PD-L1 and Survival in Solid Tumors: A Meta-Analysis.

Numerous agents targeting PD-L1/PD-1 check-point are in clinical development. However, the correlation between PD-L1 expression and prognosis of solid tumor is still in controversial. Here, we elicit a systematic review and meta-analysis to investigate the potential value of PD-L1 in the prognostic...

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Main Authors: Pin Wu, Dang Wu, Lijun Li, Ying Chai, Jian Huang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4483169?pdf=render
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spelling doaj-7217b9caa5114027a21900575b93a1ce2020-11-25T02:47:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e013140310.1371/journal.pone.0131403PD-L1 and Survival in Solid Tumors: A Meta-Analysis.Pin WuDang WuLijun LiYing ChaiJian HuangNumerous agents targeting PD-L1/PD-1 check-point are in clinical development. However, the correlation between PD-L1 expression and prognosis of solid tumor is still in controversial. Here, we elicit a systematic review and meta-analysis to investigate the potential value of PD-L1 in the prognostic prediction in human solid tumors.Electronic databases were searched for studies evaluating the expression of PD-L1 and overall survival (OS) of patients with solid tumors. Odds ratios (ORs) from individual studies were calculated and pooled by using a random-effect model, and heterogeneity and publication bias analyses were also performed.A total of 3107 patients with solid tumor from 28 published studies were included in the meta-analysis. The median percentage of solid tumors with PD-L1 overexpression was 52.5%. PD-L1 overexpression was associated with worse OS at both 3 years (OR = 2.43, 95% confidence interval (CI) = 1.60 to 3.70, P < 0.0001) and 5 years (OR = 2.23, 95% CI = 1.40 to 3.55, P = 0.0008) of solid tumors. Among the tumor types, PD-L1 was associated with worse 3 year-OS of esophageal cancer, gastric cancer, hepatocellular carcinoma, and urothelial cancer, and 5 year-OS of esophageal cancer, gastric cancer and colorectal cancer.These results suggest that expression of PD-L1 is associated with worse survival in solid tumors. However, the correlations between PD-L1 and prognosis are variant among different tumor types. More studies are needed to investigate the clinical value of PD-L1 expression in prognostic prediction and treatment option.http://europepmc.org/articles/PMC4483169?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Pin Wu
Dang Wu
Lijun Li
Ying Chai
Jian Huang
spellingShingle Pin Wu
Dang Wu
Lijun Li
Ying Chai
Jian Huang
PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
PLoS ONE
author_facet Pin Wu
Dang Wu
Lijun Li
Ying Chai
Jian Huang
author_sort Pin Wu
title PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
title_short PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
title_full PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
title_fullStr PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
title_full_unstemmed PD-L1 and Survival in Solid Tumors: A Meta-Analysis.
title_sort pd-l1 and survival in solid tumors: a meta-analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Numerous agents targeting PD-L1/PD-1 check-point are in clinical development. However, the correlation between PD-L1 expression and prognosis of solid tumor is still in controversial. Here, we elicit a systematic review and meta-analysis to investigate the potential value of PD-L1 in the prognostic prediction in human solid tumors.Electronic databases were searched for studies evaluating the expression of PD-L1 and overall survival (OS) of patients with solid tumors. Odds ratios (ORs) from individual studies were calculated and pooled by using a random-effect model, and heterogeneity and publication bias analyses were also performed.A total of 3107 patients with solid tumor from 28 published studies were included in the meta-analysis. The median percentage of solid tumors with PD-L1 overexpression was 52.5%. PD-L1 overexpression was associated with worse OS at both 3 years (OR = 2.43, 95% confidence interval (CI) = 1.60 to 3.70, P < 0.0001) and 5 years (OR = 2.23, 95% CI = 1.40 to 3.55, P = 0.0008) of solid tumors. Among the tumor types, PD-L1 was associated with worse 3 year-OS of esophageal cancer, gastric cancer, hepatocellular carcinoma, and urothelial cancer, and 5 year-OS of esophageal cancer, gastric cancer and colorectal cancer.These results suggest that expression of PD-L1 is associated with worse survival in solid tumors. However, the correlations between PD-L1 and prognosis are variant among different tumor types. More studies are needed to investigate the clinical value of PD-L1 expression in prognostic prediction and treatment option.
url http://europepmc.org/articles/PMC4483169?pdf=render
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AT lijunli pdl1andsurvivalinsolidtumorsametaanalysis
AT yingchai pdl1andsurvivalinsolidtumorsametaanalysis
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