Lou Ying, Cao Jing, Zhang Song, Ahn Chul
Department of Statistical Science, Southern Methodist University, Dallas, TX.
Department of Clinical Sciences, UT Southwestern Medical Center, Dallas, TX.
Commun Stat Theory Methods. 2017;46(1):344-353. doi: 10.1080/03610926.2014.991040. Epub 2016 Feb 18.
In clinical trials with repeated measurements, the responses from each subject are measured multiple times during the study period. Two approaches have been widely used to assess the treatment effect, one that compares the rate of change between two groups and the other that tests the time-averaged difference (TAD). While sample size calculations based on comparing the rate of change between two groups have been reported by many investigators, the literature has paid relatively little attention to the sample size estimation for time-averaged difference (TAD) in the presence of heterogeneous correlation structure and missing data in repeated measurement studies. In this study we investigate sample size calculation for the comparison of time-averaged responses between treatment groups in clinical trials with longitudinally observed binary outcomes. The GEE approach is used to derive a closed-form sample size formula, which is flexible enough to account for arbitrary missing patterns and correlation structures. In particular, we demonstrate that the proposed sample size can accommodate a mixture of missing patterns, which is frequently encountered by practitioners in clinical trials. To our knowledge, this is the first study that considers the mixture of missing patterns in sample size calculation. Our simulation shows that the nominal power and type I error are well preserved over a wide range of design parameters. Sample size calculation is illustrated through an example.
在重复测量的临床试验中,在研究期间对每个受试者的反应进行多次测量。两种方法已被广泛用于评估治疗效果,一种是比较两组之间的变化率,另一种是检验时间平均差异(TAD)。虽然许多研究者报告了基于比较两组之间变化率的样本量计算方法,但在重复测量研究中存在异质性相关结构和缺失数据的情况下,文献对时间平均差异(TAD)的样本量估计关注相对较少。在本研究中,我们研究了在具有纵向观察二元结局的临床试验中,治疗组之间时间平均反应比较的样本量计算。使用广义估计方程(GEE)方法推导出一个封闭式样本量公式,该公式足够灵活以考虑任意缺失模式和相关结构。特别是,我们证明了所提出的样本量可以适应缺失模式的混合,这在临床试验的从业者中经常遇到。据我们所知,这是第一项在样本量计算中考虑缺失模式混合的研究。我们的模拟表明,在广泛的设计参数范围内,名义检验效能和I型错误得到了很好的保持。通过一个例子说明了样本量的计算。