Using Surrogate Endpoints in Adaptive Designs with Delayed Treatment Effect

被引:10
|
作者
Li, Qing [1 ]
Lin, Jianchang [1 ]
Liu, Mengya [1 ]
Wu, Liwen [2 ]
Liu, Yingying [3 ]
机构
[1] Takeda Pharmaceut, 300 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15212 USA
[3] Biogen, Cambridge, MA 02138 USA
来源
关键词
Adaptive design; Conditional power; Delayed treatment effect; Sample; event size reestimation; Surrogate endpoint; PROGRESSION-FREE SURVIVAL; CELL LUNG-CANCER; MULTIPLE-MYELOMA; RESPONSE RATE; TIME; TRIALS; CHEMOTHERAPY; OUTCOMES; DISEASE;
D O I
10.1080/19466315.2021.1938203
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Delayed treatment effects have been commonly observed in clinical trials, which bring more challenges to the interim decision making particularly in adaptive designs setting. An improper interim analysis (IA) may falsely stop a promising study based on the traditional conditional power (CP) approach assuming the observed treatment effect will carry over for the entire study. For such scenario, a short-term surrogate endpoint which is predictive of the primary long-term outcome can be extremely useful for a more accurate CP calculation and adaptative decision. In this article, we propose using a surrogate endpoint in the IA to improve the CP calculation in designing an adaptive sample size reestimation or event size reestimation study. Through theoretical derivation and extensive simulations, we show that our proposed approach demonstrates the practical feasibility and benefits of using a surrogate endpoint for adaptive designs with delayed treatment effects. The average overall power is shown to be significantly higher than conventional event size reestimation and group sequential design when there is a delayed treatment effect in primary survival endpoint. We also demonstrate proposed approach in a case study of Phase III non-small cell lung cancer (NSCLC) trial with delayed treatment effect. Finally, we give recommendations on how this method could be implemented in confirmatory clinical trials.
引用
收藏
页码:661 / 670
页数:10
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