为连续治疗剂量反应模型提供可解释的不确定性预测区间
Conformal Prediction for Dose-Response Models with Continuous Treatments
- 将因果剂量反应问题转化为协变量偏移,用加权置信预测方法建模
- 通过核函数加权实现每个治疗值的局部覆盖率,提升预测精度
- 适用于个性化医疗等高风险决策场景,支持可信的剂量选择
理解个体层面连续治疗与结果之间的剂量-反应关系,对个性化药物剂量和健康干预决策至关重要。在高风险环境中,点估计难以满足需求,亟需不确定性量化以支持科学决策。目前,无需分布假设且模型无关的置信预测方法在连续治疗或剂量-反应模型中的应用仍有限。为此,本文提出一种新方法:将因果剂量-反应问题建模为协变量偏移,结合倾向性评分、置信预测系统和似然比,构建适用于剂量-反应模型的预测区间生成方案。通过在加权置信预测中引入核函数作为权重,实现对每个治疗值的局部覆盖近似。此外,我们使用一个新构建的合成基准数据集,验证了协变量偏移假设在获得稳健预测区间中的关键作用。
原文摘要 · Abstract (English)
Understanding the dose-response relation between a continuous treatment and the outcome for an individual can greatly drive decision-making, particularly in areas like personalized drug dosing and personalized healthcare interventions. Point estimates are often insufficient in these high-risk environments, highlighting the need for uncertainty quantification to support informed decisions. Conformal prediction, a distribution-free and model-agnostic method for uncertainty quantification, has seen limited application in continuous treatments or dose-response models. To address this gap, we propose a novel methodology that frames the causal dose-response problem as a covariate shift, leveraging weighted conformal prediction. By incorporating propensity estimation, conformal predictive systems, and likelihood ratios, we present a practical solution for generating prediction intervals for dose-response models. Additionally, our method approximates local coverage for every treatment value by applying kernel functions as weights in weighted conformal prediction. Finally, we use a new synthetic benchmark dataset to demonstrate the significance of covariate shift assumptions in achieving robust prediction intervals for dose-response models.
Thank you to arXiv for use of its open access interoperability. PaperDance 不是 arXiv 官方产品;中文卡片由大模型生成,请以原文为准。