Endoscopy 2023; 55(06): 526-534
DOI: 10.1055/a-1971-3488
Original article

Advanced serrated polyps as a target of screening: detection rate and positive predictive value within a fecal immunochemical test-based colorectal cancer screening population

David E. F. W. M. van Toledo
 1   Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands
 2   Amsterdam Gastroenterology, Endocrinology & Metabolism, Amsterdam, The Netherlands
 3   Cancer Center Amsterdam, Amsterdam University Medical Centers, Location Academic Medical Center, Amsterdam, The Netherlands
,
Emilie C. H. Breekveldt
 4   Department of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands
 5   Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands
,
Joep E. G. IJspeert
 1   Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands
 2   Amsterdam Gastroenterology, Endocrinology & Metabolism, Amsterdam, The Netherlands
 3   Cancer Center Amsterdam, Amsterdam University Medical Centers, Location Academic Medical Center, Amsterdam, The Netherlands
,
Anneke J. van Vuuren
 6   Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
Folkert J. van Kemenade
 7   Department of Pathology, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
Christian Ramakers
 8   Department of Clinical Chemistry, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
Iris D. Nagtegaal
 9   Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands
,
Monique E. van Leerdam
 5   Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands
10   Department of Gastroenterology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek, Amsterdam, The Netherlands
,
 6   Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
Iris Lansdorp-Vogelaar
 4   Department of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
Esther Toes-Zoutendijk
 4   Department of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands
,
 1   Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands
 2   Amsterdam Gastroenterology, Endocrinology & Metabolism, Amsterdam, The Netherlands
 3   Cancer Center Amsterdam, Amsterdam University Medical Centers, Location Academic Medical Center, Amsterdam, The Netherlands
› Author Affiliations
This analysis has been carried out as part of the national monitoring and evaluation of the CRC screening program, funded by the National Institute for Public Health and the Environment (RIVM). The funder was not involved in the study design, data analysis or writing of the manuscript.


Abstract

Background Advanced serrated polyps (ASPs) have a comparable risk to advanced adenomas for progression to colorectal cancer (CRC). The yield of most CRC screening programs, however, is based on advanced adenomas and CRC only. We assessed the ASP detection rate, and positive predictive value (PPV) including ASPs in a fecal immunochemical test (FIT)-based screening program.

Methods We analyzed the findings of follow-up colonoscopies of FIT-positive screenees in the Dutch CRC screening program from 2014 until 2020. Data were retrieved from the national screening and pathology database. An ASP was defined as any serrated polyp of ≥ 10 mm, sessile serrated lesion with dysplasia, or traditional serrated adenoma. The ASP detection rate was defined as the proportion of colonoscopies with ≥ 1 ASP. PPV was originally defined as the proportion of individuals with a CRC or advanced adenoma. The updated PPV definition included CRCs, advanced adenomas, and/or ASPs.

Results 322 882 colonoscopies were included in the analyses. The overall detection rate of ASPs was 5.9 %. ASPs were detected more often in women than men (6.3 % vs. 5.6 %; P < 0.001). ASP detection rates in individuals aged 55–59, 60–64, 65–69, and 70 + were 5.2 %, 6.1 %, 6.1 %, and 5.9 %, respectively (P < 0.001). The PPV for CRCs and advanced adenomas was 41.1 % and increased to 43.8 % when including ASPs. The PPV increase was larger in women than in men (3.2 vs. 2.4 percentage points).

Conclusions 5.9 % of FIT-positive screenees had ASPs, but half of these were detected in combination with a CRC or advanced adenoma. Therefore, including ASPs results in a small increase in the yield of FIT-based screening.



Publication History

Received: 04 July 2022

Accepted after revision: 02 November 2022

Accepted Manuscript online:
02 November 2022

Article published online:
12 January 2023

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71: 209-249
  • 2 van Toledo D, IJspeert JEG, Dekker E. Current approaches in managing colonic serrated polyps and serrated polyposis. Annu Rev Med 2022; 73: 293-306
  • 3 Schreiner MA, Weiss DG, Lieberman DA. Proximal and large hyperplastic and nondysplastic serrated polyps detected by colonoscopy are associated with neoplasia. Gastroenterology 2010; 139: 1497-1502
  • 4 Lu FI, van Niekerk deW, Owen D. et al. Longitudinal outcome study of sessile serrated adenomas of the colorectum: an increased risk for subsequent right-sided colorectal carcinoma. Am J Surg Pathol 2010; 34: 927-934
  • 5 Janjua HG, Høgdall E, Linnemann D. Hyperplastic polyps of the colon and rectum - reclassification, BRAF and KRAS status in index polyps and subsequent colorectal carcinoma. APMIS 2015; 123: 298-304
  • 6 Erichsen R, Baron JA, Hamilton-Dutoit SJ. et al. Increased risk of colorectal cancer development among patients with serrated polyps. Gastroenterology 2016; 150: 895-902.e895
  • 7 Holme Ø, Bretthauer M, Eide TJ. et al. Long-term risk of colorectal cancer in individuals with serrated polyps. Gut 2015; 64: 929-936
  • 8 He X, Hang D, Wu K. et al. Long-term risk of colorectal cancer after removal of conventional adenomas and serrated polyps. Gastroenterology 2020; 158: 852-861.e854
  • 9 Imperiale TF, Ransohoff DF, Itzkowitz SH. et al. Multitarget stool DNA testing for colorectal-cancer screening. NEJM 2014; 370: 1287-1297
  • 10 Chang LC, Shun CT, Hsu WF. et al. Fecal immunochemical test detects sessile serrated adenomas and polyps with a low level of sensitivity. Clin Gastroenterol Hepatol 2017; 15: 872-879.e871
  • 11 Redwood DG, Asay ED, Blake ID. et al. Stool DNA testing for screening detection of colorectal neoplasia in Alaska Native People. Mayo Clin Proc 2016; 91: 61-70
  • 12 Toes-Zoutendijk E, van Leerdam ME, Dekker E. et al. Real-time monitoring of results during first year of Dutch Colorectal Cancer Screening Program and optimization by altering fecal immunochemical test cut-off levels. Gastroenterology 2017; 152: 767-775.e762
  • 13 Bronzwaer MES, Depla A, van Lelyveld N. et al. Quality assurance of colonoscopy within the Dutch national colorectal cancer screening program. Gastrointest Endosc 2019; 89: 1-13
  • 14 IJspeert JE, Madani A, Overbeek LI. et al. Implementation of an e-learning module improves consistency in the histopathological diagnosis of sessile serrated lesions within a nationwide population screening programme. Histopathology 2017; 70: 929-937
  • 15 Clark BT, Laine L. High-quality bowel preparation is required for detection of sessile serrated polyps. Clin Gastroenterol Hepatol 2016; 14: 1155-1162
  • 16 Zorzi M, Senore C, Da Re F. et al. Detection rate and predictive factors of sessile serrated polyps in an organised colorectal cancer screening programme with immunochemical faecal occult blood test: the EQuIPE study (Evaluating Quality Indicators of the Performance of Endoscopy). Gut 2017; 66: 1233-1240
  • 17 Casparie M, Tiebosch AT, Burger G. et al. Pathology databanking and biobanking in The Netherlands, a central role for PALGA, the nationwide histopathology and cytopathology data network and archive. Cell Oncol 2007; 29: 19-24
  • 18 Lieberman DA, Rex DK, Winawer SJ. et al. Guidelines for colonoscopy surveillance after screening and polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2012; 143: 844-857
  • 19 Hassan C, Antonelli G, Dumonceau JM. et al. Post-polypectomy colonoscopy surveillance: European Society of Gastrointestinal Endoscopy (ESGE) Guideline – Update 2020. Endoscopy 2020; 52: 687-700
  • 20 Kahi CJ, Vemulapalli KC, Snover DC. et al. Findings in the distal colorectum are not associated with proximal advanced serrated lesions. Clin Gastroenterol Hepatol 2015; 13: 345-351
  • 21 IJspeert JEG, Bevan R, Senore C. et al. Detection rate of serrated polyps and serrated polyposis syndrome in colorectal cancer screening cohorts: a European overview. Gut 2017; 66: 1225-1232
  • 22 Hetzel JT, Huang CS, Coukos JA. et al. Variation in the detection of serrated polyps in an average risk colorectal cancer screening cohort. Am J Gastroenterol 2010; 105: 2656-2664
  • 23 Abdeljawad K, Vemulapalli KC, Kahi CJ. et al. Sessile serrated polyp prevalence determined by a colonoscopist with a high lesion detection rate and an experienced pathologist. Gastrointest Endosc 2015; 81: 517-524
  • 24 Lansdorp-Vogelaar I, Goede SL, Bosch LJW. et al. Cost-effectiveness of high-performance biomarker tests vs. fecal immunochemical test for noninvasive colorectal cancer screening. Clin Gastroenterol Hepatol 2018; 16: 504-512.e511
  • 25 Rasmussen SL, Krarup HB, Sunesen KG. et al. Hypermethylated DNA as a biomarker for colorectal cancer: a systematic review. Colorectal Dis 2016; 18: 549-561
  • 26 Phipps AI, Limburg PJ, Baron JA. et al. Association between molecular subtypes of colorectal cancer and patient survival. Gastroenterology 2015; 148: 77-87.e72
  • 27 Sinicrope FA, Shi Q, Smyrk TC. et al. Molecular markers identify subtypes of stage III colon cancer associated with patient outcomes. Gastroenterology 2015; 148: 88-99
  • 28 Bettington M, Walker N, Rosty C. et al. Clinicopathological and molecular features of sessile serrated adenomas with dysplasia or carcinoma. Gut 2017; 66: 97-106
  • 29 Bleijenberg AGC, JEG IJ, Mulder JBG. et al. The earliest events in BRAF-mutant colorectal cancer: exome sequencing of sessile serrated lesions with a tiny focus dysplasia or cancer reveals recurring mutations in two distinct progression pathways. J Pathol 2022; 257: 239-249
  • 30 Regula J, Rupinski M, Kraszewska E. et al. Colonoscopy in colorectal-cancer screening for detection of advanced neoplasia. NEJM 2006; 355: 1863-1872
  • 31 Brenner H, Haug U, Hundt S. Sex differences in performance of fecal occult blood testing. Am J Gastroenterol 2010; 105: 2457-2464
  • 32 Kapidzic A, van der Meulen MP, Hol L. et al. Gender differences in fecal immunochemical test performance for early detection of colorectal neoplasia. Clin Gastroenterol Hepatol 2015; 13: 1464-1471.e1464
  • 33 van Toledo DEFWM, IJspeert JEG, Bossuyt PMM. et al. Serrated polyp detection and risk of interval post-colonoscopy colorectal cancer: a population-based study. Lancet Gastroenterol Hepatol 2022; 7: 747-754
  • 34 Cock C, Anwar S, Byrne SE. et al. Low sensitivity of fecal immunochemical tests and blood-based markers of DNA hypermethylation for detection of sessile serrated adenomas/polyps. Dig Dis Sci 2019; 64: 2555-2562