奥拉帕尼
医学
卵巢癌
BRCA突变
合成致死
PARP抑制剂
癌症
聚ADP核糖聚合酶
肿瘤科
浆液性液体
浆液性卵巢癌
聚合酶
内科学
人口
妇科
癌症研究
DNA修复
遗传学
生物
DNA
环境卫生
作者
David R. Spriggs,Dan L. Longo
摘要
The article by Moore et al.1 in this issue of the Journal is the culmination of a long march for olaparib in the treatment of BRCA-mutated high-grade serous ovarian cancer — one that began with its discovery by means of synthetic lethality screening, followed by years of clinical trials to define its activity and refine its uses, and finally led to its implementation in a population of women with potentially curable ovarian cancer. Olaparib is the first in a wave of poly(adenosine diphosphate–ribose) polymerase (PARP) inhibitors, a class of agents that is changing primary treatment of ovarian cancer for the . . .
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