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Antigen-specific immunotherapy for acute myeloid leukemia: where are we now, and where do we go from here?

机译:针对急性髓性白血病的抗原特异性免疫疗法:我们现在在哪里,我们从那里去哪里?

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摘要

Antigen-specific immunotherapies have long been pursued as a means to improve the outcomes of patients with acute myeloid leukemia (AML). Success thus far has been limited, and many therapeutics have either been ineffective in the clinic or have an uncertain impact on patient outcomes. Only the CD33 antibody-drug conjugate gemtuzumab ozogamicin provided benefit in randomized studies. Here, we briefly review where we currently are with antigen-specific AML immunotherapy and where we might go from here. Besides the exploration of novel target antigens, ongoing preclinical and clinical efforts aim to improve existing immunotherapy modalities and focus on developing novel therapeutics such as bispecific antibodies and gene-modified immune effector cells. Ultimately, clinical studies need to address the question of ideal target(s) in AML, a disease of great antigenic diversity, and clarify how the upcoming immunotherapeutics should be best used and what level of supportive care is required for their safe administration.
机译:长期以来,一直追求抗原特异性免疫疗法作为改善急性髓性白血病(AML)患者预后的一种方法。迄今为止,成功是有限的,许多治疗方法要么在临床上无效,要么对患者预后产生不确定的影响。在随机研究中,只有CD33抗体-药物偶联物吉妥单抗ozogamicin提供了益处。在这里,我们简要回顾一下目前抗原特异性AML免疫治疗的现状以及我们可能从何而来。除了探索新的靶抗原外,正在进行的临床前和临床努力还旨在改善现有的免疫疗法,并致力于开发新型疗法,例如双特异性抗体和基因修饰的免疫效应细胞。最终,临床研究需要解决AML(一种具有巨大抗原多样性的疾病)中理想靶点的问题,并阐明应如何最好地使用即将到来的免疫疗法,以及对其安全管理需要何种水平的支持治疗。

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