Clinical Comparison of Safety and Efficacy of Vinorelbine/Epirubicin (NE) with Fluorouracil/Epirubicin/Cyclophosphamide (FEC)

被引:0
|
作者
Yan, Peng-Wei [1 ,2 ]
Huang, Xin-En [1 ,2 ]
Jiang, Yong [1 ,2 ]
Tang, Jin-Hai [3 ]
Xu, Hong-xia [1 ]
Xu, Xia [1 ]
Jin, Xiang [4 ]
机构
[1] Jiangsu Canc Hosp & Res Inst, Dept Chemotherapy, Nanjing, Peoples R China
[2] Nanjing Med Univ, Clin Med Coll 1, Nanjing, Peoples R China
[3] Jiangsu Canc Hosp & Res Inst, Dept Surg, Nanjing, Peoples R China
[4] Jiangsu Canc Hosp & Res Inst, Dept Res, Nanjing, Peoples R China
关键词
Vinorelbine; epirubicin; FEC; breast cancer; adjuvant chemotherapy; ADVANCED BREAST-CANCER; PHASE-II TRIAL; WEEKLY IV-VINORELBINE; INTRAVENOUS VINORELBINE; RANDOMIZED-TRIAL; FIRST-LINE; 1ST-LINE CHEMOTHERAPY; PREMENOPAUSAL WOMEN; EPIRUBICIN; CYCLOPHOSPHAMIDE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To compare the safety and efficacy of a combination of vinorelbine and epirubicin (NE) with fluorouracil/epirubicin/cyclophosphamide (FEC) as a postoperative adjuvant chemotherapy for breast cancer. Methods: Breast cancer patients were treated postoperatively in Jiangsu Cancer Hospital and Research Institute from 1997 to 2006 with either the NE regimen (vinorelbine 40mg/m(2) iv on day 1 and day 8, epirubicin 50mg/m(2) iv on day 1 and day 2, and a cycle repeated every 21-28 days for totally 4-6 cycles) or the FEC regimen (5-Fu 500mg/m(2) iv gtt on day 1, epirubicin 50mg/m(2) iv on day 1 and day 2, CTX 500mg/m(2) iv on day 1 and a cycle repeated every 21-28 days for totally 4-6 cycles). Toxicity was evaluated after each cycle of chemotherapy. Results: Main side effects in both NE and FEC groups were neutropenia and gastrointestinal syndrome, with a 5 year survival rate of 87.9% in the NE and 85.2% in the FEC group. Conclusions: NE regimen is safe with good long-term survival rate, and thus could be recommended as a postoperative chemotherapy regimen for breast cancer.
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收藏
页码:1115 / 1118
页数:4
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