Joint modeling of longitudinal and competing-risk data using cumulative incidence functions for the failure submodels accounting for potential failure cause misclassification through double sampling

被引:0
|
作者
Thomadakis, Christos [1 ]
Meligkotsidou, Loukia [2 ]
Yiannoutsos, Constantin T. [3 ]
Touloumi, Giota [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, Dept Hyg Epidemiol & Med Stat, Athens, Greece
[2] Natl & Kapodistrian Univ Athens, Dept Math, Athens, Greece
[3] Indiana Univ, Dept Biostat & Hlth Data Sci, 410 West 10th St,Suite 3000, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
Bayesian approach; Cumulative incidence function; Joint modeling; Misclassification; Multistate model; Shared parameter models; PARAMETRIC REGRESSION; INFERENCE; SURVIVAL;
D O I
10.1093/biostatistics/kxac043
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Most of the literature on joint modeling of longitudinal and competing-risk data is based on cause-specific hazards, although modeling of the cumulative incidence function (CIF) is an easier and more direct approach to evaluate the prognosis of an event. We propose a flexible class of shared parameter models to jointly model a normally distributed marker over time and multiple causes of failure using CIFs for the survival submodels, with CIFs depending on the "true" marker value over time (i.e., removing the measurement error). The generalized odds rate transformation is applied, thus a proportional subdistribution hazards model is a special case. The requirement that the all-cause CIF should be bounded by 1 is formally considered. The proposed models are extended to account for potential failure cause misclassification, where the true failure causes are available in a small random sample of individuals. We also provide a multistate representation of the whole population by defining mutually exclusive states based on the marker values and the competing risks. Based solely on the assumed joint model, we derive fully Bayesian posterior samples for state occupation and transition probabilities. The proposed approach is evaluated in a simulation study and, as an illustration, it is fitted to real data from people with HIV.
引用
收藏
页码:80 / 97
页数:18
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