Efficient nonparametric estimation of the covariate-adjusted threshold-response function, a support-restricted stochastic intervention
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Identifying a biomarker or treatment-dose threshold that marks a specified level of risk is an important problem, especially in clinical trials. This risk, viewed as a function of thresholds and possibly adjusted for covariates, we call the threshold-response function. Extending the work of Donovan, Hudgens and Gilbert (2019), we propose a nonparametric efficient estimator for the covariate-adjusted threshold-response function, which utilizes machine learning and Targeted Minimum-Loss Estimation (TMLE). We additionally propose a more general estimator, based on sequential regression, that also applies when there is outcome missingness. We show that the threshold-response for a given threshold may be viewed as the expected outcome under a stochastic intervention where all participants are given a treatment dose above the threshold. We prove the estimator is efficient and characterize its asymptotic distribution. A method to construct simultaneous 95 threshold-response function and its inverse is given. Furthermore, we discuss how to adjust our estimator when the treatment or biomarker is missing-at-random, as is the case in clinical trials with biased sampling designs, using inverse-probability-weighting. The methods are assessed in a diverse set of simulation settings with rare outcomes and cumulative case-control sampling. The methods are employed to estimate neutralizing antibody thresholds for virologically confirmed dengue risk in the CYD14 and CYD15 dengue vaccine trials.
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