Risk factors for advanced colorectal neoplasia and colorectal cancer detected at surveillance: a nationwide study in the modern era

Author:

Smits Lisanne J H1ORCID,Siebers Albert G2,Lissenberg‐Witte Birgit I3,Lansdorp‐Vogelaar Iris4,van Kouwen Mariette C A5,Tuynman Jurriaan B1,van Grieken Nicole C T6,Nagtegaal Iris D7ORCID

Affiliation:

1. Department of Surgery, Cancer Centre Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands

2. Palga: the Dutch Nationwide Pathology Databank Stichting Palga Houten The Netherlands

3. Amsterdam UMC, Vrije Universiteit Amsterdam Epidemiology and Data Science Amsterdam The Netherlands

4. Department of Public Health Erasmus University Medical Centre Rotterdam The Netherlands

5. Department of Gastroenterology Radboud University Medical Centre Nijmegen The Netherlands

6. Department of Pathology, Cancer Centre Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands

7. Department of Pathology Radboud University Medical Centre, Radboud Institute for Molecular Life Sciences Nijmegen The Netherlands

Abstract

AimRecommendations for surveillance after colonoscopy are based on risk factors for metachronous advanced colorectal neoplasia (AN) and colorectal cancer (CRC). The value of these risk factors remains unclear in populations enriched by individuals with a positive faecal immunochemical test and were investigated in a modern setting.Methods and ResultsThis population‐based cohort study included all individuals in the Netherlands of ≥55 years old with a first adenoma diagnosis in 2015. A total of 22,471 patients were included. Data were retrieved from the Dutch Nationwide Pathology Databank (Palga). Primary outcomes were metachronous AN and CRC. Patient and polyp characteristics were evaluated by multivariable Cox regression analyses. During follow‐up, 2416 (10.8%) patients were diagnosed with AN, of which 557 (2.5% from the total population) were CRC. Adenomas with high‐grade dysplasia (hazard ratio [HR] 1.60, 95% confidence interval [CI] 1.40–1.83), villous histology (HR 1.91, 95% CI 1.59–2.28), size ≥10 mm (HR 1.12, 95% CI 1.02–1.23), proximal location (HR 1.12, 95% CI 1.02–1.23), two or more adenomas (HR 1.28, 95% CI 1.16–1.41), and serrated polyps ≥10 mm (HR 1.67, 95% CI 1.42–1.97) were independent risk factors for metachronous AN. In contrast, only adenomas with high‐grade dysplasia (HR 2.49, 95% CI 1.92–3.24) were an independent risk factor for metachronous CRC.ConclusionsRisk factors for metachronous AN and CRC were identified for populations with access to a faecal immunochemical test (FIT)‐based screening programme. If only risk factors for metachronous CRC are considered, a reduction in criteria for surveillance seems reasonable.

Publisher

Wiley

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