首页> 外文期刊>Gynecologic Oncology: An International Journal >Addition of bevacizumab to weekly paclitaxel significantly improves progression-free survival in heavily pretreated recurrent epithelial ovarian cancer.
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Addition of bevacizumab to weekly paclitaxel significantly improves progression-free survival in heavily pretreated recurrent epithelial ovarian cancer.

机译:在高度预处理的复发性上皮性卵巢癌中,将贝伐单抗添加到每周紫杉醇中可显着改善无进展生存期。

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OBJECTIVE: Weekly paclitaxel has been shown to be an effective cytotoxic regimen for recurrent epithelial ovarian cancer (EOC), and may act through inhibition of angiogenesis. Bevacizumab, a potent angiogenesis inhibitor, has also been shown to have activity in patients with EOC. Therefore, we sought to determine if the addition of bevacizumab to weekly paclitaxel led to an increased survival compared to weekly paclitaxel alone. METHODS: A single institutional review was conducted for patients with recurrent EOC treated with weekly paclitaxel (60-70mg/m(2)) on days 1, 8, 15, and 22 of a 28day cycle and those treated with weekly paclitaxel and bevacizumab (10-15mg/kg on day 1 and 15). Response rates (RR) were calculated, and progression-free survival (PFS), and overall survival (OS) were compared using Kaplan-Meier survival analysis. RESULTS: Twenty-nine patients treated with weekly paclitaxel and 41 patients treated with paclitaxel/bevacizumab were identified. The groups were similar in demographics, initial optimal cytoreduction, stage, histology, grade, platinum sensitivity, and median number of previous regimens (4 vs. 4, p=0.69).The overall response rate (ORR) was 63% (complete response (CR) 34% and partial response (PR) 29%) for paclitaxel/bevacizumab and 48% (CR 17% and PR 31%) for weekly paclitaxel (p=0.23). Improvement in PFS was seen in those treated with paclitaxel/bevacizumab in comparison to weekly paclitaxel alone (median PFS 13.2 vs. 6.2months, p<.01). There was a trend towards improved OS for paclitaxel/bevacizumab (median OS 20.6 vs. 9.1months; p=0.12). Toxicities were similar between the two regimens although more bowel perforations (2 vs. 0) were seen in the paclitaxel/bevacizumab group. CONCLUSION: A significant increase in PFS with a trend towards improved OS was demonstrated in this heavily pretreated population treated with paclitaxel/bevacizumab as compared to weekly paclitaxel alone. This data should be helpful in guiding future trials to determine the optimal care for women with recurrent EOC.
机译:目的:每周紫杉醇已被证明是复发性上皮性卵巢癌(EOC)的有效细胞毒性方案,并且可能通过抑制血管生成发挥作用。贝伐单抗(一种有效的血管生成抑制剂)也已显示在EOC患者中具有活性。因此,我们试图确定与单独使用每周紫杉醇相比,在每周使用紫杉醇中添加贝伐单抗是否可以提高生存率。方法:对28天周期的第1、8、15和22天每周一次紫杉醇(60-70mg / m(2))治疗的复发性EOC以及每周一次紫杉醇和贝伐单抗治疗的复发性EOC患者进行单一机构审查(第1天和第15天为10-15mg / kg)。计算反应率(RR),并使用Kaplan-Meier生存分析比较无进展生存期(PFS)和总生存期(OS)。结果:确定了29例每周接受紫杉醇治疗的患者和41例接受紫杉醇/贝伐单抗治疗的患者。两组在人口统计学,初始最佳细胞减少,阶段,组织学,等级,铂敏感性和既往治疗方案的中位数方面相似(4 vs. 4,p = 0.69)。总缓解率(ORR)为63%(完全缓解)紫杉醇/贝伐单抗的(CR)为34%,部分缓解(PR)为29%,每周紫杉醇为48%(CR 17%和PR 31%)(p = 0.23)。与单独使用每周紫杉醇相比,用紫杉醇/贝伐单抗治疗的患者的PFS有所改善(中位PFS 13.2对6.2个月,p <.01)。紫杉醇/贝伐单抗的OS有改善的趋势(OS的中位数为20.6比9.1个月; p = 0.12)。尽管在紫杉醇/贝伐单抗组中发现更多的肠穿孔(2比0),但两种方案的毒性相似。结论:与单独使用紫杉醇相比,在用紫杉醇/贝伐单抗治疗的经过大量预处理的人群中,PFS显着增加,并且有OS改善的趋势。这些数据应有助于指导未来的试验,以确定复发性EOC妇女的最佳护理。

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