{"about":{"site":"https://codewithpapers.app","non_affiliation":"Code with Papers and Syntology are not affiliated with, endorsed by, or sponsored by Papers with Code, Meta, or the pwc-archive mirror.","licence":"CC BY-SA 4.0","licence_url":"https://creativecommons.org/licenses/by-sa/4.0/legalcode","attribution":"https://codewithpapers.app/attribution","modified":"archive material modified by Syntology; see the attribution page"},"url":"/paper/efficient-nonparametric-estimation-of-the","title":"Efficient nonparametric estimation of the covariate-adjusted threshold-response function, a support-restricted stochastic intervention","arxiv_id":"2107.11459","date":"2021-07-23","proceeding":null,"authors":["Lars van der Laan","Wenbo Zhang","Peter B. Gilbert"],"abstract":"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% confidence bands for the 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.","url_abs":"https://arxiv.org/abs/2107.11459v2","url_pdf":"https://arxiv.org/pdf/2107.11459v2.pdf","source":{"archive":"pwc-archive (Hugging Face), CC BY-SA 4.0","snapshot":"2025-07-28","licence_url":"https://creativecommons.org/licenses/by-sa/4.0/legalcode","row_kind":"links_only","authors_date_abstract":"arXiv metadata, CC0 1.0 (https://info.arxiv.org/help/license), from the Kaggle arXiv metadata snapshot of 2026-09-12"},"code_links":[{"paper_slug":"efficient-nonparametric-estimation-of-the","repo_url":"https://github.com/Larsvanderlaan/ThresholdTMLE","is_official":1,"mentioned_in_paper":1,"mentioned_in_github":1,"framework":"none","reach":null}],"tasks":[],"methods":[],"datasets_introduced":[],"methods_introduced":[],"results":[],"syntology":{"atlas_url":null,"mcp":null,"developers":"https://syntology.ai/developers"},"arxiv_metadata":null,"syntology_extracted_results":null}