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Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis

BACKGROUND: PD-L1 has been reported to be expressed in diverse human malignancies. However, the prognostic value of PD-L1 in digestive system cancers remains inconclusive. Therefore, we conducted this meta-analysis to evaluate the prognostic impact of PD-L1 expression in digestive system cancers. MA...

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Autores principales: Dai, Cong, Wang, Meng, Lu, Jun, Dai, Zhiming, Lin, Shuai, Yang, Pengtao, Tian, Tian, Liu, Xinghan, Min, Weili, Dai, Zhijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533487/
https://www.ncbi.nlm.nih.gov/pubmed/28769571
http://dx.doi.org/10.2147/OTT.S138044
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author Dai, Cong
Wang, Meng
Lu, Jun
Dai, Zhiming
Lin, Shuai
Yang, Pengtao
Tian, Tian
Liu, Xinghan
Min, Weili
Dai, Zhijun
author_facet Dai, Cong
Wang, Meng
Lu, Jun
Dai, Zhiming
Lin, Shuai
Yang, Pengtao
Tian, Tian
Liu, Xinghan
Min, Weili
Dai, Zhijun
author_sort Dai, Cong
collection PubMed
description BACKGROUND: PD-L1 has been reported to be expressed in diverse human malignancies. However, the prognostic value of PD-L1 in digestive system cancers remains inconclusive. Therefore, we conducted this meta-analysis to evaluate the prognostic impact of PD-L1 expression in digestive system cancers. MATERIALS AND METHODS: We searched the PubMed, Embase, and the Chinese National Knowledge Infrastructure for publications concerning PD-L1 expression in digestive system cancers. Correlations of PD-L1 expression level with overall survival (OS), disease-free survival (DFS), and recurrence-free survival (RFS) were analyzed. RESULTS: Finally, 32 studies with 7,308 patients were included. Our results show that PD-L1 expression was significantly associated with poorer OS (hazard ratio [HR] =1.44, 95% confidence interval [CI] =1.18–1.76, P<0.001), but not DFS (HR =0.91, 95% CI =0.61–1.37, P=0.657) or RFS (HR =1.27, 95% CI =0.75–2.14, P=0.368). Moreover, in the subgroup analysis, significant associations between PD-L1 expression and OS were found in Asians (HR =1.50, 95% CI =1.19–1.89, P=0.001), gastric cancer (HR =1.43, 95% CI =1.05–1.94, P=0.021), and pancreatic carcinoma (HR =2.64, 95% CI =1.78–3.93, P<0.001). CONCLUSION: These results suggest that the expression of PD-L1 is associated with worse OS in digestive system cancers, especially in gastric cancer and pancreatic cancer. In addition, PD-L1 may act as a new parameter for predicting poor prognosis and a promising target for anticancer therapy in digestive system cancers.
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spelling pubmed-55334872017-08-02 Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis Dai, Cong Wang, Meng Lu, Jun Dai, Zhiming Lin, Shuai Yang, Pengtao Tian, Tian Liu, Xinghan Min, Weili Dai, Zhijun Onco Targets Ther Original Research BACKGROUND: PD-L1 has been reported to be expressed in diverse human malignancies. However, the prognostic value of PD-L1 in digestive system cancers remains inconclusive. Therefore, we conducted this meta-analysis to evaluate the prognostic impact of PD-L1 expression in digestive system cancers. MATERIALS AND METHODS: We searched the PubMed, Embase, and the Chinese National Knowledge Infrastructure for publications concerning PD-L1 expression in digestive system cancers. Correlations of PD-L1 expression level with overall survival (OS), disease-free survival (DFS), and recurrence-free survival (RFS) were analyzed. RESULTS: Finally, 32 studies with 7,308 patients were included. Our results show that PD-L1 expression was significantly associated with poorer OS (hazard ratio [HR] =1.44, 95% confidence interval [CI] =1.18–1.76, P<0.001), but not DFS (HR =0.91, 95% CI =0.61–1.37, P=0.657) or RFS (HR =1.27, 95% CI =0.75–2.14, P=0.368). Moreover, in the subgroup analysis, significant associations between PD-L1 expression and OS were found in Asians (HR =1.50, 95% CI =1.19–1.89, P=0.001), gastric cancer (HR =1.43, 95% CI =1.05–1.94, P=0.021), and pancreatic carcinoma (HR =2.64, 95% CI =1.78–3.93, P<0.001). CONCLUSION: These results suggest that the expression of PD-L1 is associated with worse OS in digestive system cancers, especially in gastric cancer and pancreatic cancer. In addition, PD-L1 may act as a new parameter for predicting poor prognosis and a promising target for anticancer therapy in digestive system cancers. Dove Medical Press 2017-07-21 /pmc/articles/PMC5533487/ /pubmed/28769571 http://dx.doi.org/10.2147/OTT.S138044 Text en © 2017 Dai et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Dai, Cong
Wang, Meng
Lu, Jun
Dai, Zhiming
Lin, Shuai
Yang, Pengtao
Tian, Tian
Liu, Xinghan
Min, Weili
Dai, Zhijun
Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title_full Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title_fullStr Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title_full_unstemmed Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title_short Prognostic and predictive values of PD-L1 expression in patients with digestive system cancer: a meta-analysis
title_sort prognostic and predictive values of pd-l1 expression in patients with digestive system cancer: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533487/
https://www.ncbi.nlm.nih.gov/pubmed/28769571
http://dx.doi.org/10.2147/OTT.S138044
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