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Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis

BACKGROUND: Prognostic significance of the programmed death-ligand-1 status in non-small cell lung carcinoma remains controversial AIMS: To show the programmed death-ligand-1 expression status in patients with non-small cell lung carcinoma and its effect on the prognosis and the relationship with cl...

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Autores principales: Şahin, Songül, Batur, Şebnem, Aydın, Övgü, Öztürk, Tülin, Turna, Akif, Öz, Büge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528525/
https://www.ncbi.nlm.nih.gov/pubmed/30592196
http://dx.doi.org/10.4274/balkanmedj.galenos.2018.2018.0392
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author Şahin, Songül
Batur, Şebnem
Aydın, Övgü
Öztürk, Tülin
Turna, Akif
Öz, Büge
author_facet Şahin, Songül
Batur, Şebnem
Aydın, Övgü
Öztürk, Tülin
Turna, Akif
Öz, Büge
author_sort Şahin, Songül
collection PubMed
description BACKGROUND: Prognostic significance of the programmed death-ligand-1 status in non-small cell lung carcinoma remains controversial AIMS: To show the programmed death-ligand-1 expression status in patients with non-small cell lung carcinoma and its effect on the prognosis and the relationship with clinicopathologic data. STUDY DESIGN: Retrospective cross-sectional study. METHODS: The study included 208 cases who were diagnosed with NSCLC and who underwent surgical resection between 2001 and 2012. Programmed death-ligand-1 (SP142 clone) was applied to the histological sections acquired from the microarray paraffin blocks with immunohistochemistry. Staining intensity was scored as weak (+, 1), moderate (++, 2), and strong (+++, 3). Percentage (0%-100%) was multiplied by staining intensity (1-2-3) to calculate the H score. Four different cut-off values were used; 1: ≥1% (independent of intensity), 2: ≥5% (independent of intensity), 3: ≥5% moderate/strong staining (except for weak staining), 4: H score ≥30 values were considered positive. In this study, staining a single cell at any intensity was considered positive. RESULTS: Thirty-four out 208 cases (16.3%) had PDL-1 positive staining. PDL-1 expression was observed in patients with non-small cell lung carcinoma independent of the histological type or subtype (range; 0-25%). When the cut-off level was set to ≥5% with moderate and strong staining, the median overall survival was 45 months for the PD-L1 positive group and not reached for the PD-L1 negative group (p-value 0.024). PD-L1 positivity was significantly higher in patients over the age of 60 years and in cases with a tumor diameter of more than 5 cm (p=0.023 and 0.025, respectively). CONCLUSION: PD-L1 expression is positive in 16.3% of patients with non-small cell lung cancer and may have a negative prognostic value.
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spelling pubmed-65285252019-05-30 Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis Şahin, Songül Batur, Şebnem Aydın, Övgü Öztürk, Tülin Turna, Akif Öz, Büge Balkan Med J Original Article BACKGROUND: Prognostic significance of the programmed death-ligand-1 status in non-small cell lung carcinoma remains controversial AIMS: To show the programmed death-ligand-1 expression status in patients with non-small cell lung carcinoma and its effect on the prognosis and the relationship with clinicopathologic data. STUDY DESIGN: Retrospective cross-sectional study. METHODS: The study included 208 cases who were diagnosed with NSCLC and who underwent surgical resection between 2001 and 2012. Programmed death-ligand-1 (SP142 clone) was applied to the histological sections acquired from the microarray paraffin blocks with immunohistochemistry. Staining intensity was scored as weak (+, 1), moderate (++, 2), and strong (+++, 3). Percentage (0%-100%) was multiplied by staining intensity (1-2-3) to calculate the H score. Four different cut-off values were used; 1: ≥1% (independent of intensity), 2: ≥5% (independent of intensity), 3: ≥5% moderate/strong staining (except for weak staining), 4: H score ≥30 values were considered positive. In this study, staining a single cell at any intensity was considered positive. RESULTS: Thirty-four out 208 cases (16.3%) had PDL-1 positive staining. PDL-1 expression was observed in patients with non-small cell lung carcinoma independent of the histological type or subtype (range; 0-25%). When the cut-off level was set to ≥5% with moderate and strong staining, the median overall survival was 45 months for the PD-L1 positive group and not reached for the PD-L1 negative group (p-value 0.024). PD-L1 positivity was significantly higher in patients over the age of 60 years and in cases with a tumor diameter of more than 5 cm (p=0.023 and 0.025, respectively). CONCLUSION: PD-L1 expression is positive in 16.3% of patients with non-small cell lung cancer and may have a negative prognostic value. Galenos Publishing 2019-05 2019-05-10 /pmc/articles/PMC6528525/ /pubmed/30592196 http://dx.doi.org/10.4274/balkanmedj.galenos.2018.2018.0392 Text en ©Copyright 2019 by Trakya University Faculty of Medicine http://creativecommons.org/licenses/by/2.5/ The Balkan Medical Journal published by Galenos Publishing House.
spellingShingle Original Article
Şahin, Songül
Batur, Şebnem
Aydın, Övgü
Öztürk, Tülin
Turna, Akif
Öz, Büge
Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title_full Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title_fullStr Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title_full_unstemmed Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title_short Programmed Death-Ligand-1 Expression in Non-Small Cell Lung Cancer and Prognosis
title_sort programmed death-ligand-1 expression in non-small cell lung cancer and prognosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528525/
https://www.ncbi.nlm.nih.gov/pubmed/30592196
http://dx.doi.org/10.4274/balkanmedj.galenos.2018.2018.0392
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