期刊论文详细信息
Cancer Communications
Right- and left-sided colorectal cancers respond differently to cetuximab
Feng-Hua Wang1  Chao Ren1  De-Shen Wang1  Rui-Hua Xu1  Dong-Sheng Zhang1  Yi-Yi Yu1  Long Bai1  Miao-Zhen Qiu2  Feng Wang2  Yu-Hong Li2  Tian-Shu Liu2  Hui-Yan Luo2  Zhi-Qiang Wang2  Yin Jin2  Ming-Ming He3  Kai-Yan Liu3 
[1] Collaborative Innovation Center for Cancer Medicine, Guangzhou, P. R. China;Department of Medical Oncology, Sun Yat-sen University Cancer Center: State Key Laboratory of Oncology in South China;Department of Medical Oncology, Zhongshan Hospital, Fudan University, Shanghai, P. R. China
关键词: Colorectal neoplasms;    Cetuximab;    Left-sided;    Right-sided;    Chemotherapy;   
DOI  :  10.1186/s40880-015-0022-x
学科分类:肿瘤学
来源: Springer
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【 摘 要 】

Right-sided colon cancer (RSCC) and left-sided colorectal cancer (LSCRC) differ with respect to their biology and genomic patterns. This study aimed to examine whether the primary tumor location is associated with the response to cetuximab in patients with metastatic colorectal cancer (mCRC). Patients with mCRC treated with cetuximab and standard chemotherapy as first- or second-line treatments were compared with randomly chosen patients who were treated with chemotherapy alone between 2005 and 2013. The main outcome measures were the overall response rate (ORR), progression-free survival (PFS), and overall survival (OS). The differences in the outcome were analyzed by using the chi-squared test, Student’s t test, and Kaplan-Meier method. The treatment results of 206 patients with mCRC treated with cetuximab and standard chemotherapy as first- or second-line treatments were compared with those of 210 patients who were treated with chemotherapy alone. As a first-line treatment, cetuximab with chemotherapy was associated with a significantly higher ORR (49.4 % vs. 28.6 %, P = 0.005) as well as longer PFS (9.1 vs. 6.2 months, P = 0.002) and OS (28.9 vs. 20.1 months, P = 0.036) than chemotherapy alone in patients with LSCRC. However, cetuximab neither improved the ORR (36.4 % vs. 26.2 %, P = 0.349) nor prolonged PFS (5.6 vs. 5.7 months, P = 0.904) or OS (25.1 vs. 19.8 months, P = 0.553) in patients with RSCC. As a second-line treatment, cetuximab exhibited a tendency to improve the ORR (23.5 % vs. 10.2 %, P = 0.087) and prolong PFS (4.9 vs. 3.5 months, P = 0.064), and it significantly prolonged OS (17.1 vs. 12.4 months, P = 0.047) compared with chemotherapy alone in the patients with LSCRC. In contrast, as a second-line treatment, cetuximab neither improved the ORR (7.1 % vs. 11.4 %, P = 0.698) nor prolonged PFS (3.3 vs. 4.2 months, P = 0.761) or OS (13.4 vs. 13.0 months, P = 0.652) in patients with RSCC. The addition of cetuximab to chemotherapy in both first- and second-line treatments of mCRC may only benefit patients with primary LSCRC.

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