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A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma

BACKGROUND: For decades, tumour hypoxia has been pursued as a cancer treatment target. However, prognostic and predictive biomarkers are essential for the use of this target in the clinic. This study investigates the prognostic value of a hypoxia-induced gene profile in localised soft tissue sarcoma...

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Autores principales: Aggerholm-Pedersen, Ninna, Sørensen, Brita Singers, Overgaard, Jens, Toustrup, Kasper, Baerentzen, Steen, Nielsen, Ole Steen, Maretty-Kongstad, Katja, Nordsmark, Marianne, Alsner, Jan, Safwat, Akmal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117798/
https://www.ncbi.nlm.nih.gov/pubmed/27701385
http://dx.doi.org/10.1038/bjc.2016.310
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author Aggerholm-Pedersen, Ninna
Sørensen, Brita Singers
Overgaard, Jens
Toustrup, Kasper
Baerentzen, Steen
Nielsen, Ole Steen
Maretty-Kongstad, Katja
Nordsmark, Marianne
Alsner, Jan
Safwat, Akmal
author_facet Aggerholm-Pedersen, Ninna
Sørensen, Brita Singers
Overgaard, Jens
Toustrup, Kasper
Baerentzen, Steen
Nielsen, Ole Steen
Maretty-Kongstad, Katja
Nordsmark, Marianne
Alsner, Jan
Safwat, Akmal
author_sort Aggerholm-Pedersen, Ninna
collection PubMed
description BACKGROUND: For decades, tumour hypoxia has been pursued as a cancer treatment target. However, prognostic and predictive biomarkers are essential for the use of this target in the clinic. This study investigates the prognostic value of a hypoxia-induced gene profile in localised soft tissue sarcoma (STS). METHODS: The hypoxia-induced gene quantification was performed by real-time quantitative PCR (RT-qPCR) of formalin-fixed, paraffin-embedded tissue samples. The gene expression cut-points were determined in a test cohort of 55 STS patients and used to allocate each patient into a more or a less hypoxic group. The cut-points found in the test cohort were applied to a cohort of 77 STS patients for validation. RESULTS: For patients with localised high-grade STS treated with surgery with or without postoperative radiation therapy, the prognostic value of the hypoxia-induced gene profile was proved in the test cohort and confirmed in the validation cohort. After adjustment for confounders, the hazard ratio (HR) was 3.2 (95% CI: 1.5; 7.0) for patients with more hypoxic tumours compared with patients with less hypoxic tumours regarding disease-specific survival. Moreover, for the development of metastatic disease, the HR was 2.61 (95% CI: 1.27; 5.33). CONCLUSIONS: The hypoxia-induced gene profile is a validated independent prognostic marker that may help identify STS patients needing more aggressive or different adjuvant treatment.
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spelling pubmed-51177982017-10-25 A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma Aggerholm-Pedersen, Ninna Sørensen, Brita Singers Overgaard, Jens Toustrup, Kasper Baerentzen, Steen Nielsen, Ole Steen Maretty-Kongstad, Katja Nordsmark, Marianne Alsner, Jan Safwat, Akmal Br J Cancer Molecular Diagnostics BACKGROUND: For decades, tumour hypoxia has been pursued as a cancer treatment target. However, prognostic and predictive biomarkers are essential for the use of this target in the clinic. This study investigates the prognostic value of a hypoxia-induced gene profile in localised soft tissue sarcoma (STS). METHODS: The hypoxia-induced gene quantification was performed by real-time quantitative PCR (RT-qPCR) of formalin-fixed, paraffin-embedded tissue samples. The gene expression cut-points were determined in a test cohort of 55 STS patients and used to allocate each patient into a more or a less hypoxic group. The cut-points found in the test cohort were applied to a cohort of 77 STS patients for validation. RESULTS: For patients with localised high-grade STS treated with surgery with or without postoperative radiation therapy, the prognostic value of the hypoxia-induced gene profile was proved in the test cohort and confirmed in the validation cohort. After adjustment for confounders, the hazard ratio (HR) was 3.2 (95% CI: 1.5; 7.0) for patients with more hypoxic tumours compared with patients with less hypoxic tumours regarding disease-specific survival. Moreover, for the development of metastatic disease, the HR was 2.61 (95% CI: 1.27; 5.33). CONCLUSIONS: The hypoxia-induced gene profile is a validated independent prognostic marker that may help identify STS patients needing more aggressive or different adjuvant treatment. Nature Publishing Group 2016-10-25 2016-10-04 /pmc/articles/PMC5117798/ /pubmed/27701385 http://dx.doi.org/10.1038/bjc.2016.310 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Aggerholm-Pedersen, Ninna
Sørensen, Brita Singers
Overgaard, Jens
Toustrup, Kasper
Baerentzen, Steen
Nielsen, Ole Steen
Maretty-Kongstad, Katja
Nordsmark, Marianne
Alsner, Jan
Safwat, Akmal
A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title_full A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title_fullStr A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title_full_unstemmed A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title_short A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
title_sort prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117798/
https://www.ncbi.nlm.nih.gov/pubmed/27701385
http://dx.doi.org/10.1038/bjc.2016.310
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