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在首次人体试验中成功进行连续肿瘤活检的实用考虑因素。

Practical consideration for successful sequential tumor biopsies in first-in-human trials.

机构信息

Department of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan.

Department of Gastrointestinal Oncology, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Invest New Drugs. 2022 Aug;40(4):841-849. doi: 10.1007/s10637-022-01236-4. Epub 2022 Apr 11.

Abstract

In first-in-human (FIH) trials, sequential tumor biopsies, i.e., two consecutive tumor biopsies, the first performed at baseline (pretreatment) and the second during the early treatment period (on-treatment), provide proof of concept in investigational new drugs. We evaluated the success of sequential tumor biopsies in FIH trials, and explored approaches for improved success rates. We retrospectively reviewed the sequential tumor biopsies required in 17 of 52 FIH trials conducted from 2015 to 2020. One hundred and thirty-eight patients were identified. Success of either pretreatment or on-treatment biopsy alone, and of sequential tumor biopsies, was defined as the acquisition of viable tumor cells and as obtaining tumor cells from both biopsy specimens, respectively. The success rates of pretreatment and on-treatment biopsy were 98.6% and 94.2%, respectively, and of sequential tumor biopsies was 70.3%. Adverse events associated with the pretreatment biopsies (33.3% positive; 72.0% negative) and timing of the first imaging assessment (before on-treatment biopsy = 40.0%; after on-treatment biopsy = 82.7%) correlated with successful sequential tumor biopsies. The reasons for unsuccessful sequential tumor biopsies could be categorized into two groups: 1) patient refusal of the on-treatment biopsy (most frequently due to early disease progression); and 2) absence of tumor cells in the pretreatment or on-treatment biopsy specimen. We propose an approach to achieving greater success in sequential tumor biopsies in FIH trials; the first imaging assessment during the study should be scheduled after on-treatment biopsy. (Registration number UMIN000042487, Date of registration November 18, 2020).

摘要

在首次人体(FIH)试验中,连续肿瘤活检,即两次连续的肿瘤活检,第一次在基线(治疗前)进行,第二次在早期治疗期间(治疗中)进行,为研究性新药提供了概念验证。我们评估了 FIH 试验中连续肿瘤活检的成功率,并探讨了提高成功率的方法。我们回顾性地审查了 2015 年至 2020 年期间进行的 52 项 FIH 试验中的 17 项所需的连续肿瘤活检。确定了 138 名患者。预处理或治疗中活检单独成功,以及连续肿瘤活检成功,分别定义为获得活肿瘤细胞以及从两个活检标本中获得肿瘤细胞。预处理和治疗中活检的成功率分别为 98.6%和 94.2%,而连续肿瘤活检的成功率为 70.3%。预处理活检的不良事件(33.3%阳性;72.0%阴性)和首次影像学评估的时间(治疗前活检=40.0%;治疗后活检=82.7%)与成功的连续肿瘤活检相关。连续肿瘤活检不成功的原因可分为两类:1)患者拒绝接受治疗中活检(最常见的原因是早期疾病进展);2)预处理或治疗中活检标本中无肿瘤细胞。我们提出了一种在 FIH 试验中提高连续肿瘤活检成功率的方法;研究期间的第一次影像学评估应在治疗后活检后进行。(注册号 UMIN000042487,注册日期 2020 年 11 月 18 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e029/9288361/2272ee2d6bcb/10637_2022_1236_Fig1_HTML.jpg

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