Chimeric Antigen Receptor T-Cell Therapy

J Natl Compr Canc Netw. 2018 Sep;16(9):1092-1106. doi: 10.6004/jnccn.2018.0073.

Abstract

Patients with relapsed or refractory (R/R) cancers have a poor prognosis and limited treatment options. The recent approval of 2 chimeric antigen receptor (CAR) autologous T-cell products for R/R B-cell acute lymphoblastic leukemia and non-Hodgkin's lymphoma treatment is setting the stage for what is possible in other diseases. However, there are important factors that must be considered, including patient selection, toxicity management, and costs associated with CAR T-cell therapy. To begin to address these issues, NCCN organized a task force consisting of a multidisciplinary panel of experts in oncology, cancer center administration, and health policy, which met for the first time in March 2018. This report describes the current state of CAR T-cell therapy and future strategies that should be considered as the application of this novel immunotherapy expands and evolves.

MeSH terms

  • Advisory Committees
  • Cancer Care Facilities / organization & administration
  • Drug Resistance, Neoplasm / immunology
  • Health Policy
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Immunotherapy, Adoptive / methods*
  • Immunotherapy, Adoptive / trends
  • Interdisciplinary Communication
  • Medical Oncology / organization & administration
  • Neoplasm Recurrence, Local / immunology
  • Neoplasm Recurrence, Local / therapy*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Receptors, Chimeric Antigen / immunology
  • Societies, Medical / organization & administration
  • T-Lymphocytes / immunology
  • T-Lymphocytes / transplantation
  • Transplantation, Autologous / adverse effects
  • Transplantation, Autologous / methods
  • Transplantation, Autologous / trends
  • United States

Substances

  • Receptors, Chimeric Antigen