» Articles » PMID: 37296906

CAR-T Cells Immunotherapies for the Treatment of Acute Myeloid Leukemia-Recent Advances

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2023 Jun 10
PMID 37296906
Authors
Affiliations
Soon will be listed here.
Abstract

In order to increase the effectiveness of cancer therapies and extend the long-term survival of patients, more and more often, in addition to standard treatment, oncological patients receive also targeted therapy, i.e., CAR-T cells. These cells express a chimeric receptor (CAR) that specifically binds an antigen present on tumor cells, resulting in tumor cell lysis. The use of CAR-T cells in the therapy of relapsed and refractory B-type acute lymphoblastic leukemia (ALL) resulted in complete remission in many patients, which prompted researchers to conduct tests on the use of CAR-T cells in the treatment of other hematological malignancies, including acute myeloid leukemia (AML). AML is associated with a poorer prognosis compared to ALL due to a higher risk of relapse caused by the development of resistance to standard treatment. The 5-year relative survival rate in AML patients was estimated at 31.7%. The objective of the following review is to present the mechanism of action of CAR-T cells, and discuss the latest findings on the results of anti-CD33, -CD123, -FLT3 and -CLL-1 CAR-T cell therapy, the emerging challenges as well as the prospects for the future.

Citing Articles

Clinical Implications of Isocitrate Dehydrogenase Mutations and Targeted Treatment of Acute Myeloid Leukemia with Mutant Isocitrate Dehydrogenase Inhibitors-Recent Advances, Challenges and Future Prospects.

Kowalczyk A, Zarychta J, Lejman M, Latoch E, Zawitkowska J Int J Mol Sci. 2024; 25(14).

PMID: 39063158 PMC: 11276768. DOI: 10.3390/ijms25147916.


The Implementation of Chimeric Antigen Receptor (CAR) T-cell Therapy in Pediatric Patients: Where Did We Come From, Where Are We Now, and Where are We Going?.

Knight E T, Oluwole O, Kitko C Clin Hematol Int. 2024; 6(1):96-115.

PMID: 38817691 PMC: 11108586. DOI: 10.46989/001c.94386.


Chimeric antigen receptor (CAR) modified T Cells in acute myeloid leukemia: limitations and expectations.

Guijarro-Albaladejo B, Marrero-Cepeda C, Rodriguez-Arboli E, Sierro-Martinez B, Perez-Simon J, Garcia-Guerrero E Front Cell Dev Biol. 2024; 12:1376554.

PMID: 38694825 PMC: 11061469. DOI: 10.3389/fcell.2024.1376554.


Next-generation treatments: Immunotherapy and advanced therapies for COVID-19.

Arevalo-Romero J, Chingate-Lopez S, Camacho B, Almeciga-Diaz C, Ramirez-Segura C Heliyon. 2024; 10(5):e26423.

PMID: 38434363 PMC: 10907543. DOI: 10.1016/j.heliyon.2024.e26423.


Chimeric Antigen Receptor T Cell and Chimeric Antigen Receptor NK Cell Therapy in Pediatric and Adult High-Grade Glioma-Recent Advances.

Kowalczyk A, Zarychta J, Marszolek A, Zawitkowska J, Lejman M Cancers (Basel). 2024; 16(3).

PMID: 38339374 PMC: 10854514. DOI: 10.3390/cancers16030623.

References
1.
Ghamari A, Pakzad P, Majd A, Ebrahimi M, Hamidieh A . Design and Production An Effective Bispecific Tandem Chimeric Antigen Receptor on T Cells against CD123 and Folate Receptor ß towards B-Acute Myeloid Leukaemia Blasts. Cell J. 2021; 23(6):650-657. PMC: 8665988. DOI: 10.22074/cellj.2021.7314. View

2.
Laszlo G, Harrington K, Gudgeon C, Beddoe M, Fitzgibbon M, Ries R . Expression and functional characterization of CD33 transcript variants in human acute myeloid leukemia. Oncotarget. 2016; 7(28):43281-43294. PMC: 5190023. DOI: 10.18632/oncotarget.9674. View

3.
Harrer D, Dorrie J, Schaft N . CARs and Drugs: Pharmacological Ways of Boosting CAR-T-Cell Therapy. Int J Mol Sci. 2023; 24(3). PMC: 9916546. DOI: 10.3390/ijms24032342. View

4.
Kiyoi H, Kawashima N, Ishikawa Y . FLT3 mutations in acute myeloid leukemia: Therapeutic paradigm beyond inhibitor development. Cancer Sci. 2019; 111(2):312-322. PMC: 7004512. DOI: 10.1111/cas.14274. View

5.
Thol F, Ganser A . Treatment of Relapsed Acute Myeloid Leukemia. Curr Treat Options Oncol. 2020; 21(8):66. PMC: 7324428. DOI: 10.1007/s11864-020-00765-5. View