首页> 外文期刊>The Lancet >Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial.
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Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial.

机译:伊立替康联合氟尿嘧啶与单独的氟尿嘧啶相比是转移性结直肠癌的一线治疗:一项多中心随机试验。

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BACKGROUND: Irinotecan is active against colorectal cancer in patients whose disease is refractory to fluorouracil. We investigated the efficacy of these two agents combined for first-line treatment of metastatic colorectal cancer. METHODS: 387 patients previously untreated with chemotherapy (other than adjuvant) for advanced colorectal cancer were randomly assigned open-label irinotecan plus fluorouracil and calcium folinate (irinotecan group, n=199) or fluorouracil and calcium folinate alone (no-irinotecan group, n=188). Infusion schedules were once weekly or every 2 weeks, and were chosen by each centre. We assessed response rates and time to progression, and also response duration, survival, and quality of life. Analyses were done on the intention-to-treat population and on evaluable patients. FINDINGS: The response rate was significantly higher in patients in the irinotecan group than in those in the no-irinotecan group (49 vs 31%, p<0.001 for evaluable patients, 35 vs 22%, p<0.005 by intention to treat). Time to progression was significantly longer in the irinotecan group than in the no-irinotecan group (median 6.7 vs 4.4 months, p<0.001), and overall survival was higher (median 17.4 vs 14.1 months, p=0.031). Some grade 3 and 4 toxic effects were significantly more frequent in the irinotecan group than in the no-irinotecan group, but effects were predictible, reversible, non-cumulative, and manageable. INTERPRETATION: Irinotecan combined with fluorouracil and calcium folinate was well-tolerated and increased response rate, time to progression, and survival, with a later deterioration in quality of life. This combination should be considered as a reference first-line treatment for metastatic colorectal cancer.
机译:背景:伊立替康对患有氟尿嘧啶难治性疾病的患者具有抗结肠直肠癌的活性。我们研究了这两种药物联合用于转移性结直肠癌一线治疗的功效。方法:387例先前未接受过化疗(除辅助剂外)治疗的晚期大肠癌患者被随机分配为开放标签的伊立替康加氟尿嘧啶和叶酸钙(伊立替康组,n = 199)或仅含氟尿嘧啶和叶酸钙(无伊立替康组,n = 188)。输液时间表是每周一次或每2周一次,并由每个中心选择。我们评估了缓解率和进展时间,以及缓解持续时间,生存率和生活质量。对意向治疗人群和可评估患者进行了分析。结果:伊立替康组患者的反应率显着高于非伊立替康组(有意治疗的患者分别为49比31%,p <0.001,可治疗患者分别为35比22%,p <0.005)。伊立替康组的进展时间明显长于非伊立替康组(中位6.7 vs 4.4个月,p <0.001),总生存期更长(中位17.4 vs 14.1个月,p = 0.031)。伊立替康组的某些3级和4级毒性作用明显高于非伊立替康组,但这种作用是可预测的,可逆的,非累积的和可控制的。解释:伊立替康与氟尿嘧啶和亚叶酸钙的结合耐受性好,反应率,进展时间和生存期增加,但生活质量随后下降。该组合应被视为转移性结直肠癌的参考一线治疗。

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