癸他滨
骨髓增生异常综合症
髓系白血病
医学
低甲基化剂
临床试验
髓样
阿扎胞苷
白血病
加药
肿瘤科
重症监护医学
生物信息学
内科学
DNA甲基化
骨髓
生物
基因表达
基因
生物化学
作者
Nicholas J. Short,Hagop M. Kantarjian
摘要
Azacitidine and decitabine are hypomethylating agents that have dose-dependent epigenetic and cytotoxic effects and are widely used in the treatment of myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). In this review, we discuss the path to regulatory approval of azacitidine and decitabine, highlighting the substantial efforts that have been made to optimize the dosing schedule and administration of these drugs, including the development of new, oral formulations of both agents. We also review novel combination strategies that are being investigated in ongoing clinical trials for patients with MDS and AML, as well as efforts to expand the current indications of these agents.
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