Hospital Universitari Mútua de Terrassa, Terrassa, Spain.
Chemotherapy. 2010;56(2):142-6. doi: 10.1159/000313527. Epub 2010 Apr 21.
We gathered data from multiple institutions on the cetuximab regimen of patients with metastatic colorectal cancer.
126 patients from 19 centers were included from July 2006 to July 2007 in this prospective non-controlled study. Irinotecan-refractory metastatic colorectal cancer patients with Karnofsky >or=70 received cetuximab 500 mg/m(2) every 2 weeks (q2w) in combination with irinotecan 180 mg/m(2) q2w until disease progression or unacceptable toxicity. The primary endpoint was the progression-free rate at 12 weeks.
Median age was 65 years; 65.9% male; colon/rectum 64.3/34.1%; Karnofsky status <or=80/>or=90% in 45.3/54.7% of the patients. The progression-free rate was 42.7 (95% CI 32.8-52.6) and 22.4% (95% CI 14.2-30.7) at 12 and 24 weeks, respectively. The main grade 3 or 4 toxicities were: diarrhea 13.5% and acne-like rash 10.3%. No grade 3 or 4 infusional or allergic reactions were reported.
The progression-free rates confirm that cetuximab q2w in combination with irinotecan is an option, and is as active and safe as the standard weekly regimen.
我们从多个机构收集了转移性结直肠癌患者使用西妥昔单抗方案的数据。
本前瞻性非对照研究纳入了 2006 年 7 月至 2007 年 7 月来自 19 个中心的 126 例患者。Karnofsky 评分≥70 的对伊立替康耐药的转移性结直肠癌患者接受西妥昔单抗 500 mg/m²,每 2 周(q2w)联合伊立替康 180 mg/m²,q2w,直至疾病进展或不可接受的毒性。主要终点为 12 周时的无进展率。
中位年龄为 65 岁;65.9%为男性;结肠癌/直肠癌分别为 64.3%/34.1%;Karnofsky 状态<80%/≥90%的患者分别占 45.3%/54.7%。12 周和 24 周时的无进展率分别为 42.7%(95%CI 32.8-52.6)和 22.4%(95%CI 14.2-30.7)。主要的 3 级或 4 级毒性为:腹泻 13.5%和痤疮样皮疹 10.3%。未报告 3 级或 4 级输注相关或过敏反应。
无进展率证实,西妥昔单抗 q2w 联合伊立替康是一种选择,与标准的每周方案一样有效且安全。