Hepatobiliary and Pancreatic Oncology Division, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Jpn J Clin Oncol. 2010 Dec;40(12):1189-91. doi: 10.1093/jjco/hyq110. Epub 2010 Jul 14.
A randomized Phase II selection design trial comparing gemcitabine plus S-1 combination therapy with S-1 monotherapy for chemo-naïve unresectable or recurrent biliary tract cancer patients was started in Japan. The aim of this trial is to evaluate the efficacy and safety of the two regimens and to determine which is more promising as a test arm regimen to be compared with the current standard regimen, gemcitabine plus cisplatin, in a subsequent Phase III trial. Patients with unresectable or recurrent biliary tract cancer are randomized to either gemcitabine plus S-1 combination therapy arm or S-1 monotherapy arm. A total of 100 patients will be accrued for this study from 18 institutions over 1 year. The primary endpoint is the proportion of 1-year overall survival, and the secondary endpoints are progression-free survival, response rate and adverse events.
一项针对未经化疗的不可切除或复发性胆道癌患者的吉西他滨联合 S-1 与 S-1 单药治疗的随机 II 期选择设计试验已在日本启动。本试验的目的是评估两种方案的疗效和安全性,并确定哪种方案更有前途作为试验组方案,与随后的 III 期试验中的当前标准方案吉西他滨联合顺铂进行比较。不可切除或复发性胆道癌患者随机分配至吉西他滨联合 S-1 联合治疗组或 S-1 单药治疗组。本研究将在 1 年内从 18 个机构招募 100 名患者。主要终点是 1 年总生存率的比例,次要终点是无进展生存期、缓解率和不良事件。