[开发治疗急性髓性白血病新型药物的未来前景]。

Naoko Hosono
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引用次数: 0

摘要

近 40 年来,阿糖胞苷和蒽环类药物联合疗法一直是治疗急性髓性白血病(AML)的标准疗法。目前,人们对急性髓细胞白血病的细胞遗传学和分子生物学已经有所了解,随着FLT3抑制剂、Bcl2抑制剂和低甲基化药物等药物自2018年起在日本上市,急性髓细胞白血病的治疗也发生了巨大变化。然而,急性髓细胞白血病仍然很难治愈,复发率很高。在此,我们回顾了作为急性髓细胞白血病潜在治疗方法的尚未在日本获批的新型药物(CPX-351、IDH 抑制剂、menin 抑制剂和口服阿扎胞苷),以及目前正在临床试验或开发中的治疗性抗体(BiTE、DART、免疫检查点抑制剂)。这些新型药物不仅可作为单药治疗,还可作为与强化化疗或阿扎胞苷/韦尼妥类药物的联合疗法进行研究。新时代的急性髓细胞性白血病治疗有望实现各种目标,包括消灭白血病细胞、长期缓解和提高生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Future prospects for the development of novel agents for acute myeloid leukemia].

For nearly 40 years, combination therapy with cytarabine and anthracycline has been the standard of care for acute myeloid leukemia (AML). The cytogenetics and molecular biology of AML are now understood, and the treatment of AML has undergone dramatic changes in Japan with the launch of drugs such as FLT3 inhibitors, Bcl2 inhibitors, and hypomethylating agents since 2018. However, AML remains very difficult to cure, with a high relapse rate. Here, we review novel agents that have not yet been approved in Japan (CPX-351, IDH inhibitors, menin inhibitors, and oral azacitidine) as potential treatments for AML, as well as therapeutic antibodies (BiTEs, DARTs, immune checkpoint inhibitors) currently under investigation in clinical trials or in development. These novel agents are being investigated not only as monotherapy but also as combination therapy with intensive chemotherapy or azacitidine/venetoclax. The new era of AML treatment is expected to support a variety of goals, including leukemic cell elimination, long-term remission, and improved quality of life.

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