医学
威尼斯人
髓系白血病
米多司他林
阿糖胞苷
肿瘤科
刺猬
药理学
白血病
癌症研究
内科学
信号转导
慢性淋巴细胞白血病
生物化学
化学
作者
Antonella Bruzzese,Caterina Labanca,Enrica Antonia Martino,Francesco Mendicino,Eugenio Lucia,Virginia Olivito,Antonino Neri,Annalisa Imovilli,Fortunato Morabito,Ernesto Vigna,Massimo Gentile
标识
DOI:10.1080/14656566.2023.2272659
摘要
Traditional treatment strategies for acute myeloid leukemia (AML) have primarily relied on standard chemotherapy regimens for four decades. Indeed, the landscape of AML therapy has evolved substantially in recent years, mainly due to the introduction of hypomethylating agents and small molecules.Bcl2 inhibitor venetoclax, Fms-like tyrosine kinase 3 (FLT3) inhibitors such as midostaurin and gilteritinib, and isocitrate dehydrogenases 1 and 2 (IDH1 and IDH2) inhibitors ivosidenib and enasidenib, as well as hedgehog (HH) pathway inhibitor glasdegib represented a significant step forward in AML therapeutic armamentarium. Smoothened (SMO) inhibitor in combination with low-dose cytarabine marks a recent milestone.
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