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Comparison of short-term outcomes of D2 and D3 lymph nodes dissection for colon cancer

https://doi.org/10.17650/2949-5857-2024-14-1-51-61

Abstract

Background. D3 lymph node dissection remains controversial in colon cancer surgery.

Aim. To compare the short-term of D2 and D3 lymph nodes dissection for colon cancer.

Materials and methods. Design of the study – prospective randomize controlled study. Inclusion criteria: age over 18 years, colon adenocarcinoma cT3–4n0–2m0, patient consent to participate in the study. Exclusion criteria: distant metastases diagnosed preoperatively, cTis–T2, cT4b (pancreas, stomach, small intestine, ureter, bladder, kidney), emergent cases (limited to tumor perforation, acute bowel obstruction), history of previous chemotherapy or radiation therapy, synchronous or metachronous cancer, pregnancy or breastfeeding, refusal to participate in the study. withdrawal criteria were exploratory laparotomy/laparoscopy or other reasons for refusing resection.

Results. A total of 436 patients were included in the study no differences were found in the clinical characteristics of groups D2 and D3. In the D2 lymph node dissection group the incidence of unintentional vascular injuries was in 7 (3.2 %) patients, in the D3 lymph node dissection group – in 15 (6.9 %) patients (p = 0.12). The operating time increased by 30 minutes in D3 lymph node dissection group (p p = 0.42). Hartmann’s procedure was performed in 2 (0.9 %) patients in the D2 lymph node dissection group. Complications IIIb were recorded in 5 (2.3 %) and 9 (4.1 %) patients in lymph node dissection groups D2 and D3, respectively (p = 0.42). Anastomotic leakage was not observed in the D2 lymph node dissection group; in the D3 lymph node dissection group, it was diagnosed in 3 (1.4 %) patients (p = 0.25). postoperative multiple-organ failure (Iv) or mortality (v) were not observed. grade 3 quality of the specimen was observed in 160 (73.4 %) patients in the D2 lymph node dissection group, 163 (74.8 %) in the D3 lymph node dissection group (p = 0.79). The median number of lymph node harvested was 11 more in the D3 lymph node dissection group (p < 0.001). Apical lymph nodes were positive in 5 (2.3 %) patients in the D3 lymph node dissection group. There was no difference between the groups in R0 resection margin.

Conclusion. D3 lymph node dissection is safe in terms of short-term outcomes in the treatment of colon cancer.

About the Authors

V. V. Balaban
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Vladimir Vladimirovich Balaban

Build. 2, 8 Trubetskaya St., Moscow 119991



M. G. Mutyk
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic
Russian Federation

2a Polotskaya St., Donetsk 283092



N. V. Bondarenko
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



S. E. Zolotukhin
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



O. V. Sovpel
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



I. V. Sovpel
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



M. M. Klochkov
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



D. S. Zykov
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic
Russian Federation

2a Polotskaya St., Donetsk 283092



I. V. Rublevskyi
G.V. Bondar Republican Cancer Center, Ministry of Health of the Donetsk People’s Republic; M. Gorky Donetsk State Medical University
Russian Federation

2a Polotskaya St., Donetsk 283092

16 Ilicha Prospekt, Donetsk 283003



I. A. Tulina
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Build. 2, 8 Trubetskaya St., Moscow 119991



V. M. Nekoval
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Build. 2, 8 Trubetskaya St., Moscow 119991



S. I. Barkhatov
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Build. 2, 8 Trubetskaya St., Moscow 119991



A. E. Vasilyev
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Build. 2, 8 Trubetskaya St., Moscow 119991



P. V. Tsarkov
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Russian Federation

Build. 2, 8 Trubetskaya St., Moscow 119991



References

1. Fedyanin M.Yu., Gladkov O.A., Gordeev S.S. et al. Practical recommendations for drug treatment of cancer of the colon, rectosigmoid junction and rectum. RUSSCO practical recommendations, part 1. Zlokachestvennye opuholi = Malignant tumors 2023;13(3s2–1):425–82. (In Russ.). DOI: 10.18027/2224-5057-2023-13-3s2-1-425-482

2. Jamieson J.K., Dobson J.F. The lymphatics of the colon. Proc R Soc Med Surg Sect 1909;2:149–74. DOI: 10.1177/003591570900201506

3. Dennosuke J. General rules for clinical and pathological studies on cancer of the colon, rectum and anus. The Japanese Journal of Surgery 1983;13:557–73. DOI: https://doi.org/10.1007/BF02469505

4. Hashiguchi Y., Muro K., Saito Y. 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):1–42. DOI: 10.1007/s10147-019-01485-z

5. Toyota S., Ohta H., Anazawa S. Rationale for extent of lymph node dissection for right colon cancer. Dis Colon Rectum 1995;38(7):705–11. DOI: 10.1007/BF02048026

6. Mori T., Takahashi K., Yasuno M. Radical resection with autonomic nerve preservation and lymph node dissection techniques in lower rectal cancer surgery and its results: the impact of lateral lymph node dissection. Langenbeck’s Arch Surg 1998;383:409–15. DOI: 10.1007/s004230050153

7. Hohenberger W., Reingruber B., Merkel S. Surgery for colon cancer. Scand J Surg 2003;92(1):45–52. DOI: 10.1177/145749690309200107

8. Hohenberger W., Weber K., Matzel K. et al. Standardized surgery for colonic cancer: complete mesocolic excision and central ligation – technical notes and outcome. Colorectal Dis 2009;11(4):354–64; discussion 364-5. DOI: 10.1111/j.1463-1318.2008.01735.x

9. West N.P., Kobayashi H., Takahashi K. et al. Understanding optimal colonic cancer surgery: comparison of Japanese D3 resection and European complete mesocolic excision with central vascular ligation. J Clin Oncol 2012;30(15):1763–9. DOI: 10.1200/JCO.2011.38.3992

10. Watanabe M. Chokucho Komon Geka Shujutsu Hyojun Shujutsu to Step up Shujutsu (DS NOW-Digestive Surgery NOW-5). Tokyo, Japan, Medical View, 2009. 204 p. (In Japanese).

11. Søndenaa K., Quirke P., Hohenberger W. et al. The rationale behind complete mesocolic excision (CME) and a central vascular ligation for colon cancer in open and laparoscopic surgery: proceedings of a consensus conference. Int J Colorectal Dis 2014;29(4):419–28. DOI: 10.1007/s00384-013-1818-2

12. Abdelkhalek M., Setit A., Bianco F. et al. Complete mesocolic excision with central vascular ligation in comparison with conventional surgery for patients with colon cancer – the experiences at two centers. Ann Coloproctol 2018;34(4):180–6. DOI: 10.3393/ac.2017.08.05

13. Panayotti L.L. Immediate results of performing D2 and D3 lymph node dissections during surgical treatment of colon cancer (randomized prospective study): dissertation of a candidate of medical sciences. St. Petersburg, 2020. (In Russ.). https://www.niioncologii.ru/science/thesis/neposredstvennye-rezultatyvypolneniya-d2-i-d3-limfodissekcij-pri-hirurgicheskom-lecheniiraka-obodochnoj-kishki/dissertaciya.pdf

14. Bertelsen C.A., Neuenschwander A.U., Jansen J.E. et al. Short-term outcomes after complete mesocolic excision compared with ‘conventional’ colonic cancer surgery. Br J Surg 2016;103(5): 581–9. DOI: 10.1002/bjs.10083

15. Agalianos C., Gouvas N., Dervenis C. et al. Is complete mesocolic excision oncologically superior to conventional surgery for colon cancer? A retrospective comparative study. Ann Gastroenterol 2017;30(6):688–96. DOI: 10.20524/aog.2017.0197

16. Bertelsen C.A., Neuenschwander A.U., Jansen J.E. et al. Disease-free survival after complete mesocolic excision compared with conventional colon cancer surgery: a retrospective, population-based study. Lancet Oncol 2015;16(2):161–8. DOI: 10.1016/S1470-2045(14)71168-4

17. Balaban V., Tsugulya P., Tsarkov P. D3 lymph nodes dissection using lateral-to-medial approach in rectal cancer surgery. Dis Colon Rectum 2022;65(3):e180–1. DOI: 10.1097/DCR.0000000000002253

18. West N.P., Morris E.J., Rotimi O. et al. Pathology grading of colon cancer surgical resection and its association with survival: a retrospective observational study. Lancet Oncol 2008;9(9):857–65. DOI: 10.1016/s1470-2045(08)70181-5

19. Balaban V., Tulina I., Tsugulya P. et al. Superior mesenteric artery bleeding during D3 lymph node dissection for right colon cancer – A video vignette. Colorectal Disease 2023;25(7):1553–4. DOI: 10.1111/codi.16573

20. Xu L., Su X., He Z. et al. Short-term outcomes of complete mesocolic excision versus D2 dissection in patients undergoing laparoscopic colectomy for right colon cancer (RELARC): a randomised, controlled, phase 3, superiority trial. Lancet Oncol 2021;22(3):391–401. DOI: 10.1016/S1470-2045(20)30685-9

21. Degiuli M., Aguilar A.H.R., Solej M. et al. A randomized phase III trial of complete mesocolic excision compared with conventional surgery for right colon cancer: interim analysis of a nationwide multicenter study of the Italian Society of Surgical Oncology Colorectal Cancer Network (CoME-in trial). Ann Surg Oncol 2023. DOI: 10.1245/s10434-023-14664-0

22. Kong J.C., Prabhakaran S., Choy K.T. et al. Oncological reasons for performing a complete mesocolic excision: a systematic review and meta-analysis. ANZ J Surg 2021;91(12):124–131. DOI: 10.1111/ans.16518

23. Merkel S., Weber K., Matzel K.E. et al. Prognosis of patients with colonic carcinoma before, during and after implementation of complete mesocolic excision. Br J Surg 2016;103(9):1220–9. DOI: 10.1002/bjs.10183

24. Son G.M., Yun M.S., Lee I.Y. et al. Clinical effectiveness of fluorescence lymph node mapping using ICG for laparoscopic right hemicolectomy: a prospective case-control study. Cancers (Basel) 2023;15(20):4927. DOI: 10.3390/cancers15204927


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