Oba Masaru, Chin Keisho, Kawazoe Yoshimasa, Takagi Koichi, Ogura Mariko, Shinozaki Eiji, Suenaga Mitsukuni, Matsusaka Satoshi, Mizunuma Nobuyuki, Hatake Kiyohiko
Gastrointestinal Group, Division of Medical Oncology, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Oncol Lett. 2011 Mar;2(2):241-245. doi: 10.3892/ol.2011.242. Epub 2011 Jan 20.
The optimal regimen of chemotherapy for gastric cancer in a second-line setting remains to be clarified. The aim of this retrospective study was to evaluate the efficacy and safety of second-line irinotecan treatment. A total of 134 patients with gastric cancer who had received prior chemotherapy with fluoropyrimidine-based regimens were treated with irinotecan (150 mg/m(2) on days 1 and 15) alone every 4 weeks (Arm I) or irinotecan (70 mg/m(2) on days 1 and 15) plus cisplatin (80 mg/m(2) on day 1) every 4 weeks (Arm IP) between April, 2004 and March, 2009. Patient characteristics, response rate, progression-free survival, overall survival and safety were investigated. Of 134 patients with recurrent or unresectable gastric cancer, 92 were treated in Arm I and 42 patients in Arm IP. Overall response rate in Arm I was 8.1%, compared with 20.0% in Arm IP (P=0.65). Median progression-free survival (Arm I vs. IP; 2.6 vs. 2.7 months, P=0.73) and median overall survival (Arm I vs. IP; 9.8 vs. 8.0 months, P=0.67) did not differ between the two treatment groups. Neutropenia, leukopenia and anorexia were the most common grade 3/4 adverse events, occurring significantly more frequently in Arm IP than in Arm I (P<0.05). Irinotecan may be a key agent, and serial irinotecan monotherapy is more beneficial as compared to irinotecan plus cisplatin in the treatment of advanced gastric cancer in second-line settings. Irinotecan monotherapy is beneficial compared to irinotecan plus cisplatin in second-line settings for the treatment of advanced gastric cancer refractory to fluoropyrimidine-based regimens.
二线治疗中胃癌的最佳化疗方案仍有待明确。这项回顾性研究的目的是评估二线伊立替康治疗的疗效和安全性。2004年4月至2009年3月期间,共有134例接受过基于氟嘧啶方案的一线化疗的胃癌患者,分别接受每4周一次的伊立替康单药治疗(方案I:第1天和第15天给予150mg/m²)或每4周一次的伊立替康(第1天和第15天给予70mg/m²)联合顺铂(第1天给予80mg/m²)治疗(方案IP)。研究了患者特征、缓解率、无进展生存期、总生存期和安全性。134例复发或不可切除胃癌患者中,92例接受方案I治疗,42例接受方案IP治疗。方案I的总缓解率为8.1%,方案IP为20.0%(P = 0.65)。两个治疗组之间的中位无进展生存期(方案I vs. IP;2.6个月 vs. 2.7个月,P = 0.73)和中位总生存期(方案I vs. IP;9.8个月 vs. 8.0个月,P = 0.6)无差异。中性粒细胞减少、白细胞减少和厌食是最常见的3/4级不良事件,方案IP组的发生率显著高于方案I组(P < 0.05)。在二线治疗晚期胃癌中,伊立替康可能是关键药物,与伊立替康联合顺铂相比,序贯伊立替康单药治疗更有益。在二线治疗中,对于对基于氟嘧啶方案难治的晚期胃癌,伊立替康单药治疗比伊立替康联合顺铂更有益。