威尼斯人
髓系白血病
阿糖胞苷
医学
低甲基化剂
白血病
阿扎胞苷
肿瘤科
髓样
细胞凋亡
癌症研究
药理学
内科学
生物
基因
DNA甲基化
遗传学
慢性淋巴细胞白血病
基因表达
作者
Kapil Saxena,Courtney D. DiNardo,Naval Daver,Marina Konopleva
标识
DOI:10.1016/j.clml.2021.08.015
摘要
The treatment landscape for acute myeloid leukemia has expanded significantly in the past 5 years with the approval of several therapeutic small molecules. While agents such as FLT3 inhibitors and IDH inhibitors are restricted for patients with specific mutations, the selective BCL-2 inhibitor venetoclax combined with a hypomethylating agent or low-dose cytarabine was approved after demonstrating frontline efficacy across a molecularly heterogenous group of patients. Currently, venetoclax is being investigated in combination with multiple other therapies as the role of the intrinsic apoptotic pathway in acute myeloid leukemia continues to be explored.
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