Article Text

This article has a correction. Please see:

Download PDFPDF
Adenoma prevalence and cancer risk in familial non-polyposis colorectal cancer
  1. G Lindgren1,
  2. A Liljegren2,
  3. E Jaramillo3,
  4. C Rubio4,
  5. A Lindblom1
  1. 1Department of Clinical Genetics, Karolinska Hospital, S 171 76 Stockholm, Sweden
  2. 2Department of Clinical Genetics, Karolinska Hospital, S 171 76 Stockholm, Sweden and Department of Clinical Oncology, Danderyds Hospital, S 182 88, Stockholm, Sweden
  3. 3Department of Gastroenterology, Karolinska Hospital, S 171 76 Stockholm, Sweden
  4. 4Department of Oncology and Pathology, Karolinska Hospital, S 171 76 Stockholm, Sweden
  1. Correspondence to:
    A Lindblom, Department of Clinical Genetics, CMM L8-02, S 171 76 Stockholm, Sweden;
    annika.lindblom{at}cmm.ki.se

Abstract

Background and aims: Polypectomy in the colon has been shown to prevent colorectal cancer in both the general population and in familial colorectal cancer. Individuals with a family history of colorectal cancer have an increased risk of the disease. Over a period of 10 years, 304 subjects at risk were included in ongoing surveillance with regular colonoscopies. To compile the medical findings and experience generated during this period, a retrospective cross sectional study was performed.

Subjects: Subjects were classified into three family groups: families with hereditary non-polyposis colorectal cancer (HNPCC); families with hereditary colorectal cancer (HCC, non-Lynch syndrome); and a third group of families with only empirical risk estimates based on a family history of two close relatives (TCR) with colorectal cancer.

Methods: The risk population was studied with regard to age at onset, prevalence, number, cancer risk, size, dysplasia, and distribution of adenomas. A comparison was made within the family groups and with a reference group representing the general population.

Results: In total, 195 adenomas and six cancers were detected among 85 individuals. The relative risk of having an adenoma in the whole risk population compared with the general population was 2.6. Subjects from TCR families had most adenomas and HNPCC subjects had the least. A shift from proximal adenomas to distal carcinomas in families with HCC and TCR suggested a higher cancer risk in distal adenomas in these syndromes. HNPCC families showed a younger age at onset and adenomas with a higher degree of dysplasia. In HNPCC, there was a similar localisation of adenomas and carcinomas, suggesting a high risk of cancer in all adenomas.

Conclusions: There was clear overrepresentation of adenomas in all three family types compared with the reference population. In HNPCC, we found earlier onset of adenomas and faster progression to cancer. Families with HCC, and even more so TCR subjects, had a later onset and lower risk of cancer from proximal adenomas. Based on these results, surveillance protocols in Sweden have been revised.

  • familial colorectal cancer
  • hereditary non-polyposis colorectal cancer
  • colonoscopy
  • surveillance
  • tumour progression
  • HNPCC, hereditary non-polyposis colorectal cancer
  • HCC, hereditary colorectal cancer
  • TCR, two close relatives with colorectal cancer
  • OCR, one close relative with colorectal cancer
  • MSI, microsatellite instability
  • RR, relative risk

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

Linked Articles

  • CORRECTION
    BMJ Publishing Group Ltd and British Society of Gastroenterology