High-dimensional biomarkers such as genomics are increasingly being measured in randomized clinical trials. Consequently, there is a growing interest in developing methods that improve the power to detect biomarker-treatment interactions. We adapt recently proposed two-stage interaction detecting procedures in the setting of randomized clinical trials. We also propose a new stage 1 multivariate screening strategy using ridge regression to account for correlations among biomarkers. For this multivariate screening, we prove the asymptotic between-stage independence, required for family-wise error rate control, under biomarker-treatment independence. Simulation results show that in various scenarios, the ridge regression screening procedure can provide substantially greater power than the traditional one-biomarker-at-a-time screening procedure in highly correlated data. We also exemplify our approach in two real clinical trial data applications.
翻译:基因组学等高维生物标志越来越多地在随机临床试验中进行测量。因此,人们越来越有兴趣制定方法来改进生物标志处理相互作用的检测能力。我们最近对随机临床试验的设置中拟议的两阶段互动检测程序进行了调整。我们还提出了一个新的阶段1多变量筛选战略,使用脊柱回归法来计算生物标志的相互关系。对于这种多变量筛选,我们证明,在生物标志处理独立下,为了控制家庭错误率,需要不同阶段之间的独立。模拟结果表明,在各种情况下,山脊回归筛选程序能够提供比高度关联数据中传统的一次性生物标志实时筛选程序大得多的能量。我们还在两个真正的临床实验数据应用中举例说明了我们的方法。