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Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group
A goal of the COG Ewing Sarcoma (ES) Biology Committee is enabling identification of reliable biomarkers that can predict treatment response and outcome through the use of prospectively collected tissues and correlative studies in concert with COG therapeutic studies. In this report, we aim to provi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674398/ https://www.ncbi.nlm.nih.gov/pubmed/23761859 http://dx.doi.org/10.3389/fonc.2013.00141 |
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author | Shukla, Neerav Schiffman, Joshua D. Reed, Damon Davis, Ian J. Womer, Richard B. Lessnick, Stephen L. Lawlor, Elizabeth R. |
author_facet | Shukla, Neerav Schiffman, Joshua D. Reed, Damon Davis, Ian J. Womer, Richard B. Lessnick, Stephen L. Lawlor, Elizabeth R. |
author_sort | Shukla, Neerav |
collection | PubMed |
description | A goal of the COG Ewing Sarcoma (ES) Biology Committee is enabling identification of reliable biomarkers that can predict treatment response and outcome through the use of prospectively collected tissues and correlative studies in concert with COG therapeutic studies. In this report, we aim to provide a concise review of the most well-characterized prognostic biomarkers in ES, and to provide recommendations concerning design and implementation of future biomarker studies. Of particular interest and potentially high clinical relevance are studies of cell-cycle proteins, sub-clinical disease, and copy number alterations. We discuss findings of particular interest from recent biomarker studies and examine factors important to the success of identifying and validating clinically relevant biomarkers in ES. A number of promising biomarkers have demonstrated prognostic significance in numerous retrospective studies and now need to be validated prospectively in larger cohorts of equivalently treated patients. The eventual goal of refining the discovery and use of clinically relevant biomarkers is the development of patient specific ES therapeutic modalities. |
format | Online Article Text |
id | pubmed-3674398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36743982013-06-11 Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group Shukla, Neerav Schiffman, Joshua D. Reed, Damon Davis, Ian J. Womer, Richard B. Lessnick, Stephen L. Lawlor, Elizabeth R. Front Oncol Oncology A goal of the COG Ewing Sarcoma (ES) Biology Committee is enabling identification of reliable biomarkers that can predict treatment response and outcome through the use of prospectively collected tissues and correlative studies in concert with COG therapeutic studies. In this report, we aim to provide a concise review of the most well-characterized prognostic biomarkers in ES, and to provide recommendations concerning design and implementation of future biomarker studies. Of particular interest and potentially high clinical relevance are studies of cell-cycle proteins, sub-clinical disease, and copy number alterations. We discuss findings of particular interest from recent biomarker studies and examine factors important to the success of identifying and validating clinically relevant biomarkers in ES. A number of promising biomarkers have demonstrated prognostic significance in numerous retrospective studies and now need to be validated prospectively in larger cohorts of equivalently treated patients. The eventual goal of refining the discovery and use of clinically relevant biomarkers is the development of patient specific ES therapeutic modalities. Frontiers Media S.A. 2013-06-06 /pmc/articles/PMC3674398/ /pubmed/23761859 http://dx.doi.org/10.3389/fonc.2013.00141 Text en Copyright © 2013 Shukla, Schiffman, Reed, Davis, Womer, Lessnick, Lawlor and Committee. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Oncology Shukla, Neerav Schiffman, Joshua D. Reed, Damon Davis, Ian J. Womer, Richard B. Lessnick, Stephen L. Lawlor, Elizabeth R. Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title_full | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title_fullStr | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title_full_unstemmed | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title_short | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children’s Oncology Group |
title_sort | biomarkers in ewing sarcoma: the promise and challenge of personalized medicine. a report from the children’s oncology group |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674398/ https://www.ncbi.nlm.nih.gov/pubmed/23761859 http://dx.doi.org/10.3389/fonc.2013.00141 |
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