Abstract
Background:Cetuximab enhances the efficacy of chemotherapy in several cancer types. This trial assessed the activity of cetuximab and chemotherapy in advanced gastric cancer.Methods:Patients with previously untreated, metastatic, gastric cancer received cetuximab 400 mg m 2 at first infusion followed by weekly infusions of 250 mg m 2 combined with FUFOX (oxaliplatin 50 mg m 2, 5-FU 2000 mg m 2, and DL-folinic acid 200 mg m 2 d1, 8, 15 and 22 qd36). The primary endpoint was tumour response.Results:Overall, 52 patients were enrolled. The most common grade 3/4 toxicities were diarrhoea (33%), and skin toxicity (24%). Efficacy was evaluable in 46 patients who showed a response rate of 65% (CI 95%: 50-79%) including four complete responses. Time to progression (TTP) was 7.6 months (CI 95%: 5.0-10.1 months) and overall survival (OS) was 9.5 months (CI 95%: 7.9-11.1 months). Epidermal growth factor receptor (EGFR) was detectable in 60% of tumours but showed no correlation with treatment outcome. A KRAS mutation was found in only 1 of 32 (3%) tumour samples analysed.Conclusion: Cetuximab plus FUFOX showed an interesting high response rate in metastatic gastric cancer. Cetuximab plus platinum-fluoropyrimidine chemotherapy is at present being investigated in a phase III randomised controlled trial.
Original language | English |
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Pages (from-to) | 500-505 |
Number of pages | 6 |
Journal | British Journal of Cancer |
Volume | 102 |
Issue number | 3 |
DOIs | |
State | Published - Feb 2010 |
Keywords
- Antibody
- Cetuximab
- Chemotherapy
- EGFR
- Gastric cancer
- KRAS mutation