AI Article Synopsis

  • Epstein-Barr virus-positive gastric cancer (EBVGC) has a low chance of lymph node metastasis (LNM) compared to non-EBVGC, indicating its potential for endoscopic resection (ER).
  • A retrospective analysis of surgical cases from 2005 to 2014 revealed that EBVGC comprised 7.9% of cases, highlighting distinct demographic and pathological features, such as a higher prevalence in males and a lower rate of lymphatic invasion.
  • The study concludes that pT1b EBVGC is a good candidate for ER, particularly when lymphovascular invasion is not present, suggesting that EBV status should be considered in treatment decisions.

Article Abstract

Background: Epstein-Barr virus-positive gastric cancer (EBVGC) is associated with a low prevalence of lymph node metastasis (LNM); however, EBV status is not considered in the indication of endoscopic resection (ER). We aimed to clarify the implication of EBV status for ER of pT1b GC.

Methods: Consecutive cases of pT1b GCs treated with surgery between 2005 and 2014 were retrospectively analyzed. Clinicopathological factors and LNM status were compared between EBVGC and non-EBVGC groups.

Results: EBVGC accounted for 7.9% (71 of 898) cases. Compared to non-EBVGC, EBVGC was more frequent in males (p = 0.0055), the upper third region (p < 0.0001), showed elevated growth features (p = 0.0059), and was associated with a lower frequency of accompanying ulceration (p = 0.002), greater depth of submucosal invasion (p = 0.017), and lower frequency of lymphatic invasion (p < 0.0001). Frequency of LNM was significantly lower in EBVGC than in non-EBVGC (4.2% vs. 21.9%, p < 0.0001). In EBVGC, tumors without lymphovascular invasion showed significantly lower frequency of LNM than those with lymphovascular invasion (0 of 50, 0%; vs 3 of 21, 14.3%; p = 0.023). Histologically, 84.5% (60 of 71) of EBVGC included carcinomas with lymphoid stroma and/or lace pattern components.

Conclusions: pT1b EBVGC is a convincing candidate for ER, regardless of risk factors other than lymphovascular invasion.

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Source
http://dx.doi.org/10.1007/s00535-019-01562-0DOI Listing

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