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A review of statistical methods on testing time-to-event data


Biometrics & Biostatistics International Journal
Tu Xu,1 Danting Zhu2
Agios Pharmaceuticals, Cambridge, USA

Abstract

The proportional hazard (PH) is commonly assumed for claiming efficacy and planning sample size in randomized clinical trials with time-to-event (TTE) type of endpoints. It is well known that the log-rank test is the most powerful testing method when the PH assumption holds. In recent years, with the advancement of immuno-oncology therapies, the non-PH scenarios, such as the delayed treatment effect and the diminished treatment effect, are frequently observed. A variety of alternative methods have been proposed for testing the time-to-event data while there is no uniformly most powerful method under the non-PH setting. In this paper, six popularly used methods for testing the TTE data are reviewed followed by a numerical comparison. 

Keywords

time-to-event, proportional hazard, log-rank test, restricted mean survival time

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