| Literature DB >> 29808479 |
Yanxun Xu1, Peter Müller2, Apostolia M Tsimberidou3, Donald Berry4.
Abstract
Targeted therapies on the basis of genomic aberrations analysis of the tumor have shown promising results in cancer prognosis and treatment. Regardless of tumor type, trials that match patients to targeted therapies for their particular genomic aberrations have become a mainstream direction of therapeutic management of patients with cancer. Therefore, finding the subpopulation of patients who can most benefit from an aberration-specific targeted therapy across multiple cancer types is important. We propose an adaptive Bayesian clinical trial design for patient allocation and subpopulation identification. We start with a decision theoretic approach, including a utility function and a probability model across all possible subpopulation models. The main features of the proposed design and population finding methods are the use of a flexible nonparametric Bayesian survival regression based on a random covariate-dependent partition of patients, and decisions based on a flexible utility function that reflects the requirement of the clinicians appropriately and realistically, and the adaptive allocation of patients to their superior treatments. Through extensive simulation studies, the new method is demonstrated to achieve desirable operating characteristics and compares favorably against the alternatives.Entities:
Keywords: Bayesian adaptive designs; basket trials; subpopulation identification; targeted therapies
Mesh:
Year: 2018 PMID: 29808479 PMCID: PMC6261711 DOI: 10.1002/bimj.201700162
Source DB: PubMed Journal: Biom J ISSN: 0323-3847 Impact factor: 2.207