Abstract
We consider the situation of estimating the marginal survival distribution from censored data subject to dependent censoring using auxiliary variables. We had previously developed a nonparametric multiple imputation approach. The method used two working proportional hazards (PH) models, one for the event times and the other for the censoring times, to define a nearest neighbor imputing risk set. This risk set was then used to impute failure times for censored observations. Here, we adapt the method to the situation where the event and censoring times follow accelerated failure time models and propose to use the Buckley-James estimator as the two working models. Besides studying the performances of the proposed method, we also compare the proposed method with two popular methods for handling dependent censoring through the use of auxiliary variables, inverse probability of censoring weighted and parametric multiple imputation methods, to shed light on the use of them. In a simulation study with time-independent auxiliary variables, we show that all approaches can reduce bias due to dependent censoring. The proposed method is robust to misspecification of either one of the two working models and their link function. This indicates that a working proportional hazards model is preferred because it is more cumbersome to fit an accelerated failure time model. In contrast, the inverse probability of censoring weighted method is not robust to misspecification of the link function of the censoring time model. The parametric imputation methods rely on the specification of the event time model. The approaches are applied to a prostate cancer dataset.
Keywords
Buckley-James estimator
Cox proportional hazards model
accelerated failure time
auxiliary variables
multiple imputation
nearest neighbor
MeSH Terms
Computer Simulation
Humans
Kaplan-Meier Estimate
Male
Probability
Proportional Hazards Models
Prostatic Neoplasms/epidemiology,radiotherapy
Risk Factors
Statistics, Nonparametric
Survival Analysis
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hsu Chiu-Hsieh
Division of Epidemiology and Biostatistics, Mel and Enid Zuckerman College of Public Health, AZ, 85724, Tucson, U.S.A. | Arizona Cancer Center, University of Arizona, AZ, 85724, Tucson, U.S.A.
Taylor Jeremy M G
Department of Biostatistics, School of Public Health, University of Michigan, MI, 48109, Ann Arbor, U.S.A.
Hu Chengcheng
Division of Epidemiology and Biostatistics, Mel and Enid Zuckerman College of Public Health, AZ, 85724, Tucson, U.S.A. | Arizona Cancer Center, University of Arizona, AZ, 85724, Tucson, U.S.A.
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