Combined weekly carboplatin and paclitaxel as primary treatment of advanced epithelial ovarian carcinoma

被引:38
作者
Safra, Tamar [2 ]
Menczer, Joseph [3 ]
Bernstein, Rinat Molho [2 ]
Shpigel, Shulem [2 ]
Matcejevsky, Dianna [2 ]
Inbar, Moshe J. [2 ]
Golan, Abraham [4 ]
Grisaru, Dan [1 ]
Levy, Tally [3 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Gynecol Oncol Serv, Dept Obstet & Gynecol, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Sourasky Med Ctr, Dept Oncol, IL-64239 Tel Aviv, Israel
[3] Tel Aviv Univ, Sackler Fac Med, Wolfson Med Ctr, Div Gynecol Oncol, Holon, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Wolfson Med Ctr, Dept Obstet & Gynecol, Holon, Israel
关键词
Ovarian cancer; Weekly combined carboplatin and paclitaxel; Toxicity; CELL LUNG-CANCER; PHASE-III; 1ST-LINE CHEMOTHERAPY; RANDOMIZED-TRIAL; MITOTIC BLOCK; PHARMACOKINETICS; CISPLATIN; THERAPY; TAXOL;
D O I
10.1016/j.ygyno.2009.04.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To evaluate safety and outcome of weekly carboplatin and paclitaxel as the initial postoperative adjuvant chemotherapy for epithelial ovarian carcinoma (EOC) patients. Methods. Patients with stage IC-IV epithelial ovarian cancer (EOC) primary peritoneal of tubal carcinoma were enrolled in this phase 11 study. Intravenous carboplatin (area Under the curve 2) and paclitaxel (80 mg/m(2)) were administered on days 1, 8, and 15 of a 28-day cycle for 6-8 cycles. Cytoreductive surgery was performed as primary treatment OF after 3 cycles of weekly neoadjuvant chemotherapy, followed postoperatively by an additional 3 cycles of chemotherapy. Results. Sixty-four women (median age 65 years, range 39.9-82.8) were enrolled. Fifty-six of them (87.6%) were diagnosed with stage III-IV disease. Neutropenia was the most common hematological toxicity: 25% of the subjects had grade 3-4 neutropenia, 34.4% were supported by GCSF and 15.6% received epoetin, The majority (89%) of the patients had grade 1 and only 7.8% had grade 2 alopecia. 7.8% had grade 3 fatigue and 14.1% had grade 2 and 3.1% grade 3 neuropathy, none developed grade 4 neuropathy and only 6.3% had some residual neuropathy at >6 months after treatment. With a median follow-up of 31.5 months (range 5.9-57.3), estimated median survival was 52.0 months and median progression-free survival 25.74 (8.4-57.3) months (95% CI, 21.2-30.3). Overall and complete response rates were 92.1% and 64.1% respectively. Conclusion. Weekly carboplatin and paclitaxel as the initial chemotherapy for EOC is a feasible and well tolerated regimen and Should be further evaluated in a larger phase III study. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:215 / 218
页数:4
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