Chen Ye, Cao Dan, Bi Feng, Li Qiu, Qiu Meng
Department of Medical Oncology, Cancer Center, the State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, No. 37, Guo Xue Xiang, Chengdu, 610041, Sichuan Province, China.
Med Oncol. 2014 May;31(5):935. doi: 10.1007/s12032-014-0935-2. Epub 2014 Mar 30.
Weekly cetuximab plus irinotecan-based regiments are standard first- and second-line chemotherapy for patients with KRAS wild-type metastatic colorectal cancer (mCRC). However, the chemotherapy regimens are given every 2 weeks, which is asynchronous with cetuximab weekly administration. This study investigated the efficacy and safety of biweekly cetuximab administration in patients with mCRC. Twenty-six patients with KRAS wild-type mCRC, who received biweekly cetuximab plus FOLFIRI/irinotecan as first/second-line chemotherapy, at least three cycles of cetuximab and once CT evaluation in West China Hospital from May 2010 to February 2013, were retrospectively analyzed. The median number of cetuximab administrations was 8.3 (range 3-20). Fourteen patients received FOLFIRI as first-line therapy; response rate was 50.0%; median PFS was 8.8 months (95% CI 4.9-12.7). Ten patients received FOLFIRI and two patients received irinotecan as second-line therapy; response rate was 33.3%; median PFS was 4.6 months (95% CI 0.9-8.3). The toxicity was similar to weekly cetuximab combination schedules. Rash was observed in 69.2% of evaluable patients (grade 3 in 7.7%). Overall, our results show that biweekly cetuximab plus FOLFIRI/irinotecan may be as effective and safe as the standard weekly schedule.
对于KRAS基因野生型转移性结直肠癌(mCRC)患者,基于西妥昔单抗联合伊立替康的每周化疗方案是标准的一线和二线化疗方案。然而,化疗方案是每2周进行一次,这与西妥昔单抗的每周给药不同步。本研究调查了mCRC患者每2周给予西妥昔单抗的疗效和安全性。对2010年5月至2013年2月在华西医院接受每2周一次西妥昔单抗联合FOLFIRI/伊立替康作为一线/二线化疗、至少三个周期西妥昔单抗治疗且进行过一次CT评估的26例KRAS基因野生型mCRC患者进行回顾性分析。西妥昔单抗给药的中位数为8.3次(范围3 - 20次)。14例患者接受FOLFIRI作为一线治疗;缓解率为50.0%;中位无进展生存期(PFS)为8.8个月(95%CI 4.9 - 12.7)。10例患者接受FOLFIRI且2例患者接受伊立替康作为二线治疗;缓解率为33.3%;中位PFS为4.6个月(95%CI 0.9 - 8.3)。毒性与每周使用西妥昔单抗的联合方案相似。在可评估患者中69.