Estimating personalized treatment effects from high-dimensional observational data is essential in situations where experimental designs are infeasible, unethical, or expensive. Existing approaches rely on fitting deep models on outcomes observed for treated and control populations. However, when measuring individual outcomes is costly, as is the case of a tumor biopsy, a sample-efficient strategy for acquiring each result is required. Deep Bayesian active learning provides a framework for efficient data acquisition by selecting points with high uncertainty. However, existing methods bias training data acquisition towards regions of non-overlapping support between the treated and control populations. These are not sample-efficient because the treatment effect is not identifiable in such regions. We introduce causal, Bayesian acquisition functions grounded in information theory that bias data acquisition towards regions with overlapping support to maximize sample efficiency for learning personalized treatment effects. We demonstrate the performance of the proposed acquisition strategies on synthetic and semi-synthetic datasets IHDP and CMNIST and their extensions, which aim to simulate common dataset biases and pathologies.
翻译:在实验设计不可行、不道德或费用昂贵的情况下,从高维观测数据中估算个人化的治疗效果至关重要。现有方法依赖于对治疗和控制人口所观察到的结果进行适当的深层次模型。然而,在衡量个人结果方面成本很高,就像肿瘤生物心理一样,需要为取得每种结果制定一种抽样高效的战略。深贝耶斯积极学习通过选择高度不确定的点,为有效获取数据提供了一个框架。然而,现有方法将培训数据的获取偏向于受治疗和控制人口之间非重叠支持的区域。由于在这类区域无法辨别治疗效果,这些方法不具有样本效率。我们引入了因果性、贝耶斯获取功能,其依据是信息理论,即获取的数据偏向区域倾斜,同时支持最大限度地提高样本效率,以学习个性化治疗效果。我们展示了拟议的合成和半合成数据集IHDP和CMNIST及其扩展的获取战略的绩效,目的是模拟常见的数据偏向和病理。