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Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma
Programmed death ligand-1 (PD-L1) is a potentially important tumor immunotherapy target. However, whether PD-L1 expression is associated with survival in nasopharyngeal carcinoma (NPC) remains controversial. The aim of the present study was to investigate the association between PD-L1 expression and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530303/ https://www.ncbi.nlm.nih.gov/pubmed/28781814 http://dx.doi.org/10.3892/mco.2017.1318 |
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author | Li, Ying-Fei Ding, Jian-Wu Liao, Ling-Min Zhang, Zhi-Lin Liao, Shou-Sheng Wu, Ying Zhou, Dan-Yang Liu, An-Wen Huang, Long |
author_facet | Li, Ying-Fei Ding, Jian-Wu Liao, Ling-Min Zhang, Zhi-Lin Liao, Shou-Sheng Wu, Ying Zhou, Dan-Yang Liu, An-Wen Huang, Long |
author_sort | Li, Ying-Fei |
collection | PubMed |
description | Programmed death ligand-1 (PD-L1) is a potentially important tumor immunotherapy target. However, whether PD-L1 expression is associated with survival in nasopharyngeal carcinoma (NPC) remains controversial. The aim of the present study was to investigate the association between PD-L1 expression and prognosis in NPC. The expression of PD-L1 was assessed in tumor specimens from 120 patients with NPC using immunohistochemistry. Staining was evaluated using the H-score method. The associations between PD-L1 expression and clinical characteristics and prognosis were analyzed. Overall, 78% of the patients had stage I–III and 22% had stage IV disease. The estimated 5-year overall survival (OS) and disease-free survival (DFS) rates for the entire cohort were 87.5 and 70.1%, respectively. PD-L1 expression was detected in 85 (71%) patients and was localized to the tumor cells. High tumor expression of PD-L1 (median H-score ≥5) was associated with significantly poorer OS (P=0.023) and DFS (P=0.002). Univariate analysis indicated that low PD-L1 expression was associated with better DFS compared with high PD-L1 expression (HR=0.163, 95% CI: 0.044–0.600, P=0.006 for DFS). Multivariate analysis revealed that T stage (HR=8.190, 95% CI: 1.355–18.152; P=0.023) and PD-L1 expression level (HR=0.124, 95% CI: 0.031–0.509; P=0.001) served as independent prognostic factors for DFS. In conclusion, tumor PD-L1 expression was found to be a significant prognostic factor in NPC, and high PD-L1 expression may be of prognostic value for recurrence and metastasis following conventional treatments. |
format | Online Article Text |
id | pubmed-5530303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-55303032017-08-04 Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma Li, Ying-Fei Ding, Jian-Wu Liao, Ling-Min Zhang, Zhi-Lin Liao, Shou-Sheng Wu, Ying Zhou, Dan-Yang Liu, An-Wen Huang, Long Mol Clin Oncol Articles Programmed death ligand-1 (PD-L1) is a potentially important tumor immunotherapy target. However, whether PD-L1 expression is associated with survival in nasopharyngeal carcinoma (NPC) remains controversial. The aim of the present study was to investigate the association between PD-L1 expression and prognosis in NPC. The expression of PD-L1 was assessed in tumor specimens from 120 patients with NPC using immunohistochemistry. Staining was evaluated using the H-score method. The associations between PD-L1 expression and clinical characteristics and prognosis were analyzed. Overall, 78% of the patients had stage I–III and 22% had stage IV disease. The estimated 5-year overall survival (OS) and disease-free survival (DFS) rates for the entire cohort were 87.5 and 70.1%, respectively. PD-L1 expression was detected in 85 (71%) patients and was localized to the tumor cells. High tumor expression of PD-L1 (median H-score ≥5) was associated with significantly poorer OS (P=0.023) and DFS (P=0.002). Univariate analysis indicated that low PD-L1 expression was associated with better DFS compared with high PD-L1 expression (HR=0.163, 95% CI: 0.044–0.600, P=0.006 for DFS). Multivariate analysis revealed that T stage (HR=8.190, 95% CI: 1.355–18.152; P=0.023) and PD-L1 expression level (HR=0.124, 95% CI: 0.031–0.509; P=0.001) served as independent prognostic factors for DFS. In conclusion, tumor PD-L1 expression was found to be a significant prognostic factor in NPC, and high PD-L1 expression may be of prognostic value for recurrence and metastasis following conventional treatments. D.A. Spandidos 2017-09 2017-07-13 /pmc/articles/PMC5530303/ /pubmed/28781814 http://dx.doi.org/10.3892/mco.2017.1318 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Li, Ying-Fei Ding, Jian-Wu Liao, Ling-Min Zhang, Zhi-Lin Liao, Shou-Sheng Wu, Ying Zhou, Dan-Yang Liu, An-Wen Huang, Long Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title | Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title_full | Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title_fullStr | Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title_full_unstemmed | Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title_short | Expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
title_sort | expression of programmed death ligand-1 predicts poor outcome in nasopharyngeal carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530303/ https://www.ncbi.nlm.nih.gov/pubmed/28781814 http://dx.doi.org/10.3892/mco.2017.1318 |
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