医学
威尼斯人
髓系白血病
阿糖胞苷
肿瘤科
养生
低甲基化剂
化疗
蒽环类
药理学
白血病
内科学
癌症
乳腺癌
生物化学
基因表达
化学
慢性淋巴细胞白血病
DNA甲基化
基因
出处
期刊:PubMed
日期:2019-01-01
卷期号:60 (9): 1108-1119
被引量:4
标识
DOI:10.11406/rinketsu.60.1108
摘要
Conventional chemotherapy with cytarabine and anthracycline (often referred to as "7+3") has been used for many years in the treatment of acute myeloid leukemia (AML). Despite meaningful advances in areas of supportive care and transplantation, little progress has been made in developing new chemotherapy options. In 2018, The Food and Drug Administration (FDA) of the US approved several novel agents for AML treatment as follows: ivosidenib, an inhibitor of isocitrate dehydrogenase-1; venetoclax, a potent inhibitor of bcl2; and glasdegib, an inhibitor of hedgehog signaling pathway. Moreover, clinical trials of alvocidib (flavopiridol), an inhibitor of the CDK9, pevonedistat, an inhibitor of NEDD8, and APR-246, a reactivator of mutant p53, are in progress. These agents will either be incorporated into the conventional 7+3 regimen or combined with hypomethylating agents to improve the outcome of AML therapy, and the results will guide the next stage of precision medicine in the treatment of AML.
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