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Clinical study of irinotecan therapy in patients with fluoropyrimidine-resistant advanced colorectal cancer

机译:伊立替康治疗氟嘧啶耐药晚期大肠癌的临床研究

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The clinical efficacy and safety of irinotecan (CPT-11) therapy were studied retrospectively in patients with fluoropyrimidine-resistant advanced colorectal cancer. The subjects were 44 patients who were treated with CPT-11 alone or with a combination of CPT-11 and mitomycin C (MMC) at our institute from April 1999 to March 2003. CPT-11 (120-150 mg/m2) alone or CPT-11 with MMC (5 mg/m2) was administered every 2 weeks. The objective overall response rate was 11% (95% confidence interval, 3.8-25%). In 38 patients who were treated until October 2002, the median survival time was 12 months. Two-year survival rate was 13%. Grade 3 anorexia or diarrhea occurred in 6 patients (14%) and 5 patients (11%), respectively. There was no treatment-related death or early death within 30 days from the last administration of CPT-11 (+MMC). This retrospective study demonstrated the reproducible activity and safety of CPT-11 for the treatment of fluoropyrimidine-resistant advanced colorectal cancer in clinical practice.
机译:回顾性研究了伊立替康(CPT-11)治疗对氟嘧啶耐药的晚期大肠癌患者的临床疗效和安全性。研究对象为1999年4月至2003年3月在我院接受CPT-11单独治疗或CPT-11与丝裂霉素C(MMC)联合治疗的44例患者。CPT-11(120-150 mg / m2)单独或每2周施用一次含MMC(5 mg / m2)的CPT-11。客观总体缓解率为11%(95%置信区间为3.8-25%)。在截至2002年10月接受治疗的38例患者中,中位生存时间为12个月。两年生存率为13%。分别发生6例(14%)和5例(11%)的3级厌食或腹泻。自上次给予CPT-11(+ MMC)后的30天内,没有与治疗相关的死亡或早期死亡。这项回顾性研究证明了CPT-11在临床实践中对氟嘧啶耐药的晚期大肠癌的治疗具有可再现的活性和安全性。

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