Joint longitudinal and time-to-event models for multilevel hierarchical data

Author:

Brilleman Samuel L12ORCID,Crowther Michael J3ORCID,Moreno-Betancur Margarita245,Buros Novik Jacqueline6,Dunyak James7,Al-Huniti Nidal7,Fox Robert7,Hammerbacher Jeff68,Wolfe Rory12

Affiliation:

1. Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia

2. Victorian Centre for Biostatistics (ViCBiostat), Melbourne, Australia

3. Biostatistics Research Group, Department of Health Sciences, University of Leicester, Leicester, UK

4. Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Melbourne, Australia

5. Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia

6. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA

7. Quantitative Clinical Pharmacology, IMED Biotech Unit, AstraZeneca, Waltham, MA, USA

8. Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA

Abstract

Joint modelling of longitudinal and time-to-event data has received much attention recently. Increasingly, extensions to standard joint modelling approaches are being proposed to handle complex data structures commonly encountered in applied research. In this paper, we propose a joint model for hierarchical longitudinal and time-to-event data. Our motivating application explores the association between tumor burden and progression-free survival in non-small cell lung cancer patients. We define tumor burden as a function of the sizes of target lesions clustered within a patient. Since a patient may have more than one lesion, and each lesion is tracked over time, the data have a three-level hierarchical structure: repeated measurements taken at time points (level 1) clustered within lesions (level 2) within patients (level 3). We jointly model the lesion-specific longitudinal trajectories and patient-specific risk of death or disease progression by specifying novel association structures that combine information across lower level clusters (e.g. lesions) into patient-level summaries (e.g. tumor burden). We provide user-friendly software for fitting the model under a Bayesian framework. Lastly, we discuss alternative situations in which additional clustering factor(s) occur at a level higher in the hierarchy than the patient-level, since this has implications for the model formulation.

Funder

National Health and Medical Research Council

Medical Research Council

Publisher

SAGE Publications

Subject

Health Information Management,Statistics and Probability,Epidemiology

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