间较短的概念更有可能被制药赞助商批准(P=0.05)。对于赞助商批准的IIT概念,从初始提交到试验激活的中位总时间为18个月。结论:只有一小部分拟议的研究者发起的癌症临床试验在漫长的开发过程中成功启动。鉴于IIT在解决现实世界的实际问题和临床研究医师教师面临的日益增长的专业挑战方面的重要性,进一步关注IIT发展的促进因素和障碍是有必要的。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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