奥佐美星
威尼斯人
米多司他林
医学
阿糖胞苷
柔红霉素
CD33
髓系白血病
卡奇霉素
肿瘤科
药理学
白血病
内科学
慢性淋巴细胞白血病
生物
遗传学
干细胞
川地34
作者
Andrew H. Wei,Ing Soo Tiong
出处
期刊:Blood
[Elsevier BV]
日期:2017-12-07
卷期号:130 (23): 2469-2474
被引量:105
标识
DOI:10.1182/blood-2017-08-784066
摘要
In 2017, 4 drugs received US Food and Drug Administration marketing approval for acute myeloid leukemia (AML) treatment: targeted therapies for mutant FLT3 and IDH2, a liposomal cytarabine-daunorubicin formulation for therapy-related AML and AML with myelodysplasia-related changes, and resurgence of an antibody-drug conjugate designed to target CD33. Promising results also emerged for the BCL-2 inhibitor venetoclax combined with low-intensity therapy in older patients unfit for intensive chemotherapy. This quintet of new drugs is likely to reshape the therapeutic landscape of AML.
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