A104 ADENOMATOUS POLYPOSIS WITHIN TERTIARY GASTROENTEROLOGY PRACTICES: A RETROSPECTIVE STUDY
Abstract Background Adenomatous polyposis (AP) is defined as ≥ 10 cumulative colorectal adenomas. Despite its clinical relevance, its prevalence, genetic implications, and optimal management remains unknown. Aims Evaluate the prevalence and outcomes of AP within a tertiary gastroenterology referral center. Methods Patients with at least 1 adenomatous colorectal polyp removed by 1 of 11 gastroenterologists at a tertiary referral center between 2013-2023 were screened for AP using a validated histopathology database. Patients with a known adenomatous polyposis syndrome and/or previous colorectal surgery prior to referral were excluded from analysis. All patients with AP (defined as ≥ 10 adenomatous colorectal polyps) underwent full chart review. Data were extracted for demographic and clinical outcomes. Results Of 10,603 patients with at least 1 colorectal adenoma, 330 (3.1%) were diagnosed with AP. AP patients were diagnosed over a median of 5 years (IQR 1-9 years) and a median of 3 colonoscopies (IQR 2-4 colonoscopies). The frequencies of an advanced adenoma and colorectal cancer (CRC) were 236 (71.5%) and 23 (7.0%), respectively. 78.2% of CRC diagnosed before or concurrent to AP diagnosis. Genetic analysis was completed in 22 (6.8%) patients, with a deleterious mutation found in 10 (45.4%). 276 (83.6%) patients were managed endoscopically with 24 (7.3%) referred to surgery and 30 (9.1%) discharged due to age. 300 (90.9%) patients had 10-20 adenomas and 30 (9.1%) patients had > 20 adenomas. Patients with > 20 adenomas were more commonly referred to surgery (6, 20% vs. 18, 6%; p = 0.014). There was no difference in the frequency of CRC between groups (21, 7.0% in 10-20 adenomas and 2, 6.7% in >20 adenomas; p=0.195). Conclusions In patients with ≥ 1 colorectal adenoma, the prevalence of AP was 3.1%, with an overall CRC risk of 7.0%. The majority of patients can be successfully managed endoscopically with further evidence needed to delineate appropriate surveillance interval recommendations. Funding Agencies CAG
Authors
- Robert Enns (ORCID: https://orcid.org/0000-0002-9018-4522)
- E. G. Taylor (ORCID: https://orcid.org/0000-0001-8450-1125)
- See‐Tong Pang (ORCID: https://orcid.org/0000-0002-2064-0828)
- Douglas Motomura (ORCID: https://orcid.org/0000-0001-5688-8158)
- Shuyu Jiang (ORCID: https://orcid.org/0000-0003-4711-4112)
- Jennifer J. Telford (ORCID: https://orcid.org/0000-0002-6884-6147)
- Mei Yu (ORCID: https://orcid.org/0000-0003-0306-6817)
- Daniel Flegg
- Wei Xiong (ORCID: https://orcid.org/0000-0003-0669-5029)
- Neal Shahidi (ORCID: https://orcid.org/0000-0002-4536-0515)
- Micah Ten-Pow
- Eric Lam
- P Tavakoli (ORCID: https://orcid.org/0000-0003-4558-9122)
- Arman Walia
Institutions
- University of British Columbia (CA)
- St. Paul's Hospital (CA)
Publication Details
- Journal
- Journal of the Canadian Association of Gastroenterology
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1093/jcag/gwae059.104
- Primary Topic
- Genetic factors in colorectal cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- McMaster University