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Uncovering PD-L1 and CD8(+) TILS Expression and Clinical Implication in Cervical Squamous Cell Carcinoma

OBJECTIVE: To investigate the association between programmed death-ligand 1 (PD-L1) coupled with CD8(+) tumor-infiltrating lymphocytes (TILS) and the clinicopathological features, along with prognosis of cervical squamous cell carcinoma (CSCC). METHODS: 95 patients of CSCC received tumor resection a...

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Detalles Bibliográficos
Autores principales: Chen, Jingjing, Gu, Ping, Wu, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455844/
https://www.ncbi.nlm.nih.gov/pubmed/32884946
http://dx.doi.org/10.1155/2020/8164365
Descripción
Sumario:OBJECTIVE: To investigate the association between programmed death-ligand 1 (PD-L1) coupled with CD8(+) tumor-infiltrating lymphocytes (TILS) and the clinicopathological features, along with prognosis of cervical squamous cell carcinoma (CSCC). METHODS: 95 patients of CSCC received tumor resection at the Department of Pathology of the First Affiliated Hospital of University of Science and Technology of China (USTC) from 2015 to 2020. Full-automatic immunohistochemistry was applied to measure PD-L1 expression and CD8(+) TILS density. Our literature deeply assessed the links between PD-L1 expression, clinicopathological features, and the influences of combination of PD-L1 and CD8(+) TILS (PD-L1(+)/CD8(+) TILS) on the prognosis of CSCC. RESULTS: 64.21% of CSCC patients (61/95) expressed PD-L1, and PD-L1 expression was related to the Federation of Gynecology and Obstetrics (FIGO) stage, tumor size, invasion depth, differentiation degree, metastasis of lymph node, and vascular invasion (P < 0.05). Dramatic correlation between PD-L1 expression and CD8(+) TILS density was illustrated in CSCC patients (r = −0.461, P < 0.001). Obvious differences in differentiation degree, FIGO stage, infiltration depth, and lymph node metastasis were shown between patients with PD-L1 coupled with high-density of CD8(+) TILS and those with PD-L1 coupled with low-density of CD8(+) TILS (P < 0.05). Patients with PD-L1 negative expression exhibited better prognosis compared with those with PD-L1 positive expression (P < 0.05). Patients with PD-L1 coupled with high-density of CD8(+) TILS showed better prognostic status, while those with PD-L1 coupled with low-density of CD8(+) TILS had worse prognostic condition (P < 0.05). Differentiation, metastasis of lymph node, and FIGO stage were substantive impact elements of a CSCC patient's overall survival (OS) by Cox multivariate analysis. CONCLUSIONS: CD8(+) TILS density is related to PD-L1 expression in carcinoma. PD-L1/CD8(+) TILS density can be regarded as evaluation for the prognosis of patients with CSCC, providing a new therapeutic target in clinical application.