Using modified intention-to-treat as a principal stratum estimator for failure to initiate treatment

Author:

Kahan Brennan C1ORCID,White Ian R1ORCID,Edwards Mark2,Harhay Michael O34

Affiliation:

1. MRC Clinical Trials Unit at UCL, London, UK

2. Department of Anaesthesia, University Hospital Southampton NHS Foundation Trust, Southampton, UK

3. Clinical Trials Methods and Outcomes Lab, PAIR (Palliative and Advanced Illness Research) Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

4. Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Background: A common intercurrent event affecting many trials is when some participants do not begin their assigned treatment. For example, in a double-blind drug trial, some participants may not receive any dose of study medication. Many trials use a ‘modified intention-to-treat’ approach, whereby participants who do not initiate treatment are excluded from the analysis. However, it is not clear (a) the estimand being targeted by such an approach and (b) the assumptions necessary for such an approach to be unbiased. Methods: Using potential outcome notation, we demonstrate that a modified intention-to-treat analysis which excludes participants who do not begin treatment is estimating a principal stratum estimand (i.e. the treatment effect in the subpopulation of participants who would begin treatment, regardless of which arm they were assigned to). The modified intention-to-treat estimator is unbiased for the principal stratum estimand under the assumption that the intercurrent event is not affected by the assigned treatment arm, that is, participants who initiate treatment in one arm would also do so in the other arm (i.e. if someone began the intervention, they would also have begun the control, and vice versa). Results: We identify two key criteria in determining whether the modified intention-to-treat estimator is likely to be unbiased: first, we must be able to measure the participants in each treatment arm who experience the intercurrent event, and second, the assumption that treatment allocation will not affect whether the participant begins treatment must be reasonable. Most double-blind trials will satisfy these criteria, as the decision to start treatment cannot be influenced by the allocation, and we provide an example of an open-label trial where these criteria are likely to be satisfied as well, implying that a modified intention-to-treat analysis which excludes participants who do not begin treatment is an unbiased estimator for the principal stratum effect in these settings. We also give two examples where these criteria will not be satisfied (one comparing an active intervention vs usual care, where we cannot identify which usual care participants would have initiated the active intervention, and another comparing two active interventions in an unblinded manner, where knowledge of the assigned treatment arm may affect the participant’s choice to begin or not), implying that a modified intention-to-treat estimator will be biased in these settings. Conclusion: A modified intention-to-treat analysis which excludes participants who do not begin treatment can be an unbiased estimator for the principal stratum estimand. Our framework can help identify when the assumptions for unbiasedness are likely to hold, and thus whether modified intention-to-treat is appropriate or not.

Funder

Medical Research Council

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

Reference16 articles.

1. CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials

2. Nonadherence to treatment protocol in published randomised controlled trials: a review

3. A systematic review finds variable use of the intention-to-treat principle in musculoskeletal randomized controlled trials with missing data

4. Non-inferiority trials: are they inferior? A systematic review of reporting in major medical journals

5. European Medicines Agency. ICH E9 (R1) addendum on estimands sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials, https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e9-r1-addendum-estimands-sensitivity-analysis-clinical-trials-guideline-statistical-principles_en.pdf

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