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Emergency surgeries for rectal cancer complicated by intestinal obstruction: long-term outcomes and prognostic factors

https://doi.org/10.17650/2686-9594-2020-10-1-11-19

Abstract

The aim of the study: to examine the indicators of relapse-free survival and evaluate prognostic factors that had the greatest impact on relapse- free survival in patients with rectal cancer complicated by obstructive obstruction and undergoing emergency surgery.

Materials and methods. The analysis of the immediate and long-term results of treatment – relapse-free survival of patients undergoing emergency surgery for rectal cancer complicated by obstructive obstruction in general surgical and specialized hospitals in Smolensk from 2001 to 2017 is presented. Relapse-free survival was analyzed by the Kaplan–Meier method. To determine the influence of potential risk factors on the rate of occurrence of the studied event, Cox regression was used.

Results. Postoperative complications of the III–IV degree according to Clavien–Dindo were more common in patients undergoing emergency surgery for complicated rectal cancer in general surgical hospitals (p = 0.0056). In specialized hospitals, anastomosis leakage in 5.3 % (1 of 19 cases), in general surgical hospitals – 16.3 % (9 of 55 cases). Five-year relapse-free survival in general surgical hospitals at the IIB stage was 18.3 %, median survival – 32 months; in specialized hospitals at stage IIB 5‑year relapse-free was 45.8 %, median survival – 52 months (p = 0.028 and 0.011, respectively). A multivariate analysis confirmed the influence of the following factors on the performance of a 5‑year relapse-free survival: hospital specialization (risk ratio (RR) 1.35; 95 % confidence interval (CI) 1.18–1.55; p <0.001), type of surgery – one-stage operations (RR 1.13; 95 % CI 1.05–1.22; p = 0.001), the presence of metastases in the lymph nodes (RR 0.77; 95 % CI 0.71–0.84; p <0.0001), the number of examined lymph nodes (RR 0.79; 95 % CI 0.72–0.87; p <0.001).

Conclusions. It is advisable to carry out two-stage surgical treatment with the formation of a colostomy at the first stage; the main stage of radical intervention should be performed in a specialized hospital.

About the Authors

S. N. Shchaeva
Smolensk State Medical University, Ministry of Health of Russia
Russian Federation
28 Krupskoy St., Smolensk 214019, Russia


E. A. Kazantseva
Clinical Hospital No. 1
Russian Federation
40 Frunze St., Smolensk 214004, Russia


E. V. Gordeeva
Smolensk State Medical University, Ministry of Health of Russia
Russian Federation
28 Krupskoy St., Smolensk 214019, Russia


References

1. Situation with cancer care in Russia in 2017. Ed. by A.D. Kaprin, V.V. Starinskiy, G.V. Petrova. Moscow: P.A. Herzen Moscow Oncology Research Institute, 2018. 236 p. (In Russ.)

2. Biondo S., Kreisler E., Millan M. et al. Differences in patient postoperative and long-term outcomes between obstructive and perforated colonic cancer. Am J Surg 2008;195:427–32.

3. Shabunin A.V., Bagateliya Z.A. Algorithm of surgical care for complicated colorectal cancer. Koloproktologiya = Coloproctology 2019;18(1):66–73. (In Russ.). DOI: 10.33878/2073-7556-2019-18-1-66-73.

4. Iversen L.H., Bülow S., Christensen I.J. et al. Danish Colorectal Cancer Group Postoperative medical complications are the main cause of early death after emergency surgery for colonic cancer. Br J Surg 2008;95:1012–9. DOI: 10.1002/bjs.6114.

5. Shchaeva S.N. Emergency surgeries for complicated colorectal cancer performed in hospitals for general surgery: multivariate analysis of short-term and long-term treatment outcomes. Tazovaya khirurgiya i onkologiya = Pelvic Surgery and Oncology 2019;9(2):38–46. (In Russ.). DOI: 10.17650/2220-3478-2019-9-2-38-46.

6. Barsukov Yu.A., Tkachev S.I., Mamedli Z.Z. et al. Combination treatment of rectal cancer using polyradiomodification and short courses of neoadjuvant radiotherapy. Tazovaya khirurgiya i onkologiya = Pelvic Surgery and Oncology 2019;9(3):34–45. (In Russ.). DOI: 10.17650/2686-9594-2019-9-3-34-45.

7. Meshikhes A.W. Evidence-based surgery: the obstacles and solutions. Int J Surg 2015;18:159–62.

8. Felli E., Brunetti F., Disabato M. et al. Robotic right colectomy for hemorrhagic right colon cancer: a case report and review of the literature of minimally invasive urgent colectomy. World J Emerg Surg 2014;9:32.

9. Harji D.P., Griffiths B., Burke D. et al. Systematic review of emergency laparoscopic colorectal resection. Br J Surg 2014;101(1):e126–33. DOI: 10.1002/bjs.9348.

10. Weixler B., Warschkow R., Ramser M. et al. Urgent surgery after emergency presentation for colorectal cancer has no impact on overall and disease-free survival: a propensity score analysis. BMC Cancer 2016;16:208. DOI: 10.1186/s12885-016-2239-8.

11. Chang G.J., Kaiser A.M., Mills S. et al. Practice parameters for the management of colon cancer. Dis Colon Rectum 2012;55(8):831–43. DOI: 10.1097/DCR.0b013e3182567e13.

12. Brehant O., Fuks D., Bartoli E. et al. Elective (planned) colectomy in patients with colorectal obstruction after placement of a self-expanding metallic stent as a bridge to surgery: the results of a prospective study. Colorectal Dis 2009;11:178–83 DOI: 10.1111/j.1463-1318.2008.01578.x.

13. Chen T.M., Huang Y.T., Wang G.C. Outcome of colon cancer initially presenting as colon perforation and obstruction. World J Surg Oncol 2017;15:164. DOI: 10.1186/s12957-017-1228-y.

14. Ho Y.H., Siu S.K., Buttner P. et al. The effect of obstruction and perforation on colorectal cancer disease-free survival. World J Surg 2010;34:1091–101.

15. Crozier J.E., Leitch E.F., McKee R.F. et al. Relationship between emergency presentation, systemic inflammatory response, and cancer-specific survival in patients undergoing potentially curative surgery for colon cancer. Am J Surg 2009;197(4):544–9. DOI: 10.1016/j.amjsurg.2007.12.052.

16. Manfredi S., Bouvier A.M., Lepage C. et al. Incidence and patterns of recurrence after resection for cure of colonic cancer in a well-defined population. Br J Surg 2006;93(9):1115–22. DOI: 10.1002/bjs.5349.

17. Read T.E., Mutch M.G., Chang B.W. et al. Locoregional recurrence and survival after curative resection of adenocarcinoma of the colon. J Am Coll Surg 2002;195(1):33–40. DOI: 10.1016/s1072-7515(02)01224-3.

18. Harris G.J.C., Church J.M., Senagore A.J. et al. Factors affecting local recurrence of colonic adenocarcinoma. Dis Colon Rectum 2002;45(8):1029–34. DOI: 10.1007/s10350-004-6355-1.

19. Sjövall A., Granath F., Cedermark B. et al. Loco-regional recurrence from colon cancer: a population-based study. Ann Surg Oncol 2007;14(2):432–40. DOI: 10.1245/s10434-006-9243-1.

20. Biondo S., Martí-Ragué J., Kreisler E. et al. A prospective study of outcomes of emergency and elective surgeries for complicated colonic cancer. Am J Surg 2005;189(4):377–83. DOI: 10.1016/j.amjsurg.2005.01.009.

21. Biondo S., Kreisler E., Millan M. Impact of surgical specialization on emergency colorectal surgery outcomes. Arch Surg 2010;145(1):79–86. DOI: 10.1001/archsurg.2009.208.

22. Smith J.A.E., King P.M., Lane R.H.S. Evidence of the effect of “specialization” on the management, surgical outcome and survival from colorectal cancer in Wessex. Br J Surg 2003;90:583–92. DOI: 10.1002/bjs.4085.

23. Asano H., Kojima K., Ogino N. et al. Postoperative recurrence and risk factors of colorectal cancer perforation. Int J Colorectal Dis 2017;32(3):419–24. DOI: 10.1007/s00384-016-2694-3.

24. Cortet M., Grimault A., Cheynel N. et al. Patterns of recurrence of obstructing colon cancers after surgery for cure: a population- based study. Colorectal Dis 2013;15(9):1100–6. DOI: 10.1111/codi.12268.

25. Sugawara K., Kawaguchi Y., Nomura Y. et al. Insufficient lymph node sampling in patients with colorectal cancer perforation is associated with an adverse oncological outcome. World J Surg 2017;32(3):419–24. DOI: 10.1007/s00384-016-2694-3.

26. Shchaeva S.N., Achkasov S.I. Assessment of the efficacy of emergency surgeries in patients with complicated colorectal cancer. Koloproktologiya = Coloproctology 2017;60(2):30–5. (In Russ.).

27. Runkel N.S., Hinz U., Lehnert T. et al. Improved outcome after emergency surgery for cancer of the large intestine. Br J Surg 1998;85:1260–5 DOI: 10.1046/j.1365-2168.1998.00855.x.

28. Barbas A.S., Turley R.S., Mantyh C.R. et al. Effect ofsurgeon specialization on long-term survival following colon cancer resection at an NCI-designated cancer center. J Surg Oncol 2012;106: 219–23. DOI: 10.1002/jso.22154.

29. Oliphant R., Nicholson G.A., Horgan P.G. et al. West of Scotland Colorectal Cancer Managed Clinical Network. Contribution of surgical specialization to improved colorectal cancer survival. Br J Surg 2013;100: 1388–95. DOI: 10.1002/bjs.9227.

30. Hall G.M., Shanmugan S., Bleier J.I. et al. Colorectal specialization and survival in colorectal cancer. Colorectal Dis 2016;18:O51–60. DOI: 10.1111/codi.13246.


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