Original article
Vol. 154 No. 7 (2024)
Detection rate of colorectal cancer by routine colonoscopy is comparable in patients aged 45–49 and 50–54 years
- Carla Ammann
- Rina Maqkaj
- Marcel Andre Schneider
- Stefanie Josefine Hehl
- Ralph Fritsch
- Daniel Pohl
- Gerhard Rogler
- Christoph Gubler
- Matthias Turina
- Michael Scharl
Summary
OBJECTIVES: Colorectal carcinoma remains one of the most common malignancies worldwide. Colonoscopy screening is most effective for early detection and tumour prevention and is currently recommended in Europe for adults aged over 50 years. However, given that an increasing proportion of patients are diagnosed before the age of 50, we set out to determine the detection rate of colorectal carcinoma in patients younger than 50 years and to determine the best threshold for starting colonoscopy screening.
METHODS: Single-centre, retrospective cohort study of all colonoscopies performed, regardless of indication, in our department at a tertiary Swiss university hospital in patients aged ≥18 and <60 years between 2016 and 2021. Colorectal cancer detection rate was calculated per 5-year age group and analysed separately by sex.
RESULTS: The current analysis included 2846 colonoscopies performed for any indication. Colorectal carcinoma was found in 5/366 (1.4%) patients aged 45–49 years (3/210 or 1.4% of males and 2/156 or 1.3% of females) and in 9/819 (1.1%) patients aged 50–54 years (5/495 or 1.0% of males and 4/324 or 1.2% of females). Adenomas with high-grade dysplasia were found in 5/366 (1.4%) patients aged 45–49 years and in 11/819 (1.3%) aged 50–54 years; by sex, in 4/210 or 1.9% of males and 1/156 or 0.6% of females aged 45–49 years, and in 6/495 or 1.2% of males and 5/324 or 1.5% of females aged 50–54 years. Detection of adenoma with low-grade dysplasia increased from 14.6% (21/144) at age <30 years to 41% (150/366) at 45–49 years and 43.5% (356/819) at 50–54 years. A similar increasing trend was also seen if we analysed these groups by sex.
CONCLUSIONS: The detection rate of colorectal carcinoma, but also adenomas, in our patients aged 45–49 years was similar to that in patients aged over 50, in both sexes. Thus our data are in line with the assumption that lowering the screening age to 45 years might be reasonable from a medical point of view for achieving a reduction in disease-specific mortality by improved screening strategies.
References
- Dekker E, Tanis PJ, Vleugels JL, Kasi PM, Wallace MB. Colorectal cancer. Lancet. 2019 Oct;394(10207):1467–80. 10.1016/S0140-6736(19)32319-0
DOI: https://doi.org/10.1016/S0140-6736(19)32319-0
- Guo F, Chen C, Holleczek B, Schöttker B, Hoffmeister M, Brenner H. Strong Reduction of Colorectal Cancer Incidence and Mortality After Screening Colonoscopy: Prospective Cohort Study From Germany. Am J Gastroenterol. 2021 May;116(5):967–75. 10.14309/ajg.0000000000001146
DOI: https://doi.org/10.14309/ajg.0000000000001146
- Krebsliga. https://www.krebsliga.ch/ueber-krebs/frueherkennung/darmkrebs/darmkrebs-screening-programm [
- Bretthauer M, Løberg M, Wieszczy P, Kalager M, Emilsson L, Garborg K, et al.; NordICC Study Group. Effect of Colonoscopy Screening on Risks of Colorectal Cancer and Related Death. N Engl J Med. 2022 Oct;387(17):1547–56. 10.1056/NEJMoa2208375
DOI: https://doi.org/10.1056/NEJMoa2208375
- Sehgal M, Ladabaum U, Mithal A, Singh H, Desai M, Singh G. Colorectal Cancer Incidence After Colonoscopy at Ages 45-49 or 50-54 Years. Gastroenterology. 2021 May;160(6):2018–2028.e13. 10.1053/j.gastro.2021.02.015
DOI: https://doi.org/10.1053/j.gastro.2021.02.015
- Siegel RL, Torre LA, Soerjomataram I, Hayes RB, Bray F, Weber TK, et al. Global patterns and trends in colorectal cancer incidence in young adults. Gut. 2019 Dec;68(12):2179–85. 10.1136/gutjnl-2019-319511
DOI: https://doi.org/10.1136/gutjnl-2019-319511
- Vuik FE, Nieuwenburg SA, Bardou M, Lansdorp-Vogelaar I, Dinis-Ribeiro M, Bento MJ, et al. Increasing incidence of colorectal cancer in young adults in Europe over the last 25 years. Gut. 2019 Oct;68(10):1820–6. 10.1136/gutjnl-2018-317592
DOI: https://doi.org/10.1136/gutjnl-2018-317592
- Siegel RL, Miller KD, Jemal A. Colorectal Cancer Mortality Rates in Adults Aged 20 to 54 Years in the United States, 1970-2014. JAMA. 2017 Aug;318(6):572–4. 10.1001/jama.2017.7630
DOI: https://doi.org/10.1001/jama.2017.7630
- Mueller M, Schneider MA, Deplazes B, Cabalzar-Wondberg D, Rickenbacher A, Turina M. Colorectal cancer of the young displays distinct features of aggressive tumor biology: A single-center cohort study. World J Gastrointest Surg. 2021 Feb;13(2):164–75. 10.4240/wjgs.v13.i2.164
DOI: https://doi.org/10.4240/wjgs.v13.i2.164
- Davidson KW, Barry MJ, Mangione CM, Cabana M, Caughey AB, Davis EM, et al.; US Preventive Services Task Force. Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement. JAMA. 2021 May;325(19):1965–77. 10.1001/jama.2021.6238
DOI: https://doi.org/10.1001/jama.2021.6238
- Zaborowski AM, Abdile A, Adamina M, Aigner F, d’Allens L, Allmer C, et al.; REACCT Collaborative. Characteristics of Early-Onset vs Late-Onset Colorectal Cancer: A Review. JAMA Surg. 2021 Sep;156(9):865–74. 10.1001/jamasurg.2021.2380
- Bhandari A, Woodhouse M, Gupta S. Colorectal cancer is a leading cause of cancer incidence and mortality among adults younger than 50 years in the USA: a SEER-based analysis with comparison to other young-onset cancers. J Investig Med. 2017 Feb;65(2):311–5. 10.1136/jim-2016-000229
DOI: https://doi.org/10.1136/jim-2016-000229
- Siegel RL, Miller KD, Goding Sauer A, Fedewa SA, Butterly LF, Anderson JC, et al. Colorectal cancer statistics, 2020. CA Cancer J Clin. 2020 May;70(3):145–64. 10.3322/caac.21601
DOI: https://doi.org/10.3322/caac.21601
- Araghi M, Soerjomataram I, Bardot A, Ferlay J, Cabasag CJ, Morrison DS, et al. Changes in colorectal cancer incidence in seven high-income countries: a population-based study. Lancet Gastroenterol Hepatol. 2019 Jul;4(7):511–8. 10.1016/S2468-1253(19)30147-5
DOI: https://doi.org/10.1016/S2468-1253(19)30147-5
- Ladabaum U, Mannalithara A, Meester RG, Gupta S, Schoen RE. Cost-Effectiveness and National Effects of Initiating Colorectal Cancer Screening for Average-Risk Persons at Age 45 Years Instead of 50 Years. Gastroenterology. 2019 Jul;157(1):137–48. 10.1053/j.gastro.2019.03.023
DOI: https://doi.org/10.1053/j.gastro.2019.03.023
- Gheysariyeha F, Rahimi F, Tabesh E, Hemami MR, Adibi P, Rezayatmand R. Cost-effectiveness of colorectal cancer screening strategies: A systematic review. Eur J Cancer Care (Engl). 2022 Nov;31(6):e13673. 10.1111/ecc.13673
DOI: https://doi.org/10.1111/ecc.13673
- Cardoso R, Guo F, Heisser T, Hackl M, Ihle P, De Schutter H, et al. Colorectal cancer incidence, mortality, and stage distribution in European countries in the colorectal cancer screening era: an international population-based study. Lancet Oncol. 2021 Jul;22(7):1002–13. 10.1016/S1470-2045(21)00199-6
DOI: https://doi.org/10.1016/S1470-2045(21)00199-6
- Holme Ø, Løberg M, Kalager M, Bretthauer M, Hernán MA, Aas E, et al.; NORCCAP Study Group†. Long-Term Effectiveness of Sigmoidoscopy Screening on Colorectal Cancer Incidence and Mortality in Women and Men: A Randomized Trial. Ann Intern Med. 2018 Jun;168(11):775–82. 10.7326/M17-1441
DOI: https://doi.org/10.7326/M17-1441
- Ko CW, Doria-Rose VP, Barrett MJ, Kamineni A, Enewold L, Weiss NS. Screening flexible sigmoidoscopy versus colonoscopy for reduction of colorectal cancer mortality. Int J Colorectal Dis. 2019 Jul;34(7):1273–81. 10.1007/s00384-019-03300-7
DOI: https://doi.org/10.1007/s00384-019-03300-7
- Cheng TI, Wong JM, Hong CF, Cheng SH, Cheng TJ, Shieh MJ, et al. Colorectal cancer screening in asymptomaic adults: comparison of colonoscopy, sigmoidoscopy and fecal occult blood tests. J Formos Med Assoc. 2002 Oct;101(10):685–90.
- Segnan N, Senore C, Andreoni B, Azzoni A, Bisanti L, Cardelli A, et al.; SCORE3 Working Group-Italy. Comparing attendance and detection rate of colonoscopy with sigmoidoscopy and FIT for colorectal cancer screening. Gastroenterology. 2007 Jun;132(7):2304–12. 10.1053/j.gastro.2007.03.030
DOI: https://doi.org/10.1053/j.gastro.2007.03.030
- Baldacchini F, Bucchi L, Giuliani O, Mancini S, Ravaioli A, Vattiato R, et al.; Emilia-Romagna Region Workgroup for Colorectal Screening Evaluation. Effects of Attendance to an Organized Fecal Immunochemical Test Screening Program on the Risk of Colorectal Cancer: An Observational Cohort Study. Clin Gastroenterol Hepatol. 2022 Oct;20(10):2373–82. 10.1016/j.cgh.2022.01.053
- Shaukat A, Kaalby L, Baatrup G, Kronborg O, Duval S, Shyne M, et al. Effects of Screening Compliance on Long-term Reductions in All-Cause and Colorectal Cancer Mortality. Clin Gastroenterol Hepatol. 2021 May;19(5):967–975.e2. 10.1016/j.cgh.2020.06.019
DOI: https://doi.org/10.1016/j.cgh.2020.06.019
- Buskermolen M, Cenin DR, Helsingen LM, Guyatt G, Vandvik PO, Haug U, et al. Colorectal cancer screening with faecal immunochemical testing, sigmoidoscopy or colonoscopy: a microsimulation modelling study. BMJ. 2019 Oct;367:l5383. 10.1136/bmj.l5383
DOI: https://doi.org/10.1136/bmj.l5383
- Shaukat A, Mongin SJ, Geisser MS, Lederle FA, Bond JH, Mandel JS, et al. Long-term mortality after screening for colorectal cancer. N Engl J Med. 2013 Sep;369(12):1106–14. 10.1056/NEJMoa1300720
DOI: https://doi.org/10.1056/NEJMoa1300720
- Patel SG, May FP, Anderson JC, Burke CA, Dominitz JA, Gross SA, et al. Updates on Age to Start and Stop Colorectal Cancer Screening: Recommendations From the U.S. Multi-Society Task Force on Colorectal Cancer. Gastroenterology. 2022 Jan;162(1):285–99. 10.1053/j.gastro.2021.10.007
DOI: https://doi.org/10.1053/j.gastro.2021.10.007
- Sinicrope FA. Increasing Incidence of Early-Onset Colorectal Cancer. N Engl J Med. 2022 Apr;386(16):1547–58. 10.1056/NEJMra2200869
DOI: https://doi.org/10.1056/NEJMra2200869