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Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy
The incidence of malignant melanoma is rising worldwide and survival for metastatic disease is still poor. Recently, new treatment options have become available. Still, predictive biomarkers are needed to optimise treatment for this patient group. In this study, we investigated the predictive value...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317286/ https://www.ncbi.nlm.nih.gov/pubmed/30225999 http://dx.doi.org/10.1002/cjp2.116 |
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author | Schuster, Cornelia Akslen, Lars A Stokowy, Tomasz Straume, Oddbjørn |
author_facet | Schuster, Cornelia Akslen, Lars A Stokowy, Tomasz Straume, Oddbjørn |
author_sort | Schuster, Cornelia |
collection | PubMed |
description | The incidence of malignant melanoma is rising worldwide and survival for metastatic disease is still poor. Recently, new treatment options have become available. Still, predictive biomarkers are needed to optimise treatment for this patient group. In this study, we investigated the predictive value of 60 angiogenic factors in patients with metastatic melanoma treated with the anti‐vascular endothelial growth factor A antibody bevacizumab. Thirty‐five patients were included in a clinical phase II trial and baseline serum samples were analysed by multiplex protein array. High‐serum concentration of Activin A was significantly associated with objective response (OR) to treatment (p = 0.014). Candidate proteins that indicated a borderline association with treatment response were further investigated by immunohistochemistry. Strong expression of Activin A, interleukin‐1β, and urokinase‐type plasminogen activator receptor in metastases was significantly associated with OR (p = 0.011, p = 0.003, and p = 0.007, respectively), as well as with markers of activated angiogenesis, such as higher number of proliferating vessels and the presence of glomeruloid microvascular proliferations. Our findings indicate that these proteins may be potential predictive markers for treatment with bevacizumab monotherapy. |
format | Online Article Text |
id | pubmed-6317286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63172862019-01-08 Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy Schuster, Cornelia Akslen, Lars A Stokowy, Tomasz Straume, Oddbjørn J Pathol Clin Res Original Articles The incidence of malignant melanoma is rising worldwide and survival for metastatic disease is still poor. Recently, new treatment options have become available. Still, predictive biomarkers are needed to optimise treatment for this patient group. In this study, we investigated the predictive value of 60 angiogenic factors in patients with metastatic melanoma treated with the anti‐vascular endothelial growth factor A antibody bevacizumab. Thirty‐five patients were included in a clinical phase II trial and baseline serum samples were analysed by multiplex protein array. High‐serum concentration of Activin A was significantly associated with objective response (OR) to treatment (p = 0.014). Candidate proteins that indicated a borderline association with treatment response were further investigated by immunohistochemistry. Strong expression of Activin A, interleukin‐1β, and urokinase‐type plasminogen activator receptor in metastases was significantly associated with OR (p = 0.011, p = 0.003, and p = 0.007, respectively), as well as with markers of activated angiogenesis, such as higher number of proliferating vessels and the presence of glomeruloid microvascular proliferations. Our findings indicate that these proteins may be potential predictive markers for treatment with bevacizumab monotherapy. John Wiley & Sons, Inc. 2018-11-09 /pmc/articles/PMC6317286/ /pubmed/30225999 http://dx.doi.org/10.1002/cjp2.116 Text en © 2018 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Schuster, Cornelia Akslen, Lars A Stokowy, Tomasz Straume, Oddbjørn Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title | Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title_full | Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title_fullStr | Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title_full_unstemmed | Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title_short | Predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
title_sort | predictive value of angiogenic proteins in patients with metastatic melanoma treated with bevacizumab monotherapy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317286/ https://www.ncbi.nlm.nih.gov/pubmed/30225999 http://dx.doi.org/10.1002/cjp2.116 |
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