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Prevalence and characteristics of post‐colonoscopy colorectal cancers in a New Zealand regional centre: a 10‐year analysis
Author(s) -
Willington Adam J.,
Cosgrove Samuel,
Davison Polly,
Cunliffe Robert N.
Publication year - 2021
Publication title -
internal medicine journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 70
eISSN - 1445-5994
pISSN - 1444-0903
DOI - 10.1111/imj.14811
Subject(s) - medicine , colonoscopy , colorectal cancer , diverticular disease , stage (stratigraphy) , cancer , disease , gastroenterology , paleontology , biology
Abstract Background Post‐colonoscopy colorectal cancers (PCCRC) are cancers that appear following a colonoscopy in which no cancer is diagnosed. The occurrence of PCCRC is thought to be multifactorial, reflecting both endoscopy quality and potential differences in tumour biology between detected colorectal cancers and PCCRC. Aim To identify the prevalence and characteristics of PCCRC in a New Zealand regional centre over a 10‐year period. Method All cases of colorectal cancer ( n = 1055) in the Bay of Plenty region between 1 February 2009 and 1 February 2019 were cross‐referenced with endoscopy coding records to identify patients who had undergone colonoscopy within the preceding 6–60 months in which cancer was not identified. Results A total of 46 patients were identified to have PCCRC, giving a prevalence of 4.4%. The majority of these patients were older (80% aged 65 years or over) and female (67%). The mean interval between index colonoscopy and diagnosis of PCCRC was 3.03 years. Most (80%) patients had existent pathology (diverticular disease or colonic polyps) at index colonoscopy, and a significant proportion (43%) developed cancer in the same colonic segment. PCCRC were evenly distributed between the left (50%) and right (50%) colon. The majority of patients (63%) had early‐stage cancer. Conclusions The prevalence of PCCRC in a New Zealand cohort is consistent with other international reports. Most patients with PCCRC are older, female and have early‐stage disease. Of interest, a high proportion of patients developed cancer within a colonic segment with existent pathology, suggesting either missed lesions or incomplete polyp resection.