Summary measures in non-inferiority clinical trials with a time-to-event outcome: an empirical comparison of power

Our results empirically corroborate the theoretical advantage of difference in restricted mean survival time over the hazard ratio and difference in survival in non-inferiority clinical trials. This advantage is most apparent when estimation is done under proportional hazards. Choosing a relevant time point at which to evaluate the survival-based summary measures is an important aspect that should be carefully considered. We recommend incorporation of the difference in restricted mean survival time in the design and analysis of non-inferiority clinical trials when clinically justifiable. If appropriate, estimation under proportional hazards is preferable.

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Journal
BMC Medical Research Methodology
Published
2025-05-24
DOI
https://doi.org/10.1186/s12874-025-02576-4
Primary Topic
Statistical Methods in Clinical Trials
Type
article
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article

Summary measures in non-inferiority clinical trials with a time-to-event outcome: an empirical comparison of power

Marta Fiocco, Matteo Quartagno, Shole D.L. Broer, Ian R. White et al.
BMC Medical Research Methodology
Statistical Methods in Clinical Trials
article

Summary measures in non-inferiority clinical trials with a time-to-event outcome: an empirical comparison of power

Marta Fiocco, Matteo Quartagno, Shole D.L. Broer, Ian R. White, Isabelle R. Weir, Tim P. Morris
article en

Abstract

Our results empirically corroborate the theoretical advantage of difference in restricted mean survival time over the hazard ratio and difference in survival in non-inferiority clinical trials. This advantage is most apparent when estimation is done under proportional hazards. Choosing a relevant time point at which to evaluate the survival-based summary measures is an important aspect that should be carefully considered. We recommend incorporation of the difference in restricted mean survival time in the design and analysis of non-inferiority clinical trials when clinically justifiable. If appropriate, estimation under proportional hazards is preferable.

BMC Medical Research MethodologyVol. 25(1)
Leiden University (NL), Leiden University Medical Center (NL), MRC Clinical Trials Unit at UCL (GB), Edwards Lifesciences (United States) (US), University College London (GB), Edwards Lifesciences (Switzerland) (CH)
Gender equality
Openalex Percentile: Top 89%
Statistical Methods in Clinical Trials
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