Duration of response (DOR) and time to response (TTR) are typically evaluated as secondary endpoints in early-stage clinical studies in oncology when efficacy is assessed by the best overall response (BOR) and presented as the overall response rate (ORR). Despite common use of DOR and TTR in particular in single-arm studies, the definition of these endpoints and the questions they are intended to answer remain unclear. Motivated by the estimand framework, we present relevant scientific questions of interest for DOR and TTR and propose corresponding estimand definitions. We elaborate on how to deal with relevant intercurrent events which should follow the same considerations as implemented for the primary response estimand. A case study in mantle cell lymphoma illustrates the implementation of relevant estimands of DOR and TTR. We close the paper with practical recommendations to implement DOR and TTR in clinical study protocols.
翻译:反应期限(DOR)和反应时间(TTR)通常在肿瘤学早期临床临床研究中被评为二级终点,因为效率是通过最佳总体反应(BOR)评估的,作为总体反应(ORR)提出。尽管在单臂研究中通常使用DOR和TR(TR),但这些终点的定义和它们打算回答的问题仍然不清楚。我们受到最高框架的激励,提出DOR和TTR感兴趣的相关科学问题,并提出相应的估计定义。我们详细说明如何处理相关的经常间事件,这些活动应该遵循对主要反应估计执行的同样考虑。关于人造细胞淋巴的案例研究说明了DOR和TTR(TR)相关估计值和问题的执行情况。我们以在临床研究协议中执行DOR和TTR的切实建议来结束该文件。