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Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy
BACKGROUND: The prognostic and predictive value of multiple serum biomarkers was evaluated using samples from a randomised phase III study (HORIZON II) investigating chemotherapy with or without cediranib in metastatic colorectal cancer (mCRC). METHODS: Baseline levels of 207 protein markers were me...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844909/ https://www.ncbi.nlm.nih.gov/pubmed/24149180 http://dx.doi.org/10.1038/bjc.2013.649 |
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author | Spencer, S K M Pommier, A J C Morgan, S R Barry, S T Robertson, J D Hoff, P M Jürgensmeier, J M |
author_facet | Spencer, S K M Pommier, A J C Morgan, S R Barry, S T Robertson, J D Hoff, P M Jürgensmeier, J M |
author_sort | Spencer, S K M |
collection | PubMed |
description | BACKGROUND: The prognostic and predictive value of multiple serum biomarkers was evaluated using samples from a randomised phase III study (HORIZON II) investigating chemotherapy with or without cediranib in metastatic colorectal cancer (mCRC). METHODS: Baseline levels of 207 protein markers were measured in serum samples from 582 HORIZON II (FOLFOX/XELOX plus cediranib 20 mg (n=330) or placebo (n=252)) patients. Median baseline values of each biomarker were used to categorise patients as high or low. Markers were then assessed for their association with efficacy, defined by progression-free survival (PFS) and overall survival (OS). A generalised boosted regression model identified markers of particular interest. RESULTS: Correlation of protein levels with PFS and OS suggested that multiple factors had a prognostic value, independent of treatment arm, including IL-6, IL-8, C-reactive protein (CRP), ICAM-1 and carcinoembryonic antigen (CEA). Among the angiogenesis regulators, low levels of vascular endothelial growth factor (VEGF), VEGF-D, VEGFR-1, VEGFR-3, NRP1 and Tie-2 correlated with better outcome. CONCLUSION: This large data set generated using serum samples from mCRC patients treated with chemotherapy and VEGF inhibitors, defines baseline characteristics for 207 serum proteins. Multiple prognostic factors were identified that could be disease related or predict which patients derive most benefit from 5-fluorouracil (5-FU)-based chemotherapy, meriting further exploration in prospective studies. |
format | Online Article Text |
id | pubmed-3844909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38449092014-11-26 Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy Spencer, S K M Pommier, A J C Morgan, S R Barry, S T Robertson, J D Hoff, P M Jürgensmeier, J M Br J Cancer Clinical Study BACKGROUND: The prognostic and predictive value of multiple serum biomarkers was evaluated using samples from a randomised phase III study (HORIZON II) investigating chemotherapy with or without cediranib in metastatic colorectal cancer (mCRC). METHODS: Baseline levels of 207 protein markers were measured in serum samples from 582 HORIZON II (FOLFOX/XELOX plus cediranib 20 mg (n=330) or placebo (n=252)) patients. Median baseline values of each biomarker were used to categorise patients as high or low. Markers were then assessed for their association with efficacy, defined by progression-free survival (PFS) and overall survival (OS). A generalised boosted regression model identified markers of particular interest. RESULTS: Correlation of protein levels with PFS and OS suggested that multiple factors had a prognostic value, independent of treatment arm, including IL-6, IL-8, C-reactive protein (CRP), ICAM-1 and carcinoembryonic antigen (CEA). Among the angiogenesis regulators, low levels of vascular endothelial growth factor (VEGF), VEGF-D, VEGFR-1, VEGFR-3, NRP1 and Tie-2 correlated with better outcome. CONCLUSION: This large data set generated using serum samples from mCRC patients treated with chemotherapy and VEGF inhibitors, defines baseline characteristics for 207 serum proteins. Multiple prognostic factors were identified that could be disease related or predict which patients derive most benefit from 5-fluorouracil (5-FU)-based chemotherapy, meriting further exploration in prospective studies. Nature Publishing Group 2013-11-26 2013-10-22 /pmc/articles/PMC3844909/ /pubmed/24149180 http://dx.doi.org/10.1038/bjc.2013.649 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Clinical Study Spencer, S K M Pommier, A J C Morgan, S R Barry, S T Robertson, J D Hoff, P M Jürgensmeier, J M Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title | Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title_full | Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title_fullStr | Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title_full_unstemmed | Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title_short | Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
title_sort | prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844909/ https://www.ncbi.nlm.nih.gov/pubmed/24149180 http://dx.doi.org/10.1038/bjc.2013.649 |
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