Classification of gallbladder cancer by assessment of CD8+ TIL and PD-L1 expression

BMC Cancer. 2018 Jul 28;18(1):766. doi: 10.1186/s12885-018-4651-8.

Abstract

Background: Programmed death ligand 1/2 (PD-L1/PD-L2) expression has been established as a prognostic factor for various solid tumors and as a predictive factor for PD-1 blockade therapy, but scant data on its role in gallbladder cancer (GBC). The aims of this study were to assess the expression of PD-L1/PD-L2 and the density of CD8+ tumor-infiltrating lymphocytes (TIL) from GBC samples and to quantify the association between survival prognosis and these factors.

Methods: CD8+ TILs density and the expression of PD-1, PD-L1, PD-L2 and CD133 were assessed using immunohistochemistry in tumor specimens from 66 patients with gallbladder adenocarcinoma. These indexes were correlated with the clinicopathological features.

Results: The rate of PD-L1-positive (PD-L1+) was 54%, which included 18% positivity in tumor cells, and 36% in peritumoral immune stroma. High CD8+ TIL density (CD8high) was observed in PD-L1+ GBC, and PD-L1+ was positively associated with PD-L2+ expression. Regarding prognostic factors, PD-L1+ expression was related to worse overall survival (OS), and CD8high indicated better OS and progression-free survival (PFS). The combination of CD8high with PD-L1+ serves as a prognostic factor for improved OS (P < 0.001) and PFS (P = 0.014).

Conclusion: Analysis of the tumor immune microenvironment based on CD8+ TIL and PD-L1 expression is a promising independent predictor for the clinical outcome of GBC patients.

Keywords: CD8+ TILs; Gallbladder cancer; Immune microenvironment; Immunohistochemistry; PD-L1.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • B7-H1 Antigen / blood
  • B7-H1 Antigen / metabolism*
  • CD8-Positive T-Lymphocytes / metabolism*
  • Female
  • Gallbladder Neoplasms* / diagnosis
  • Gallbladder Neoplasms* / epidemiology
  • Gallbladder Neoplasms* / metabolism
  • Gallbladder Neoplasms* / mortality
  • Humans
  • Immunohistochemistry
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Prognosis
  • Progression-Free Survival

Substances

  • B7-H1 Antigen
  • CD274 protein, human