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Analysis of two-phase sampling data with semiparametric additive hazards models

机译:用半参数加性危害模型分析两相采样数据

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Under the case-cohort design introduced by Prentice (Biometrica 73:1-11, 1986), the covariate histories are ascertained only for the subjects who experience the event of interest (i.e., the cases) during the follow-up period and for a relatively small random sample from the original cohort (i.e., the subcohort). The case-cohort design has been widely used in clinical and epidemiological studies to assess the effects of covariates on failure times. Most statistical methods developed for the case-cohort design use the proportional hazards model, and few methods allow for time-varying regression coefficients. In addition, most methods disregard data from subjects outside of the subcohort, which can result in inefficient inference. Addressing these issues, this paper proposes an estimation procedure for the semiparametric additive hazards model with case-cohort/two-phase sampling data, allowing the covariates of interest to be missing for cases as well as for non-cases. A more flexible form of the additive model is considered that allows the effects of some covariates to be time varying while specifying the effects of others to be constant. An augmented inverse probability weighted estimation procedure is proposed. The proposed method allows utilizing the auxiliary information that correlates with the phase-two covariates to improve efficiency. The asymptotic properties of the proposed estimators are established. An extensive simulation study shows that the augmented inverse probability weighted estimation is more efficient than the widely adopted inverse probability weighted complete-case estimation method. The method is applied to analyze data from a preventive HIV vaccine efficacy trial.
机译:根据Prentice提出的病例队列设计(Biometrica 73:1-11,1986),仅针对在随访期内经历了关注事件(即病例)的受试者确定协变量历史。来自原始队列(即子队列)的相对较小的随机样本。病例组设计已广泛用于临床和流行病学研究,以评估协变量对失败时间的影响。为案例队列设计开发的大多数统计方法都使用比例风险模型,很少有方法允许随时间变化的回归系数。此外,大多数方法都忽略了来自亚人群之外的受试者的数据,这可能导致推理效率低下。针对这些问题,本文提出了一个具有病例队列/两阶段抽样数据的半参数加性危害模型的估计程序,该方法可以使病例以及非病例都缺少相关的协变量。考虑了加性模型的一种更灵活的形式,该形式允许某些协变量的效果随时间变化,同时将其他协变量指定为常数。提出了一种增强的逆概率加权估计程序。所提出的方法允许利用与第二阶段协变量相关的辅助信息来提高效率。提出了估计量的渐近性质。广泛的仿真研究表明,增强的逆概率加权完整案例估计方法比广泛采用的逆概率加权完整案例估计方法更有效。该方法适用于分析预防性HIV疫苗功效试验的数据。

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