[未来急性髓性白血病的治疗策略]。

Yuho Najima
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引用次数: 0

摘要

随着日本人口的老龄化,急性髓性白血病(AML)变得越来越普遍,这凸显了基于年龄、合并症和遗传异常的个体化治疗的重要性。这篇综述概述了引入阿扎胞苷联合venetoclax、FLT3抑制剂和CPX-351后AML管理的重大转变。它还讨论了在日本开发的下一代测序小组HEM-SIGHT,该小组于2025年被日本国民健康保险覆盖,使分子分层的诊断方法成为可能。尽管治疗取得了进展,但包括tp53突变和mecom过表达在内的几种亚型AML仍然高度难治性,即使采用同种异体干细胞移植和靶向治疗。这些高风险实体构成了持续的治疗挑战。当前AML治疗模式已转向战略性个性化,包括分子异常识别、可测量的残留疾病评估和基于这些发现的治疗适应。为了在临床实践中更广泛地采用精准医学,日本必须继续加强其诊断系统,在常规实践中简化基因组检测,并将这些策略与新的治疗开发相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Future treatment strategies for acute myeloid leukemia].

Acute myeloid leukemia (AML) is becoming more prevalent as the Japanese population ages, highlighting the growing importance of individualized treatment based on age, comorbidities, and genetic abnormalities. This review outlines the significant transformation in AML management after the introduction of azacitidine plus venetoclax, FLT3 inhibitors, and CPX-351. It also discusses HEM-SIGHT, a next-generation sequencing panel developed in Japan that became covered by Japanese national health insurance in 2025, enabling a molecularly stratified approach to diagnosis. Despite advances in treatment, several subtypes including TP53-mutated and MECOM-overexpressing AML remain highly refractory, even with allogeneic stem cell transplantation and targeted therapies. These high-risk entities pose ongoing therapeutic challenges. The current paradigm in AML treatment has shifted toward strategic personalization, encompassing molecular abnormality identification, measurable residual disease assessment, and treatment adaptation based on these findings. To achieve wider adoption of precision medicine in clinical practice, Japan must continue strengthening its diagnostic systems, streamlining genomic testing in routine practice, and integrating these strategies with novel therapeutic development.

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