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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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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