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  4. Clinical risk factors of colorectal cancer in patients with serrated polyposis syndrome: a multicentre cohort analysis
 
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Clinical risk factors of colorectal cancer in patients with serrated polyposis syndrome: a multicentre cohort analysis
File(s)
SPS Clinical Risk Factors (Final).pdf (223.66 KB)
Accepted version
Author(s)
IJspeert, JE
Rana, SA
Atkinson, NS
van Herwaarden, YJ
Bastiaansen, BA
more
Type
Journal Article
Abstract
OBJECTIVE: Serrated polyposis syndrome (SPS) is accompanied by an increased risk of colorectal cancer (CRC). Patients fulfilling the clinical criteria, as defined by the WHO, have a wide variation in CRC risk. We aimed to assess risk factors for CRC in a large cohort of patients with SPS and to evaluate the risk of CRC during surveillance. DESIGN: In this retrospective cohort analysis, all patients with SPS from seven centres in the Netherlands and two in the UK were enrolled. WHO criteria were used to diagnose SPS. Patients who only fulfilled WHO criterion-2, with IBD and/or a known hereditary CRC syndrome were excluded. RESULTS: In total, 434 patients with SPS were included for analysis; 127 (29.3%) were diagnosed with CRC. In a per-patient analysis ≥1 serrated polyp (SP) with dysplasia (OR 2.07; 95% CI 1.28 to 3.33), ≥1 advanced adenoma (OR 2.30; 95% CI 1.47 to 3.67) and the fulfilment of both WHO criteria 1 and 3 (OR 1.60; 95% CI 1.04 to 2.51) were associated with CRC, while a history of smoking was inversely associated with CRC (OR 0.36; 95% CI 0.23 to 0.56). Overall, 260 patients underwent surveillance after clearing of all relevant lesions, during which two patients were diagnosed with CRC, corresponding to 1.9 events/1000 person-years surveillance (95% CI 0.3 to 6.4). CONCLUSION: The presence of SPs containing dysplasia, advanced adenomas and/or combined WHO criteria 1 and 3 phenotype is associated with CRC in patients with SPS. Patients with a history of smoking show a lower risk of CRC, possibly due to a different pathogenesis of disease. The risk of developing CRC during surveillance is lower than previously reported in literature, which may reflect a more mature multicentre cohort with less selection bias.
Date Issued
2015-11-24
Date Acceptance
2015-10-28
Citation
Gut, 2015, 66, pp.278-284
URI
http://hdl.handle.net/10044/1/39517
DOI
https://www.dx.doi.org/10.1136/gutjnl-2015-310630
ISSN
1468-3288
Publisher
BMJ Publishing Group
Start Page
278
End Page
284
Journal / Book Title
Gut
Volume
66
Copyright Statement
© 2015 The Authors. Produced by BMJ Publishing Group Ltd (& BSG) under licence. This article has been accepted for publication in Gut following peer review. The definitive copyedited, typeset version is available online at: http://dx.doi.org/10.1136/gutjnl-2015-310630.
Subjects
COLONIC POLYPS
COLONOSCOPY
COLORECTAL CANCER
POLYPOSIS
SURVEILLANCE
Dutch workgroup serrated polyps & polyposis (WASP)
Gastroenterology & Hepatology
Clinical Sciences
Paediatrics And Reproductive Medicine
Publication Status
Published
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