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

被引:25
|
作者
Rose, Peter G. [1 ]
Ali, Shamshad [2 ]
Moslemi-Kebria, Mehdi [3 ]
Simpkins, Fiona [4 ]
机构
[1] Cleveland Clin Fdn, 9500 Euclid Ave A81, Cleveland, OH 44195 USA
[2] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[3] City Hope Natl Med Ctr, Natl Med Ctr, Dept Surg, Div Gynecol Oncol, Duarte, CA USA
[4] Univ Penn, Philadelphia, PA 19104 USA
关键词
Endometrial cancer; Bevacizumab; Carboplatin; Chemotherapy; First-line; Paclitaxel; Second-line; PHASE-II TRIAL; CANCER; CHEMOTHERAPY; TEMSIROLIMUS; OVARIAN;
D O I
10.1097/IGC.0000000000000891
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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(2) 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, 0-45 courses) 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 bevacizumabas 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.
引用
收藏
页码:452 / 458
页数:7
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