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急性髓系白血病中不断演变的范式:跨年龄与风险分层的个体化治疗策略

英文原题:Evolving Paradigms in Acute Myeloid Leukemia: Personalized Approaches to Therapy Across Age and Risk Groups.

查看英文原题

Evolving Paradigms in Acute Myeloid Leukemia: Personalized Approaches to Therapy Across Age and Risk Groups.

PubMed 2025/08/28(内容时间) Cancers (Basel) Q2 · IF 4.8(JCR 2025)

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中文摘要

急性髓系白血病(AML)是一种侵袭性血液系统恶性肿瘤,特征为髓系前体细胞克隆性增殖和疾病进展迅速。历史上AML治疗主要依赖强化化疗,但分子诊断和风险分层进展显著改变了疾病管理。本综述讨论AML当前治疗模式,强调个体化医疗在不同年龄和风险人群中的作用日益增加。对于较年轻且身体状况适合的患者,“7+3”等强化方案仍为标准治疗,常联合FMS样酪氨酸激酶3(FLT3)和IDH抑制剂等靶向药。老年或不适合强化治疗者可从低强度疗法中获益,例如去甲基化药物联合venetoclax,目前已成为一线标准治疗。脂质体化疗(CPX-351)、可测量微小残留病(MRD)监测和维持治疗进一步优化了缓解后策略。menin抑制剂、抗体药物偶联物以及CAR-T 细胞和疫苗等免疫疗法属于新兴治疗,为复发/难治性疾病患者提供更多选择。本综述全面概述AML治疗现状和未来方向,强调治疗正转向个体化、突变驱动的策略。

展开英文摘要原文

Acute myeloid leukemia (AML) is an aggressive hematologic malignancy characterized by the clonal proliferation of myeloid precursors and rapid progression. Historically consisting of intensive chemotherapy, AML management has evolved significantly due to advances in molecular diagnostics and risk stratification. This review discusses current therapeutic paradigms in AML, emphasizing the growing role of personalized medicine across age and risk groups. For younger, fit patients, intensive regimens such as the "7 + 3" protocol remain the standard, often enhanced by targeted agents like FMS-like tyrosine kinase 3 (FLT3) and IDH inhibitors.

Older or unfit individuals benefit from low-intensity treatments such as hypomethylating agents combined with venetoclax, now considered a frontline standard of care. The use of liposomal chemotherapy (CPX-351), measurable residual disease (MRD) monitoring, and maintenance therapy further refine post-remission strategies.

Emerging therapies, including menin inhibitors, antibody-drug conjugates, and immunotherapies like CAR-T cells and vaccines, offer additional options, especially in relapsed/refractory settings. This comprehensive review outlines the current landscape and future directions in AML therapy, emphasizing the transition toward individualized, mutation-driven treatment strategies.

论文信息

作者
Yadav SK、Joshi U、Hussein G、Warsame M、Liu B、Shrestha A、Krastev P、Korsapati HR
第一作者单位
Hospital Internal Medicine, Mayo Clinic Health System, Mankato, MN 56001, USA.United States
通讯作者单位
Department of Hematology and Oncology, Mayo Clinic Health System, Mankato, MN 56001, USA.United States
文献类型
综述
期刊
Cancers2025 Aug 28
原文标识
PubMed 40940920 · DOI 10.3390/cancers17172824