Clinicopathological and Prognostic Significance of Programmed Death Ligand-1 SP142 Expression in 132 Patients With Triple-negative Breast Cancer

In Vivo. 2022 Nov-Dec;36(6):2890-2898. doi: 10.21873/invivo.13030.

Abstract

Background/aim: The prognostic value of programmed death ligand-1 (PD-L1) expression in triple-negative breast cancer (TNBC) has not been sufficiently investigated. In this study, we examined whether PD-L1 expression status is associated with clinicopathological features and outcomes of patients with TNBC.

Patients and methods: Immunostaining for PD-L1 SP142 was performed on tissue microarrays containing 132 TNBC samples. High PD-L1 expression was defined as ≥10% of the tumor area occupied by PD-L1-expressing cells.

Results: Thirty-five (26.5%) patients showed high PD-L1 SP142 expression on immune cells (ICs). High IC PD-L1 expression was significantly correlated with smaller tumor size (p=0.030), absence of lymphovascular invasion (p=0.024), and fewer lymph node metastases (p=0.002). Multivariate survival analysis revealed that high IC PD-L1 expression independently predicted better disease-free survival (DFS) of TNBC patients.

Conclusion: High PD-L1 SP142 expression on ICs was significantly associated with favorable clinicopathological parameters and better outcomes in patients with TNBC. Our observations suggest that high IC PD-L1 expression can be used as an independent prognostic marker for predicting better DFS in patients with TNBC.

Keywords: Breast; SP142; prognosis; programmed death ligand-1; triple-negative breast cancer.

MeSH terms

  • B7-H1 Antigen* / genetics
  • Humans
  • Lymphatic Metastasis
  • Prognosis
  • Triple Negative Breast Neoplasms* / metabolism

Substances

  • CD274 protein, human
  • B7-H1 Antigen