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Bayesian joint modeling of longitudinal patient-reported outcomes and survival: an application to chronic obstructive pulmonary disease

Abstract

Questionnaire-based patient-reported outcomes (PROs) are discrete, bounded and overdispersed, yet joint models relating them to survival may ignore these features or estimate both processes sequentially. We propose a Bayesian joint model combining a beta-binomial mixed-effects submodel with a Weibull proportional hazards submodel, linked through the subject-specific response probability. Simulations show that simultaneous estimation reduces bias in the longitudinal slope and yields practically unbiased association estimates, unlike two-stage estimation. In a cohort of 543 patients with chronic obstructive pulmonary disease, the model identified associations for all eight SF-36 dimensions and for two of three SGRQ dimensions, including several associations not detected by the two-stage approach, and provided dynamic survival predictions.

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BibTeX
@misc{galanarcicollar2026bayesian,
  title = {{Bayesian joint modeling of longitudinal patient-reported outcomes and survival: an application to chronic obstructive pulmonary disease}},
  author = {Cristina Galán-Arcicollar and Danilo Alvares and Josu Najera-Zuloaga and Dae-Jin Lee},
  howpublished = {arXiv},
  year = {2026},
  month = sep,
  doi = {10.48550/arxiv.2609.30188},
  eprint = {2609.30188},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.30188},
}
RIS
TY  - UNPB
TI  - Bayesian joint modeling of longitudinal patient-reported outcomes and survival: an application to chronic obstructive pulmonary disease
AU  - Cristina Galán-Arcicollar
AU  - Danilo Alvares
AU  - Josu Najera-Zuloaga
AU  - Dae-Jin Lee
PY  - 2026
DA  - 2026/09/24
PB  - arXiv
DO  - 10.48550/arxiv.2609.30188
UR  - https://arxiv.org/abs/2609.30188
AB  - Questionnaire-based patient-reported outcomes (PROs) are discrete, bounded and overdispersed, yet joint models relating them to survival may ignore these features or estimate both processes sequentially. We propose a Bayesian joint model combining a beta-binomial mixed-effects submodel with a Weibull proportional hazards submodel, linked through the subject-specific response probability. Simulations show that simultaneous estimation reduces bias in the longitudinal slope and yields practically unbiased association estimates, unlike two-stage estimation. In a cohort of 543 patients with chronic obstructive pulmonary disease, the model identified associations for all eight SF-36 dimensions and for two of three SGRQ dimensions, including several associations not detected by the two-stage approach, and provided dynamic survival predictions.
ER  -