Department of Gastroenterology and Hematology, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Gastroenterol Res Pract. 2012;2012:640401. doi: 10.1155/2012/640401. Epub 2012 Feb 15.
Background. S-1 plus cisplatin has been established to be standard first-line chemotherapy for advanced gastric cancer in Japan. The optimal second-line treatment refractory to S-1 plus cisplatin remains unclear. Methods. We retrospectively studied the efficacy, toxicity, and survival of irinotecan plus mitomycin C in patients with advanced gastric cancer refractory to a fluoropyrimidine plus cisplatin. Results. Twenty-four patients were studied. Prior chemotherapy was S-1 plus cisplatin in 15 patients, S-1 plus cisplatin and docetaxel in 8, and 5-fluorouracil plus cisplatin with radiotherapy in 1. The overall response rate was 17.4%. The median overall survival was 8.6 months, and the median progression-free survival was 3.6 months. Grade 3 or 4 toxicities included leukopenia (33%), neutropenia (50%), anemia (33%), thrombocytopenia (4%), anorexia (13%), diarrhea (4%), and febrile neutropenia (13%). Conclusion. A combination of irinotecan and mitomycin C is potentially effective in patients with advanced gastric cancer refractory to a fluoropyrimidine plus cisplatin.
S-1 联合顺铂已被确立为日本晚期胃癌的标准一线化疗方案。对于对 S-1 联合顺铂耐药的最佳二线治疗仍不清楚。
我们回顾性研究了伊立替康联合丝裂霉素 C 在晚期胃癌患者中的疗效、毒性和生存情况,这些患者对氟嘧啶加顺铂耐药。
24 例患者接受了研究。15 例患者先前接受过 S-1 联合顺铂化疗,8 例患者接受过 S-1 联合顺铂和多西紫杉醇化疗,1 例患者接受过氟尿嘧啶联合顺铂联合放疗。总体缓解率为 17.4%。中位总生存期为 8.6 个月,中位无进展生存期为 3.6 个月。3 级或 4 级毒性包括白细胞减少(33%)、中性粒细胞减少(50%)、贫血(33%)、血小板减少(4%)、厌食(13%)、腹泻(4%)和发热性中性粒细胞减少(13%)。
伊立替康联合丝裂霉素 C 对氟嘧啶加顺铂耐药的晚期胃癌患者可能有效。