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Estimation of Treatment Policy Estimands for Continuous Outcomes Using Off-Treatment Sequential Multiple Imputation. | LitMetric

AI Article Synopsis

  • - The ICH E9 (R1) estimands framework focuses on defining clinical trial effects and managing post-baseline intercurrent events, like treatment discontinuation, using treatment policy strategies that analyze outcomes regardless of these events.
  • - Traditional estimation methods, like mixed models and multiple imputation, can be biased as they often ignore the differences in outcomes for patients who discontinued treatment compared to those who continued.
  • - The study proposes new multiple imputation models that account for these differences in outcomes post-discontinuation, demonstrating that while they can reduce bias, they may also increase variability; the choice of model depends on trial specifics, disease type, and data completeness.

Article Abstract

The 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11602932PMC
http://dx.doi.org/10.1002/pst.2411DOI Listing

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