Abstract
As data-rich medical datasets are becoming routinely collected, there is a growing demand for regression methodology that facilitates variable selection over a large number of predictors. Bayesian variable selection algorithms offer an attractive solution, whereby a sparsity inducing prior allows inclusion of sets of predictors simultaneously, leading to adjusted effect estimates and inference of which covariates are most important. We present a new implementation of Bayesian variable selection, based on a Reversible Jump MCMC algorithm, for survival analysis under the Weibull regression model. A realistic simulation study is presented comparing against an alternative LASSO-based variable selection strategy in datasets of up to 20,000 covariates. Across half the scenarios, our new method achieved identical sensitivity and specificity to the LASSO strategy, and a marginal improvement otherwise. Runtimes were comparable for both approaches, taking approximately a day for 20,000 covariates. Subsequently, we present a real data application in which 119 protein-based markers are explored for association with breast cancer survival in a case cohort of 2287 patients with oestrogen receptor-positive disease. Evidence was found for three independent prognostic tumour markers of survival, one of which is novel. Our new approach demonstrated the best specificity.
| Original language | English |
|---|---|
| Pages (from-to) | 414-436 |
| Number of pages | 23 |
| Journal | Statistical Methods in Medical Research |
| Volume | 26 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Feb 2017 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© The Author(s) 2014.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Bayesian variable selection
- MCMC
- breast cancer
- gene expression
- penalised regression
- reversible jump
- stability selection
- survival analysis
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