ArticleBiometrics2025
Design of platform trials with a change in the control treatment arm.
Article in Biometrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- A statistical evaluation of decision-making methods and the efficiency of Bayesian multi-arm multi-stage trials.Clinical trials (London, England) · 2026Article
- A Multi-Stage Drop-the-Loser Design With Superiority Boundaries.Statistics in medicine · 2026Article
- On the Inclusion of Non-Concurrent Controls in Platform Trials With an Interim Analysis.Statistics in medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Platform trials are an efficient way of testing multiple treatments. We consider platform trials where, if a treatment is found to be superior to the control, it will become the new standard of care. The remaining treatments are then tested against this new control. In this setting, one can either keep the information on both the new standard of care and the other active treatments before the control is changed or discard this information when testing for benefit of the remaining treatments. We show analytically and numerically, retaining the information collected before the change in control can be detrimental to the power in a frequentist multi-arm multi-stage trial. Specifically, we consider the overall power, the probability that the active treatment with the greatest treatment effect is found during the trial, and the conditional power, the probability a given treatment is found superior against the current control. Also studied is the conditional type I error, the probability a given treatment is incorrectly found superior against the current control. We prove when retaining the information decreases both the overall and conditional power but also decreases the conditional type I error. A motivating example is then studied. Based on these observations, we discuss different aspects to consider when deciding whether to run a continuous platform trial or run an inherently new trial using the same trial infrastructure.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.