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PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study
BACKGROUND: The prognostic value of programmed death-ligand 1 (PD-L1) expression in patients with malignant pleural mesothelioma (MPM) has been controversial according to previous investigations. Therefore, we conducted a meta-analysis to assess the potential prognostic significance of PD-L1 express...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533928/ https://www.ncbi.nlm.nih.gov/pubmed/33062064 http://dx.doi.org/10.1177/1758835920962362 |
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author | Jin, Liu Gu, Weiling Li, Xueqin Xie, Liang Wang, Linhong Chen, Zhongwen |
author_facet | Jin, Liu Gu, Weiling Li, Xueqin Xie, Liang Wang, Linhong Chen, Zhongwen |
author_sort | Jin, Liu |
collection | PubMed |
description | BACKGROUND: The prognostic value of programmed death-ligand 1 (PD-L1) expression in patients with malignant pleural mesothelioma (MPM) has been controversial according to previous investigations. Therefore, we conducted a meta-analysis to assess the potential prognostic significance of PD-L1 expression in MPM. METHODS: PubMed, Embase, Web of Science, Scopus, and the Cochrane Library were thoroughly searched for relevant original articles published before 9 April 2020. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) of overall survival (OS) and progression-free survival (PFS) were calculated. The results of the meta-analysis were verified using The Cancer Genome Atlas (TCGA) dataset. RESULTS: In total 16 studies were included in our meta-analysis. A high PD-L1 expression was associated with a poor OS (HR = 1.53, 95% CI = 1.28–1.83, p < 0.001), but not a grave PFS (HR = 1.07, 95% CI = 0.82–1.39, p = 0.643) in MPM. Furthermore, the PD-L1 expression correlated with the sarcomatoid + biphasic type of MPM (odds ratio = 4.32, 95% CI = 2.16–8.64, p < 0.001). TCGA data indicated that PD-L1 was a significant prognostic factor for OS (HR = 2.069, 95% CI = 1.136–3.769, p = 0.0175), but not for PFS (HR = 1.205, 95% CI = 0.572–2.539, p = 0.624), which was in accordance with the results of the meta-analysis. CONCLUSION: A high PD-L1 expression is a significant prognostic factor for poor OS of patients with MPM. We therefore suggest that PD-L1 expression levels can be used to predict the clinical outcomes of patients with MPM in the future. |
format | Online Article Text |
id | pubmed-7533928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75339282020-10-14 PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study Jin, Liu Gu, Weiling Li, Xueqin Xie, Liang Wang, Linhong Chen, Zhongwen Ther Adv Med Oncol Meta-Analysis BACKGROUND: The prognostic value of programmed death-ligand 1 (PD-L1) expression in patients with malignant pleural mesothelioma (MPM) has been controversial according to previous investigations. Therefore, we conducted a meta-analysis to assess the potential prognostic significance of PD-L1 expression in MPM. METHODS: PubMed, Embase, Web of Science, Scopus, and the Cochrane Library were thoroughly searched for relevant original articles published before 9 April 2020. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) of overall survival (OS) and progression-free survival (PFS) were calculated. The results of the meta-analysis were verified using The Cancer Genome Atlas (TCGA) dataset. RESULTS: In total 16 studies were included in our meta-analysis. A high PD-L1 expression was associated with a poor OS (HR = 1.53, 95% CI = 1.28–1.83, p < 0.001), but not a grave PFS (HR = 1.07, 95% CI = 0.82–1.39, p = 0.643) in MPM. Furthermore, the PD-L1 expression correlated with the sarcomatoid + biphasic type of MPM (odds ratio = 4.32, 95% CI = 2.16–8.64, p < 0.001). TCGA data indicated that PD-L1 was a significant prognostic factor for OS (HR = 2.069, 95% CI = 1.136–3.769, p = 0.0175), but not for PFS (HR = 1.205, 95% CI = 0.572–2.539, p = 0.624), which was in accordance with the results of the meta-analysis. CONCLUSION: A high PD-L1 expression is a significant prognostic factor for poor OS of patients with MPM. We therefore suggest that PD-L1 expression levels can be used to predict the clinical outcomes of patients with MPM in the future. SAGE Publications 2020-09-29 /pmc/articles/PMC7533928/ /pubmed/33062064 http://dx.doi.org/10.1177/1758835920962362 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Meta-Analysis Jin, Liu Gu, Weiling Li, Xueqin Xie, Liang Wang, Linhong Chen, Zhongwen PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title | PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title_full | PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title_fullStr | PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title_full_unstemmed | PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title_short | PD-L1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
title_sort | pd-l1 and prognosis in patients with malignant pleural mesothelioma: a meta-analysis and bioinformatics study |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533928/ https://www.ncbi.nlm.nih.gov/pubmed/33062064 http://dx.doi.org/10.1177/1758835920962362 |
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