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低甲基化剂的临床最新进展。

Clinical update on hypomethylating agents.

机构信息

INSERM/CNRS UMR 944/7212, Saint-Louis Research Institute, Paris Diderot University, Paris, France.

Hematology Laboratory, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, Paris, France.

出版信息

Int J Hematol. 2019 Aug;110(2):161-169. doi: 10.1007/s12185-019-02651-9. Epub 2019 Apr 24.

Abstract

Hypomethylating agents (HMAs), azacitidine and decitabine, are standards of care in higher-risk myelodysplastic syndromes and in acute myeloid leukemia patients ineligible for intensive therapy. Over the last 10 years, research efforts have sought to better understand their mechanism of action, both at the molecular and cellular level. These efforts have yet to robustly identify biomarkers for these agents. The clinical activity of HMAs in myeloid neoplasms has been firmly established now but still remains of limited magnitude. Besides optimized use at different stages of the disease, most of the expected clinical progress with HMAs will come from the development of second-generation compounds orally available and/or with improved pharmacokinetics, and from the search, so far mostly empirical, of HMA-based synergistic drug combinations.

摘要

低甲基化药物(HMAs),阿扎胞苷和地西他滨,是高危骨髓增生异常综合征和不适合强化治疗的急性髓系白血病患者的标准治疗方法。在过去的 10 年中,研究人员努力更好地了解它们在分子和细胞水平上的作用机制。这些努力尚未为这些药物强有力地确定生物标志物。HMAs 在髓系肿瘤中的临床活性现已得到充分确立,但仍然有限。除了在疾病的不同阶段优化使用外,HMAs 的大部分预期临床进展将来自第二代化合物的开发,这些化合物口服且/或具有更好的药代动力学特性,以及迄今为止主要是经验性的寻找基于 HMA 的协同药物组合。

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