Volume 30, Issue 7 pp. 1147-1154
Gastroenterology

Ideal colonoscopic surveillance intervals to reduce incidence of advanced adenoma and colorectal cancer

Norm M Good

Corresponding Author

Norm M Good

CSIRO Digital Productivity, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia

Australian e-Health Research Centre, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia

Correspondence

Mr Norm M Good, Australian e-Health Research Centre, Lvl 5, UQ Health Sciences Building 901/16, Royal Brisbane and Womens' Hospital, Herston, QLD 4029, Australia. Email: [email protected]

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Finlay A Macrae

Finlay A Macrae

Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, Victoria, Australia

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Graeme P Young

Graeme P Young

Flinders Centre for Innovation in Cancer, Flinders University, Bedford Park, South Australia, Australia

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John O'Dywer

John O'Dywer

Australian e-Health Research Centre, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia

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Masha Slattery

Masha Slattery

Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, Victoria, Australia

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William Venables

William Venables

CSIRO Digital Productivity, Ecosciences Precinct, Dutton Park, Queensland, Australia

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Trevor J Lockett

Trevor J Lockett

CSIRO Food & Nutrition, Riverside Corporate Park, North Ryde, New South Wales, Australia

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Marilla O'Dwyer

Marilla O'Dwyer

I&D, Rio Tinto, Brisbane, Queensland, Australia

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First published: 22 January 2015
Citations: 21
Disclosures: No conflicts of interest from any authors.
Grant support: None.

Abstract

Background and Aims

There is limited information about the interplay between multiple risk factors contributing to the risk of advanced neoplasia. We determined the actual risk for advanced neoplasia in relation to lapsed time between colonoscopies in people enrolled in a structured surveillance program. This risk information can be used to guide the selection of optimal surveillance intervals.

Methods

Patients were recruited into programs at two major tertiary hospitals, with a personal or family history of advanced neoplasia. Five thousand one hundred forty-one patients had an index and one or more surveillance colonoscopies. Fifty-one percent had a family history of colorectal neoplasia while the remainder had a personal history.

Results

Patients with an immediately prior colonoscopy result (prior result) of advanced adenoma had a risk for advanced neoplasia 7.1 times greater than those with a normal prior result. Cancer as a prior result did not confer a greater risk than either a hyperplastic polyp or a nonadvanced adenoma. Being female reduced risk, age increased risk. Only a family history of a first-degree relative diagnosed under 55, or definite or suspected hereditary nonpolyposis colorectal cancer (HNPCC) conferred an increased risk over a personal history of advanced neoplasia.

Conclusions

Most family history categories did not confer excess risk above personal history of advanced neoplasia. A prior cancer poses less of a risk than a prior advanced adenoma. Based on our models, a person with an advanced adenoma should be scheduled for colonoscopy at 3 years, corresponding to a 15% risk of advanced neoplasia for a male aged under 56. Guidelines should be updated that uses a 15% risk as a benchmark for calculating surveillance intervals.

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