Phase II trial of combination chemotherapy with gemcitabine, 5-fluorouracil and cisplatin for advanced cancers of the bile duct, gallbladder, and ampulla of Vater

被引:0
作者
Sohn, Byeong Seok [1 ]
Yuh, Young Jin [1 ]
Kim, Ki-hwan [2 ]
Jeon, Tae Joo [1 ]
Kim, Nam Sun [1 ]
Kim, Sung Rok [1 ]
机构
[1] Inje Univ, Sanggye Paik Hosp, Dept Internal Med, Coll Med, Seoul 139707, South Korea
[2] Inje Univ, Sanggye Paik Hosp, Dept Surg, Coll Med, Seoul 139707, South Korea
来源
TUMORI JOURNAL | 2013年 / 99卷 / 02期
关键词
biliary tract cancer; cisplatin; 5-fluorouracil; gemcitabine; overall survival; response; BILIARY-TRACT CARCINOMA; HIGH-DOSE; 5-FLUOROURACIL; 1ST-LINE CHEMOTHERAPY; CAPECITABINE; OXALIPLATIN; INFUSION; EPIRUBICIN; GFP;
D O I
10.1177/030089161309900203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims, and background. For advanced cancers of the bile duct, gallbladder and ampulla of Vater, there are only a few treatment options. We explored the efficacy of the combination of gemcitabine, 5-fluorouracil and cisplatin for advanced binary cancers. Methods. From September 2003 to April 2010, 28 patients with recurrent or metastatic binary tract cancer were enrolled. A treatment regimen consisting of gemcitabine (800 mg/m(2) at a fixed dose rate on days 1 and 8), 5-fluorouracil (1 g/m(2)/day continuous infusion for 4 days) and cisplatin (60 mg/m2 on day 2) was repeated every 3 weeks. Results. One (3.6%) patient showed complete response, 8 (28.6%) partial response, 14 (50%) stable disease and 5 (17.9%) disease progression. Overall, the objective response rate was 32.1% (95% CI, 17.9-50.6%) and the disease control rate was 82.1% (95% CI, 64.4-92.1%). Median progression-free survival and overall survival were 7.6 months (95% CI, 5.5-9.7) and 11.2 months (95% CI, 6.8-15.5), respectively. G3/4 neutropenia was observed in 44 (24.3%) of 181 cycles and G3/4 thrombocytopenia in 48 (26.5%) of 181 cycles. There was no treatment-related mortality. Conclusions. The combined regimen of gemcitabine, 5-fluorouracil and cisplatin has comparable activity for patients with advanced cancer of the bile duct, gallbladder and ampulla of Vater. Toxicity was tolerable but substantial.
引用
收藏
页码:139 / 144
页数:6
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