Multistate modeling of clinical hold in randomized clinical trials
- PMID: 31820541
- DOI: 10.1002/pst.1989
Multistate modeling of clinical hold in randomized clinical trials
Abstract
A clinical hold order by the Food and Drug Administration (FDA) to the sponsor of a clinical trial is a measure to delay a proposed or to suspend an ongoing clinical investigation. The phase III clinical trial START serves as motivating data example to explore implications and potential statistical approaches for a trial continuing after a clinical hold is lifted. In spite of a modified intention-to-treat (ITT) analysis introduced to account for the clinical hold by excluding patients potentially affected most by the clinical hold, results of the trial did not show a significant improvement of overall survival duration, and the question remains whether the negative result was an effect of the clinical hold. In this paper, we propose a multistate model incorporating the clinical hold as well as disease progression as intermediate events to investigate the impact of the clinical hold on the treatment effect. Moreover, we consider a simple counterfactual censoring approach as alternative strategy to the modified ITT analysis to deal with a clinical hold. Using a realistic simulation study informed by the START data and with a design based on our multistate model, we show that the modified ITT analysis used in the START trial was reasonable. However, the censoring approach will be shown to have some benefits in terms of power and flexibility.
Keywords: clinical hold; overall survival; progression-free survival; proportional hazards model; time-dependent covariates.
© 2019 The Authors. Pharmaceutical Statistics published by John Wiley & Sons Ltd.
References
-
- U.S. Food and Drug Administration. IND Application Procedures: Clinical Hold. 2013. http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDeveloped....
-
- Boudes PF. An Analysis of US Food and Drug Administration Clinical Hold Orders for Drugs and Biologics: A Prospective Study Between 2008 and 2014. Pharmaceutical Medicine. 2015;29(4):203-209.
-
- Butts C. others. Tecemotide (L-BLP25) versus placebo after chemoradiotherapy for stage III non-small-cell lung cancer (START): a randomised, double-blind, phase 3 trial. Lancet Oncology. 2014;15(1):59-68.
-
- Fu H, Wang Y, Liu J, Kulkarni PM, Melemed AS. Joint modeling of progression-free survival and overall survival by a Bayesian normal induced copula estimation model. Statistics in Medicine. 2013;32(2):240-254.
-
- Fleischer F, Gaschler-Markefski B, Bluhmki E. A statistical model for the dependence between progression-free survival and overall survival. Statistics in Medicine. 2009;28(21):2669-2686.
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