Mismatch repair deficiency and its relationship with histopathological features in gastric cancer patients

被引:0
作者
Nguyen, Thi Hong Chuyen [1 ]
Nguyen, Tran Bao Song [2 ]
Nguyen, Thanh Phuc [3 ]
Ha, Thi Minh Thi [4 ]
Pham, Nguyen Cuong [5 ]
Nguyen, Thi Thu Giang [6 ]
Phan, Minh Tri [1 ]
Le, Thanh Huy [1 ]
Ha, Thanh Thanh [1 ]
Nguyen, Tran Thuc Huan [1 ]
Dang, Cong Thuan [2 ]
机构
[1] Hue Univ, Univ Med & Pharm, Dept Oncol, Hue, Vietnam
[2] Hue Univ, Univ Med & Pharm, Dept Histol Embryol Pathol & Forens Med, 06 Ngo Quyen St, Hue 530000, Vietnam
[3] Hue Univ, Univ Med & Pharm, Dept Anat Surg Training, Hue, Vietnam
[4] Hue Univ, Univ Med & Pharm, Dept Med Genet, Hue, Vietnam
[5] Hue Cent Hosp, Dept Pathol, Hue, Vietnam
[6] Vinmec Cent Pk Int Hosp, Oncol Ctr, Ho Chi Minh City, Vietnam
关键词
gastric cancer; microsatellite instability; mismatch repair deficiency; histopathological features; immunohistochemical; MICROSATELLITE INSTABILITY; PROGNOSTIC VALUE; CHEMOTHERAPY;
D O I
10.18999/nagjms.87.1.93
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Gastric cancer is a common malignancy disease with a poor prognosis. Deficient mismatch repair is a prognostic and predictive marker of response to systemic therapies. However, deficient mismatch repair frequency and the relationship between this status and microscopic characteristics are inconsistent across nations. We aimed to determine the rate of deficient mismatch repair and its association with histopathological features in gastric cancer patients. A cross-sectional study was conducted on 226 gastric cancer patients January 2024. Mismatch repair protein expression was evaluated using immunohistochemical staining, and any absence of mismatch repair proteins was regarded as deficient mismatch repair. The deficient mismatch repair rate was 12.8%. Deficient mismatch repair appeared to be more frequent in the intestinal subtype of Lauren classification odds ratio (OR) = 4.767 (95% confidence interval [CI], 1.086-20.921; p = 0.039), tubular/papillary adenocarcinoma (OR = 5.25; 95% CI, 1.185-23.251; p = 0.029), mucinous adenocarcinoma (OR = 6.19; 95% CI, 1.113-34.445; p = 0.037), and differentiated type (OR = 3.24; 95% CI, 1.324-7.931; p = 0.01). No statistically significant association was detected with histopathological features according to the Tumor Location-Modified Lauren classification and mucinous secreting morphology. Deficient mismatch repair status was unusual in gastric cancer. The degree of cell differentiation and microscopic characteristics based on the World Health Organization and Lauren classification could all impact the predictive power for microsatellite-instable status.
引用
收藏
页码:93 / 104
页数:12
相关论文
共 36 条
  • [1] Sung H, Ferlay J, Siegel RL, Et al., Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries, CA Cancer J Clin, 71, 3, pp. 209-249, (2021)
  • [2] Sitarz R, Skierucha M, Mielko J, Offerhaus GJA, Maciejewski R, Polkowski WP., Gastric cancer: epidemiology, prevention, classification, and treatment, Cancer Manag Res, 10, pp. 239-248, (2018)
  • [3] Bray F, Laversanne M, Sung H, Et al., Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries, CA Cancer J Clin, 74, 3, pp. 229-263, (2024)
  • [4] Nie RC, Chen GM, Yuan SQ, Et al., Adjuvant Chemotherapy for Gastric Cancer Patients with Mismatch Repair Deficiency or Microsatellite Instability: Systematic Review and Meta-Analysis, Ann Surg Oncol, 29, 4, pp. 2324-2331, (2022)
  • [5] Pietrantonio F, Miceli R, Raimondi A, Et al., Individual Patient Data Meta-Analysis of the Value of Microsatellite Instability As a Biomarker in Gastric Cancer, J Clin Oncol, 37, 35, pp. 3392-3400, (2019)
  • [6] Sohn BH, Hwang JE, Jang HJ, Et al., Clinical significance of four molecular subtypes of gastric cancer identified by The Cancer Genome Atlas project, Clin Cancer Res, 23, 15, pp. 4441-4449, (2017)
  • [7] Polom K, Marrelli D, Smyth EC, Et al., The Role of Microsatellite Instability in Positive Margin Gastric Cancer Patients, Surg Innov, 25, 2, pp. 99-104, (2018)
  • [8] Ratti M, Lampis A, Hahne JC, Passalacqua R, Valeri N., Microsatellite instability in gastric cancer: molecular bases, clinical perspectives, and new treatment approaches, Cell Mol Life Sci, 75, 22, pp. 4151-4162, (2018)
  • [9] Jaffrelot M, Fares N, Brunac AC, Et al., An unusual phenotype occurs in 15% of mismatch repair-deficient tumors and is associated with non-colorectal cancers and genetic syndromes, Mod Pathol, 35, 3, pp. 427-437, (2022)
  • [10] Smyth EC, Wotherspoon A, Peckitt C, Et al., Mismatch Repair Deficiency, Microsatellite Instability, and Survival: An Exploratory Analysis of the Medical Research Council Adjuvant Gastric Infusional Chemotherapy (MAGIC) Trial, JAMA Oncol, 3, 9, pp. 1197-1203, (2017)