Authors
Christos S Karapetis, Shirin Khambata-Ford, Derek J Jonker, Chris J O'Callaghan, Dongsheng Tu, Niall C Tebbutt, R John Simes, Haji Chalchal, Jeremy D Shapiro, Sonia Robitaille, Timothy J Price, Lois Shepherd, Heather-Jane Au, Christiane Langer, Malcolm J Moore, John R Zalcberg
Publication date
2008/10/23
Journal
New England Journal of Medicine
Volume
359
Issue
17
Pages
1757-1765
Publisher
Massachusetts Medical Society
Description
Background
Treatment with cetuximab, a monoclonal antibody directed against the epidermal growth factor receptor, improves overall and progression-free survival and preserves the quality of life in patients with colorectal cancer that has not responded to chemotherapy. The mutation status of the K-ras gene in the tumor may affect the response to cetuximab and have treatment-independent prognostic value.
Methods
We analyzed tumor samples, obtained from 394 of 572 patients (68.9%) with colorectal cancer who were randomly assigned to receive cetuximab plus best supportive care or best supportive care alone, to look for activating mutations in exon 2 of the K-ras gene. We assessed whether the mutation status of the K-ras gene was associated with survival in the cetuximab and supportive-care groups.
Results
Of the tumors evaluated for K-ras mutations, 42.3% had at least one mutation in exon 2 of the …
Total citations
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Scholar articles
CS Karapetis, S Khambata-Ford, DJ Jonker… - New England Journal of Medicine, 2008