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      The diagnostic yield of colonoscopic surveillance following resection of early age onset colorectal cancer

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          Abstract

          Background

          The primary benefit of post‐colorectal cancer (CRC) colonoscopic surveillance is to detect and remove premalignant lesions to prevent metachronous CRC. Current guidelines for long‐term colonoscopic surveillance post early age onset CRC (EOCRC) resection are based on limited evidence. The aims of this study were to assess the diagnostic yield of colonoscopic surveillance post‐EOCRC resection and identify molecular and clinicopathological risk factors associated with advanced neoplasia.

          Methodology

          A retrospective cohort study of prospectively collected data was conducted at St Mark's hospital, London, United Kingdom, for patients diagnosed with EOCRC who underwent at least one episode of post‐CRC colonoscopic surveillance between 1978 and 2022. We collected clinicopathological data including tumour molecular status and neoplasia detection rates.

          Results

          In total, 908 colonoscopic surveillance procedures were performed in 195 patients over 2581.3 person‐years of follow‐up. The diagnostic yields of metachronous CRC, advanced adenomas and non‐advanced adenomas were 1.76%, 3.41% and 22.69% respectively. Sixteen patients (8.21%) developed metachronous CRC, and the majority (87.5%) were detected more than 3 years post index EOCRC diagnosis. Detection of advanced neoplasia was significantly higher in EOCRC patients with Lynch syndrome (26.15%) compared with those in whom Lynch syndrome was excluded (13.13%) (OR, 2.343; 95% CI, 1.014–5.256; p = 0.0349).

          Conclusions

          During colonoscopic surveillance post‐EOCRC resection, the long‐term risk of developing metachronous advanced neoplasia remains high in the context of Lynch syndrome, but this trend is not as clearly evident when Lynch syndrome has been excluded.

          Abstract

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          Most cited references27

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          Colorectal cancer statistics, 2020

          Colorectal cancer (CRC) is the second most common cause of cancer death in the United States. Every 3 years, the American Cancer Society provides an update of CRC occurrence based on incidence data (available through 2016) from population-based cancer registries and mortality data (through 2017) from the National Center for Health Statistics. In 2020, approximately 147,950 individuals will be diagnosed with CRC and 53,200 will die from the disease, including 17,930 cases and 3,640 deaths in individuals aged younger than 50 years. The incidence rate during 2012 through 2016 ranged from 30 (per 100,000 persons) in Asian/Pacific Islanders to 45.7 in blacks and 89 in Alaska Natives. Rapid declines in incidence among screening-aged individuals during the 2000s continued during 2011 through 2016 in those aged 65 years and older (by 3.3% annually) but reversed in those aged 50 to 64 years, among whom rates increased by 1% annually. Among individuals aged younger than 50 years, the incidence rate increased by approximately 2% annually for tumors in the proximal and distal colon, as well as the rectum, driven by trends in non-Hispanic whites. CRC death rates during 2008 through 2017 declined by 3% annually in individuals aged 65 years and older and by 0.6% annually in individuals aged 50 to 64 years while increasing by 1.3% annually in those aged younger than 50 years. Mortality declines among individuals aged 50 years and older were steepest among blacks, who also had the only decreasing trend among those aged younger than 50 years, and excluded American Indians/Alaska Natives, among whom rates remained stable. Progress against CRC can be accelerated by increasing access to guideline-recommended screening and high-quality treatment, particularly among Alaska Natives, and elucidating causes for rising incidence in young and middle-aged adults.
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            Global patterns and trends in colorectal cancer incidence in young adults

            Early-onset colorectal cancer (CRC) is increasing in the USA despite rapid declines in older ages. Similar patterns are reported in Australia and Canada, but a comprehensive global analysis of contemporary data is lacking. We extracted long-term data from Cancer Incidence in Five Continents and supplemental sources to report on worldwide CRC incidence rates and trends by age (20–49 years and ≥50 years) through diagnosis year 2012 or beyond (Australia, Finland, New Zealand, Norway, Sweden, USA). During 2008–2012, age-standardised CRC incidence rates in adults <50 ranged from 3.5 per 100 000 (95% CI 3.2 to 3.9) in India (Chennai) to 12.9 (95% CI 12.6 to 13.3) in Korea. During the most recent decade of available data, incidence in adults <50 was stable in 14 of 36 countries; declined in Austria, Italy and Lithuania; and increased in 19 countries, nine of which had stable or declining trends in older adults (Australia, Canada, Denmark, Germany, New Zealand, Slovenia, Sweden, UK and USA). In Cyprus, Netherlands and Norway, inclines in incidence in young adults were twice as rapid as those in older adults (eg, Norway average annual per cent change (AAPC), 1.9 (95% CI 1.4 to 2.5) vs 0.5 (95% CI 0.3 to 0.7)). Among most high-income countries with long-term data, the uptick in early-onset disease began in the mid-1990s. The steepest increases in young adults were in Korea (AAPC, 4.2 (95% CI 3.4 to 5.0)) and New Zealand (AAPC, 4.0 (95% CI 2.1 to 6.0)). CRC incidence increased exclusively in young adults in nine high-income countries spanning three continents, potentially signalling changes in early-life exposures that influence large bowel carcinogenesis.
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              Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010.

              The overall incidence of colorectal cancer (CRC) has been decreasing since 1998 but there has been an apparent increase in the incidence of CRC in young adults.
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                Author and article information

                Contributors
                Husam.al-maliki21@imperial.ac.uk
                k.monahan@imperial.ac.uk
                Journal
                United European Gastroenterol J
                United European Gastroenterol J
                10.1002/(ISSN)2050-6414
                UEG2
                United European Gastroenterology Journal
                John Wiley and Sons Inc. (Hoboken )
                2050-6406
                2050-6414
                03 January 2024
                May 2024
                : 12
                : 4 ( doiID: 10.1002/ueg2.v12.4 )
                : 469-476
                Affiliations
                [ 1 ] Department of Surgery and Cancer Imperial College London London UK
                [ 2 ] Centre for Familial Intestinal Cancer St Mark's Hospital London UK
                Author notes
                [*] [* ] Correspondence

                Husam Al Maliki, Department of Surgery and Cancer, Imperial College London, London, UK.

                Email: Husam.al-maliki21@ 123456imperial.ac.uk

                Kevin J. Monahan, The St Mark’s Centre for Familial Intestinal Cancer, Lynch Syndrome & Family Cancer Clinic & Polyposis Registry, St Mark’s: The National Bowel Hospital, Central Middlesex Hospital Site, Acton Lane, Park Royal, London NW10 7NS, UK.

                Email: k.monahan@ 123456imperial.ac.uk

                Author information
                https://orcid.org/0009-0005-3803-1376
                http://orcid.org/0000-0002-7918-4003
                Article
                UEG212516
                10.1002/ueg2.12516
                11091789
                38170450
                57ed2995-4793-40c1-b145-a1c3506000de
                © 2024 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 30 August 2023
                : 20 November 2023
                Page count
                Figures: 3, Tables: 4, Pages: 8, Words: 5241
                Categories
                Original Article
                Luminal
                Custom metadata
                2.0
                May 2024
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.4.2 mode:remove_FC converted:14.05.2024

                adenoma,colorectal cancer,crc,early‐age onset,eocrc,lynch,metachronous,neoplasia,polyps,surveillance

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