医学
贝伐单抗
内科学
危险系数
肿瘤科
卵巢癌
卡铂
无进展生存期
临床终点
安慰剂
化疗
癌症
随机对照试验
顺铂
病理
置信区间
替代医学
作者
Benoît You,Christopher Purdy,Larry J. Copeland,Elizabeth M. Swisher,Michael A. Bookman,Gini F. Fleming,Robert L. Coleman,Leslie M. Randall,Krishnansu S. Tewari,Bradley J. Monk,Robert S. Mannel,Joan L. Walker,Fabio Cappuccini,David E. Cohn,Mahvish Muzaffar,David G. Mutch,Andrea E. Wahner Hendrickson,Lainie P. Martin,Olivier Colomban,Robert A. Burger
摘要
In patients with high-grade ovarian cancer, predictors of bevacizumab efficacy in first-line setting are needed. In the ICON-7 trial, a poor tumor intrinsic chemosensitivity (defined by unfavorable modeled cancer antigen-125 [CA-125] ELIMination rate constant K [KELIM] score) was a predictive biomarker. Only the patients with high-risk disease (suboptimally resected stage III, or stage IV) exhibiting unfavorable KELIM score < 1.0 had overall survival (OS) benefit from bevacizumab (median: 29.7
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