Quality assessment of rectal cancer surgery: how are we doing?

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Nabil Haloui
Mohamed Mehdi Trabelsi
Mehdi Khalfallah
Annouar Oueslati
Ibtissem Bouasker
Ramzi Nouira

Abstract

Introduction: Surgery remains a cornerstone in the treatment of rectal cancer. Optimal surgical resection implies respect for carcinologic principles. The best way to evaluate a good quality of resection requires certainly an exhaustive evaluation of the surgical specimen by the surgeon and the pathologist.


Aim: To assess the quality of resected rectal cancers.


Methods: This study included patients operated on for rectal malignant epithelial tumors, between January 1st, 2015 and December 31st, 2020, in the general surgery department B at Charles Nicolle’s Hospital in Tunis. Data relevant to the pathologic examination were recorded. We performed a descriptive study and an analytic bivariate study comparing the two groups "number of lymph nodes harvested less than 12" versus "number of lymph nodes harvested higher than or equal to 12".


Results: Neoadjuvant therapy was performed in 39 patients (79%). Anterior resection (AR) was performed in 43 patients (43%) and abdominoperineal resection (APR) was performed in 11 patients (20%). There were no invaded margins. The mean distal surgical margin was 3±1.4 cm. Mesorectum was complete in 38 surgical specimens (70%). The median number of lymph nodes harvested was 14. Resection was considered R0 in 47 patients (87%). In bivariate analysis, there was no difference between the "number of harvested lymph nodes <12" and the "number of harvested lymph nodes ≥ 12" groups for the variables: laparotomy, laparoscopic approach, conversion to laparotomy and chemoradiotherapy


Conclusion: Quality of surgical resection of rectal cancer in our department was in accordance with recommendations.

Keywords:

rectal neoplasms, surgery, proctectomy, pathology, quality improvement, lymph node excision, chemoradiotherapy

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References

  1. Demir A, Alan O, Oruc E. Tumor budding for predicting prognosis of resected rectum
  2. cancer after neoadjuvant treatment. World journal of surgical oncology 2019;14;17(1):50.
  3. Bridoux V, de Chaisemartin C, Beyer L, et al. Recommandations pour la pratique clinique.
  4. Cancer du rectum 2016;10(1):12-27
  5. Bozzetti F, Andreola S, Bertario L. Pathological features of rectal cancer after preoperative
  6. radiochemotherapy. International journal of colorectal disease 1998;13(1):54-5.
  7. Heald RJ. A new approach to rectal cancer. British journal of hospital medicine
  8. ;22(3):277-81.
  9. Heald RJ, Ryall RD. Recurrence and survival after total mesorectal excision for rectal
  10. cancer. Lancet (London, England) 1986;1(8496):1479-82.
  11. Institut national du cancer. Mise à jour 2011 des comptes rendus d’anatomopathologie :
  12. données minimales à renseigner pour une tumeur primitive, traitements, soins et innovations.
  13. Kirkham N, Lemoine NR. The pathologist, the surgeon and colorectal cancer: get it right
  14. because it matters. Progress in Pathology 1998;201–213.
  15. Brierley J, Gospodarowicz MK, Wittekind C. TNM classification des tumeurs malignes
  16. huitième édition Cassini 2017.
  17. Mandard AM, Dalibard F, Mandard JC, et al. Pathologic assessment of tumor regression
  18. after preoperative chemoradiotherapy of esophageal carcinoma, Clinicopathologic
  19. correlations. Cancer 1994;1;73(11):2680-6.
  20. Jackson C, Sharples K, Firth M, et al. The PIPER Project: An Internal Examination of
  21. Colorectal Cancer Management in New Zealand 2015.
  22. Keane C, Lin AY, Kramer N, Bissett I. Can pathological reports of rectal cancer provide
  23. national quality indicators? ANZ journal of surgery. 2018;88(9):E639-E43.
  24. Frederick L, DAVID L, Irvin D, et al AJCC CANCER STAGING MANUAL sixth Edition
  25. Ha YH, Jeong SY, Lim SB, et al. Influence of preoperative chemoradiotherapy on the
  26. number of lymph nodes retrieved in rectal cancer. Annals of surgery 2010;252(2):336-40.
  27. Baxter NN, Virnig DJ, Rothenberger DA, Morris AM, Jessurun J, Virnig BA. Lymph node
  28. evaluation in colorectal cancer patients: a population-based study. Journal of the National Cancer Institute 2005;97(3):219-25.
  29. da Costa DW, van Dekken H, Witte BI, van Wagensveld BA, van Tets WF, Vrouenraets BC. Lymph Node Yield in Colon Cancer: Individuals Can Make the Difference.
  30. Digestive surgery 2015;32(4):269-74.
  31. Morris EJ, Maughan NJ, Forman D, Quirke P. Identifying stage III colorectal cancer patients: the influence of the patient, surgeon, and pathologist. Journal of clinical oncology 2007;25(18):2573-9.
  32. Mechera R, Schuster T, Rosenberg R, Speich B. Lymph node yield after rectal resection in patients treated with neoadjuvant radiation for rectal cancer: A systematic review and meta-analysis. European journal of cancer 2017;72:84-94.
  33. Cotte E, Artru P, Bachet JB, et al . Cancer du rectum : Thésaurus National de Cancérologie Digestive 2021
  34. Nikberg M, Kindler C, Chabok A, Letocha H, Shetye J, Smedh K. Circumferential resection margin as a prognostic marker in the modern multidisciplinary management of rectal cancer. Diseases of the colon and rectum 2015;58(3):275-82.
  35. Leite JS, Martins SC, Oliveira J, Cunha MF, Castro-Sousa F. Clinical significance of macroscopic completeness of mesorectal resection in rectal cancer. Colorectal disease 2011;13(4):381-6.
  36. Maslekar S, Sharma A, Macdonald A, Gunn J, Monson JR, Hartley JE. Mesorectal grades predict recurrences after curative resection for rectal cancer. Diseases of the colon and rectum 2007;50(2):168-75.
  37. Quirke P, Steele R, Monson J, et al. Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the
  38. MRC CR07 and NCIC-CTG CO16 randomised clinical trial. Lancet 2009;373(9666):821-8.
  39. Nessar G, Demirbag AE, Celep B, Elbir OH, Kayaalp C. Extralevator abdominoperineal excision versus conventional surgery for low rectal cancer: a single surgeon experience. Ulus Cerrahi Derg 2016;32(4):244-7.