Journal of Clinical Medicine (Feb 2019)

Chimeric Antigen Receptor (CAR) T Cell Therapy in Acute Myeloid Leukemia (AML)

  • Susanne Hofmann,
  • Maria-Luisa Schubert,
  • Lei Wang,
  • Bailin He,
  • Brigitte Neuber,
  • Peter Dreger,
  • Carsten Müller-Tidow,
  • Michael Schmitt

DOI
https://doi.org/10.3390/jcm8020200
Journal volume & issue
Vol. 8, no. 2
p. 200

Abstract

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Despite high response rates after initial chemotherapy in patients with acute myeloid leukemia (AML), relapses occur frequently, resulting in a five-year-survival by <30% of the patients. Hitherto, allogeneic hemotopoietic stem cell transplantation (allo-HSCT) is the best curative treatment option in intermediate and high risk AML. It is the proof-of-concept for T cell-based immunotherapies in AML based on the graft-versus-leukemia (GvL)-effect, but it also bears the risk of graft-versus-host disease. CD19-targeting therapies employing chimeric antigen receptor (CAR) T cells are a breakthrough in cancer therapy. A similar approach for myeloid malignancies is highly desirable. This article gives an overview on the state-of-the art of preclinical and clinical studies on suitable target antigens for CAR T cell therapy in AML patients.

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