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PD-L1 expression patterns in oral cancer as an integrated approach for further prognostic classification.
Miranda-Galvis, Marisol; Rumayor Piña, Alicia; Sales de Sá, Raísa; Almeida Leite, Amanda; Agustin Vargas, Pablo; Calsavara, Vinicius Fernando; Lópes Pinto, Clóvis A; Teng, Yong; Kowalski, Luiz Paulo.
Afiliación
  • Miranda-Galvis M; Oral Diagnosis Department, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, Brazil.
  • Rumayor Piña A; Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA, USA.
  • Sales de Sá R; Faculty of Dentistry, Autonomous University of Coahuila, Saltillo, Mexico.
  • Almeida Leite A; Oral Diagnosis Department, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, Brazil.
  • Agustin Vargas P; Oral Diagnosis Department, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, Brazil.
  • Calsavara VF; Oral Diagnosis Department, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, Brazil.
  • Lópes Pinto CA; Department of Epidemiology and Statistics, A.C. Camargo Cancer Center, São Paulo, Brazil.
  • Teng Y; Department of Anatomic Pathology, A.C. Camargo Cancer Center, São Paulo, Brazil.
  • Kowalski LP; Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA, USA.
Oral Dis ; 27(7): 1699-1710, 2021 Oct.
Article en En | MEDLINE | ID: mdl-33169454
ABSTRACT

BACKGROUND:

Despite the well-known role of programmed cell death ligand 1 (PD-L1) in promoting immune resistance in oral squamous cell carcinoma (OSCC), its potential utility as a prognostic biomarker is undetermined. We evaluated PD-L1 expression as predictor of survival in patients with OSCC and explored PD-L1 expression patterns.

METHODS:

We conducted a retrospective cohort study that assessed PD-L1 expression through immunohistochemistry in 123 surgical specimens of OSCC. A first approach evaluated tumor proportion scores (TPS) and combined proportion scores (CPS). Next, expression patterns were examined by evaluating PD-L1 localization in tumor nests, as well as the interfaces of tumor cells (TC) and immune cells (IC) in the tumor microenvironment.

RESULTS:

High-level PD-L1 expression determined by TPS and CPS using variable cutoffs was not associated with survival. Immunohistochemistry revealed that TC expressed PD-L1 in either patchy or diffuse patterns. The patchy pattern was an independent risk factor for overall survival. Furthermore, expression patterns in the tumor immune microenvironment showed that most cases expressed PD-L1 on both TC and IC, while PD-L1 non-expressors had the lowest overall survival.

CONCLUSION:

PD-L1 expression patterns in the context of localization in tumor nests and TC-IC interactions represent antitumor immune responses better than either TPS or CPS. Our suggested classification system may have important implications for the characterization of OSCC and for the use of PD-L1 as a prognostic biomarker.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Carcinoma de Células Escamosas / Neoplasias de Cabeza y Cuello Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Carcinoma de Células Escamosas / Neoplasias de Cabeza y Cuello Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article