Revolutionizing acute myeloid leukemia treatment: a systematic review of immune-based therapies.

IF 2.9 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Discover. Oncology Pub Date : 2025-01-26 DOI:10.1007/s12672-025-01797-9
Ugochi Ebinama, Binsah George
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Abstract

The established protocol for the management of acute myeloid leukemia (AML) has traditionally involved the administration of induction chemotherapy, followed by consolidation chemotherapy, and subsequent allogeneic stem cell transplantation for eligible patients. However, the prognosis for individuals with relapsed and refractory AML remains unfavorable. In response to the necessity for more efficacious therapeutic modalities, targeted immunotherapy has emerged as a promising advancement in AML treatment. This comprehensive review article specifically examines classical unconjugated and toxin-conjugated monoclonal antibodies, which are currently in the preclinical phase or undergoing evaluation in clinical trials. The review delves into the proposed mechanisms through which these monoclonal antibodies elicit anti-tumor activity and identifies the challenges associated with designing targeted immunotherapy. The review focuses on targeting specific antigens in AML, including FLT3/CD125, CLL-1, CD33, CD38, CD47, CD70, and CD123.

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革新急性髓性白血病治疗:免疫疗法的系统综述。
传统的急性髓性白血病(AML)治疗方案包括诱导化疗,然后是巩固化疗,然后对符合条件的患者进行同种异体干细胞移植。然而,复发和难治性AML患者的预后仍然不利。由于需要更有效的治疗方式,靶向免疫治疗已成为AML治疗中有希望的进展。这篇全面的综述文章专门研究了经典的非偶联和毒素偶联单克隆抗体,这些抗体目前处于临床前阶段或正在临床试验中进行评估。这篇综述深入探讨了这些单克隆抗体引发抗肿瘤活性的机制,并确定了与设计靶向免疫治疗相关的挑战。本综述的重点是针对AML中的特异性抗原,包括FLT3/CD125、CLL-1、CD33、CD38、CD47、CD70和CD123。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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