PD-L1 expression characteristics in colorectal adenocarcinoma

  • Lê Thị Thanh Xuân Khoa Giải phẫu bệnh, Bệnh viện Trung ương quân đội 108; Bộ môn Giải phẫu bệnh, Trường Đại học Y Hà Nộ
  • Nguyễn Văn Chủ Bộ môn Giải phẫu bệnh, Trường Đại học Y Hà Nội; Khoa Giải phẫu bệnh, bệnh viện K cơ sở Quán s
  • Ngô Thị Minh Hạnh Khoa Giải phẫu bệnh, Bệnh viện Trung ương quân đội 108
  • Lê Thị Huệ Khoa Giải phẫu bệnh, Bệnh viện Trung ương quân đội 108
  • Nghiêm Xuân Hoàn Phòng khoa học Quân sự, Bệnh viện Trung ương quân đội 108

Main Article Content

Keywords

PD-L1, colorectal adenocarcinoma, immunohistochemistry

Abstract

Background: Colorectal cancer (CRC) is a global health burden. The role of the tumor microenvironment and the immune checkpoint molecule Programmed Death-Ligand 1 (PD-L1) as a prognostic marker in colorectal adenocarcinoma remains a topic of controversy. Objective: To describe the expression characteristics of the PD-L1 marker in colorectal adenocarcinoma and to evaluate the correlation between PD-L1 expression and the clinical and histopathological features of the tumor. Subject and method: A cross-sectional descriptive study was conducted on 80 cases of colorectal adenocarcinoma at various disease stages, classified according to the 8th edition of the AJCC cTNM staging system, treated at the 108 Military Central Hospital from August 2023 to December 2024. Immunohistochemistry (IHC) was used to detect PD-L1 expression using the Dako PD-L1 IHC 22C3 pharmDx assay monoclonal antibody. The correlation between PD-L1 status, assessed by the Combined Positive Score (CPS), and clinicopathological variables (age, gender, tumor location, histological grade, TNM stage, perineural invasion, lymphovascular invasion, tumor necrosis) was analyzed using SPSS 25.0 statistical software, the Chi-square and Fisher’s exact tests. Result: Positive PD-L1 expression (CPS ≥ 1) was observed in 57 out of 80 cases (71.3%). Statistical analysis revealed a highly significant correlation between positive PD-L1 expression and poor differentiation (p = 0.003), advanced TNM stage (III/IV) (p = 0.001; OR = 0.04), and the presence of perineural invasion (p = 0.039; OR=3.7). No statistically significant association was found between PD-L1 expression and age, gender, tumor location, lymphovascular invasion, or tumor necrosis. Conclusion: mPD-L1 expression is a prognostic biomarker associated with poor outcomes and aggressive tumor biology in colorectal adenocarcinoma.

Article Details

References

1. Sung H, Ferlay J, Siegel RL et al (2021) Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 71(3): 209-249.
2. Baran B, Mert Ozupek N, Tetik NY et al (2018) Difference Between Left-Sided and Right-Sided Colorectal Cancer: A Focused Review of Literature. Gastroenterology Res 11(4): 264-273.
3. Paijens ST, Vledder A, de Bruyn M et al (2021) Tumor-infiltrating lymphocytes in the immunotherapy era. Cell Mol Immunol 18(4): 842-859.
4. Li Y, Liang L, Dai W et al (2019) The Prognostic and Clinicopathological Roles of PD-L1 Expression in Colorectal Cancer: A Systematic Review and Meta-Analysis. Front Pharmacol 10: 139.
5. Shen H, Wei Z, Zou B et al (2019) The prognostic role of programmed death-ligand 1 in colorectal cancer: A systematic review and meta-analysis. J Gastrointest Oncol 10(4): 671-681.
6. Wang Z, Zhang C, Xu Z et al (2020) PD-L1 expression in colon cancer and its relationship with clinical-pathological features. J Immunoassay Immunochem 41(1): 57-65.
7. Ganesh K, Stadler ZK, Cercek A et al (2019) Immunotherapy in colorectal cancer: rationale, challenges and potential. Nat Rev Gastroenterol Hepatol 16(6): 361-375.
8. Karpathiou G, Camy F, Gkolfinopoulos S et al (2024) Evaluation of PD-L1 Expression in Colorectal Carcinomas by Comparing Scoring Methods and Their Significance in Relation to Clinicopathologic Parameters. Diagnostics (Basel) 14(10): 1031.
9. Kim JH, Park HE, Cho NY, Lee HS, Kang GH (2016) Characterisation of PD-L1-positive subsets of microsatellite-unstable colorectal cancers. Br J Cancer 115(4): 490-496.
10. Al-Jussani GN, Alsughayer A, Yousuf MS, Mullahuwash Y, Dabbagh T, Sughayer MAJTIJoBM (2022) The clinicopathological features of programmed death ligand-1 expression in colorectal carcinoma. Int J Biol Markers 37(3): 322-327.
11. Rosenbaum MW, Bledsoe JR, Morales-Oyarvide V, Huynh TG, Mino-Kenudson MJMp (2016) PD-L1 expression in colorectal cancer is associated with microsatellite instability, BRAF mutation, medullary morphology and cytotoxic tumor-infiltrating lymphocytes. Mod Pathol 29(9): 1104-1112.
12. Das S, Sahoo S, Singh S et al (2025) Programmed Cell Death Ligand-1 (PD-L1) Expression in Colorectal Carcinoma and Its Correlation with Clinicopathological Variables. Cureus 14(10): 30491.
13. Tadachina S, Devi Shivalingaiah S, Shetty M (2024) Immunohistochemical Expression of Programmed Death Ligand- 1 (PD-L1) in Colorectal Carcinoma; A Cross-sectional Study. Iran J Pathol Winter; 19(1):22-30. doi: 10.30699/IJP.2023.1988660.3054.