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Targeting CD38 for acute leukemia

Acute leukemia (AL) is a hematological malignancy, and the prognosis of most AL patients hasn’t improved significantly, particularly for relapsed or refractory (R/R) AL. Therefore, new treatments for R/R adult acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) are urgently necessary...

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Detalles Bibliográficos
Autores principales: Zhong, Xushu, Ma, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597453/
https://www.ncbi.nlm.nih.gov/pubmed/36313735
http://dx.doi.org/10.3389/fonc.2022.1007783
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author Zhong, Xushu
Ma, Hongbing
author_facet Zhong, Xushu
Ma, Hongbing
author_sort Zhong, Xushu
collection PubMed
description Acute leukemia (AL) is a hematological malignancy, and the prognosis of most AL patients hasn’t improved significantly, particularly for relapsed or refractory (R/R) AL. Therefore, new treatments for R/R adult acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) are urgently necessary. Novel developments have been made in AL treatment, including target and immune therapies. CD38 is one of the targets due to its high expression in many hematological malignancies, including multiple myeloma, ALL and a subset of AML. Consequently, targeting CD38 therapies, including CD38 monoclonal antibodies (mAbs), bispecific antibodies, and CAR-T cell therapy, exhibit promising efficacy in treating multiple myeloma without significant toxicity and are being explored in other hematological malignancies and nonhematological diseases. Herein, this review focuses on targeting CD38 therapies in ALL and AML, which demonstrate sound antileukemic effects in acute leukemia and are expected to become effective treatment methods.
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spelling pubmed-95974532022-10-27 Targeting CD38 for acute leukemia Zhong, Xushu Ma, Hongbing Front Oncol Oncology Acute leukemia (AL) is a hematological malignancy, and the prognosis of most AL patients hasn’t improved significantly, particularly for relapsed or refractory (R/R) AL. Therefore, new treatments for R/R adult acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) are urgently necessary. Novel developments have been made in AL treatment, including target and immune therapies. CD38 is one of the targets due to its high expression in many hematological malignancies, including multiple myeloma, ALL and a subset of AML. Consequently, targeting CD38 therapies, including CD38 monoclonal antibodies (mAbs), bispecific antibodies, and CAR-T cell therapy, exhibit promising efficacy in treating multiple myeloma without significant toxicity and are being explored in other hematological malignancies and nonhematological diseases. Herein, this review focuses on targeting CD38 therapies in ALL and AML, which demonstrate sound antileukemic effects in acute leukemia and are expected to become effective treatment methods. Frontiers Media S.A. 2022-10-12 /pmc/articles/PMC9597453/ /pubmed/36313735 http://dx.doi.org/10.3389/fonc.2022.1007783 Text en Copyright © 2022 Zhong and Ma https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zhong, Xushu
Ma, Hongbing
Targeting CD38 for acute leukemia
title Targeting CD38 for acute leukemia
title_full Targeting CD38 for acute leukemia
title_fullStr Targeting CD38 for acute leukemia
title_full_unstemmed Targeting CD38 for acute leukemia
title_short Targeting CD38 for acute leukemia
title_sort targeting cd38 for acute leukemia
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597453/
https://www.ncbi.nlm.nih.gov/pubmed/36313735
http://dx.doi.org/10.3389/fonc.2022.1007783
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