CC BY-NC-ND 4.0 · Endosc Int Open 2021; 09(10): E1472-E1479
DOI: 10.1055/a-1518-6754
Original article

Clinical and endoscopic characteristics of post-colonoscopy colorectal cancers detected within 10 years after a previous negative examination[*]

Kenta Kodama
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
2   Division of Gastroenterology, Japanese Red Cross Society Fukushima Hospital, Fukushima, Japan
,
Shin-ei Kudo
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Hideyuki Miyachi
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Kunihiko Wakamura
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yasuharu Maeda
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Katsuro Ichimasa
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yushi Ogawa
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yuta Kouyama
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Masahiro Abe
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yohei Ogura
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Taishi Okumura
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Kenichi Mochizuki
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yosuke Minegishi
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Misaki Ishiyama
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Yuichi Mori
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Masashi Misawa
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Toyoki Kudo
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Takemasa Hayashi
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Fumio Ishida
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
Daisuke Watanabe
3   Division of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan
4   Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States
› Author Affiliations

Abstract

Background and study aims We sometimes encounter colorectal cancer (CRC) that is discovered during the time interval between initial colonoscopy and the recommended follow-up examination. Although several studies reported such cases of CRC, most were based on registry data, which implied that the endoscopic quality was not consistent or guaranteed. We aimed to clarify these clinical and endoscopic characteristics at our high-volume center where a retrospective survey could be precisely performed.

Patients and methods We retrospectively analyzed patients with CRC who underwent endoscopic resection or surgery from April 2002 to December 2010, categorizing them into two groups: a “study group” of patients with a negative colonoscopy during the previous 10 years, and a “control group” of patients without a previous colonoscopy or with a previous colonoscopy more than 10 years prior.

Results A total of 2042 patients had CRC, among which 55 patients were classified into the study group and the remaining 1989 into the control group. The CRC cases in the study group showed a significant association with smaller (< 30 mm) tumor size (odds ratio [OR] 2.3; 95 % confidence interval [CI] 1.3–4.0) and proximal tumor site (OR 1.7; 95 %CI 0.9–2.9). In addition, right-sided and depressed-type T1 CRCs were significantly more common in the study group.

Conclusions Tumor size and location were associated with CRCs detected within 10 years after the negative examination. In addition, depressed-type T1 CRCs were more common. Therefore, we should pay more attention to small, right-sided, or depressed-type tumors in daily colonoscopy.

* Meeting presentations: Part of the present study was presented at the United European Gastroenterology Week 2013, Berlin, Germany, 16th October 2013 (poster presentation).




Publication History

Received: 29 June 2020

Accepted: 01 February 2021

Article published online:
16 September 2021

© 2021. The Author (s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Katanoda K, Hori M, Matsuda T. et al. An updated report on the trends in cancer incidence and mortality in Japan, 1958–2013. Jpn J Clin Oncol 2015; 45: 390-401
  • 2 Fearon ER, Vogelstein B. A genetic model for colorectal tumorigenesis. Cell 1990; 61: 759-767
  • 3 Winawer S, Fletcher R, Rex D. et al. Colorectal cancer screening and surveillance: clinical guidelines and rationale-Update based on new evidence. Gastroenterology 2003; 124: 544-560
  • 4 Zauber AG, Winawer SJ, OʼBrien MJ. et al. Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med 2012; 366: 687-696
  • 5 Rutter MD, Beintaris I, Valori R. et al. World Endoscopy Organization Consensus Statements on Post-Colonoscopy and Post-Imaging Colorectal Cancer. Gastroenterology 2018; 155: 909-925.e903
  • 6 Samadder NJ, Curtin K, Tuohy TM. et al. Characteristics of missed or interval colorectal cancer and patient survival: a population-based study. Gastroenterology 2014; 146: 950-960
  • 7 Robertson DJ, Lieberman DA, Winawer SJ. et al. Colorectal cancers soon after colonoscopy: a pooled multicohort analysis. Gut 2014; 63: 949-956
  • 8 Baxter NN, Sutradhar R, Forbes SS. et al. Analysis of administrative data finds endoscopist quality measures associated with postcolonoscopy colorectal cancer. Gastroenterology 2011; 140: 65-72
  • 9 Lakoff J, Paszat LF, Saskin R. et al. Risk of developing proximal versus distal colorectal cancer after a negative colonoscopy: a population-based study. Clin Gastroenterol Hepatol 2008; 6: 1117-1121 quiz 1064
  • 10 Singh H, Nugent Z, Mahmud SM. et al. Predictors of colorectal cancer after negative colonoscopy: a population-based study. Am J Gastroenterol 2010; 105: 663-673 quiz 674
  • 11 Rex DK, Johnson DA, Anderson JC. et al. American College of Gastroenterology guidelines for colorectal cancer screening 2009 [corrected]. Am J Gastroenterol 2009; 104: 739-750
  • 12 Miyachi H, Kudo SE, Ichimasa K. et al. Management of T1 colorectal cancers after endoscopic treatment based on the risk stratification of lymph node metastasis. J Gastroenterol Hepatol 2016; 31: 1126-1132
  • 13 Kudo S, Lambert R, Allen JI. et al. Nonpolypoid neoplastic lesions of the colorectal mucosa. Gastrointest Endosc 2008; 68: S3-47
  • 14 Kudo S, Tamura S, Hirota S. et al. The problem of de novo colorectal carcinoma. European journal of cancer 1995; 31A: 1118-1120
  • 15 Kudo SE, Sugihara Y, Kida H. et al. Depressed-Type Colonic Lesions and "De Novo" Cancer in Familial Adenomatous Polyposis: A Colonoscopist's Viewpoint. ISRN gastroenterology 2013; 2013: 838134
  • 16 Kudo S, Tamura S, Nakajima T. et al. Diagnosis of colorectal tumorous lesions by magnifying endoscopy. Gastrointest Endosc 1996; 44: 8-14
  • 17 Sanduleanu S, le Clercq CM, Dekker E. et al. Definition and taxonomy of interval colorectal cancers: a proposal for standardising nomenclature. Gut 2015; 64: 1257-1267
  • 18 Imperiale TF, Glowinski EA, Lin-Cooper C. et al. Five-year risk of colorectal neoplasia after negative screening colonoscopy. N Engl J Med 2008; 359: 1218-1224
  • 19 Cooper GS, Xu F, Barnholtz Sloan JS. et al. Prevalence and predictors of interval colorectal cancers in medicare beneficiaries. Cancer 2012; 118: 3044-3052
  • 20 le Clercq CM, Bouwens MW, Rondagh EJ. et al. Postcolonoscopy colorectal cancers are preventable: a population-based study. Gut 2014; 63: 957-963
  • 21 Singh S, Singh PP, Murad MH. et al. Prevalence, risk factors, and outcomes of interval colorectal cancers: a systematic review and meta-analysis. Am J Gastroenterol 2014; 109: 1375-1389
  • 22 Kaminski MF, Regula J, Kraszewska E. et al. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med 2010; 362: 1795-1803
  • 23 Dekker E, Sanduleanu S. Colorectal cancer: Strategies to minimize interval CRC in screening programmes. Nat Rev Gastroenterol Hepatol 2016; 13: 10-12
  • 24 Moss S, Ancelle-Park R, Brenner H. European guidelines for quality assurance in colorectal cancer screening and diagnosis. First Edition--Evaluation and interpretation of screening outcomes. Endoscopy 2012; 44 (Suppl. 03) Se49-64
  • 25 Brenner H, Chang-Claude J, Seiler CM. et al. Interval cancers after negative colonoscopy: population-based case-control study. Gut 2012; 61: 1576-1582
  • 26 Richter JM, Campbell EJ, Chung DC. Interval colorectal cancer after colonoscopy. Clin Colorectal Cancer 2015; 14: 46-51
  • 27 Hasegawa S, Mitsuyama K, Kawano H. et al. Endoscopic discrimination of sessile serrated adenomas from other serrated lesions. Oncol Lett 2011; 2: 785-789
  • 28 Kashida H, Ikehara N, Hamatani S. et al. Endoscopic characteristics of colorectal serrated lesions. Hepatogastroenterology 2011; 58: 1163-1167
  • 29 Snover DC. Update on the serrated pathway to colorectal carcinoma. Hum Pathol 2011; 42: 1-10
  • 30 Arain MA, Sawhney M, Sheikh S. et al. CIMP status of interval colon cancers: another piece to the puzzle. Am J Gastroenterol 2010; 105: 1189-1195
  • 31 Rondagh EJ, Bouwens MW, Riedl RG. et al. Endoscopic appearance of proximal colorectal neoplasms and potential implications for colonoscopy in cancer prevention. Gastrointest Endosc 2012; 75: 1218-1225
  • 32 Farrar WD, Sawhney MS, Nelson DB. et al. Colorectal cancers found after a complete colonoscopy. Clin Gastroenterol Hepatol 2006; 4: 1259-1264
  • 33 Haug U, Regula J. Interval cancer: nightmare of colonoscopists. Gut 2014; 63: 865-866
  • 34 le Clercq CM, Winkens B, Bakker CM. et al. Metachronous colorectal cancers result from missed lesions and non-compliance with surveillance. Gastrointest Endosc 2015; 82: 325-333.e322
  • 35 Church JM, Muto T, Appau K. Flat lesions of the colorectal mucosa: differences in recognition between Japanese and American endoscopists. Diseases of the colon and rectum 2004; 47: 1462-1466
  • 36 Soetikno RM, Kaltenbach T, Rouse RV. et al. Prevalence of nonpolypoid (flat and depressed) colorectal neoplasms in asymptomatic and symptomatic adults. Jama 2008; 299: 1027-1035
  • 37 Voorham QJ, Carvalho B, Spiertz AJ. et al. Chromosome 5q loss in colorectal flat adenomas. Clin Cancer Res 2012; 18: 4560-4569
  • 38 Rutter MD, Beintaris I, Valori R. et al. World Endoscopy Organization Consensus Statements on Post-Colonoscopy and Post-Imaging Colorectal Cancer. Gastroenterology 2018; 155: 909-925