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Estimating mean potential outcome under adaptive treatment length strategies in continuous time

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  • Hao Sun
  • Ashkan Ertefaie
  • Brent A. Johnson

Abstract

An adaptive treatment length strategy is a sequential stage‐wise treatment strategy where a subject's treatment begins at baseline and one chooses to stop or continue treatment at each stage provided the subject has been continuously treated. The effects of treatment are assumed to be cumulative and, therefore, the effect of treatment length on clinical endpoint, measured at the end of the study, is of primary scientific interest. At the same time, adverse treatment‐terminating events may occur during the course of treatment that require treatment be stopped immediately. Because the presence of a treatment‐terminating event may be strongly associated with the study outcome, the treatment‐terminating event is informative. In observational studies, decisions to stop or continue treatment depend on covariate history that confounds the relationship between treatment length on outcome. We propose a new risk‐set weighted estimator of the mean potential outcome under the condition that time‐dependent covariates update at a set of common landmarks. We show that our proposed estimator is asymptotically linear given mild assumptions and correctly specified working models. Specifically, we study the theoretical properties of our estimator when the nuisance parameters are modeled using either parametric or semiparametric methods. The finite sample performance and theoretical results of the proposed estimator are evaluated through simulation studies and demonstrated by application to the Enhanced Suppression of the Platelet Receptor IIb/IIIa with Integrilin Therapy (ESPRIT) infusion trial data.

Suggested Citation

  • Hao Sun & Ashkan Ertefaie & Brent A. Johnson, 2022. "Estimating mean potential outcome under adaptive treatment length strategies in continuous time," Biometrics, The International Biometric Society, vol. 78(4), pages 1503-1514, December.
  • Handle: RePEc:bla:biomet:v:78:y:2022:i:4:p:1503-1514
    DOI: 10.1111/biom.13504
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    References listed on IDEAS

    as
    1. Brent A. Johnson & Heather Ribaudo & Roy M. Gulick & Joseph J. Eron Jr., 2013. "Modeling Clinical Endpoints as a Function of Time of Switch to Second-Line ART with Incomplete Data on Switching Times," Biometrics, The International Biometric Society, vol. 69(3), pages 732-740, September.
    2. Brent A. Johnson & Anastasios A. Tsiatis, 2005. "Semiparametric inference in observational duration-response studies, with duration possibly right-censored," Biometrika, Biometrika Trust, vol. 92(3), pages 605-618, September.
    3. Xin Lu & Brent A. Johnson, 2017. "Direct estimation for adaptive treatment length policies: Methods and application to evaluating the effect of delayed PEG insertion," Biometrics, The International Biometric Society, vol. 73(3), pages 981-989, September.
    4. Brent A. Johnson & Anastasios A. Tsiatis, 2004. "Estimating Mean Response as a Function of Treatment Duration in an Observational Study, Where Duration May Be Informatively Censored," Biometrics, The International Biometric Society, vol. 60(2), pages 315-323, June.
    5. Liangyuan Hu & Joseph W. Hogan & Ann W. Mwangi & Abraham Siika, 2018. "Modeling the causal effect of treatment initiation time on survival: Application to HIV/TB co†infection," Biometrics, The International Biometric Society, vol. 74(2), pages 703-713, June.
    6. Shu Yang & Anastasios A. Tsiatis & Michael Blazing, 2018. "Modeling survival distribution as a function of time to treatment discontinuation: A dynamic treatment regime approach," Biometrics, The International Biometric Society, vol. 74(3), pages 900-909, September.
    7. Xin Lu & Brent A. Johnson, 2015. "Direct estimation of the mean outcome on treatment when treatment assignment and discontinuation compete," Biometrika, Biometrika Trust, vol. 102(4), pages 797-807.
    8. Edward H. Kennedy & Zongming Ma & Matthew D. McHugh & Dylan S. Small, 2017. "Non-parametric methods for doubly robust estimation of continuous treatment effects," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 79(4), pages 1229-1245, September.
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