论文标题
关于在随机临床试验中的限制平均生存时间测试的样本量确定
On sample size determination for restricted mean survival time-based tests in randomized clinical trials
论文作者
论文摘要
限制的平均生存时间(RMST)正在引起人们的注意,以量化随机临床试验中对生存结果的治疗效果。已经提出了几种基于基于RMST的测试来确定样本量的方法。但是,据我们所知,尚无关于基于RMST的测试的功率和样本量的讨论,该测试的增强版本利用基线协变量来提高估计效率和测试无治疗效果的权力。基于对数秩检验的常规事件驱动的研究设计使我们能够在不指定生存功能的情况下计算给定危险比的功率。相反,基于RMST的测试的现有样本量确定方法取决于两组整个生存曲线的假设的适当性。此外,为了处理增强测试,必须处理基线协变量与马丁莱尔残差之间的相关性。为了解决这些问题,我们为基于RMST的测试的增强版本提出了一个近似样本量公式,该公式不需要指定治疗组中的整个生存曲线,还需要一种样本量重估算方法,以更新基线协变量与具有盲数据数据的Martingale残差之间的相关性。所提出的程序将使研究能够在给定的RMST差异的目标功能中具有目标能力,即使在设计阶段无法指定正确的生存功能。
Restricted mean survival time (RMST) is gaining attention as a measure to quantify the treatment effect on survival outcomes in randomized clinical trials. Several methods to determine sample size based on the RMST-based tests have been proposed. However, to the best of our knowledge, there is no discussion about the power and sample size regarding the augmented version of RMST-based tests, which utilize baseline covariates for a gain in estimation efficiency and in power for testing the no treatment effect. The conventional event-driven study design based on the log-rank test allows us to calculate the power for a given hazard ratio without specifying the survival functions. In contrast, the existing sample size determination methods for the RMST-based tests relies on the adequacy of the assumptions of the entire survival curves of two groups. Furthermore, to handle the augmented test, the correlation between the baseline covariates and the martingale residuals must be handled. To address these issues, we propose an approximated sample size formula for the augmented version of the RMST-based test, which does not require specifying the entire survival curve in the treatment group, and also a sample size recalculation approach to update the correlations between the baseline covariates and the martingale residuals with the blinded data. The proposed procedure will enable the studies to have the target power for a given RMST difference even when correct survival functions cannot be specified at the design stage.