Bayesian additive regression trees for evaluating treatment benefit predictors using observational data
用贝叶斯加性回归树评估观察数据中的治疗获益预测器AI 解读 ↓
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A treatment benefit predictor (TBP) is an algorithm that maps a patient's characteristics to their putative benefit from a given treatment, which can be used to inform treatment decisions. However, a TBP must be evaluated in the target population before being adopted for patient care. When only observational data are available, evaluating TBPs requires standard causal identification assumptions, as treatment assignment in such settings is not random. We obtain the posterior distributions of predictive performance measures to evaluate prespecified TBPs using observational data, by taking advantage of Bayesian additive regression trees (BART). We illustrate the evaluation of TBPs using selected measures and graphical visualizations: the concentration of benefit ($C_b$) index and the moderate calibration curve. Simulation studies of binary and continuous outcomes settings, including balanced and imbalanced treatment allocation in the binary setting, establish the validity of the proposed approach. In a case study, we use this approach to assess a TBP for systemic antibiotic therapy for patients with chronic obstructive pulmonary disease (COPD). We show that the constructed TBP does not in fact make calibrated predictions, because it both makes optimistic predictions of risks and exaggerates the risk reduction due to treatment. We conclude that flexible Bayesian approaches have the potential to assess TBPs, offering opportunities for flexible model specifications, adjustment for confounding, and uncertainty characterization.
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Estimating the causal effect of fertility on women's employment is challenging because fertility and labour-market decisions are jointly determined. Instrumental-variable strategies are widely used, but credible instruments are rare and their validity often depends on covariates. Two-stage least squares, the dominant implementation, does not flexibly accommodate covariate-dependent instrument validity and is poorly suited to count-valued treatment and effect heterogeneity…