Journal
CLINICAL COLORECTAL CANCER
Volume 14, Issue 2, Pages 81-90Publisher
CIG MEDIA GROUP, LP
DOI: 10.1016/j.clcc.2014.12.011
Keywords
Bevacizumab; Cetuximab; Chemotherapy; Colorectal cancer; Panitumumab
Categories
Funding
- Merck Serono
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Studies comparing first-line monoclonal antibodies in advanced colorectal cancer (CRC) have yielded conflicting results. The results of our meta-analysis show superior response rates and overall survival (OS) with first-line anti epidermal growth factor receptor (anti-EGFR) therapy compared with anti vascular endothelial growth factor (anti-VEGF) therapy but no difference in progression-free survival (PFS). Anti-EGFR monoclonal antibodies in combination with chemotherapy may be an alternative option as initial treatment of CRC. Background: Monoclonal antibodies targeting epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) have demonstrated efficacy in combination with chemotherapy in the first-line therapy of advanced colorectal cancer (CRC). Data from randomized studies comparing these monoclonal antibodies as initial therapy is conflicting, and their comparative efficacy remains unclear. We aimed to evaluate the impact of these targeted therapies on patient outcomes by combining the data from randomized clinical trials. Materials and Methods: MEDLINE, PubMed, EMBASE, and meeting proceedings within the past 12 months were searched to identify relevant studies. All randomized phase II/III clinical trials of advanced CRC comparing an anti-EGFR therapy with an anti-VEGF agent in the first-line setting were included. Data were extracted on sample size, objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Results: Three randomized studies comprising 2014 participants were included in the meta-analysis. For patients with KRAS wild type (KRAS-WT) CRC, the ORR was superior in patients who received first-line anti-EGFR therapy compared with those who received anti-VEGF therapy (odds ratio [OR], 1.31; 95% confidence interval [Cl], 1.09-1.58; P =.004). This effect was even stronger for all RAS-WT patients (OR, 1.46; 95% Cl, 1.13-1.90; P =.004). There was no difference in PFS overall irrespective of the KRAS-WT (HR, 1.03; 95% Cl, 0.93-1.13; P =.61) or all RAS-WT (HR, 0.92; 95% Cl, 0.71-1.18; P =.50) status. The OS was significantly longer in the patients who received first-line anti-EGFR therapy compared with those who received anti-VEGF therapy (KRAS-WT: HR, 0.79; 95% Cl, 0.65-0.97; P =.026; all RAS-WT: HR, 0.77; 95% Cl, 0.63-0.95; P =.016). Conclusion: The results of our research show superior ORR and OS with first-line anti-EGFR therapy compared with anti-VEGF therapy in both KRAS-WT and all RAS-WT patients with advanced CRC. These results suggest that anti-EGFR monoclonal antibodies may be a real alternative to anti-VEGF therapy as initial treatment of advanced CRC.
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