嵌合抗原受体T细胞治疗急性髓性白血病:试验和磨难

Swati Garg, Wei Ni, James D. Griffin, Martin Sattler
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引用次数: 0

摘要

急性髓系白血病(AML)是一种异质性的血液系统恶性肿瘤,通常与标准化疗或靶向治疗后的复发和耐药有关,特别是在老年患者中。造血干细胞移植被认为是具有治疗目的的最终挽救选择。使用嵌合抗原受体(CAR)的过继细胞疗法在B细胞恶性肿瘤中显示出希望,目前正在研究AML。AML的初步临床试验结果令人失望,我们回顾了目前提高CAR疗法疗效的策略。针对不同抗原的大量临床试验可能反映了AML的遗传异质性。在多个早期临床研究中报告的患者数量有限,因此很难得出CAR安全性的结论,但它确实表明这种方法在AML中的疗效落后于在B细胞恶性肿瘤中观察到的成功。显然,不仅需要改进CAR的设计,而且还需要确定AML中在正常髓系细胞中表达有限的靶标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chimeric Antigen Receptor T Cell Therapy in Acute Myeloid Leukemia: Trials and Tribulations
Acute myeloid leukemia (AML) is a heterogeneous hematological malignancy that is often associated with relapse and drug resistance after standard chemotherapy or targeted therapy, particularly in older patients. Hematopoietic stem cell transplants are looked upon as the ultimate salvage option with curative intent. Adoptive cell therapy using chimeric antigen receptors (CAR) has shown promise in B cell malignancies and is now being investigated in AML. Initial clinical trials have been disappointing in AML, and we review current strategies to improve efficacy for CAR approaches. The extensive number of clinical trials targeting different antigens likely reflects the genetic heterogeneity of AML. The limited number of patients reported in multiple early clinical studies makes it difficult to draw conclusions about CAR safety, but it does suggest that the efficacy of this approach in AML lags behind the success observed in B cell malignancies. There is a clear need not only to improve CAR design but also to identify targets in AML that show limited expression in normal myeloid lineage cells.
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