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Point estimation following two-stage adaptive threshold enrichment clinical trials.
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- Author(s): Kimani PK;Kimani PK; Todd S; Todd S; Renfro LA; Renfro LA; Stallard N; Stallard N
- Source:
Statistics in medicine [Stat Med] 2018 Sep 30; Vol. 37 (22), pp. 3179-3196. Date of Electronic Publication: 2018 May 31.- Publication Type:
Journal Article; Research Support, Non-U.S. Gov't- Language:
English - Source:
- Additional Information
- Source: Publisher: Wiley Country of Publication: England NLM ID: 8215016 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0258 (Electronic) Linking ISSN: 02776715 NLM ISO Abbreviation: Stat Med Subsets: MEDLINE
- Publication Information: Original Publication: Chichester ; New York : Wiley, c1982-
- Subject Terms:
- Abstract: Recently, several study designs incorporating treatment effect assessment in biomarker-based subpopulations have been proposed. Most statistical methodologies for such designs focus on the control of type I error rate and power. In this paper, we have developed point estimators for clinical trials that use the two-stage adaptive enrichment threshold design. The design consists of two stages, where in stage 1, patients are recruited in the full population. Stage 1 outcome data are then used to perform interim analysis to decide whether the trial continues to stage 2 with the full population or a subpopulation. The subpopulation is defined based on one of the candidate threshold values of a numerical predictive biomarker. To estimate treatment effect in the selected subpopulation, we have derived unbiased estimators, shrinkage estimators, and estimators that estimate bias and subtract it from the naive estimate. We have recommended one of the unbiased estimators. However, since none of the estimators dominated in all simulation scenarios based on both bias and mean squared error, an alternative strategy would be to use a hybrid estimator where the estimator used depends on the subpopulation selected. This would require a simulation study of plausible scenarios before the trial.
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Br J Psychiatry. 2009 Mar;194(3):252-9. (PMID: 19252156) - Grant Information: MR/N028309/1 United Kingdom MRC_ Medical Research Council; MR/N028309/1 International UK Medical Research Council
- Contributed Indexing: Keywords: biomarker; multistage; personalized medicine; subgroup or subpopulation selection; targeted therapy
- Accession Number: 0 (Biomarkers)
- Publication Date: Date Created: 20180602 Date Completed: 20191107 Latest Revision: 20240402
- Publication Date: 20240402
- Accession Number: PMC6175016
- Accession Number: 10.1002/sim.7831
- Accession Number: 29855066
- Source:
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