Yamashita Tatsuya, Arai Kuniaki, Terashima Takeshi, Sunagozaka Hajime, Shimakami Tetsuro, Yamashita Taro, Mizukoshi Eishiro, Sakai Akito, Honda Masao, Kaneko Shuichi
Dept. of Gastroenterology, Kanazawa University Hospital.
Gan To Kagaku Ryoho. 2012 Sep;39(9):1435-7.
We describe our experience with a patient who had advanced hepatocellular carcinoma (HCC) that responded markedly to treatment with the oral fluoropyrimidine anticancer drug S-1 (120mg/day/body bid on day 1 through 28 followed by a 14-day recovery period). The patient was enrolled in a phase I / II study designed to evaluate the safety and efficacy of S-1 in patients with advanced HCC. The best overall efficacy was confirmed to be a partial response (PR). After a total of 6 courses of treatment given on an outpatient basis, the target lesion volume decreased by 73. 8%. With regard to adverse events, the patient did not develop Grade 3 or higher adverse drug reactions. Therefore, the patient continued outpatient treatment for a total of 6 courses. The duration of survival from the start of treatment until death was 820 days, suggesting that S-1 is moderately effective and well tolerated in patients with advanced HCC.
我们描述了一名患有晚期肝细胞癌(HCC)患者的治疗经历,该患者对口服氟嘧啶类抗癌药物S-1治疗有显著反应(第1至28天每天120mg/体,每日两次,随后为14天恢复期)。该患者参加了一项I/II期研究,旨在评估S-1对晚期HCC患者的安全性和疗效。确认最佳总体疗效为部分缓解(PR)。在门诊总共进行6个疗程的治疗后,靶病灶体积减少了73.8%。关于不良事件,该患者未发生3级或更高级别的药物不良反应。因此,该患者继续进行了总共6个疗程的门诊治疗。从治疗开始到死亡的生存期为820天,表明S-1对晚期HCC患者有中度疗效且耐受性良好。