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Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis
Accumulated evidence has shown that the programmed cell death receptor 1/programmed cell death receptor 1 ligand 1 (PD-1/PD-L1) pathway is a promising therapeutic target for cancer immunotherapy. However, the association between PD-L1 and esophageal squamous cell carcinoma (ESCC) patient survival re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862626/ https://www.ncbi.nlm.nih.gov/pubmed/29568405 http://dx.doi.org/10.18632/oncotarget.23810 |
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author | Guo, Wei Wang, Pan Li, Ning Shao, Fei Zhang, Hao Yang, Zhenlin Li, Renda Gao, Yibo He, Jie |
author_facet | Guo, Wei Wang, Pan Li, Ning Shao, Fei Zhang, Hao Yang, Zhenlin Li, Renda Gao, Yibo He, Jie |
author_sort | Guo, Wei |
collection | PubMed |
description | Accumulated evidence has shown that the programmed cell death receptor 1/programmed cell death receptor 1 ligand 1 (PD-1/PD-L1) pathway is a promising therapeutic target for cancer immunotherapy. However, the association between PD-L1 and esophageal squamous cell carcinoma (ESCC) patient survival remains unclear. We performed a meta-analysis to investigate the prognostic value of PD-L1 in ESCC. We searched PubMed, Embase, Web of Knowledge, and Cochrane Central Register of Controlled Trials databases for relevant studies that evaluated PD-L1 expression and ESCC patient survival. Fixed- and random-effects meta-analyses were conducted according to the heterogeneity of the included studies. Sensitivity analysis was performed according to Metan-based influence analysis. Publication bias was evaluated using Egger’s and Begg’s tests. Overall, 13 studies with 2,877 patients were included. Twelve studies demonstrated the association between overall survival (OS), and 6 studies described the relation between disease-free survival (DFS). PD-L1 overexpression was found in 43.7% (1,258 of 2,877) of the patients with ESCC. High PD-L1 expression was associated with distant metastasis in patients with ESCC (P = 0.04). Moreover, high PD-L1 expression was significantly associated with poor OS (hazard ratio [HR] 1.38, 95% confidence interval [CI] = 1.02–1.86, P = 0.04) and especially in Asian populations (HR 1.49, 95% CI = 1.11–1.99, P = 0.008). But it did not have an impact on disease-free survival (HR 1.15, 95% CI = 0.76–1.74, P = 0.52). Further well-designed clinical studies with uniform assessment approaches for PD-L1 expression are warranted to verify its prognostic value. |
format | Online Article Text |
id | pubmed-5862626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58626262018-03-22 Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis Guo, Wei Wang, Pan Li, Ning Shao, Fei Zhang, Hao Yang, Zhenlin Li, Renda Gao, Yibo He, Jie Oncotarget Meta-Analysis Accumulated evidence has shown that the programmed cell death receptor 1/programmed cell death receptor 1 ligand 1 (PD-1/PD-L1) pathway is a promising therapeutic target for cancer immunotherapy. However, the association between PD-L1 and esophageal squamous cell carcinoma (ESCC) patient survival remains unclear. We performed a meta-analysis to investigate the prognostic value of PD-L1 in ESCC. We searched PubMed, Embase, Web of Knowledge, and Cochrane Central Register of Controlled Trials databases for relevant studies that evaluated PD-L1 expression and ESCC patient survival. Fixed- and random-effects meta-analyses were conducted according to the heterogeneity of the included studies. Sensitivity analysis was performed according to Metan-based influence analysis. Publication bias was evaluated using Egger’s and Begg’s tests. Overall, 13 studies with 2,877 patients were included. Twelve studies demonstrated the association between overall survival (OS), and 6 studies described the relation between disease-free survival (DFS). PD-L1 overexpression was found in 43.7% (1,258 of 2,877) of the patients with ESCC. High PD-L1 expression was associated with distant metastasis in patients with ESCC (P = 0.04). Moreover, high PD-L1 expression was significantly associated with poor OS (hazard ratio [HR] 1.38, 95% confidence interval [CI] = 1.02–1.86, P = 0.04) and especially in Asian populations (HR 1.49, 95% CI = 1.11–1.99, P = 0.008). But it did not have an impact on disease-free survival (HR 1.15, 95% CI = 0.76–1.74, P = 0.52). Further well-designed clinical studies with uniform assessment approaches for PD-L1 expression are warranted to verify its prognostic value. Impact Journals LLC 2017-12-27 /pmc/articles/PMC5862626/ /pubmed/29568405 http://dx.doi.org/10.18632/oncotarget.23810 Text en Copyright: © 2018 Guo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Guo, Wei Wang, Pan Li, Ning Shao, Fei Zhang, Hao Yang, Zhenlin Li, Renda Gao, Yibo He, Jie Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title | Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title_full | Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title_fullStr | Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title_full_unstemmed | Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title_short | Prognostic value of PD-L1 in esophageal squamous cell carcinoma: a meta-analysis |
title_sort | prognostic value of pd-l1 in esophageal squamous cell carcinoma: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862626/ https://www.ncbi.nlm.nih.gov/pubmed/29568405 http://dx.doi.org/10.18632/oncotarget.23810 |
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