[Chimeric antigen receptor T-cell therapy for hematological malignancies]

Rinsho Ketsueki. 2019;60(9):1351-1357. doi: 10.11406/rinketsu.60.1351.
[Article in Japanese]

Abstract

The adoptive transfer of chimeric antigen receptor (CAR)-modified autologous T cells targeted at the B-cell antigen CD19 is highly effective in patients with relapsed or refractory B-cell malignancies. In Japan, tisagenlecleucel has been approved in March 2019, whereas axicabtagene ciloleucel, lisocabtagene maraleucel, and TBI-1501 have been tested in clinical trials. In addition, allogeneic CD19 CAR T cells from family or third-party donors have been developed for treating B-cell malignancies. Moreover, CAR T-cell therapies for acute myeloid leukemia (AML), T-cell leukemia, and multiple myeloma are still under development. Our group is currently preparing a phase I study on granulocyte macrophage colony-stimulating factor receptor-targeted CAR T cells in pediatric and adult patients with AML.

Keywords: ALL; AML; Chimeric antigen receptor.

Publication types

  • Review

MeSH terms

  • Adult
  • Child
  • Clinical Trials, Phase I as Topic
  • Hematologic Neoplasms / therapy*
  • Humans
  • Immunotherapy, Adoptive*
  • Japan
  • Receptors, Antigen, T-Cell / therapeutic use*
  • Receptors, Chimeric Antigen / therapeutic use*

Substances

  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen
  • tisagenlecleucel