Building a CAR Garage: Preparing for the Delivery of Commercial CAR T Cell Products at Memorial Sloan Kettering Cancer Center. Review uri icon

Overview

abstract

  • Two commercial chimeric antigen receptor (CAR) T cell therapies for CD19-expressing B cell malignancies, Kymriah and Yescarta, have recently been approved by the Food and Drug Administration. The administration of CAR T cells is a complex endeavor involving cell manufacture, tracking and shipping of apheresis products, and management of novel and severe toxicities. At Memorial Sloan Kettering Cancer Center, we have identified 8 essential tasks that define the CAR T cell workflow. In this review, we discuss practical aspects of CAR T cell program development, including clinical, administrative, and regulatory challenges for successful implementation.

publication date

  • March 1, 2018

Research

keywords

  • Cancer Care Facilities
  • Immunotherapy, Adoptive
  • Receptors, Chimeric Antigen
  • Workflow

Identity

PubMed Central ID

  • PMC6625528

Scopus Document Identifier

  • 85044642728

Digital Object Identifier (DOI)

  • 10.1016/j.bbmt.2018.02.018

PubMed ID

  • 29499327

Additional Document Info

volume

  • 24

issue

  • 6