Abstract
The immune checkpoint PD-1 and its ligand PD-L1 are involved in the induction of immunological tolerance of solid tumors including oral squamous cell carcinoma (OSCC). The aim of the study was to establish the clinical and prognostic significance of PD-L1 in OSCC. Tissue microarrays of 125 resected OSCC were stained with two different commercially available PD-L1 antibodies (clones E1L3N and 22C3), alongside PD-1 immunostaining. PD-L1 expression in more than 10% of tumor cells was associated with poorer survival, and established as a clinically relevant cut-off point. This relevant PD-L1 expression was detected in 10% to 15% OSCC specimens depending on the anti-PD-L1 antibody, and showed an inverse correlation with tobacco and alcohol consumption. We consistently found that PD-L1 expression was associated with tumor recurrence and lower disease-specific survival. Multivariate analysis further revealed that neck node metastasis (HR 2.304; P = 0.009) and tumor PD-L1 expression (HR 2.571; P = 0.01) were significant independent factors for poor prognosis. PD-L1 expression in more than 10% of tumor cells was a significant and independent factor of poor prognosis in OSCC. PD-L1 expression in more than 10% of tumor cells was consistently established as a clinically relevant cut-off point by using two different antibodies. Remarkably, PD-L1 expression emerges as an independent poor prognosis marker in patients with OSCC.
MeSH Terms
Adult
Aged
Aged, 80 and over
B7-H1 Antigen/metabolism
Biomarkers, Tumor/metabolism
Carcinoma, Squamous Cell/metabolism,secondary,surgery
Female
Follow-Up Studies
Humans
Lymphatic Metastasis
Male
Middle Aged
Mouth Neoplasms/metabolism,pathology,surgery
Neoplasm Invasiveness
Neoplasm Recurrence, Local/metabolism,pathology,surgery
Prognosis
Programmed Cell Death 1 Receptor/metabolism
Retrospective Studies
Survival Rate
Chemicals
B7-H1 Antigen
Biomarkers, Tumor
CD274 protein, human
PDCD1 protein, human
Programmed Cell Death 1 Receptor
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
de Vicente Juan C
ORCID
Department of Oral and Maxillofacial Surgery, Hospital Universitario Central de Asturias, Asturias, Spain. jvicente@uniovi.es juanagp.finba@gmail.com. | Instituto de Investigación Sanitaria del Principado de Asturias, Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Asturias. Spain.
Rodríguez-Santamarta Tania
Department of Oral and Maxillofacial Surgery, Hospital Universitario Central de Asturias, Asturias, Spain.
Rodrigo Juan P
ORCID
Instituto de Investigación Sanitaria del Principado de Asturias, Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Asturias. Spain. | Department of Otolaryngology, Hospital Universitario Central de Asturias, Asturias. Spain. | Ciber de Cáncer, Instituto de Salud Carlos III, Madrid, Spain.
Blanco-Lorenzo Verónica
Department of Pathology, Hospital Universitario Central de Asturias, Asturias. Spain.
Allonca Eva
Instituto de Investigación Sanitaria del Principado de Asturias, Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Asturias. Spain. | Department of Otolaryngology, Hospital Universitario Central de Asturias, Asturias. Spain. | Ciber de Cáncer, Instituto de Salud Carlos III, Madrid, Spain.
García-Pedrero Juana M
ORCID
Instituto de Investigación Sanitaria del Principado de Asturias, Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Asturias. Spain. jvicente@uniovi.es juanagp.finba@gmail.com. | Department of Otolaryngology, Hospital Universitario Central de Asturias, Asturias. Spain. | Ciber de Cáncer, Instituto de Salud Carlos III, Madrid, Spain.