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The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis

OBJECTIVE: Although the prognostic value of programmed cell death-ligand 1 (PD-L1) expression in non-Hodgkin lymphoma (NHL) has been evaluated in many studies, the results remain controversial. To investigate the prognostic role of PD-L1 expression and the association between PD-L1 expression and cl...

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Autores principales: Zhao, Shu, Zhang, Minghui, Zhang, Yu, Meng, Hongxue, Wang, Yan, Liu, Yupeng, Jing, Jing, Huang, Lan, Sun, Mengqi, Zhang, Yue, Zhang, Qingyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121049/
https://www.ncbi.nlm.nih.gov/pubmed/30197796
http://dx.doi.org/10.20892/j.issn.2095-3941.2018.0047
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author Zhao, Shu
Zhang, Minghui
Zhang, Yu
Meng, Hongxue
Wang, Yan
Liu, Yupeng
Jing, Jing
Huang, Lan
Sun, Mengqi
Zhang, Yue
Zhang, Qingyuan
author_facet Zhao, Shu
Zhang, Minghui
Zhang, Yu
Meng, Hongxue
Wang, Yan
Liu, Yupeng
Jing, Jing
Huang, Lan
Sun, Mengqi
Zhang, Yue
Zhang, Qingyuan
author_sort Zhao, Shu
collection PubMed
description OBJECTIVE: Although the prognostic value of programmed cell death-ligand 1 (PD-L1) expression in non-Hodgkin lymphoma (NHL) has been evaluated in many studies, the results remain controversial. To investigate the prognostic role of PD-L1 expression and the association between PD-L1 expression and clinicopathological features of NHL, we performed a meta-analysis. METHODS: The PubMed, EMBASE, and Cochrane Library databases were searched up to November 30, 2017. The hazard ratio (HR), 95% confidence interval (CI), and odds ratios (OR) with 95% CIs were combined to evaluate the association of PD-L1 expression with overall survival (OS) and clinicopathological features. Review manager 5.3 and STATA 12.0 were used in this meta-analysis. RESULTS: A total of 2,005 patients across nine studies were enrolled in our meta-analysis, and the pooled results showed that high PD-L1 expression was associated with a poor prognosis (HR=2.04, 95% CI: 1.18–3.54, P=0.01). In the subgroup analysis according to histology types, pooled results demonstrated that an increased PD-L1 expression was an unfavorable prognostic factor for diffuse large B-cell lymphoma (HR=1.92, 95% CI: 1.06–3.48, P=0.03) but not for natural killer/T-cell lymphoma (HR=2.41, 95% CI: 0.47–12.22, P=0.29). Pooled ORs indicated that PD-L1 expression was higher in NHL with international prognostic indices of ≥3. However, PD-L1 expression had no correlation with gender, age, disease stage, lactate dehydrogenase level, B symptoms, and germinal center B-cell-like lymphoma. CONCLUSIONS: High PD-L1 expression was a poor prognostic biomarker in patients with NHL. Because of our limited sample size, high-quality studies with larger sample sizes are needed to validate our results.
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spelling pubmed-61210492018-09-07 The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis Zhao, Shu Zhang, Minghui Zhang, Yu Meng, Hongxue Wang, Yan Liu, Yupeng Jing, Jing Huang, Lan Sun, Mengqi Zhang, Yue Zhang, Qingyuan Cancer Biol Med Original Article OBJECTIVE: Although the prognostic value of programmed cell death-ligand 1 (PD-L1) expression in non-Hodgkin lymphoma (NHL) has been evaluated in many studies, the results remain controversial. To investigate the prognostic role of PD-L1 expression and the association between PD-L1 expression and clinicopathological features of NHL, we performed a meta-analysis. METHODS: The PubMed, EMBASE, and Cochrane Library databases were searched up to November 30, 2017. The hazard ratio (HR), 95% confidence interval (CI), and odds ratios (OR) with 95% CIs were combined to evaluate the association of PD-L1 expression with overall survival (OS) and clinicopathological features. Review manager 5.3 and STATA 12.0 were used in this meta-analysis. RESULTS: A total of 2,005 patients across nine studies were enrolled in our meta-analysis, and the pooled results showed that high PD-L1 expression was associated with a poor prognosis (HR=2.04, 95% CI: 1.18–3.54, P=0.01). In the subgroup analysis according to histology types, pooled results demonstrated that an increased PD-L1 expression was an unfavorable prognostic factor for diffuse large B-cell lymphoma (HR=1.92, 95% CI: 1.06–3.48, P=0.03) but not for natural killer/T-cell lymphoma (HR=2.41, 95% CI: 0.47–12.22, P=0.29). Pooled ORs indicated that PD-L1 expression was higher in NHL with international prognostic indices of ≥3. However, PD-L1 expression had no correlation with gender, age, disease stage, lactate dehydrogenase level, B symptoms, and germinal center B-cell-like lymphoma. CONCLUSIONS: High PD-L1 expression was a poor prognostic biomarker in patients with NHL. Because of our limited sample size, high-quality studies with larger sample sizes are needed to validate our results. Chinese Anti-Cancer Association 2018-08 /pmc/articles/PMC6121049/ /pubmed/30197796 http://dx.doi.org/10.20892/j.issn.2095-3941.2018.0047 Text en
spellingShingle Original Article
Zhao, Shu
Zhang, Minghui
Zhang, Yu
Meng, Hongxue
Wang, Yan
Liu, Yupeng
Jing, Jing
Huang, Lan
Sun, Mengqi
Zhang, Yue
Zhang, Qingyuan
The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title_full The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title_fullStr The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title_full_unstemmed The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title_short The prognostic value of programmed cell death ligand 1 expression in non-Hodgkin lymphoma: a meta-analysis
title_sort prognostic value of programmed cell death ligand 1 expression in non-hodgkin lymphoma: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121049/
https://www.ncbi.nlm.nih.gov/pubmed/30197796
http://dx.doi.org/10.20892/j.issn.2095-3941.2018.0047
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