Estimation of Treatment Policy Estimands for Continuous Outcomes Using Off‐Treatment Sequential Multiple Imputation

Author:

Drury Thomas1ORCID,Abellan Juan J.1ORCID,Best Nicky1ORCID,White Ian R.2

Affiliation:

1. GSK London UK

2. MRC Clinical Trials Unit at UCL University College London London UK

Abstract

ABSTRACTThe estimands framework outlined in ICH E9 (R1) describes the components needed to precisely define the effects to be estimated in clinical trials, which includes how post‐baseline ‘intercurrent’ events (IEs) are to be handled. In late‐stage clinical trials, it is common to handle IEs like ‘treatment discontinuation’ using the treatment policy strategy and target the treatment effect on outcomes regardless of treatment discontinuation. For continuous repeated measures, this type of effect is often estimated using all observed data before and after discontinuation using either a mixed model for repeated measures (MMRM) or multiple imputation (MI) to handle any missing data. In basic form, both these estimation methods ignore treatment discontinuation in the analysis and therefore may be biased if there are differences in patient outcomes after treatment discontinuation compared with patients still assigned to treatment, and missing data being more common for patients who have discontinued treatment. We therefore propose and evaluate a set of MI models that can accommodate differences between outcomes before and after treatment discontinuation. The models are evaluated in the context of planning a Phase 3 trial for a respiratory disease. We show that analyses ignoring treatment discontinuation can introduce substantial bias and can sometimes underestimate variability. We also show that some of the MI models proposed can successfully correct the bias, but inevitably lead to increases in variance. We conclude that some of the proposed MI models are preferable to the traditional analysis ignoring treatment discontinuation, but the precise choice of MI model will likely depend on the trial design, disease of interest and amount of observed and missing data following treatment discontinuation.

Funder

Medical Research Council

Publisher

Wiley

Reference10 articles.

1. ICH “E9(R1) Addendum on Estimands and Sensitivity Analysis in Clinical Trials ”2019 https://www.ich.org/page/efficacy‐guidelines.

2. Treatment policy estimands for recurrent event data using data collected after cessation of randomised treatment

3. Estimation of a treatment policy estimand for time to event data using data collected post discontinuation of randomised treatment

4. J. H.Roger “Joint Modelling of On‐Treatment and Off‐Treatment Data” (poster presentation PSI Annual Conference 2017).

5. Aligning Treatment Policy Estimands and Estimators—A Simulation Study in Alzheimer’s Disease

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