Division of Biostatistics, College of Public Health, The Ohio State University, 1841 Neil Ave., Columbus, OH, 43210, USA.
Lifetime Data Anal. 2021 Jan;27(1):177-194. doi: 10.1007/s10985-020-09514-0. Epub 2021 Jan 8.
Time-to-event data often violate the proportional hazards assumption inherent in the popular Cox regression model. Such violations are especially common in the sphere of biological and medical data where latent heterogeneity due to unmeasured covariates or time varying effects are common. A variety of parametric survival models have been proposed in the literature which make more appropriate assumptions on the hazard function, at least for certain applications. One such model is derived from the First Hitting Time (FHT) paradigm which assumes that a subject's event time is determined by a latent stochastic process reaching a threshold value. Several random effects specifications of the FHT model have also been proposed which allow for better modeling of data with unmeasured covariates. While often appropriate, these methods often display limited flexibility due to their inability to model a wide range of heterogeneities. To address this issue, we propose a Bayesian model which loosens assumptions on the mixing distribution inherent in the random effects FHT models currently in use. We demonstrate via simulation study that the proposed model greatly improves both survival and parameter estimation in the presence of latent heterogeneity. We also apply the proposed methodology to data from a toxicology/carcinogenicity study which exhibits nonproportional hazards and contrast the results with both the Cox model and two popular FHT models.
时间事件数据通常违反了流行的 Cox 回归模型中固有的比例风险假设。这种违反情况在生物医学数据领域尤为常见,因为未测量的协变量或时变效应会导致潜在的异质性。文献中提出了各种参数生存模型,这些模型对危险函数的假设更加合适,至少对于某些应用程序是这样。一种这样的模型源自第一到达时间 (FHT) 范式,该范式假设受试者的事件时间由到达阈值的潜在随机过程决定。还提出了几种 FHT 模型的随机效应规格,这些规格允许更好地对具有未测量协变量的数据进行建模。虽然这些方法通常是合适的,但由于它们无法对广泛的异质性进行建模,因此往往缺乏灵活性。为了解决这个问题,我们提出了一种贝叶斯模型,该模型放宽了当前使用的随机效应 FHT 模型中对混合分布的假设。通过模拟研究,我们证明了在存在潜在异质性的情况下,所提出的模型极大地提高了生存和参数估计的效果。我们还将所提出的方法应用于显示非比例风险的毒理学/致癌性研究的数据,并将结果与 Cox 模型和两种流行的 FHT 模型进行对比。