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Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma

Surgery followed by chemoradiation and adjuvant chemotherapy is standard of care for patients with a glioblastoma (GBM). Due to its limited benefit, an upfront method to predict dismal outcome would prevent unnecessary toxic treatment. We searched for a predictive blood derived biomarker in a cohort...

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Autores principales: van Linde, Myra E., van der Mijn, Johannes C., Pham, Thang V., Knol, Jaco C., Wedekind, Laurine E., Hovinga, Koos E., Aliaga, Esther Sanchez, Buter, Jan, Jimenez, Connie R., Reijneveld, Jaap C., Verheul, Henk M. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992035/
https://www.ncbi.nlm.nih.gov/pubmed/27444431
http://dx.doi.org/10.1007/s11060-016-2178-x
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author van Linde, Myra E.
van der Mijn, Johannes C.
Pham, Thang V.
Knol, Jaco C.
Wedekind, Laurine E.
Hovinga, Koos E.
Aliaga, Esther Sanchez
Buter, Jan
Jimenez, Connie R.
Reijneveld, Jaap C.
Verheul, Henk M. W.
author_facet van Linde, Myra E.
van der Mijn, Johannes C.
Pham, Thang V.
Knol, Jaco C.
Wedekind, Laurine E.
Hovinga, Koos E.
Aliaga, Esther Sanchez
Buter, Jan
Jimenez, Connie R.
Reijneveld, Jaap C.
Verheul, Henk M. W.
author_sort van Linde, Myra E.
collection PubMed
description Surgery followed by chemoradiation and adjuvant chemotherapy is standard of care for patients with a glioblastoma (GBM). Due to its limited benefit, an upfront method to predict dismal outcome would prevent unnecessary toxic treatment. We searched for a predictive blood derived biomarker in a cohort of 55 patients with GBM. Increasing age (HR 1.03, 95 % CI 1.01–1.06), and postoperative tumor residue (HR 1.07, 95 % CI 1.02–1.15) were independently associated with unfavourable progression free survival (PFS) in these patients. Corticosteroid use before start of chemoradiaton was strongly predictive for outcome (HR 3.26, 95 % CI 1.67–6.39) with a mean PFS and OS in patients using corticosteroids of 7.3 and 14.6 months, versus 16.1 and 21.6 months in patients not using corticosteroids (p = 0.0005, p < 0.0067 respectively). Despite earlier reports, blood concentrations of YKL-40, Fetuin-a and haptoglobin were not predictive for response. In addition, serum peptide profiles, determined by MALDI-TOF mass spectroscopy, were not predictive as well. In conclusion, further biomarker discovery studies are needed to predict treatment outcome for patients with GBM in the near future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-016-2178-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-49920352016-09-06 Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma van Linde, Myra E. van der Mijn, Johannes C. Pham, Thang V. Knol, Jaco C. Wedekind, Laurine E. Hovinga, Koos E. Aliaga, Esther Sanchez Buter, Jan Jimenez, Connie R. Reijneveld, Jaap C. Verheul, Henk M. W. J Neurooncol Laboratory Investigation Surgery followed by chemoradiation and adjuvant chemotherapy is standard of care for patients with a glioblastoma (GBM). Due to its limited benefit, an upfront method to predict dismal outcome would prevent unnecessary toxic treatment. We searched for a predictive blood derived biomarker in a cohort of 55 patients with GBM. Increasing age (HR 1.03, 95 % CI 1.01–1.06), and postoperative tumor residue (HR 1.07, 95 % CI 1.02–1.15) were independently associated with unfavourable progression free survival (PFS) in these patients. Corticosteroid use before start of chemoradiaton was strongly predictive for outcome (HR 3.26, 95 % CI 1.67–6.39) with a mean PFS and OS in patients using corticosteroids of 7.3 and 14.6 months, versus 16.1 and 21.6 months in patients not using corticosteroids (p = 0.0005, p < 0.0067 respectively). Despite earlier reports, blood concentrations of YKL-40, Fetuin-a and haptoglobin were not predictive for response. In addition, serum peptide profiles, determined by MALDI-TOF mass spectroscopy, were not predictive as well. In conclusion, further biomarker discovery studies are needed to predict treatment outcome for patients with GBM in the near future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-016-2178-x) contains supplementary material, which is available to authorized users. Springer US 2016-07-21 2016 /pmc/articles/PMC4992035/ /pubmed/27444431 http://dx.doi.org/10.1007/s11060-016-2178-x Text en © The Author(s) 2016 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.
spellingShingle Laboratory Investigation
van Linde, Myra E.
van der Mijn, Johannes C.
Pham, Thang V.
Knol, Jaco C.
Wedekind, Laurine E.
Hovinga, Koos E.
Aliaga, Esther Sanchez
Buter, Jan
Jimenez, Connie R.
Reijneveld, Jaap C.
Verheul, Henk M. W.
Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title_full Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title_fullStr Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title_full_unstemmed Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title_short Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
title_sort evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma
topic Laboratory Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992035/
https://www.ncbi.nlm.nih.gov/pubmed/27444431
http://dx.doi.org/10.1007/s11060-016-2178-x
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