Sun Yanqing, Qi Li, Yang Guangren, Gilbert Peter B
Department of Mathematics and Statistics, University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Biostatistics and Programming, Sanofi, Bridgewater, NJ, 08807, USA.
Biom J. 2018 May;60(3):516-536. doi: 10.1002/bimj.201700002. Epub 2018 Feb 28.
This article develops hypothesis testing procedures for the stratified mark-specific proportional hazards model with missing covariates where the baseline functions may vary with strata. The mark-specific proportional hazards model has been studied to evaluate mark-specific relative risks where the mark is the genetic distance of an infecting HIV sequence to an HIV sequence represented inside the vaccine. This research is motivated by analyzing the RV144 phase 3 HIV vaccine efficacy trial, to understand associations of immune response biomarkers on the mark-specific hazard of HIV infection, where the biomarkers are sampled via a two-phase sampling nested case-control design. We test whether the mark-specific relative risks are unity and how they change with the mark. The developed procedures enable assessment of whether risk of HIV infection with HIV variants close or far from the vaccine sequence are modified by immune responses induced by the HIV vaccine; this question is interesting because vaccine protection occurs through immune responses directed at specific HIV sequences. The test statistics are constructed based on augmented inverse probability weighted complete-case estimators. The asymptotic properties and finite-sample performances of the testing procedures are investigated, demonstrating double-robustness and effectiveness of the predictive auxiliaries to recover efficiency. The finite-sample performance of the proposed tests are examined through a comprehensive simulation study. The methods are applied to the RV144 trial.
本文针对具有缺失协变量的分层标记特定比例风险模型开发了假设检验程序,其中基线函数可能因分层而异。标记特定比例风险模型已被用于评估标记特定的相对风险,其中标记是感染的HIV序列与疫苗中所代表的HIV序列的遗传距离。这项研究的动机是分析RV144三期HIV疫苗疗效试验,以了解免疫反应生物标志物与HIV感染的标记特定风险之间的关联,其中生物标志物是通过两阶段抽样嵌套病例对照设计进行采样的。我们检验标记特定的相对风险是否为1以及它们如何随标记变化。所开发的程序能够评估与疫苗序列接近或远离的HIV变体感染HIV的风险是否会因HIV疫苗诱导的免疫反应而改变;这个问题很有趣,因为疫苗保护是通过针对特定HIV序列的免疫反应实现的。检验统计量是基于增强的逆概率加权完全病例估计量构建的。研究了检验程序的渐近性质和有限样本性能,证明了预测辅助变量恢复效率的双重稳健性和有效性。通过全面的模拟研究检验了所提出检验的有限样本性能。这些方法应用于RV144试验。