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The necessity of intensive surveillance colonoscopy for patients with a remaining right colon after resection of colorectal cancer: a retrospective cohort study

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Abstract

Purpose

To clarify how often postoperative surveillance colonoscopy should be undertaken based on the risk factors for the development of metachronous cancer (MC) and advanced adenoma (AA) after surgery for colorectal cancer.

Methods

We collected data of consecutive patients who underwent curative resection for primary colorectal cancer between 2005 and 2012, with preoperative colonoscopy and surveillance colonoscopy at 1 year after surgery (406 patients, mean age: 69 years, 59% male). The detection rates of AA (with villous features, > 10 mm or high-grade dysplasia) and MC by surveillance colonoscopy were the primary outcomes.

Results

At 5 years, colonoscopy was performed as postoperative surveillance an average of 3.2 times. AA and MC were detected in 57 (14.0%) and 18 patients (4.4%), respectively. Both lesions were more common in the right colon (n = 43) than in the left colon (n = 28). The detection rate did not differ to a statistically significant extent according to the number of colonoscopies performed for surveillance (p = 0.21). However, after left-sided colectomy, both types of lesions were more commonly detected in those who received ≥ 3 colonoscopies than in those with one or two colonoscopies (p = 0.04).

Conclusion

A remaining right colon after left-sided colectomy was associated with a higher risk of develo** AA and MC. Physicians should consider performing surveillance colonoscopy more frequently if the right colon remains after surgery.

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References

  1. Togashi K, Konishi F, Ozawa A, Sato T, Shito K, Kashiwagi H, et al. Predictive factors for detecting colorectal carcinomas in surveillance colonoscopy after colorectal cancer surgery. Dis Colon Rectum. 2000;43:S47–53.

    Article  CAS  Google Scholar 

  2. Tjandra JJ, Chan MK. Follow-up after curative resection of colorectal cancer: a meta-analysis. Dis Colon Rectum. 2007;50:1783–99.

    Article  Google Scholar 

  3. Rodriguez-Moranta F, Salo J, Arcusa A, Boadas J, Piñol V, Bessa X, et al. Postoperative surveillance in patients with colorectal cancer who have undergone curative resection: a prospective, multicenter, randomized, controlled trial. J Clin Oncol. 2006;24:386–93.

    Article  Google Scholar 

  4. Pita-Fernandez S, Alhayek-Ai M, Gonzalez-Martin C, López-Calviño B, Seoane-Pillado T, Pértega-Díaz S. Intensive follow-up strategies improve outcomes in nonmetastatic colorectal cancer patients after curative surgery: a systematic review and meta-analysis. Ann Oncol. 2015;26:644–56.

    Article  CAS  Google Scholar 

  5. Kjeldsen BJ, Kronborg O, Fenger C, Jørgensen OD. The pattern of recurrent colorectal cancer in a prospective randomised study and the characteristics of diagnostic tests. Int J Colorectal Dis. 1997;12:329–34.

    Article  CAS  Google Scholar 

  6. Green RJ, Metlay JP, Propert K, Catalano PJ, Macdonald JS, Mayer RJ, et al. Surveillance for second primary colorectal cancer after adjuvant chemotherapy: an analysis of Intergroup 0089. Ann Intern Med. 2002;136:261–9.

    Article  CAS  Google Scholar 

  7. Kahi CJ, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, Kaltenbach T, et al. Colonoscopy surveillance after colorectal cancer resection: recommendations of the US multi-society task force on colorectal cancer. Gastroenterology. 2016;150:758-768.e711.

    Article  Google Scholar 

  8. Glynne-Jones R, Wyrwicz L, Tiret E, Brown G, Rödel C, Cervantes A, et al. Rectal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018;29:iv263.

    Article  CAS  Google Scholar 

  9. Labianca R, Nordlinger B, Beretta GD, Mosconi S, Mandalà M, Cervantes A, et al. Early colon cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2013;24:vi64-72 (Suppl 6).

    Article  Google Scholar 

  10. Hashiguchi Y, Muro K, Saito Y, Ito Y, Ajioka Y, Hamaguchi T, et al. Japanese society for cancer of the colon and rectum (JSCCR) guidelines 2019 for the treatment of colorectal cancer. Int J Clin Oncol. 2020;25:1–42.

    Article  Google Scholar 

  11. Meyerhardt JA, Mangu PB, Flynn PJ, Korde L, Loprinzi CL, Minsky BD, et al. Follow-up care, surveillance protocol, and secondary prevention measures for survivors of colorectal cancer: American society of clinical oncology clinical practice guideline endorsement. J Clin Oncol. 2013;31:4465–70.

    Article  Google Scholar 

  12. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®). Colon Cancer. Version 2. 2020.

  13. Winawer SJ, Zauber AG. The advanced adenoma as the primary target of screening. Gastrointest Endosc Clin N Am. 2002;12:1–9.

    Article  Google Scholar 

  14. Winawer SJ, Zauber AG, Fletcher RH, Stillman JS, O’Brien MJ, Levin B, et al. Guidelines for colonoscopy surveillance after polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer and the American Cancer Society. Gastroenterology. 2006;130:1872–85.

    Article  Google Scholar 

  15. Winawer SJ, Zauber AG, O’Brien MJ, Ho MN, Gottlieb L, Sternberg SS, The National Polyp Study Workgroup, et al. Randomized comparison of surveillance intervals after colonoscopic removal of newly diagnosed adenomatous polyps. N Engl J Med. 1993;328:901–6.

    Article  CAS  Google Scholar 

  16. Sano Y, Fujii T, Matsuda T, Oda Y, Kudo S, Igarashi M, et al. Study design and patient recruitment for the Japan Polyp Study. Open Access J Clin Trials. 2014;6:37–44.

    Article  Google Scholar 

  17. Singh S, Singh PP, Murad MH, Singh H, Samadder NJ. Prevalence, risk factors, and outcomes of interval colorectal cancers: a systematic review and meta-analysis. Am J Gastroenterol. 2014;109:1375–89.

    Article  Google Scholar 

  18. Samadder NJ, Curtin K, Tuohy TM, Pappas L, Boucher K, Provenzale D, et al. Characteristics of missed or interval colorectal cancer and patient survival: a population-based study. Gastroenterology. 2014;146:950–60.

    Article  Google Scholar 

  19. Spratt JS Jr, Ackerman LV, Moyer CA. Relationship of polyps of the colon to colonic cancer. Ann Surg. 1958;148:682–96 (discussion 696-688).

    Article  Google Scholar 

  20. Sadahiro S, Ohmura T, Saito T, Suzuki S. Relationship between length and surface area of each segment of the large intestine and the incidence of colorectal cancer. Cancer. 1991;68:84–7.

    Article  CAS  Google Scholar 

  21. Matsuda T, Fujii T, Sano Y, Kudo SE, Oda Y, Kaneko K, et al. Randomized comparison of surveillance intervals after colonoscopic removal of adenomatous polyps: results from the Japan Polyp Study. Gastroenterology. 2014;146:S161–2.

    Article  Google Scholar 

  22. Thomas-Gibson S, Rogers P, Cooper S, Man R, Rutter MD, Suzuki N, et al. Judgement of the quality of bowel preparation at screening flexible sigmoidoscopy is associated with variability in adenoma detection rates. Endoscopy. 2006;38:456–60.

    Article  CAS  Google Scholar 

  23. Chandran S, Parker F, Vaughan R, Mitchell B, Fanning S, Brown G, et al. Right-sided adenoma detection with retroflexion versus forward-view colonoscopy. Gastrointest Endosc. 2015;81:608–13.

    Article  Google Scholar 

  24. Chokshi RV, Hovis CE, Hollander T, Early DS, Wang JS. Prevalence of missed adenomas in patients with inadequate bowel preparation on screening colonoscopy. Gastrointest Endosc. 2012;75:1197–203.

    Article  Google Scholar 

  25. Hong SN, Sung IK, Kim JH, Choe WH, Kim BK, Ko SY, et al. The Effect of the bowel preparation status on the risk of missing polyp and adenoma during screening colonoscopy: a tandem colonoscopic study. Clin Endosc. 2012;45:404–11.

    Article  Google Scholar 

  26. Rondagh EJ, Bouwens MW, Riedl RG, Winkens B, de Ridder R, Kaltenbach T, et al. Endoscopic appearance of proximal colorectal neoplasms and potential implications for colonoscopy in cancer prevention. Gastrointest Endosc. 2012;75:1218–25.

    Article  Google Scholar 

  27. Heresbach D, Barrioz T, Lapalus MG, Coumaros D, Bauret P, Potier P, et al. Miss rate for colorectal neoplastic polyps: a prospective multicenter study of back-to-back video colonoscopies. Endoscopy. 2008;40:284–90.

    Article  CAS  Google Scholar 

  28. Payne SR, Church TR, Wandell M, Rösch T, Osborn N, Snover D, et al. Endoscopic detection of proximal serrated lesions and pathologic identification of sessile serrated adenomas/polyps vary on the basis of center. Clin Gastroenterol Hepatol. 2014;12:1119–26.

    Article  Google Scholar 

  29. Kahi CJ, Hewett DG, Norton DL, Eckert GJ, Rex DK. Prevalence and variable detection of proximal colon serrated polyps during screening colonoscopy. Clin Gastroenterol Hepatol. 2011;9:42–6.

    Article  Google Scholar 

  30. Guinney J, Dienstmann R, Wang X, de Reyniès A, Schlicker A, Soneson C, et al. The consensus molecular subtypes of colorectal cancer. Nat Med. 2015;21:1350–6.

    Article  CAS  Google Scholar 

  31. Minamoto T, Sawaguchi K, Ohta T, Itoh T, Mai M. Superficial-type adenomas and adenocarcinomas of the colon and rectum: a comparative morphological study. Gastroenterology. 1994;106:1436–43.

    Article  CAS  Google Scholar 

  32. Sakashita M, Aoyama N, Maekawa S, Kuroda K, Shirasaka D, Ichihara T, et al. Flat-elevated and depressed, subtypes of flat early colorectal cancers, should be distinguished by their pathological features. Int J Colorectal Dis. 2000;15:275–81.

    Article  CAS  Google Scholar 

  33. Torlakovic E, Skovlund E, Snover DC, Torlakovic G, Nesland JM. Morphologic reappraisal of serrated colorectal polyps. Am J Surg Pathol. 2003;27:65–81.

    Article  Google Scholar 

  34. Bosman F, Carneiro F, Hruban R, et al. WHO classification of tumours of the digestive system. Lyon (France): IARC Press; 2010.

  35. Kambara T, Simms LA, Whitehall VL, Spring KJ, Wynter CV, Walsh MD, et al. BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum. Gut. 2004;53:1137–44.

    Article  CAS  Google Scholar 

  36. O’Brien MJ, Yang S, Mack C, Xu H, Huang CS, Mulcahy E, et al. Comparison of microsatellite instability, CpG island methylation phenotype, BRAF and KRAS status in serrated polyps and traditional adenomas indicates separate pathways to distinct colorectal carcinoma end points. Am J Surg Pathol. 2006;30:1491–501.

    Article  Google Scholar 

  37. Murakami T, Mitomi H, Yao T, Saito T, Shibuya T, Sakamoto N, et al. Distinct histopathological characteristics in colorectal submucosal invasive carcinoma arising in sessile serrated adenoma/polyp and conventional tubular adenoma. Virchows Arch. 2018;472:383–93.

    Article  Google Scholar 

  38. Snover DC. Update on the serrated pathway to colorectal carcinoma. Hum Pathol. 2010;42:1–10.

    Article  Google Scholar 

  39. Rastogi A, Bansal A, Wani S, Callahan P, McGregor DH, Cherian R, et al. Narrow-band imaging colonoscopy—a pilot feasibility study for the detection of polyps and correlation of surface patterns with polyp histologic diagnosis. Gastrointest Endosc. 2008;67:280–6.

    Article  Google Scholar 

  40. Inoue T, Murano M, Murano N, Kuramoto T, Kawakami K, Abe Y, et al. Comparative study of conventional colonoscopy and pan-colonic narrow-band imaging system in the detection of neoplastic colonic polyps: a randomized, controlled trial. J Gastroenterol. 2008;43:45–50.

    Article  Google Scholar 

  41. ** XF, Chai TH, Shi JW, Yang XC, Sun QY. Meta-analysis for evaluating the accuracy of endoscopy with narrow band imaging in detecting colorectal adenomas. J Gastroenterol Hepatol. 2012;27:882–7.

    Article  Google Scholar 

  42. Nakamura H, Ikematsu H, Osera S, Ito R, Sato D, Minamide T, et al. Visual assessment of colorectal flat and depressed lesions by using narrow band imaging. Endosc Int Open. 2017;05:E1284–8.

    Article  Google Scholar 

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Correspondence to Mitsuru Yokota.

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Mitsuru Yokota and other co-authors declare no conflicts of interest in association with the present study.

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Yokota, M., Muto, J., Hashida, K. et al. The necessity of intensive surveillance colonoscopy for patients with a remaining right colon after resection of colorectal cancer: a retrospective cohort study. Surg Today 52, 502–509 (2022). https://doi.org/10.1007/s00595-021-02372-9

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