K-ras mutations in patients with early colorectal cancers

• Published in: Gut Vol. 41; no. 3; pp. 323 - 329
• Main Authors: Andreyev, H J N, Tilsed, J V T, Cunningham, D, Sampson, S A, Norman, A R, Schneider, H J, Clarke, P A
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Society of Gastroenterology 01.09.1997; BMJ; BMJ Publishing Group LTD
• Subjects: Adenocarcinoma - genetics; Adenocarcinoma - pathology; Adult; Aged; Aged, 80 and over; Biological and medical sciences; Cancer; Cancer therapies; Chemotherapy; Colorectal cancer; Colorectal Neoplasms - genetics; Colorectal Neoplasms - pathology; Dukes’ stage; Female; Gastroenterology. Liver. Pancreas. Abdomen; Genes; Genes, ras - genetics; Humans; K-ras; Male; Medical sciences; microdissection; Middle Aged; Mutation; Neoplasm Recurrence, Local - genetics; Neoplasm Staging; Point Mutation - genetics; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Studies; Surgery; Tumors; Human; Rectal disease; Carcinoma; Early stage; Tumoral marker; Malignant tumor; Result; Colonic disease; Clinical stage; Rectum; Predictive value; Digestive diseases; Genetics; Intestinal disease; Colon; Mutation
• ISSN: 0017-5749; 1468-3288; 1458-3288
• DOI: 10.1136/gut.41.3.323

Background—Published data are contradictory about the importance of K-ras mutations in advanced tumours and are not available for early cancers. Aims—To establish whether specific K-ras mutations are prognostic markers in early stage colorectal adenocarcinoma. Methods—The presence of K-ras exon 1 mutations were correlated with tumour recurrence in two groups of patients: group 1 was a consecutive series of patients with resected colorectal adenocarcinoma at low risk of recurrence; group 2 were patients referred for chemotherapy after relapse of previously resected early stage tumours. K-ras mutations were detected by direct sequencing of whole tissue samples in all patients and in some, the leading edge and centre of the tumour were also microdissected out individually and sequenced. Results—Mutations were present in 26 (26.5%) of 98 patients in group 1; 14 patients developed a recurrence, four (28.5%) of whom had a K-ras mutation. Seventy nine patients have not developed tumour recurrence, 22 (28%) of whom had a mutation (p=0.84). K-ras mutations were present in five of 14 patients in group 2. Microdissection did not increase the number of mutations detected. Conclusions—Individual K-ras genotypes are distributed homogeneously throughout early stage colorectal adenocarcinomas, but detection of a mutation has no apparent prognostic value.