伊立替康
医学
西妥昔单抗
内科学
结直肠癌
奥沙利铂
危险系数
肿瘤科
临床终点
中性粒细胞减少症
胃肠病学
癌症
毒性
随机对照试验
置信区间
作者
Alberto Sobrero,Joan Maurel,Louis Fehrenbacher,Werner Scheithauer,Yousif Abubakr,Manfred P. Lutz,M. E. Vega-Villegas,Cathy Eng,E.U. Steinhauer,Jana Prausová,Heinz‐Josef Lenz,Christophe Borg,Gary Middleton,H. Kröning,Gabriele Luppi,O. Kisker,Angela Zubel,Christiane Langer,Justin Kopit,Howard A. Burris
标识
DOI:10.1200/jco.2007.13.1193
摘要
To determine whether adding cetuximab to irinotecan prolongs survival in patients with metastatic colorectal cancer (mCRC) previously treated with fluoropyrimidine and oxaliplatin.This multicenter, open-label, phase III study randomly assigned 1,298 patients with epidermal growth factor receptor-expressing mCRC who had experienced first-line fluoropyrimidine and oxaliplatin treatment failure to cetuximab (400 mg/m(2) day 1 followed by 250 mg/m(2) weekly) plus irinotecan (350 mg/m(2) every 3 weeks) or irinotecan alone. Primary end point was overall survival (OS); secondary end points included progression-free survival (PFS), response rate (RR), and quality of life (QOL).Median OS was comparable between treatments: 10.7 months (95% CI, 9.6 to 11.3) with cetuximab/irinotecan and 10.0 months (95% CI, 9.1 to 11.3) with irinotecan alone (hazard ratio [HR], 0.975; 95% CI, 0.854 to 1.114; P = .71). This lack of difference may have been due to post-trial therapy: 46.9% of patients assigned to irinotecan eventually received cetuximab (87.2% of those who did, received it with irinotecan). Cetuximab added to irinotecan significantly improved PFS (median, 4.0 v 2.6 months; HR, 0.692; 95% CI, 0.617 to 0.776; P
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