Abstract

BackgroundThe application of adaptive design methodology within a clinical trial setting is becoming increasingly popular. However the application of these methods within trials is not being reported as adaptive designs hence making it more difficult to capture the emerging use of these designs. Within this review, we aim to understand how adaptive design methodology is being reported, whether these methods are explicitly stated as an ‘adaptive design’ or if it has to be inferred and to identify whether these methods are applied prospectively or concurrently.MethodsThree databases; Embase, Ovid and PubMed were chosen to conduct the literature search. The inclusion criteria for the review were phase II, phase III and phase II/III randomised controlled trials within the field of Oncology that published trial results in 2015. A variety of search terms related to adaptive designs were used.ResultsA total of 734 results were identified, after screening 54 were eligible. Adaptive designs were more commonly applied in phase III confirmatory trials. The majority of the papers performed an interim analysis, which included some sort of stopping criteria. Additionally only two papers explicitly stated the term ‘adaptive design’ and therefore for most of the papers, it had to be inferred that adaptive methods was applied. Sixty-five applications of adaptive design methods were applied, from which the most common method was an adaptation using group sequential methods.ConclusionsThis review indicated that the reporting of adaptive design methodology within clinical trials needs improving. The proposed extension to the current CONSORT 2010 guidelines could help capture adaptive design methods. Furthermore provide an essential aid to those involved with clinical trials.

Highlights

  • IntroductionAny changes during the trial should be reported as an adaptive method

  • Background and objectivesScientific background and explanation of rationaleRational for implementing an adaptive designSpecific objectives or hypotheses Trial designDescription of trial design including allocation ratioDefine what adaptive design/ adaptive method will be appliedImportant changes to methods after trial commencement, with reasonsAny changes during the trial should be reported as an adaptive method

  • This review aims to understand how adaptive design methodology is currently being reported within journals, whether these methods are being applied prospectively or concurrently, what methods are commonly applied and to understand whether the use of adaptive design methodology is being explicitly stated or whether it has to be inferred

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Summary

Introduction

Any changes during the trial should be reported as an adaptive method. The application of adaptive design methodology within a clinical trial setting is becoming increasingly popular. We aim to understand how adaptive design methodology is being reported, whether these methods are explicitly stated as an ‘adaptive design’ or if it has to be inferred and to identify whether these methods are applied prospectively or concurrently. Chow and Chang (2008) have broadened this definition by classifying adaptive designs as any modifications made prospectively, concurrently or retrospectively during the conduct of a trial. Adaptive design methods may appeal more to clinical investigators due to the flexibility and prospect of making changes based on data at an interim stage of the trial

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