急性髓性白血病的当前治疗策略

N. Suvajdžić-Vuković, M. Mitrović, M. Virijević, A. Vidović, Z. Cvetković
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摘要

介绍。急性髓性白血病是一种罕见的恶性肿瘤,诊断时平均年龄为70岁。直到最近,尽管接受同种异体造血干细胞移植治疗,患有这种疾病的年轻患者的5年生存率< 30%,而60岁以上患者的5年生存率< 10%。治疗概述。由于急性髓系白血病的异质性,几十年来一直没有新的药物用于治疗这种疾病。2017年开始引入新药:midoshuin、gilteritinib、CPX351、enasidenib、ivosidenib、venetoclax、glasdegib,同时重新引入了吉妥珠单抗ozogamicin。现代治疗策略需要个性化的方法,基于预后参数,如诊断时急性髓系白血病的细胞遗传学和分子谱,以及两个化疗周期后评估的最小残留疾病。此外,确定患者是否有资格接受“强化”治疗。根据老年患者的功能状态、合并症和老年评估进行治疗是必要的。对于急性早幼粒细胞白血病的治疗,三氧化二砷联合全反式维甲酸是公认的非高危患者(WBC为10x109/L)的治疗标准。结论。新的治疗方式以及同种异体造血干细胞移植已经改变了AML患者的预后。然而,治疗不适合强化化疗的患者,以及复发/难治性疾病的患者,仍然具有挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current strategies for the treatment of acute myeloid leukemia
Introduction. Acute myeloid leukemia is a rare malignancy with an average age of 70 years at diagnosis. Until recently, five-year survival of younger patients with this disease, despite being treated with allogenic hematopoietic stem cell transplantation, was < 30%, while in patients older than 60 years it was < 10%. Treatment overview. Due to the heterogeneity of acute myeloid leukemia no new drugs for treating this disease have been introduced for decades. The introduction of new drugs began from 2017: midostaurin, gilteritinib, CPX351, enasidenib, ivosidenib, venetoclax, glasdegib, while gemtuzumab ozogamicin has been reintroduced. Modern treatment strategies require an individual approach, based on prognostic parameters such as cytogenetical and molecular profile of acute myeloid leukemia at diagnosis and the assessment of minimal residual disease evaluated after two cycles of chemotherapy. Moreover, determining the eligibility of patients for ??intensive?? treatment, based on functional status, comorbidities and geriatric assessment of older patients, is necessary. Regarding the treatment of acute promyelocytic leukemia, the combination of arsenic trioxide and all-trans retinoic acid is universally accepted as the standard of care for non-high risk patients (WBC < 10x109/L), while standard chemotherapy combined with all-trans retinoic acid is still used for high-risk patients (WBC >10x109/L). Conclusion. Novel therapeutic modalities, along with allo-HSCT have changed the outcome of AML patients. However, treating patients unfit for intensive chemotherapy, as well as patients with relapse/refractory disease, is still challenging.
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