The risk of subsequent primary cancers after colorectal cancer in southeast England. (1st May 2002)

• Record Type: Journal Article
• Authors: Evans, H S; Møller, H; Robinson, D; Lewis, C M; Bell, C M J; Hodgson, S V
• Is Part Of: Gut. Volume 50:(2002)Supplement 5
• Page Start: 647
• Page End: 652
• Publication Date: 2002-05-01
• Subjects: primary cancers -- colorectal cancer -- cancer genetics; TCR, Thames Cancer Registry -- HNPCC, hereditary non-polyposis colorectal cancer -- ICD, International Classification of Diseases -- SIR, standardised incidence ratio; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gut.50.5.647
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : Background: Multiple cancers may occur in an individual because of a genetic predisposition, environmental exposure, cancer therapy, or immunological deficiency. Colorectal cancer is one of the most commonly diagnosed cancers, and inherited factors play an important role in its aetiology. Aims: To characterise the occurrence of multiple primary cancers in patients diagnosed with colorectal cancer and explore the possibility of a common aetiology for different cancer sites. Patients: The Thames Cancer Registry database was used to identify patients with a first colorectal cancer, resident in the North or South Thames region, diagnosed between 1 January 1961 and 31 December 1995. A total of 127 281 patients were included, 61 433 men and 65 848 women. Methods: Observed numbers of cancers occurring after the diagnosis of colorectal cancer were compared with expected numbers, calculated using appropriate age, sex, and period specific rates, to obtain standardised incidence ratios. The occurrence of colorectal cancers subsequent to cancers at other sites was also examined. Results: Small intestinal cancer was significantly increased in men diagnosed with colorectal cancer before the age of 60 years and in women diagnosed with colorectal cancer after the age of 65 years. Colorectal cancer was also significantly increased after a first diagnosis of cancer of the small intestine. Other cancer sites with a significant increase after colorectal cancer included the cervix uteri, corpus uteri, and ovary. Conclusions: Patients with colorectal cancer are at increased risk of developing cancer at a number of other sites. Some of these associations are consistent with the effects of known inherited cancer susceptibility genes.