Articles Vol. 67 No. Số CĐ12- Bệnh viện Ung bướu Nghệ An (2026) 14/08/2026

EVALUATION OF MICROSATELLITE INSTABILITY STATUS AND ASSOCIATED FACTORS IN COLORECTAL CANCER AT NGHE AN ONCOLOGY HOSPITAL

Viet Phan Dinh1,2, Mai Nguyen Thi1,2, Giang Phan Thi1,2
1 Nghe An Oncology Hospital
2 Bệnh viện Ung Bướu Nghệ An
DOI: 10.52163/yhc.v67iCD12.6142
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Abstract

Objective: To determine the rate of microsatellite instability (MSI) and its association with clinical, subclinical, and molecular features (RAS/BRAF mutations) and disease stage in colorectal cancer (CRC) patients at Nghe An Oncology Hospital.

Methods: A cross-sectional, combined retrospective-prospective study was conducted at Internal Medicine Department III, Nghe An Oncology Hospital, from January 1, 2023 to June 30, 2026, on 174 CRC patients assessed for MSI/MMR status (convenience sampling). Data were analyzed using SPSS 20.0, with Chi-square/Fisher's Exact tests (significance at p < 0.05).

Results: Among 174 patients, the MSI-H/dMMR rate was 14.4% (25 cases); RAS mutation rate was 49.2% (KRAS 47.4%, NRAS 1.8%) and BRAF mutation was 5.3%. Most patients presented at stage II (42.0%) and III (30.5%); left-sided colon tumors were most common (45.4%), and adenocarcinoma was the predominant histological type (92.0%). MSI was significantly more frequent in patients under 50 years old (28.6% vs. 12.4% in those ≥50, p = 0.048), in right-sided colon tumors (34.1% vs. 7.6% left-sided and 9.3% rectal, p = 0.001), and in early-stage I-II disease (19.8% vs. 8.4% in stage III-IV, p = 0.033). No significant associations were found between MSI and sex, ECOG status, CEA level, endoscopic lesion type, histological type, differentiation grade, or RAS/BRAF mutations (p > 0.05 for all).

Conclusion: The MSI-H/dMMR rate among CRC patients at Nghe An Oncology Hospital was 14.4%, significantly associated with younger age, right-sided tumor location, and earlier disease stage - supporting the value of routine MSI testing to guide appropriate immunotherapy decisions.

References
[1]
F. Bray và c.s., “Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries”, CA. Cancer J. Clin., tập 74, số 3, tr 229–263, 2024, doi: 10.3322/caac.21834. Google Scholar
[2]
Akira Ooki, Eiji Shinozaki, Kensei Yamaguchi, Immunotherapy in Colorectal Cancer: Current and Future Strategies, Journal of the Anus, Rectum and Colon, 2021, Volume 5, Issue 1, Pages 11-24, Released on J-STAGE January 28, 2021, https://doi.org/10.23922/jarc.2020-064, Google Scholar
[3]
X. Y. Chen, H. X. Li, H. Cheng, X. Y. Wang, và S. J. Zhang, “Microsatellite instability in colorectal cancer”, Indian J. Pathol. Microbiol., tập 68, số 2, tr 255, thg. 6 2025, doi: 10.4103/ijpm.ijpm_651_23. Google Scholar
[4]
H. Kawakami, A. Zaanan, và F. A. Sinicrope, “Microsatellite Instability Testing and Its Role in the Management of Colorectal Cancer”, Curr. Treat. Options Oncol., tập 16, số 7, tr 30, thg. 6 2015, doi: 10.1007/s11864-015-0348-2. Google Scholar
[5]
Y. Schwitalle và c.s., “Immune response against frameshift-induced neopeptides in HNPCC patients and healthy HNPCC mutation carriers”, Gastroenterology, tập 134, số 4, tr 988–997, thg. 4 2008, doi: 10.1053/j.gastro.2008.01.015. Google Scholar
[6]
F. Battaglin, M. Naseem, H.-J. Lenz, và M. E. Salem, “Microsatellite instability in colorectal cancer: overview of its clinical significance and novel perspectives”, Clin. Adv. Hematol. Oncol. HO, tập 16, số 11, tr 735–745, thg. 11 2018. Google Scholar
[7]
“ĐÁNH GIÁ MỐI LIÊN QUAN GIỮA SỰ MẤT ỔN ĐỊNH VI VỆ TINH VỚI MỘT SỐ ĐẶC ĐIỂM LÂM SÀNG, CẬN LÂM SÀNG TRONG UNG THƯ ĐẠI TRỰC TRÀNG | Tạp chí Y học Việt Nam”. Truy cập: 23 Tháng Bảy 2026. [Online]. Có tại: https://tapchiyhocvietnam.vn/index.php/vmj/article/view/7154 Google Scholar
[8]
Trà Đ. T., Thịnh P. V., và Dũng T. N., “Nghiên cứu sự mất ổn định vi vệ tinh trong ung thư biểu mô tuyến đại trực tràng bằng phương pháp hóa mô miễn dịch”, J. 108 - Clin. Med. Phamarcy, thg. 2 2023, doi: 10.52389/ydls.v18i1.1627. Google Scholar
[9]
H. D. Trinh và c.s., “Deficient Mismatch Repair Subtypes in Vietnamese Colorectal Cancer: Clinicopathologic Associations, Predictive Modeling, and IHC-PCR Concordance”, Cancer Manag. Res., tập 18, tr 1–12, thg. 3 2026, doi: 10.2147/CMAR.S587649. Google Scholar
[10]
Y. Chen và c.s., “Clinicopathological and molecular characteristics of early-onset vs late-onset colorectal cancer according to tumor location”, Int. J. Clin. Oncol., tập 27, số 4, tr 749–755, thg. 4 2022, doi: 10.1007/s10147-021-02101-9. Google Scholar