A two-stage approach for dynamic prediction of time-to-event distributions

被引:16
|
作者
Huang, Xuelin [1 ]
Yan, Fangrong [1 ,4 ]
Ning, Jing [1 ]
Feng, Ziding [1 ]
Choi, Sangbum [2 ]
Cortes, Jorge [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77230 USA
[2] Univ Texas Hlth Sci Ctr Houston, Dept Internal Med, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77230 USA
[4] China Pharmaceut Univ, Res Ctr Biostat & Computat Pharm, Nanjing 210009, Jiangsu, Peoples R China
基金
美国国家卫生研究院;
关键词
biomarker; dynamic prediction; landmark analysis; longitudinal data; survival analysis; time-dependent covariate; LONGITUDINAL DATA; SURVIVAL; MODEL; ACCURACY; LEUKEMIA;
D O I
10.1002/sim.6860
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dynamic prediction uses longitudinal biomarkers for real-time prediction of an individual patient's prognosis. This is critical for patients with an incurable disease such as cancer. Biomarker trajectories are usually not linear, nor even monotone, and vary greatly across individuals. Therefore, it is difficult to fit them with parametric models. With this consideration, we propose an approach for dynamic prediction that does not need to model the biomarker trajectories. Instead, as a trade-off, we assume that the biomarker effects on the risk of disease recurrence are smooth functions over time. This approach turns out to be computationally easier. Simulation studies show that the proposed approach achieves stable estimation of biomarker effects over time, has good predictive performance, and is robust against model misspecification. It is a good compromise between two major approaches, namely, (i) joint modeling of longitudinal and survival data and (ii) landmark analysis. The proposed method is applied to patients with chronic myeloid leukemia. At any time following their treatment with tyrosine kinase inhibitors, longitudinally measured BCR-ABL gene expression levels are used to predict the risk of disease progression. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:2167 / 2182
页数:16
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