Auxiliary variable-enriched biomarker-stratified design.

TitleAuxiliary variable-enriched biomarker-stratified design.
Publication TypeJournal Article
Year of Publication2018
AuthorsWang, Ting, Xiaofei Wang, Haibo Zhou, Jianwen Cai, and Stephen L. George
JournalStat Med
Date Published2018 12 30
KeywordsBayes Theorem, Biomarkers, Cost Savings, Humans, Models, Statistical, Precision Medicine, Randomized Controlled Trials as Topic, Treatment Outcome

Clinical trials in the era of precision medicine require assessment of biomarkers to identify appropriate subgroups of patients for targeted therapy. In a biomarker-stratified design (BSD), biomarkers are measured on all patients and used as stratification variables. However, such a trial can be both inefficient and costly, especially when the prevalence of the subgroup of primary interest is low and the cost of assessing the biomarkers is high. Efficiency can be improved and costs reduced by using enriched biomarker-stratified designs, in which patients of primary interest, typically the biomarker-positive patients, are oversampled. We consider a special type of enrichment design, an auxiliary variable-enriched design (AEBSD), in which enrichment is based on some inexpensive auxiliary variable that is positively correlated with the true biomarker. The proposed AEBSD reduces the total cost of the trial compared with a standard BSD when the prevalence rate of true biomarker positivity is small and the positive predictive value (PPV) of the auxiliary biomarker is larger than the prevalence rate. In addition, for an AEBSD, we can immediately randomize the patients selected in the screening process without waiting for the result of the true biomarker test, reducing the treatment waiting time. We propose an adaptive Bayesian method to adjust the assumed PPV while the trial is ongoing. Numerical studies and an example illustrate the approach. An R package is available.

Alternate JournalStat Med
Original PublicationAuxiliary variable-enriched biomarker-stratified design.
PubMed ID30221368
PubMed Central IDPMC6279614
Grant ListP30 ES010126 / ES / NIEHS NIH HHS / United States
R21 AG042894 / AG / NIA NIH HHS / United States
P01 CA142538 / CA / NCI NIH HHS / United States
R01 ES021900 / ES / NIEHS NIH HHS / United States