A Bayesian adaptive phase 1 design to determine the optimal dose and schedule of an adoptive T-cell therapy in a mixed patient population

Contemp Clin Trials. 2016 May:48:153-65. doi: 10.1016/j.cct.2016.04.004. Epub 2016 Apr 19.

Abstract

We present a novel Bayesian adaptive phase 1 design to determine the optimal dosing regimen for an adoptive T-cell therapy in a mixed patient population. Our design is motivated by a B-cell Non-Hodgkin Lymphoma trial evaluating multiple dosing regimens within multiple disease subtypes. A utility score is calculated from both safety and efficacy utility functions and used to guide dose-escalation decisions. We pool safety data across disease subtypes and use a single dose-toxicity model while sharing efficacy information between disease subtypes using a hierarchical dose-response model. In addition, an adaptive randomization approach is applied to dynamically assign patients to a regimen when more than one regimen is open for enrollment. We illustrate this study design through a simulated trial example, and we investigate the operating characteristics using simulation studies.

Keywords: Adaptive randomization; Bayesian adaptive; Hierarchical modeling; Mixed population; Phase 1; Utility score.

Publication types

  • Adaptive Clinical Trial
  • Clinical Trial, Phase I

MeSH terms

  • Adoptive Transfer / methods*
  • Antigens, CD19 / metabolism
  • Bayes Theorem
  • CD4 Antigens / metabolism
  • CD8 Antigens / metabolism
  • Humans
  • Lymphoma, Large B-Cell, Diffuse / therapy*
  • Lymphoma, Mantle-Cell / therapy*
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / transplantation*
  • Transplantation, Autologous

Substances

  • Antigens, CD19
  • CD19 molecule, human
  • CD4 Antigens
  • CD8 Antigens