摘要
Introduction Right-sided colon cancer (RSCC) and left-sided colorectal cancer (LSCRC) differ with respect to theirbiology and genomic patterns. This study aimed to examine whether the primary tumor location is associated withthe response to cetuximab in patients with metastatic colorectal cancer (mCRC).Methods: Patients with mCRC treated with cetuximab and standard chemotherapy as first- or second-line treatmentswere 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.Results: The treatment results of 206 patients with mCRC treated with cetuximab and standard chemotherapy asfirst- or second-line treatments were compared with those of 210 patients who were treated with chemotherapyalone. 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) inpatients 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) orOS (13.4 vs. 13.0 months, P=0.652) in patients with RSCC.Conclusions: The addition of cetuximab to chemotherapy in both first- and second-line treatments of mCRC may onlybenefit patients with primary LSCRC.
基金
supported by grants from National Natural Science Foundation of China (No. 81302194 and 81372570)
the Specialized Research Fund for the Doctoral Program of Higher Education (No. 20130171120047)
the Fundamental Research Funds for the Central Universities (No.14ykpy40)
the Young Talent Fund of Sun Yat-sen University Cancer Center