Frequency of familial colorectal cancer

Author:

Stephenson B M12,Finan P J1,Gascoyne J2,Garbett F2,Murday V A2,Bishop D T2

Affiliation:

1. Department of Surgery, Leeds General Infirmary, University of Leeds, Leeds, UK

2. Imperial Cancer Research Fund, Genetic Epidemiology Laboratory, University of Leeds, Leeds, UK

Abstract

Abstract Familial clustering of cancer is not uncommon. The frequency of familial colorectal cancer was estimated by taking family histories from 100 patients presenting with apparently sporadic colorectal cancer. Compared with controls, the relative risk of a positive family history for colorectal cancer was 4·6. Life-table methods were used to examine the observed to expected mortality from colorectal cancer. Overall there was a fourfold increase in mortality rate (P < 0·0001), which was greatest in female relatives of patients with colonic cancer (P < 0·001). Three families with dominant inheritance of colorectal cancer and one family with Lynch type II syndrome were identified. Nine per cent of patients had siblings who had developed colorectal cancer a median of 4 years before the diagnosis of the index patient (range 1–17 years). It is recommended that a careful family history should be obtained from all patients with colorectal cancer. Where a positive history is obtained a geneticist may determine empirical risks for the development of colorectal cancer and the appropriate method of surveillance may be selected.

Funder

Imperial Cancer Research Fund

Publisher

Oxford University Press (OUP)

Subject

Surgery

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