Abstract

BackgroundPlatform trials allow adding new experimental treatments to an on-going trial. This feature is attractive to practitioners due to improved efficiency. Nevertheless, the operating characteristics of a trial that adds arms have not been well-studied. One controversy is whether just the concurrent control data (i.e. of patients who are recruited after a new arm is added) should be used in the analysis of the newly added treatment(s), or all control data (i.e. non-concurrent and concurrent).MethodsWe investigate the benefits and drawbacks of using non-concurrent control data within a two-stage setting. We perform simulation studies to explore the impact of a linear and a step trend on the inference of the trial. We compare several analysis approaches when one includes all the control data or only concurrent control data in the analysis of the newly added treatment.ResultsWhen there is a positive trend and all the control data are used, the marginal power of rejecting the corresponding hypothesis and the type one error rate can be higher than the nominal value. A model-based approach adjusting for a stage effect is equivalent to using concurrent control data; an adjustment with a linear term may not guarantee valid inference when there is a non-linear trend.ConclusionsIf strict error rate control is required then non-concurrent control data should not be used; otherwise it may be beneficial if the trend is sufficiently small. On the other hand, the root mean squared error of the estimated treatment effect can be improved through using non-concurrent control data.

Highlights

  • Platform trials allow adding new experimental treatments to an on-going trial

  • Within a two-stage setting where a new treatment is added at the end of stage one [25, 28], we explore the impact of i) the timing of adding a new arm ii) the sample size of the new arm and iii) the magnitude of a linear or a step trend [15] on the inference about the newly added experimental treatment

  • Analytical power and borrowing of strength (BoS) when there is no trend We compare BoS and the power of rejecting H02 when there is no trend and either all, or only concurrent control data are used in the inference

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Summary

Methods

We investigate the benefits and drawbacks of using non-concurrent control data within a two-stage setting. We compare several analysis approaches when one includes all the control data or only concurrent control data in the analysis of the newly added treatment

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