Paclitaxel, Carboplatin, and Bevacizumab in Advanced and Recurrent Endometrial Carcinoma.

Peter G Rose, Shamshad Ali, Mehdi Moslemi-Kebria, Fiona Simpkins
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Abstract

Objective: The aim of this study was to evaluate the efficacy of adding bevacizumab to paclitaxel and carboplatin and as maintenance in a larger cohort of patients with advanced or recurrent endometrial carcinoma.

Methods: We retrospectively identified endometrial cancer patients treated with paclitaxel (175 mg/m per 3 hours), carboplatin (area under the curve, 5) and bevacizumab (15 mg/kg) and maintenance bevacizumab treated in a post-protocol treatment cohort and evaluated them with our previously published phase 2 trial of this regimen.

Results: Twenty-seven additional patients were identified; 19 received the regimen as first-line therapy, and 8 received the regimen as second-line therapy after prior paclitaxel and carboplatin. The 19 patients who received first-line therapy were analyzed alone and with the 15 patients enrolled on protocol. The 2 cohorts were similar with respect to risk factors. Overall survival curves were not statistically different between the protocol and the postprotocol patients (log-rank test; P > 0.1). Collectively, a total of 266 courses (median, 6 courses; range, 1-20 courses) of carboplatin, paclitaxel, and bevacizumab combination therapy and 305 courses (median, 16 courses; range, 0-45courses) of bevacizumab maintenance therapy were administered as first-line therapy. Collectively, the median progression-free survival was 20 months, and median overall survival was 56 months. Among 29 patients with measurable disease, the response rate was 82.8% (95% confidence interval, 69.0%-96.5%; 15 complete responses and 9 partial responses). Among the 8 patients who received paclitaxel and carboplatin and bevacizumab as second-line therapy after paclitaxel and carboplatin, the response rate was 87.5% (6 complete responses, 1 partial response). Their median progression-free survival and median overall survival were not reached after a median follow-up of 23.5 months.

Conclusions: Although there are inherent limitations to small retrospective studies, this second analysis confirms the high response rate, progression-free survival, and overall survival in the bevacizumab, paclitaxel, and carboplatin regimen as first-line therapy in advanced and recurrent endometrial carcinoma.

紫杉醇、卡铂和贝伐单抗在晚期和复发性子宫内膜癌中的应用。
目的:本研究的目的是评估将贝伐单抗加入紫杉醇和卡铂的疗效,并在更大的晚期或复发性子宫内膜癌患者队列中进行维持。方法:我们回顾性地确定了在方案后治疗队列中接受紫杉醇(175 mg/m / 3小时)、卡铂(曲线下面积5)和贝伐单抗(15 mg/kg)治疗的子宫内膜癌患者,并使用我们之前发表的该方案的2期试验对其进行评估。结果:新增27例患者;19人接受该方案作为一线治疗,8人在既往紫杉醇加卡铂治疗后接受该方案作为二线治疗。接受一线治疗的19例患者单独分析,15例患者加入方案。两个队列的危险因素相似。方案患者和方案后患者的总生存曲线无统计学差异(log-rank检验;P > 0.1)。共266门课程(中位数为6门;卡铂、紫杉醇和贝伐单抗联合治疗的范围,1-20个疗程,305个疗程(中位数,16个疗程;贝伐单抗维持治疗的范围(0-45个疗程)作为一线治疗。总的来说,中位无进展生存期为20个月,中位总生存期为56个月。在29例可测量疾病的患者中,有效率为82.8%(95%可信区间,69.0%-96.5%;15个完整回答和9个部分回答)。在紫杉醇卡铂后接受紫杉醇卡铂+贝伐单抗二线治疗的8例患者中,有效率为87.5%(完全缓解6例,部分缓解1例)。他们的中位无进展生存期和中位总生存期在中位随访23.5个月后未达到。结论:尽管小型回顾性研究存在固有的局限性,但第二项分析证实了贝伐单抗、紫杉醇和卡铂方案作为晚期和复发性子宫内膜癌一线治疗的高缓解率、无进展生存期和总生存期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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