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About this Publication
Title
Estimation and inference of predictive discrimination for survival outcome risk prediction models.
Pubmed ID
35061146 (View this publication on the PubMed website)
Digital Object Identifier
Publication
Lifetime Data Anal. 2022 Jan 21
Authors
Li R, Ning J, Feng Z
Affiliations
  • Department of Biostatistics and Data Science, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA. ruosha.li@uth.tmc.edu.
  • Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
  • Division of Public Health Sciences, Fred Hutchison Cancer Research Center, Seattle, WA, USA.
Abstract

Accurate risk prediction has been the central goal in many studies of survival outcomes. In the presence of multiple risk factors, a censored regression model can be employed to estimate a risk prediction rule. Before the prediction tool can be popularized for practical use, it is crucial to rigorously assess its prediction performance. In our motivating example, researchers are interested in developing and validating a risk prediction tool to identify future lung cancer cases by integrating demographic information, disease characteristics and smoking-related data. Considering the long latency period of cancer, it is desirable for a prediction tool to achieve discriminative performance that does not weaken over time. We propose estimation and inferential procedures to comprehensively assess both the overall predictive discrimination and the temporal pattern of an estimated prediction rule. The proposed methods readily accommodate commonly used censored regression models, including the Cox proportional hazards model and the accelerated failure time model. The estimators are consistent and asymptotically normal, and reliable variance estimators are also developed. The proposed methods offer an informative tool for inferring time-dependent predictive discrimination, as well as for comparing the discrimination performance between candidate models. Applications of the proposed methods demonstrate enduring performance of the risk prediction tool in the PLCO study and detected decaying performance in a study of liver disease.

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