Cunningham D, Glimelius B
Royal Marsden Hospital, London, UK.
Semin Oncol. 1999 Feb;26(1 Suppl 5):6-12.
In a prospective multicenter trial, 279 patients with metastatic colorectal cancer who had failed 5-fluorouracil therapy were randomized 2:1 to receive either best supportive care (BSC) plus treatment with the topoisomerase I inhibitor, irinotecan (CPT-11; Rhône-Poulenc Rorer, Antony, France), at a dose of 350 mg/m2 every 3 weeks or BSC alone. Overall survival, the primary end point of the study, was significantly improved in patients receiving the irinotecan treatment. Only 14% of patients receiving BSC alone were alive at 1 year compared with 36% in the irinotecan group. After adjustment for prognostic factors such as performance status, the difference in survival favoring irinotecan remained highly significant (P = .001). The benefit of irinotecan was also observed through significantly longer survival without performance status deterioration, longer survival without more than 5% weight loss, and longer duration of pain-free survival. Appreciable deterioration in global quality of life (50% reduction from baseline) occurred significantly later in the irinotecan-treated patients than in the controls. Additionally, quality of life analyses of all symptoms, except diarrhea, mean scores were significantly in favor of patients assigned to irinotecan treatment than those assigned to BSC. This is the first time that the benefit of second-line chemotherapy has been demonstrated by a randomized controlled trial in advanced colorectal cancer.
在一项前瞻性多中心试验中,279例5-氟尿嘧啶治疗失败的转移性结直肠癌患者按2:1随机分组,分别接受最佳支持治疗(BSC)加拓扑异构酶I抑制剂伊立替康(CPT-11;法国安托尼罗纳普朗克-罗瑞尔公司)治疗,剂量为每3周350mg/m²,或仅接受BSC。该研究的主要终点总生存期在接受伊立替康治疗的患者中显著改善。仅接受BSC的患者1年时只有14%存活,而伊立替康组为36%。在对诸如体能状态等预后因素进行校正后,伊立替康组在生存方面的差异仍非常显著(P = 0.001)。通过无体能状态恶化的生存期显著延长、无体重减轻超过5%的生存期延长以及无痛生存期延长,也观察到了伊立替康的益处。伊立替康治疗的患者总体生活质量出现明显恶化(较基线降低50%)的时间明显晚于对照组。此外,除腹泻外所有症状的生活质量分析显示,接受伊立替康治疗患者的平均得分明显优于接受BSC的患者。这是首次通过随机对照试验在晚期结直肠癌中证明二线化疗的益处。