Defining resection margins for benign rectal tumors in transanal endoscopic microsurgery

April 17, 2025
171
УДК:  616.351-006.03-089.819-072
Specialities :
Resume

Aim: to enhance the effectiveness of surgical treatment for benign rectal tumors by optimizing transanal endoscopic microsurgery (TEM).

Materials and methods. From 2007 to 2024, a total of 153 patients with benign rectal tumors underwent TEM. The cohort comprised 80 men and 73 women, aged between 37 and 76 years, with a mean age of 58,4±11,7 years. Based on the surgical method, the patients were divided into two groups. The first group included 75 patients who underwent traditional TEM tumor resection. The second group consisted of 78 patients who underwent surgery using an advanced TEM technique. This approach involved preoperative marking of the mucous membrane surrounding the tumor, utilizing endoscopic refinement methods within healthy tissues. The effectiveness of the procedure was assessed through morphological examination of the excised tumors and the analysis of recurrence rates.

Results. In the first group, en-bloc tumor resection was performed on 62 patients (82.6%), while fragmentation resection was conducted on 13 patients (17.4%). Among those who underwent en-bloc resections, R0 (complete resection) was achieved in 59 cases (95.1%), and R1 (incomplete resection) occurred in 3 patients (4.8%). Local recurrence was noted in 11 patients (14.0%). In the second group, en-bloc tumor resection was conducted on 70 patients (89.7%), with fragmentation resection performed on 8 patients (10.3%). For the en-bloc resections in this group, R0 was achieved in 69 cases (98.5%), and R1 was observed in 1 patient (1.5%). Local recurrence was detected in 3 patients (3.8%).

Conclusion. Optimizing TEM for benign rectal tumors, which includes preoperative determination of resection margins, improves treatment efficacy by 73.7% compared to conventional techniques. Additionally, this approach significantly reduces recurrence rates from 14.6% to 3.8%.

References

  • 1. Berger Y., Gingold-Belfer R., Khatib M. et al. (2021) Transanal endoscopic microsurgery under spinal anaesthesia. J. Minimal Access Surg., 17(4): 490–494.
  • 2. Bloomfield I., Van Dalen R., Lolohea S., Wu L. (2018) Transanal endoscopic microsurgery: a New Zealand experience. ANZ J. Surg., 88(6): 592–596.
  • 3. Click B., Pinsky P.F., Hickey T. et al. (2018) Association of Colonoscopy Adenoma Findings With Long-term Colorectal Cancer Incidence. JAMA, 319(19): 2021–2031.
  • 4. Middleton P.F., Sutherland L.M., Maddern G.J. (2005) Transanal endoscopic microsurgery: a systematic review. Diseases of the colon and rectum., 48(2): 270–284.
  • 5. Hakiman H., Pendola M., Fleshman J.W. (2015) Replacing Transanal Excision with Transanal Endoscopic Microsurgery and/or Transanal Minimally Invasive Surgery for Early Rectal Cancer. Clin. Colon Rectal Surg., 28(1): 38–42.
  • 6. Heidary B., Phang T.P., Raval M.J., Brown C.J. (2014) Transanal endoscopic microsurgery: a review. Canadian journal of surgery. J. Can. Chirurg., 57(2): 127–138.
  • 7. Kouladouros K., Baral J. (2022) Transanal endoscopic microsurgical submucosal dissection (TEM-ESD) for rectal adenomas: a retrospective cohort study of 145 consecutive cases. Langenbeck’s archives of surgery, 407(6): 2423–2430.
  • 8. Laurent-Puig P., Agostini J., Maley K. (2010) Colorectal oncogenesis. Bull. Cancer, 97(11): 1311–1321. doi.org/10.1684/bdc.2010.1216.
  • 9. Mohamed B., Aung M., Mohammed A. et al. (2022) Initial Experience With Trans-anal Minimally Invasive Surgery (TAMIS) for Rectal Polyps and Early Colorectal Cancers at Cumberland Infirmary, Carlisle. Cureus., 14(11): e31958.
  • 10. Ortenzi M., Arezzo A., Ghiselli R. et al. (2022) Transanal endoscopic microsurgery after the attempt of endoscopic removal of rectal polyps. Surg. Endoscop., 36(10): 7738–7746. doi.org/10.1007/s00464-022-09162-5.
  • 11. Bains L., Lal P., Vindal A., Singh M. (2019) Giant villous adenoma of rectum- what is the malignant potential and what is the optimal treatment? A case and review of literature. World J. Surg. Oncol., 17(1): 109.
  • 12. Doyle J.B., Krigel A., Lebwohl B. (2022) Prevalence of Adenomas on Surveillance Colonoscopies for Patients with a History of Colonic Polyps of Unknown Histology. Digestive diseases and sciences, 67(7): 3239–3243.
  • 13. Gong Y., Zheng Y., Wu R. et al. (2023) Detection rates of adenomas, advanced adenomas, and colorectal cancers among the opportunistic colonoscopy screening population: a single-center, retrospective study. Chinese Med. J., 136(2): 159–166.
  • 14. Rocha Ramírez J.L., Peña J.P., Franco Gutiérrez J.R. et al. (1996) Colonic adenoma: risk factors for their malignant transformation. Revista de gastroenterologia de Mexico, 61(3): 178–183.
  • 15. Sninsky J.A., Shore B.M., Lupu G.V., Crockett S.D. (2022) Risk Factors for Colorectal Polyps and Cancer. Gastroint. Endoscop. Clin. North Am., 32(2): 195–213.
  • 16. Wang F.G., Jiang Y., Liu C., Qi H. (2023) Comparison between Endoscopic Submucosal Dissection and Transanal Endoscopic Microsurgery in Early Rectal Neuroendocrine Tumor Patients: A Meta-Analysis. J. Invest. Surg., 36(1).
  • 17. Zhang Y., Yu P., Wang P. et al. (2022) Analysis of the therapeutic effect of transanal endoscopic microsurgery on large rectal adenoma. J. Min. Access Surg., 18: 571–577.
  • 18. Feleshtynskyi Y.P., Pyrogovsky V., Lutsenko D. (2024) Method of transanal endoscopic microsurgical excision of benign rectal tumors. Ukrainian National Office of Intellectual Property and Innovation. Certificate of copyright registration No. 132473.
  • 19. Pearce S., Daneshmand S. (2018) Enhanced Endoscopy in Bladder Cancer. Curr. Urol. Rep., 19(10): 84. doi.org/10.1007/s11934-018-0833-9.
  • 20. Ray-Offor E., Abdulkareem F.B., Jebbin N.J. (2022) Pit Pattern Analysis of Colorectal Polyps using Storz Professional Image Enhancement System (SPIES) Endoscopy: A Pilot Study. J. West African Coll. Surg., 12(2): 17–22.
  • 21. Ali S., Khetpal N., Idrisov E. et al. (2021) Endoscopic Mucosal Resection for Colonic Mucosal Neoplasia and Evaluation of Long-Term Recurrence: A Single-Center Experience of 500 Cases. Southern Med. J., 114(4): 199–206.
  • 22. Rubio C.A., Nesi G., Messerini L. et al. (2006) The Vienna classification applied to colorectal adenomas. J. Gastroenterol. Hepatol., 21(11): 1697–1703.
  • 23. World Health Organization (2019) International Classification of Diseases for Oncology. A. Fritz, C. Percy, A. Jacket al. (Eds.).
  • 24. Yadav A., Vallabu S., Kumar D. et al. (2010) HIVAN phenotype: consequence of epithelial mesenchymal transdifferentiation. Am. J. Physiol. Ren. Physiol., 298(3): F734–F744.
  • 25. Kumar V., Abbas A.K., Aster J.C. (2015) Robbins and Cotran pathologic basis of disease. Edited by Vinay Kumar, Abul K. Abbas, Jon C. Aster. Ninth edition: 1379.
  • 26. Rosai J. (2011) Rosai and Ackerman’s Surgical Pathology Seven edition. J. Rosai (Ed.). Elsevier Inc., 2: 25–93.