首页> 美国卫生研究院文献>Oncology Letters >Irinotecan monotherapy offers advantage over combination therapy with irinotecan plus cisplatin in second-line setting for treatment of advanced gastric cancer following failure of fluoropyrimidine-based regimens
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Irinotecan monotherapy offers advantage over combination therapy with irinotecan plus cisplatin in second-line setting for treatment of advanced gastric cancer following failure of fluoropyrimidine-based regimens

机译:在基于氟嘧啶的治疗方案失败后二线治疗中伊立替康单药治疗优于伊立替康加顺铂联合治疗的晚期胃癌

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摘要

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/m2 on days 1 and 15) alone every 4 weeks (Arm I) or irinotecan (70 mg/m2 on days 1 and 15) plus cisplatin (80 mg/m2 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.
机译:二线治疗胃癌的最佳化疗方案仍有待阐明。这项回顾性研究的目的是评估伊立替康二线治疗的疗效和安全性。总共134例先前接受过氟嘧啶基方案化疗的胃癌患者,每4周(手臂I)或仅在第1天和第15天接受伊立替康(150 mg / m 2 )治疗,或在2004年4月之间,每4周(Arm IP)给予伊立替康(第1天和第15天为70 mg / m 2 )和顺铂(第1天为80 mg / m 2 )和2009年3月。调查了患者特征,缓解率,无进展生存期,总体生存期和安全性。在134例复发或不可切除的胃癌患者中,第I臂接受了92例治疗,而IP臂接受了42例治疗。第一组的总体缓解率为8.1%,而第一组的总体缓解率为20.0%(P = 0.65)。两种疗法的中位无进展生存期(Arm I vs. IP; 2.6 vs. 2.7个月,P = 0.73)和中位总生存期(Arm I vs. IP; 9.8 vs. 8.0个月,P = 0.67)没有差异组。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,在Arm IP中发生的频率明显高于在Arm I中(P <0.05)。伊立替康可能是关键药物,与伊立替康加顺铂相比,伊立替康单药治疗在二线治疗晚期胃癌中更有益。在二线治疗中,与伊立替康加顺铂相比,伊立替康单药治疗对于难治性基于氟嘧啶治疗的晚期胃癌具有优势。

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