Jing Xu, Camden Bay, Bingxia Wang, Guohui Liu, Cong Li
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Application of marginal structural models for causal inference on the treatment effect for overall survival in randomized controlled trials with control arm patients switching to active intervention after disease progression.
This research explores the application of marginal structural models (MSMs) in evaluating the causal treatment effect of active intervention versus control on overall survival in randomized clinical trials (RCTs) allowing for control arm patients to switch to active intervention after disease progression. When MSMs are applied in RCTs under this type of treatment switching setting, the question of interest and model specifications differ from both observational studies and from RCTs where patients in both arms are permitted to take alternative treatments after disease progression. A violation of structural positivity may result as an undesired consequence if MSM model weights are constructed using data directly from both arms. This research proposes a two-step approach to avoid this issue. Through simulation studies, it is demonstrated that the proposed approach allows for MSM to be used for analyzing survival data to detect causal active treatment effects under this one-way treatment switching setting. Additionally, estimation for the causal effect of the active intervention as the next line (post-disease progression) therapy can also be obtained from the MSM approach. A case study is presented to illustrate the application of MSMs under this type of treatment switching setting.
期刊介绍:
The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers:
Drug, device, and biological research and development;
Drug screening and drug design;
Assessment of pharmacological activity;
Pharmaceutical formulation and scale-up;
Preclinical safety assessment;
Bioavailability, bioequivalence, and pharmacokinetics;
Phase, I, II, and III clinical development including complex innovative designs;
Premarket approval assessment of clinical safety;
Postmarketing surveillance;
Big data and artificial intelligence and applications.