A Retrospective Study of Gemcitabine and Cisplatin Combination Therapy as Second-Line Treatment for Advanced Biliary Tract Cancer

被引:14
|
作者
Sasaki, Takashi [1 ]
Isayama, Hiroyuki [1 ]
Nakai, Yousuke [1 ]
Takahara, Naminatsu [1 ]
Akiyama, Dai [2 ]
Yagioka, Hiroshi [3 ]
Kogure, Hirofumi [1 ]
Matsubara, Saburo [4 ]
Ito, Yukiko [2 ]
Yamamoto, Natsuyo [1 ]
Sasahira, Naoki [1 ]
Hirano, Kenji [1 ]
Toda, Nobuo [5 ]
Tada, Minoru [1 ]
Koike, Kazuhiko [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Tokyo 1138655, Japan
[2] Japanese Red Cross Med Ctr, Dept Gastroenterol, Tokyo, Japan
[3] JR Tokyo Gen Hosp, Dept Gastroenterol, Tokyo, Japan
[4] Kanto Cent Hosp, Dept Gastroenterol, Tokyo, Japan
[5] Mitsui Mem Hosp, Dept Gastroenterol, Tokyo 101, Japan
来源
CHEMOTHERAPY | 2013年 / 59卷 / 02期
关键词
Biliary tract cancer; Gemcitabine; Cisplatin; Second-line treatment; PHASE-II TRIAL; S-1; MONOTHERAPY; 1ST-LINE CHEMOTHERAPY; PROGNOSTIC-FACTORS; PLUS GEMCITABINE; SINGLE-CENTER; CAPECITABINE; MULTICENTER; CHOLANGIOCARCINOMA; 5-FLUOROURACIL;
D O I
10.1159/000354209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To evaluate the treatment outcome of gemcitabine and cisplatin combination therapy as second-line treatment for advanced biliary tract cancer. Patients and Methods: Patients with advanced biliary tract cancer who were refractory to gemcitabine-based first-line chemotherapy were treated with gemcitabine and cisplatin combination therapy. Gemcitabine (1,000 mg/m(2)) and cisplatin (25 mg/m(2)) were administered intravenously on days 1 and 8, repeated every 3 weeks. Results: Sixty patients were included. The tumor response and disease control rates were 1.7 and 58.3%, respectively. The median overall survival and time to progression were 6.7 months (95% CI 14.9-8.1) and 3.5 months (95% CI 2.5-5.0), respectively. Grade 3/4 toxicities included leucopenia (20%), neutropenia (25%), anemia (23%), thrombocytopenia (17%), nausea (2%), anorexia (2%), and liver dysfunction (2%). Conclusions: Gemcitabine and cisplatin combination therapy showed moderate efficacy and safety as second-line treatment for advanced biliary tract cancer that is refractory to gemcitabine-based first-line chemotherapy. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:106 / 111
页数:6
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