Martín-Martorell P, Roselló S, Rodríguez-Braun E, Chirivella I, Bosch A, Cervantes A
Department of Haematology and Medical Oncology, Hospital Clínico Universitario, University of Valencia, Valencia, Spain.
Br J Cancer. 2008 Aug 5;99(3):455-8. doi: 10.1038/sj.bjc.6604530.
This is a phase II institutional exploratory trial of biweekly irinotecan and cetuximab administration regimen in metastatic colorectal cancer patients progressing to at least one previous chemotherapy line. A total of 40 patients were treated between November 2005 and November 2007 with irinotecan 180 mg m-2 and cetuximab 500 mg m-2 q2w (every 2 weeks), in every 21-day cycles, until unacceptable toxicity or progressive disease. An overall response rate of 22.5% was obtained (two complete and seven partial responses). The disease control rate was 60%. The time to progression was 3.4 months and the overall survival was 8 months. The toxicity compared very favourably to weekly cetuximab combination schedules. Grade 3/4 adverse effects were observed in 12 patients. Overall, our results turn up very similar both in terms of toxicity and efficacy to those obtained by weekly and biweekly administration regimens.
这是一项针对至少接受过一线化疗后病情进展的转移性结直肠癌患者,每两周使用伊立替康和西妥昔单抗给药方案的II期机构探索性试验。2005年11月至2007年11月期间,共有40例患者接受治疗,每21天为一个周期,伊立替康剂量为180 mg/m²,西妥昔单抗剂量为500 mg/m²,每2周(q2w)给药一次,直至出现不可接受的毒性或疾病进展。总体缓解率为22.5%(2例完全缓解和7例部分缓解)。疾病控制率为60%。疾病进展时间为3.4个月,总生存期为8个月。与每周使用西妥昔单抗的联合方案相比,该方案的毒性表现良好。12例患者出现3/4级不良反应。总体而言,我们的结果在毒性和疗效方面与每周和每两周给药方案所获得的结果非常相似。