INSERM, Centre de Recherche des Cordeliers, Sorbonne Université, USPC, Université de Paris, F-75006 Paris, France.
Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan.
Int J Environ Res Public Health. 2021 Feb 9;18(4):1639. doi: 10.3390/ijerph18041639.
Bridging studies are designed to fill the gap between two populations in terms of clinical trial data, such as toxicity, efficacy, comorbidities and doses. According to ICH-E5 guidelines, clinical data can be extrapolated from one region to another if dose-reponse curves are similar between two populations. For instance, in Japan, Phase I clinical trials are often repeated due to this physiological/metabolic paradigm: the maximum tolerated dose (MTD) for Japanese patients is assumed to be lower than that for Caucasian patients, but not necessarily for all molecules. Therefore, proposing a statistical tool evaluating the similarity between two populations dose-response curves is of most interest. The aim of our work is to propose several indicators to evaluate the distance and the similarity of dose-toxicity curves and MTD distributions at the end of some of the Phase I trials, conducted on two populations or regions. For this purpose, we extended and adapted the commensurability criterion, initially proposed by Ollier et al. (2019), in the setting of completed phase I clinical trials. We evaluated their performance using three synthetic sets, built as examples, and six case studies found in the literature. Visualization plots and guidelines on the way to interpret the results are proposed.
桥接研究旨在填补临床试验数据(如毒性、疗效、合并症和剂量)方面两个人群之间的差距。根据 ICH-E5 指南,如果两个人群之间的剂量-反应曲线相似,则可以从一个地区推断到另一个地区的临床数据。例如,在日本,由于这种生理/代谢模式,通常会重复进行 I 期临床试验:日本患者的最大耐受剂量(MTD)假设低于白种人患者,但不一定适用于所有分子。因此,提出一种评估两个人群剂量-反应曲线相似性的统计工具是最感兴趣的。我们的工作旨在提出几种指标,以评估两个人群或两个地区的一些 I 期临床试验结束时的剂量-毒性曲线和 MTD 分布的距离和相似性。为此,我们在已完成的 I 期临床试验的背景下扩展和调整了 Ollier 等人最初提出的(2019 年)一致性标准。我们使用三个合成数据集和文献中发现的六个案例研究来评估它们的性能。还提出了可视化图和解释结果的指南。