A combined test for a generalized treatment effect in clinical trials with a time-to-event outcome

Patrick Royston ()
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Patrick Royston: MRC Clinical Trials Unit

Stata Journal, 2017, vol. 17, issue 2, 405-421

Abstract: Most randomized controlled trials with a time-to-event outcome are designed and analyzed assuming proportional hazards of the treatment effect. The sample-size calculation is based on a log-rank test or the equivalent Cox test. Nonproportional hazards are seen increasingly in trials and are recognized as a potential threat to the power of the log-rank test. To address the issue, Roys- ton and Parmar (2016, BMC Medical Research Methodology 16: 16) devised a new “combined test” of the global null hypothesis of identical survival curves in each trial arm. The test, which combines the conventional Cox test with a new formulation, is based on the maximal standardized difference in restricted mean survival time (RMST) between the arms. The test statistic is based on evaluations of RMST over several preselected time points. The combined test involves the min- imum p-value across the Cox and RMST-based tests, appropriately standardized to have the correct null distribution. In this article, I outline the combined test and introduce a command, stctest, that implements the combined test. I point the way to additional tools currently under development for power and sample-size calculation for the combined test.

Keywords: stctest; randomized controlled trial; time-to-event outcome; restricted mean survival time; treatment effect; hypothesis testing; flexible para- metric model; jackknife (search for similar items in EconPapers)
Date: 2017
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