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Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis

BACKGROUND: Programmed cell death-ligand 1 (PD-L1) may be a useful molecule for targeted immunotherapy. Therefore, this meta-analysis aimed to investigate PD-L1 expression in breast cancer and its associations with clinicopathological factors and outcomes, which may help determine whether PD-L1 expr...

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Autores principales: Kim, Hye Min, Lee, Jinae, Koo, Ja Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645886/
https://www.ncbi.nlm.nih.gov/pubmed/29041905
http://dx.doi.org/10.1186/s12885-017-3670-1
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author Kim, Hye Min
Lee, Jinae
Koo, Ja Seung
author_facet Kim, Hye Min
Lee, Jinae
Koo, Ja Seung
author_sort Kim, Hye Min
collection PubMed
description BACKGROUND: Programmed cell death-ligand 1 (PD-L1) may be a useful molecule for targeted immunotherapy. Therefore, this meta-analysis aimed to investigate PD-L1 expression in breast cancer and its associations with clinicopathological factors and outcomes, which may help determine whether PD-L1 expression is a useful prognostic marker. METHODS: The Medline Ovid, Cochrane, PubMed, Google Scholar, and Web of Knowledge databases were searched for studies that evaluated the prognostic or clinicopathological significance of PD-L1 expression in patients with breast cancer, and reported at least one survival-related outcome. RESULTS: Six studies that included 7877 cases were selected for the analysis. Higher PD-L1 expression in all cells was related to higher histological grade and lymph node metastasis. Higher PD-L1 expression in tumor cell was related to larger tumor size, estrogen receptor negativity, progesterone receptor negativity, human epidermal growth factor type-2 positivity, and triple-negative breast cancer. PD-L1 positivity in all cells was associated with poorer disease-free survival, although it was not significantly associated with overall survival. CONCLUSION: The present meta-analysis revealed that cases of breast cancer with PD-L1 positivity in all cells exhibited higher histological grades, lymph node metastasis, and poorer disease-free survival. Therefore, positive expression of PD-L1 may be a useful prognostic marker in breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-017-3670-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-56458862017-10-26 Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis Kim, Hye Min Lee, Jinae Koo, Ja Seung BMC Cancer Research Article BACKGROUND: Programmed cell death-ligand 1 (PD-L1) may be a useful molecule for targeted immunotherapy. Therefore, this meta-analysis aimed to investigate PD-L1 expression in breast cancer and its associations with clinicopathological factors and outcomes, which may help determine whether PD-L1 expression is a useful prognostic marker. METHODS: The Medline Ovid, Cochrane, PubMed, Google Scholar, and Web of Knowledge databases were searched for studies that evaluated the prognostic or clinicopathological significance of PD-L1 expression in patients with breast cancer, and reported at least one survival-related outcome. RESULTS: Six studies that included 7877 cases were selected for the analysis. Higher PD-L1 expression in all cells was related to higher histological grade and lymph node metastasis. Higher PD-L1 expression in tumor cell was related to larger tumor size, estrogen receptor negativity, progesterone receptor negativity, human epidermal growth factor type-2 positivity, and triple-negative breast cancer. PD-L1 positivity in all cells was associated with poorer disease-free survival, although it was not significantly associated with overall survival. CONCLUSION: The present meta-analysis revealed that cases of breast cancer with PD-L1 positivity in all cells exhibited higher histological grades, lymph node metastasis, and poorer disease-free survival. Therefore, positive expression of PD-L1 may be a useful prognostic marker in breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-017-3670-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-17 /pmc/articles/PMC5645886/ /pubmed/29041905 http://dx.doi.org/10.1186/s12885-017-3670-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kim, Hye Min
Lee, Jinae
Koo, Ja Seung
Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title_full Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title_fullStr Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title_full_unstemmed Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title_short Clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
title_sort clinicopathological and prognostic significance of programmed death ligand-1 expression in breast cancer: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645886/
https://www.ncbi.nlm.nih.gov/pubmed/29041905
http://dx.doi.org/10.1186/s12885-017-3670-1
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