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Risk Factors of Microscopic Invasion in Early Gastric Cancer

  • Choi, Jong-Ho (Department of Surgery, Seoul National University College of Medicine) ;
  • Suh, Yun-Suhk (Department of Surgery, Seoul National University College of Medicine) ;
  • Park, Shin-Hoo (Department of Surgery, Seoul National University College of Medicine) ;
  • Kong, Seong-Ho (Department of Surgery, Seoul National University College of Medicine) ;
  • Lee, Hyuk-Joon (Department of Surgery, Seoul National University College of Medicine) ;
  • Kim, Woo Ho (Department of Pathology, Seoul National University College of Medicine) ;
  • Yang, Han-Kwang (Department of Surgery, Seoul National University College of Medicine)
  • Received : 2017.09.11
  • Accepted : 2017.11.27
  • Published : 2017.12.31

Abstract

Purpose: This study aimed to evaluate the clinical significance of microscopic invasion to determine the adequate resection margin in early gastric cancer (EGC). Materials and Methods: A retrospective review was performed that included patients who underwent gastrectomy for clinical early gastric cancer (cEGC) at Seoul National University Hospital between January 2007 and December 2010. After subtracting the microscopic resection margin from the gross resection margin for each proximal or distal resection margin, microscopic invasion was represented by the larger value. Microscopic invasion and its risk factors were analyzed according to the clinicopathologic characteristics. Results: In total, 861 patients were enrolled in the study. Microscopic invasion of cEGC was $6.0{\pm}12.8mm$, and the proportion of patients with microscopic invasion ${\geq}0mm$ was 78.4%. In the risk group, tumor location, pT stage, and differentiation did not significantly discriminate the presence of microscopic invasion. The microscopic invasion of EGC-IIb was $13.9{\pm}16.8mm$, which was significantly greater than that of EGC-I. No linear correlation was observed between the overall tumor size and microscopic invasion (R=0.030). The independent risk factors for microscopic invasion ${\geq}20mm$ were EGC-IIb vs. EGC-I/IIa/IIc/III (odds ratio [OR], 3.103; 95% confidence interval [CI], 1.533-6.282; P=0.002) and male vs. female sex (OR, 1.655; 95% CI, 1.012-2.705; P=0.045). Conclusions: Male sex and EGC-IIb were independent risk factors for microscopic invasion ${\geq}20mm$. Examination of intraoperative frozen sections is highly recommended to avoid resection margin involvement, especially in cases of EGC-IIb.

Keywords

References

  1. Yang HK, Suh YS, Lee HJ. Minimally invasive approaches for gastric cancer-Korean experience. J Surg Oncol 2013;107:277-281. https://doi.org/10.1002/jso.23179
  2. Suh YS, Yang HK. Screening and early detection of gastric cancer: East versus West. Surg Clin North Am 2015;95:1053-1066. https://doi.org/10.1016/j.suc.2015.05.012
  3. Raziee HR, Cardoso R, Seevaratnam R, Mahar A, Helyer L, Law C, et al. Systematic review of the predictors of positive margins in gastric cancer surgery and the effect on survival. Gastric Cancer 2012;15 Suppl 1:S116-S124. https://doi.org/10.1007/s10120-011-0112-7
  4. Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines 2014 (ver. 4). Gastric Cancer 2017;20:1-19.
  5. National Comprehensive Cancer Network (US). NCCN Clinical Practice Guidelines in Oncology. Gastric Cancer, Version 2.2017. Fort Washington (PA): National Comprehensive Cancer Network, 2017.
  6. Chen XZ, Zhang WH, Hu JK. Individualized proximal margin for early gastric cancer patients. World J Gastroenterol 2014;20:16793-16794. https://doi.org/10.3748/wjg.v20.i44.16793
  7. Kim BS, Oh ST, Yook JH, Kim HS, Lee IS, Kim BS. Appropriate gastrectomy resection margins for early gastric carcinoma. J Surg Oncol 2014;109:198-201. https://doi.org/10.1002/jso.23483
  8. Squires MH 3rd, Kooby DA, Poultsides GA, Pawlik TM, Weber SM, Schmidt CR, et al. Is it time to abandon the 5-cm margin rule during resection of distal gastric adenocarcinoma? A multi-institution study of the U.S. Gastric Cancer Collaborative. Ann Surg Oncol 2015;22:1243-1251. https://doi.org/10.1245/s10434-014-4138-z
  9. Luo Y, Gao P, Song Y, Sun J, Huang X, Zhao J, et al. Clinicopathologic characteristics and prognosis of Borrmann type IV gastric cancer: a meta-analysis. World J Surg Oncol 2016;14:49. https://doi.org/10.1186/s12957-016-0805-9
  10. Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A, et al. AJCC Cancer Staging Manual. 7th ed. New York (NY): Springer, 2010.
  11. Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer 2011;14:101-112. https://doi.org/10.1007/s10120-011-0041-5
  12. Bosman FT, Carneiro F, Hruban RH, Theise ND. WHO Classification of Tumours of the Digestive System. 4th ed. Lyon: IARC Press, 2010.
  13. Lee JH, Kim YI. Which is the optimal extent of resection in middle third gastric cancer between total gastrectomy and subtotal gastrectomy? J Gastric Cancer 2010;10:226-233. https://doi.org/10.5230/jgc.2010.10.4.226
  14. Ryu KW, Lee JH, Choi IJ, Bae JM. Preoperative endoscopic clipping: localizing technique of early gastric cancer. J Surg Oncol 2003;82:75-77. https://doi.org/10.1002/jso.10191
  15. Park DJ, Lee HJ, Kim SG, Jung HC, Song IS, Lee KU, et al. Intraoperative gastroscopy for gastric surgery. Surg Endosc 2005;19:1358-1361. https://doi.org/10.1007/s00464-004-2217-0
  16. The Paris endoscopic classification of superficial neoplastic lesions: esophagus, stomach, and colon: November 30 to December 1, 2002. Gastrointest Endosc 2003;58:S3-S43. https://doi.org/10.1016/S0016-5107(03)02159-X
  17. Ang TL, Fock KM, Teo EK, Tan J, Poh CH, Ong J, et al. The diagnostic utility of narrow band imaging magnifying endoscopy in clinical practice in a population with intermediate gastric cancer risk. Eur J Gastroenterol Hepatol 2012;24:362-367.
  18. Eleftheriadis N, Inoue H, Ikeda H, Onimaru M, Yoshida A, Maselli R, et al. Effective optical identification of type "0-IIb" early gastric cancer with narrow band imaging magnification endoscopy, successfully treated by endoscopic submucosal dissection. Ann Gastroenterol 2015;28:72-80.
  19. Aquino PF, Fischer JS, Neves-Ferreira AG, Perales J, Domont GB, Araujo GD, et al. Are gastric cancer resection margin proteomic profiles more similar to those from controls or tumors? J Proteome Res 2012;11:5836-5842. https://doi.org/10.1021/pr300612x
  20. Woo JW, Ryu KW, Park JY, Eom BW, Kim MJ, Yoon HM, et al. Prognostic impact of microscopic tumor involved resection margin in advanced gastric cancer patients after gastric resection. World J Surg 2014;38:439-446. https://doi.org/10.1007/s00268-013-2301-5
  21. Lee JH, Ahn SH, Park DJ, Kim HH, Lee HJ, Yang HK. Clinical impact of tumor infiltration at the transected surgical margin during gastric cancer surgery. J Surg Oncol 2012;106:772-776. https://doi.org/10.1002/jso.23123
  22. Squires MH 3rd, Kooby DA, Pawlik TM, Weber SM, Poultsides G, Schmidt C, et al. Utility of the proximal margin frozen section for resection of gastric adenocarcinoma: a 7-Institution Study of the US Gastric Cancer Collaborative. Ann Surg Oncol 2014;21:4202-4210. https://doi.org/10.1245/s10434-014-3834-z
  23. Information Committee of Korean Gastric Cancer Association. Korean Gastric Cancer Association nationwide survey on gastric cancer in 2014. J Gastric Cancer 2016;16:131-140. https://doi.org/10.5230/jgc.2016.16.3.131

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