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The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer
In breast cancer (BC), elevated levels of urokinase-type plasminogen activator (uPA) in tumor tissue have been confirmed as a strong prognostic factor in level-of-evidence-1 studies. The aim of the present study was to evaluate the clinical relevance of uPA levels in serum of metastatic BC patients...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381129/ https://www.ncbi.nlm.nih.gov/pubmed/30783124 http://dx.doi.org/10.1038/s41598-018-37259-2 |
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author | Banys-Paluchowski, Malgorzata Witzel, Isabell Aktas, Bahriye Fasching, Peter A. Hartkopf, Andreas Janni, Wolfgang Kasimir-Bauer, Sabine Pantel, Klaus Schön, Gerhard Rack, Brigitte Riethdorf, Sabine Solomayer, Erich-Franz Fehm, Tanja Müller, Volkmar |
author_facet | Banys-Paluchowski, Malgorzata Witzel, Isabell Aktas, Bahriye Fasching, Peter A. Hartkopf, Andreas Janni, Wolfgang Kasimir-Bauer, Sabine Pantel, Klaus Schön, Gerhard Rack, Brigitte Riethdorf, Sabine Solomayer, Erich-Franz Fehm, Tanja Müller, Volkmar |
author_sort | Banys-Paluchowski, Malgorzata |
collection | PubMed |
description | In breast cancer (BC), elevated levels of urokinase-type plasminogen activator (uPA) in tumor tissue have been confirmed as a strong prognostic factor in level-of-evidence-1 studies. The aim of the present study was to evaluate the clinical relevance of uPA levels in serum of metastatic BC patients and to compare uPA with other blood-based biomarkers. 252 patients were enrolled in this prospective, multicentre study. Blood samples were collected before begin of first-line or later-line systemic treatment. Serum uPA was quantified by a commercially available ELISA. Circulating tumor cells (CTCs) were detected using CellSearch; other biomarkers (EGFR, VEGF, HER2, RAS p21, TIMP1, CAIX) by ELISA. Using the ROC analysis, the optimal cut-off value (determined by the Youden index) of serum uPA was 2.52 ng/ml. Using this value, 26% of patients had elevated uPA levels. Patients with visceral metastasis and more than one metastatic site were significantly more likely to present with elevated uPA levels. CTC status, serum HER2, RAS p21, CAIX, TIMP1 and VEGF correlated significantly with uPA levels. Elevated uPA levels predicted shorter overall and progression-free survival in univariate analysis (median OS: 7.5 months [95%-CI 4.5–10.5 months] vs. not reached, p < 0.001; PFS: 4.8 [95%-CI: 3.1–6.5] vs. 9.1 [7.4–10.8] months, p < 0.001). In multivariate analysis, elevated uPA, presence of ≥5 CTCs, elevated RAS p21, higher grading and higher line of therapy were independent predictors of shorter OS, while elevated CTC counts, higher line of therapy and negative estrogen receptor status were independent predictors of shorter PFS. In conclusion, elevated uPA levels independently predict reduced overall survival and improved prognostication in patients with known CTC status. Whether high serum uPA might identify patients most likely to benefit from therapies targeting uPA, remains to be evaluated in future trials. |
format | Online Article Text |
id | pubmed-6381129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63811292019-02-22 The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer Banys-Paluchowski, Malgorzata Witzel, Isabell Aktas, Bahriye Fasching, Peter A. Hartkopf, Andreas Janni, Wolfgang Kasimir-Bauer, Sabine Pantel, Klaus Schön, Gerhard Rack, Brigitte Riethdorf, Sabine Solomayer, Erich-Franz Fehm, Tanja Müller, Volkmar Sci Rep Article In breast cancer (BC), elevated levels of urokinase-type plasminogen activator (uPA) in tumor tissue have been confirmed as a strong prognostic factor in level-of-evidence-1 studies. The aim of the present study was to evaluate the clinical relevance of uPA levels in serum of metastatic BC patients and to compare uPA with other blood-based biomarkers. 252 patients were enrolled in this prospective, multicentre study. Blood samples were collected before begin of first-line or later-line systemic treatment. Serum uPA was quantified by a commercially available ELISA. Circulating tumor cells (CTCs) were detected using CellSearch; other biomarkers (EGFR, VEGF, HER2, RAS p21, TIMP1, CAIX) by ELISA. Using the ROC analysis, the optimal cut-off value (determined by the Youden index) of serum uPA was 2.52 ng/ml. Using this value, 26% of patients had elevated uPA levels. Patients with visceral metastasis and more than one metastatic site were significantly more likely to present with elevated uPA levels. CTC status, serum HER2, RAS p21, CAIX, TIMP1 and VEGF correlated significantly with uPA levels. Elevated uPA levels predicted shorter overall and progression-free survival in univariate analysis (median OS: 7.5 months [95%-CI 4.5–10.5 months] vs. not reached, p < 0.001; PFS: 4.8 [95%-CI: 3.1–6.5] vs. 9.1 [7.4–10.8] months, p < 0.001). In multivariate analysis, elevated uPA, presence of ≥5 CTCs, elevated RAS p21, higher grading and higher line of therapy were independent predictors of shorter OS, while elevated CTC counts, higher line of therapy and negative estrogen receptor status were independent predictors of shorter PFS. In conclusion, elevated uPA levels independently predict reduced overall survival and improved prognostication in patients with known CTC status. Whether high serum uPA might identify patients most likely to benefit from therapies targeting uPA, remains to be evaluated in future trials. Nature Publishing Group UK 2019-02-19 /pmc/articles/PMC6381129/ /pubmed/30783124 http://dx.doi.org/10.1038/s41598-018-37259-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Banys-Paluchowski, Malgorzata Witzel, Isabell Aktas, Bahriye Fasching, Peter A. Hartkopf, Andreas Janni, Wolfgang Kasimir-Bauer, Sabine Pantel, Klaus Schön, Gerhard Rack, Brigitte Riethdorf, Sabine Solomayer, Erich-Franz Fehm, Tanja Müller, Volkmar The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title | The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title_full | The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title_fullStr | The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title_full_unstemmed | The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title_short | The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer |
title_sort | prognostic relevance of urokinase-type plasminogen activator (upa) in the blood of patients with metastatic breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381129/ https://www.ncbi.nlm.nih.gov/pubmed/30783124 http://dx.doi.org/10.1038/s41598-018-37259-2 |
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