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Prognostic score matching methods for estimating the average effect of a non-reversible binary time-dependent treatment on the survival function.
He, Kevin; Li, Yun; Rao, Panduranga S; Sung, Randall S; Schaubel, Douglas E.
Affiliation
  • He K; Department of Biostatistics, University of Michigan, 1415 Washington Hts., Ann Arbor, MI, 48109-2029, USA.
  • Li Y; Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania Perelman School of Medicine, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.
  • Rao PS; Department of Internal Medicine, University of Michigan, 1500 East Medical Center Dr., Ann Arbor, MI, 48109-5361, USA.
  • Sung RS; Department of Surgery, University of Michigan, 1500 East Medical Center Dr., Ann Arbor, MI, 48109-5334, USA.
  • Schaubel DE; Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania Perelman School of Medicine, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA. douglas.schaubel@pennmedicine.upenn.edu.
Lifetime Data Anal ; 26(3): 451-470, 2020 07.
Article in En | MEDLINE | ID: mdl-31576491
In evaluating the benefit of a treatment on survival, it is often of interest to compare post-treatment survival with the survival function that would have been observed in the absence of treatment. In many practical settings, treatment is time-dependent in the sense that subjects typically begin follow-up untreated, with some going on to receive treatment at some later time point. In observational studies, treatment is not assigned at random and, therefore, may depend on various patient characteristics. We have developed semi-parametric matching methods to estimate the average treatment effect on the treated (ATT) with respect to survival probability and restricted mean survival time. Matching is based on a prognostic score which reflects each patient's death hazard in the absence of treatment. Specifically, each treated patient is matched with multiple as-yet-untreated patients with similar prognostic scores. The matched sets do not need to be of equal size, since each matched control is weighted in order to preserve risk score balancing across treated and untreated groups. After matching, we estimate the ATT non-parametrically by contrasting pre- and post-treatment weighted Nelson-Aalen survival curves. A closed-form variance is proposed and shown to work well in simulation studies. The proposed methods are applied to national organ transplant registry data.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Survival Analysis / Treatment Outcome Type of study: Observational_studies / Prognostic_studies Limits: Humans Language: En Journal: Lifetime Data Anal Year: 2020 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Survival Analysis / Treatment Outcome Type of study: Observational_studies / Prognostic_studies Limits: Humans Language: En Journal: Lifetime Data Anal Year: 2020 Document type: Article Affiliation country: United States Country of publication: United States