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Updated results from OCTAVIA (front-line bevacizumab, carboplatin and weekly paclitaxel therapy for ovarian cancer)

机译:OCTAVIA的最新结果(一线贝伐单抗,卡铂和每周紫杉醇疗法治疗卵巢癌)

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Sir, Recently in this journal, we reported the primary efficacy and safety results from the single-arm OCTAVIA study evaluating the combination of bevacizumab, car-boplatin and weekly paclitaxel as front-line treatment for ovarian cancer [1]. At the primary PFS analysis, median progression-free survival (PFS) was 23.7 months (90% confidence interval [CI] 19.9-26.4 months; 95% CI 19.8-26.4 months; PFS events in 52% of patients) in the overall population and 18.1 months (95% CI 16.0— 19.6 months; PFS events in 69% of patients) in the subgroup at high risk of progression (original ICON7 definition [2]).
机译:主席先生,最近在该杂志上,我们报道了单臂OCTAVIA研究的主要疗效和安全性结果,该研究评估了贝伐单抗,卡铂和每周紫杉醇联合治疗卵巢癌的一线治疗[1]。在主要的PFS分析中,总人群中位无进展生存期(PFS)为23.7个月(90%置信区间[CI] 19.9-26.4个月; 95%CI 19.8-26.4个月; 52%的患者发生PFS事件)在亚组中有进展的高风险(原始ICON7定义[2])和18.1个月(95%CI 16.0-19.6个月; PFS事件占69%的患者)。

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