CAR T-cell therapy in acute myeloid leukemia.

Saudi Med J

From the Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Shaqra University, Shaqra, Kingdom of Saudi Arabia.

Published: October 2024

AI Article Synopsis

  • Acute myeloid leukemia (AML) is a serious blood cancer affecting myeloid progenitor cells, with patients facing poor outcomes when the disease relapses or resists treatment.
  • Chimeric antigen receptor (CAR) T-cell therapy is being explored as a potential new treatment, with early clinical trials showing promising results targeting specific AML markers like CD33, CD123, and CLL-1.
  • However, challenges remain due to the variability of AML and the risk of harmful effects on healthy cells, highlighting the need for further research and improvements in CAR T-cell technology.

Article Abstract

Acute myeloid leukemia (AML) is an aggressive leukemic malignancy that affects myeloid lineage progenitors. Relapsed or refractory AML patients continue to have poor prognoses, necessitating the development of novel therapy alternatives. Adoptive T-cell therapy with chimeric antigen receptors (CARs) is an intriguing possibility in the field of leukemia treatment. Chimeric antigen receptor T-cell therapy is now being tested in clinical trials (mostly in phase I and phase II) using AML targets including CD33, CD123, and CLL-1. Preliminary data showed promising results. However, due to the cellular and molecular heterogeneity of AML and the co-expression of some AML targets on hematopoietic stem cells, these clinical investigations have shown substantial "on-target off-tumor" toxicities, indicating that more research is required. In this review, the latest significant breakthroughs in AML CAR T cell therapy are presented. Furthermore, the limitations of CAR T-cell technology and future directions to overcome these challenges are discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11463564PMC
http://dx.doi.org/10.15537/smj.2024.45.10.20240330DOI Listing

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