奥拉帕尼
医学
贝伐单抗
肿瘤科
卵巢癌
内科学
临床终点
人口
BRCA突变
化疗
无进展生存期
癌症
胃肠病学
随机对照试验
基因
生物化学
化学
聚合酶
聚ADP核糖聚合酶
环境卫生
作者
Isabelle Laure Ray-Coquard,Alexandra Léary,Sandro Pignata,Claire Cropet,Andrew Martin,Gerhard Bogner,Hiroyuki Yoshida,Ignace Vergote,N. Colombo,Jenni Mäenpää,Frédèric Selle,Barbara Schmalfeldt,Giovanni Scambia,Eva María Guerra Alia,Claudia Lefeuvre‐Plesse,A. Belau,Alain Lortholary,Martina Gropp‐Meier,Éric Pujade-Lauraine,P. Harter
标识
DOI:10.1016/j.annonc.2022.08.025
摘要
In the PAOLA-1/ENGOT-ov25 (NCT02477644) primary analysis, adding ola to maintenance bev after first-line (1L) platinum-based chemotherapy (PBC) + bev led to a significant progression-free survival (PFS) benefit in AOC (HR 0.59, 95% CI 0.49–0.72; P<0.001), particularly in pts with homologous recombination deficiency (HRD+; BRCA1/2 mutation [BRCAm] and/or genomic instability; Ray-Coquard et al NEJM 2019). Here, we report the prespecified final OS analysis.
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