Programmed death-ligand 1 expression in tumor cells and tumor-infiltrating lymphocytes are associated with depth of tumor invasion in penile cancer

2Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

The present study aimed to demonstrate the propor-tion of the programmed death-ligand 1 (PD-L1) expression in penile cancer patients and the association with clinico-pathological parameters. Formalin-fixed paraffin-embedded specimens were obtained from 43 patients with primary penile squamous cell carcinoma t reated at Srinagarind Hospit al, Facult y of Medici ne, Khon Kaen Universit y, between 2008 and 2018. PD-L1 expression was evaluated by the immunohistochemistry using an SP263 monoclonal antibody. PD-L1 positivity was defined as >25% tumor cell staining or >25% tumor-associated immune cell staining. The correlation between PD-L1 expression and clinico-pathological parameters was analyzed. A total of eight of 43 patients (18.6%) were identified as positive for PD-L1 expression in tumor cells and tumor-infiltrating lympho-cytes. In the PD-L1 positive group, there was a significant association with pathological T stage (P=0.014) with a higher percentage of PD-L1 positive tumors in T1 stage compared with T2-T4 stage. In this cohort, there was a trend towards longer survival in patients with positive PD-L1 expression (5-year OS: 75% vs. 61.2%, P=0.19). Lymph node involve-ment and the location of tumor at the shaft of penis were two independent prognostic factors for survival. In conclusion, the PD-L1 expression was detected in 18% of penile cancer patients and high expression of PD-L1 was associated with the early T stage.

Cite

CITATION STYLE

APA

Sangkhamanon, S., Kotano, N., Sirithanaphol, W., Rompsaithong, U., Kiatsopit, P., Sookprasert, A., … Chindaprasirt, J. (2023). Programmed death-ligand 1 expression in tumor cells and tumor-infiltrating lymphocytes are associated with depth of tumor invasion in penile cancer. Biomedical Reports, 19(1). https://doi.org/10.3892/br.2023.1627

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free