Douillard J Y, Cunningham D, Roth A D, Navarro M, James R D, Karasek P, Jandik P, Iveson T, Carmichael J, Alakl M, Gruia G, Awad L, Rougier P
Centre René Gauducheau, Saint Herblain, France.
Lancet. 2000 Mar 25;355(9209):1041-7. doi: 10.1016/s0140-6736(00)02034-1.
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.
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.
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.
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.
伊立替康对氟尿嘧啶难治的结直肠癌患者有效。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疗效。
387例既往未接受过晚期结直肠癌化疗(辅助化疗除外)的患者被随机分配接受开放标签的伊立替康联合氟尿嘧啶和亚叶酸钙(伊立替康组,n = 199)或仅接受氟尿嘧啶和亚叶酸钙(非伊立替康组,n = 188)。输注方案为每周一次或每2周一次,由各中心选择。我们评估了缓解率和疾病进展时间,以及缓解持续时间、生存率和生活质量。分析在意向性治疗人群和可评估患者中进行。
伊立替康组患者的缓解率显著高于非伊立替康组(可评估患者中分别为49%对31%,p<0.001;意向性治疗分析中分别为35%对22%,p<0.005)。伊立替康组的疾病进展时间显著长于非伊立替康组(中位数6.7个月对4.4个月,p<0.001),总生存率也更高(中位数17.4个月对14.1个月,p = 0.031)。伊立替康组3级和4级毒性反应的发生率显著高于非伊立替康组,但这些反应是可预测、可逆、非累积且可控制的。
伊立替康联合氟尿嘧啶和亚叶酸钙耐受性良好,提高了缓解率、疾病进展时间和生存率,生活质量后期有所下降。这种联合方案应被视为转移性结直肠癌的一线参考治疗方案。