Brückner Matthias, Brannath Werner
Competence Center for Clinical Trials, University of Bremen, Linzer Str. 4, 28359, Bremen, Germany.
Lifetime Data Anal. 2017 Jul;23(3):339-352. doi: 10.1007/s10985-016-9360-5. Epub 2016 Mar 11.
In clinical trials survival endpoints are usually compared using the log-rank test. Sequential methods for the log-rank test and the Cox proportional hazards model are largely reported in the statistical literature. When the proportional hazards assumption is violated the hazard ratio is ill-defined and the power of the log-rank test depends on the distribution of the censoring times. The average hazard ratio was proposed as an alternative effect measure, which has a meaningful interpretation in the case of non-proportional hazards, and is equal to the hazard ratio, if the hazards are indeed proportional. In the present work we prove that the average hazard ratio based sequential test statistics are asymptotically multivariate normal with the independent increments property. This allows for the calculation of group-sequential boundaries using standard methods and existing software. The finite sample characteristics of the new method are examined in a simulation study in a proportional and a non-proportional hazards setting.
在临床试验中,生存终点通常使用对数秩检验进行比较。对数秩检验和Cox比例风险模型的序贯方法在统计文献中有大量报道。当比例风险假设被违反时,风险比定义不明确,对数秩检验的功效取决于删失时间的分布。平均风险比被提议作为一种替代效应量度,在非比例风险情况下具有有意义的解释,并且如果风险确实成比例,则等于风险比。在本研究中,我们证明基于平均风险比的序贯检验统计量渐近地服从具有独立增量性质的多元正态分布。这允许使用标准方法和现有软件来计算组序贯界值。在比例风险和非比例风险设定的模拟研究中检验了新方法的有限样本特征。