J Gastric Cancer.  2019 Dec;19(4):427-437. 10.5230/jgc.2019.19.e38.

Clinical Implications of Microsatellite Instability in Early Gastric Cancer

• Kim DG
• An JY
• Kim H
• Shin SJ
• Choi S
• Seo WJ
• Roh CK
• Cho M
• Son T
• Kim HI
• Cheong JH
• Hyung WJ
• Noh SH
• Choi YY

• KMID: 2466031
• DOI: http://doi.org/10.5230/jgc.2019.19.e38

Abstract

PURPOSE
We aimed to evaluate the clinical characteristics of microsatellite instability in early gastric cancer.
MATERIALS AND METHODS
The microsatellite instability status of resected early gastric tumors was evaluated using two mononucleotide repeat markers (BAT25 and BAT26) and three dinucleotide repeat markers (D5S346, D2S123, and D17S250). Tumors with instability in two or more markers were defined as microsatellite instability-high (MSI-H) and others were classified as microsatellite stable (MSS).
RESULTS
Overall, 1,156 tumors were included in the analysis, with 85 (7.4%) classified as MSI-H compared with MSS tumors. For MSI-H tumors, there was a significant correlation with the female sex, older age, tumor location in the lower gastric body, intestinal histology, lymphovascular invasion (LVI), and submucosal invasion (P<0.05). There was also a trend toward an association with lymph node (LN) metastasis (P=0.056). In mucosal gastric cancer, there was no significant difference in MSI status in tumors with LN metastasis or tumors with LVI. In submucosal gastric cancer, LVI was more frequently observed in MSI-H than in MSS tumors (38.9% vs. 25.0%, P=0.027), but there was no difference in the presence of LN metastases. The prognosis of MSI-H tumors was similar to that of MSS tumors (log-rank test, P=0.797, the hazard ratio for MSI-H was adjusted by age, sex, pT stage, and the number of metastatic LNs, 0.932; 95% confidence interval, 0.423-2.054; P=0.861).
CONCLUSIONS
MSI status was not useful in predicting prognosis in early gastric cancer. However, the frequent presence of LVI in early MSI-H gastric cancer may help guide the appropriate treatment for patients, such as endoscopic treatment or limited LN surgical dissection.

Keyword

Microsatellite instability; Gastric cancer; Prognosis; Lymph nodes

MeSH Terms

Dinucleotide Repeats
Female
Humans
Lymph Nodes
Microsatellite Instability*
Microsatellite Repeats*
Neoplasm Metastasis
Prognosis
Stomach Neoplasms*

Figure

• 

  Fig. 1 DFS Kaplan-Meier curves (A) in overall cohort, (B) in stage I. DFS = disease-free survival; HR = hazard ratio; CI = confidence interval; MSS = microsatellite stable; MSI-H = microsatellite instability-high.

• 

  Fig. 2 Kaplan-Meier curve for histologic type, pT stage, pN stage. LN = lymph node; DFS = disease-free survival; HR = hazard ratio; CI = confidence interval; MSS = microsatellite stable; MSI-H = microsatellite instability-high.

• 

  Fig. 3 Patient distribution based on extended ESD indication. A. Tumor size ≤2 cm, histologically of differentiated type, pT1a, UL(−). B. Tumor size >2 cm, histologically of differentiated type, pT1a, UL(−). C. Tumor size ≤3 cm, histologically of differentiated type, pT1a, UL(+). D. Tumor size ≤2 cm, histologically of undifferentiated type, pT1a, UL(−). E. Tumor size ≤3 cm, histologically of differentiated type, pT1b (Sm1, ≤500 μm from the muscularis mucosae). ESD = endoscopic submucosal dissection; LNM = lymph node metastasis; MSS = microsatellite stable; MSI-H = microsatellite instability-high; UL = ulcerative lesion.

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