Volume 62, Issue 2 pp. 398-413
RESEARCH PAPER
Open Access

A tutorial on dynamic risk prediction of a binary outcome based on a longitudinal biomarker

Rana Dandis

Corresponding Author

Rana Dandis

Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands

Correspondence

Rana Dandis, Radboud Institute for Health Sciences, Radboud University Medical Center, Geert Grooteplein noord 21, 6500 HB Nijmegen, The Netherlands.

Email: [email protected]

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Steven Teerenstra

Steven Teerenstra

Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands

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Leon Massuger

Leon Massuger

Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, The Netherlands

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Fred Sweep

Fred Sweep

Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands

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Yalck Eysbouts

Yalck Eysbouts

Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, The Netherlands

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Joanna IntHout

Joanna IntHout

Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands

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First published: 28 November 2019
Citations: 5

Abstract

Dynamic risk predictions based on all available information are useful in timely identification of high-risk patients. However, in contrast with time to event outcomes, there is still a lack of studies that clearly demonstrate how to obtain and update predictions for a future binary outcome using a repeatedly measured biomarker. The aim of this study is to give an illustrative overview of four approaches to obtain such predictions: likelihood based two-stage method (2SMLE), likelihood based joint model (JMMLE), Bayesian two-stage method (2SB), and Bayesian joint model (JMB). We applied the approaches to provide weekly updated predictions of post–molar gestational trophoblastic neoplasia (GTN) based on age and repeated measurements of human chorionic gonadotropin (hCG). Discrimination and calibration measures were used to compare the accuracy of the weekly predictions. Internal validation of the models was conducted using bootstrapping. The four approaches resulted in the same predictive and discriminative performance in predicting GTN. A simulation study showed that the joint models outperform the two-stage methods when we increase the within- and the between-patients variability of the biomarker. The applicability of these models to produce dynamic predictions has been illustrated through a comprehensive explanation and accompanying syntax (R and SAS®).

CONFLICT OF INTEREST

The authors have declared no conflict of interest.

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