Regeneron Pharmaceuticals, Inc., 110 Allen Road, Basking Ridge, NJ 07920, USA.
Contemp Clin Trials. 2013 Nov;36(2):642-50. doi: 10.1016/j.cct.2013.09.009. Epub 2013 Sep 25.
Clinical trial designs for targeted therapy development are progressing toward the goal of personalized medicine. Motivated by the need of ongoing efforts to develop targeted agents for lung cancer patients, we propose a Bayesian two-step Lasso procedure for biomarker selection under the proportional hazards model. We seek to identify the key markers that are either prognostic or predictive with respect to treatment from a large number of biomarkers. In the first step of our two-step strategy, we use the Bayesian group Lasso to identify the important marker groups, wherein each group contains the main effect of a single marker and its interactions with treatments. Applying a loose selection criterion in the first step, the goal of first step is to screen out unimportant biomarkers. In the second step, we zoom in to select the individual markers and interactions between markers and treatments in order to identify prognostic or predictive markers using the Bayesian adaptive Lasso. Our strategy takes a full Bayesian approach and is built upon rapid advancement of Lasso methodologies with variable selection. The proposed method is generally applicable to the development of targeted therapies in clinical trials. Our simulation study demonstrates the good performance of the two-step Lasso: Important biomarkers can typically be selected with high probabilities, and unimportant markers can be effectively eliminated from the model.
针对靶向治疗开发的临床试验设计正在朝着个性化医学的目标推进。鉴于不断努力为肺癌患者开发靶向药物的需要,我们提出了一种基于比例风险模型的贝叶斯两步 Lasso 方法,用于生物标志物选择。我们试图从大量生物标志物中确定与治疗相关的关键预后或预测标志物。在两步策略的第一步中,我们使用贝叶斯组 Lasso 来识别重要的标记组,其中每个组包含单个标记的主效应及其与治疗的相互作用。在第一步中应用宽松的选择标准,第一步的目标是筛选出不重要的生物标志物。在第二步中,我们使用贝叶斯自适应 Lasso 对标记和治疗之间的个体标记和相互作用进行放大,以确定预后或预测标记。我们的策略采用了全贝叶斯方法,并建立在带有变量选择的 Lasso 方法的快速发展之上。所提出的方法通常适用于临床试验中靶向治疗的开发。我们的模拟研究表明两步 Lasso 具有良好的性能:重要的生物标志物通常可以以高概率选择,并且不重要的标记可以有效地从模型中消除。