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Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer

Epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis. The emerging role of treatments co-targeting the EGFR system in breast cancer has increased the need to identify companion biomarkers. The aim of this study is to investigate whether pretreatment serum level...

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Autores principales: Kjær, Ina Mathilde, Olsen, Dorte Aalund, Brandslund, Ivan, Bechmann, Troels, Jakobsen, Erik Hugger, Bogh, Søren Bie, Madsen, Jonna Skov
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538553/
https://www.ncbi.nlm.nih.gov/pubmed/33024132
http://dx.doi.org/10.1038/s41598-020-72944-1
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author Kjær, Ina Mathilde
Olsen, Dorte Aalund
Brandslund, Ivan
Bechmann, Troels
Jakobsen, Erik Hugger
Bogh, Søren Bie
Madsen, Jonna Skov
author_facet Kjær, Ina Mathilde
Olsen, Dorte Aalund
Brandslund, Ivan
Bechmann, Troels
Jakobsen, Erik Hugger
Bogh, Søren Bie
Madsen, Jonna Skov
author_sort Kjær, Ina Mathilde
collection PubMed
description Epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis. The emerging role of treatments co-targeting the EGFR system in breast cancer has increased the need to identify companion biomarkers. The aim of this study is to investigate whether pretreatment serum levels of EGFR and EGFR ligands in early-stage breast cancer patients might provide prognostic information as a stepping stone for further investigation. The study, which included 311 early-stage breast cancer patients, investigated associations between preoperative serum levels of EGFR and EGFR ligands (epidermal growth factor, heparin-binding epidermal growth factor (HBEGF), amphiregulin, transforming growth factor-α and betacellulin) and survival. Cutoffs were determined using Youden’s method, and overall survival (OS) and invasive disease-free survival (IDFS) were evaluated using Cox regression. Preoperative S-EGFR < 60.3 ng/mL was associated with shorter OS and IDFS in both univariate analyses and when adjusting for standard prognostic factors (p < 0.05). Preoperative S-HBEGF < 21.4 pg/mL was associated with shorter OS in both univariate and multivariate analyses, whereas association with shorter IDFS could only be demonstrated in the univariate analysis. In conclusion, our study demonstrated shorter survival in early-stage breast cancer patients who had low pretreatment levels of either S-EGFR or S-HBEGF.
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spelling pubmed-75385532020-10-07 Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer Kjær, Ina Mathilde Olsen, Dorte Aalund Brandslund, Ivan Bechmann, Troels Jakobsen, Erik Hugger Bogh, Søren Bie Madsen, Jonna Skov Sci Rep Article Epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis. The emerging role of treatments co-targeting the EGFR system in breast cancer has increased the need to identify companion biomarkers. The aim of this study is to investigate whether pretreatment serum levels of EGFR and EGFR ligands in early-stage breast cancer patients might provide prognostic information as a stepping stone for further investigation. The study, which included 311 early-stage breast cancer patients, investigated associations between preoperative serum levels of EGFR and EGFR ligands (epidermal growth factor, heparin-binding epidermal growth factor (HBEGF), amphiregulin, transforming growth factor-α and betacellulin) and survival. Cutoffs were determined using Youden’s method, and overall survival (OS) and invasive disease-free survival (IDFS) were evaluated using Cox regression. Preoperative S-EGFR < 60.3 ng/mL was associated with shorter OS and IDFS in both univariate analyses and when adjusting for standard prognostic factors (p < 0.05). Preoperative S-HBEGF < 21.4 pg/mL was associated with shorter OS in both univariate and multivariate analyses, whereas association with shorter IDFS could only be demonstrated in the univariate analysis. In conclusion, our study demonstrated shorter survival in early-stage breast cancer patients who had low pretreatment levels of either S-EGFR or S-HBEGF. Nature Publishing Group UK 2020-10-06 /pmc/articles/PMC7538553/ /pubmed/33024132 http://dx.doi.org/10.1038/s41598-020-72944-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kjær, Ina Mathilde
Olsen, Dorte Aalund
Brandslund, Ivan
Bechmann, Troels
Jakobsen, Erik Hugger
Bogh, Søren Bie
Madsen, Jonna Skov
Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title_full Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title_fullStr Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title_full_unstemmed Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title_short Prognostic impact of serum levels of EGFR and EGFR ligands in early-stage breast cancer
title_sort prognostic impact of serum levels of egfr and egfr ligands in early-stage breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538553/
https://www.ncbi.nlm.nih.gov/pubmed/33024132
http://dx.doi.org/10.1038/s41598-020-72944-1
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