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Sarcoma Immunotherapy

Much of our knowledge regarding cancer immunotherapy has been derived from sarcoma models. However, translation of preclinical findings to bedside success has been limited in this disease, though several intriguing clinical studies hint at the potential efficacy of this treatment modality. The rarit...

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Detalles Bibliográficos
Autores principales: Gouw, Launce G., Jones, Kevin B., Sharma, Sunil, Randall, R. Lor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763415/
https://www.ncbi.nlm.nih.gov/pubmed/24213130
http://dx.doi.org/10.3390/cancers3044139
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author Gouw, Launce G.
Jones, Kevin B.
Sharma, Sunil
Randall, R. Lor
author_facet Gouw, Launce G.
Jones, Kevin B.
Sharma, Sunil
Randall, R. Lor
author_sort Gouw, Launce G.
collection PubMed
description Much of our knowledge regarding cancer immunotherapy has been derived from sarcoma models. However, translation of preclinical findings to bedside success has been limited in this disease, though several intriguing clinical studies hint at the potential efficacy of this treatment modality. The rarity and heterogeneity of tumors of mesenchymal origin continues to be a challenge from a therapeutic standpoint. Nonetheless, sarcomas remain attractive targets for immunotherapy, as they can be characterized by specific epitopes, either from their mesenchymal origins or specific alterations in gene products. To date, standard vaccine trials have proven disappointing, likely due to mechanisms by which tumors equilibrate with and ultimately escape immune surveillance. More sophisticated approaches will likely require multimodal techniques, both by enhancing immunity, but also geared towards overcoming innate mechanisms of immunosuppression that favor tumorigenesis.
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spelling pubmed-37634152013-09-05 Sarcoma Immunotherapy Gouw, Launce G. Jones, Kevin B. Sharma, Sunil Randall, R. Lor Cancers (Basel) Review Much of our knowledge regarding cancer immunotherapy has been derived from sarcoma models. However, translation of preclinical findings to bedside success has been limited in this disease, though several intriguing clinical studies hint at the potential efficacy of this treatment modality. The rarity and heterogeneity of tumors of mesenchymal origin continues to be a challenge from a therapeutic standpoint. Nonetheless, sarcomas remain attractive targets for immunotherapy, as they can be characterized by specific epitopes, either from their mesenchymal origins or specific alterations in gene products. To date, standard vaccine trials have proven disappointing, likely due to mechanisms by which tumors equilibrate with and ultimately escape immune surveillance. More sophisticated approaches will likely require multimodal techniques, both by enhancing immunity, but also geared towards overcoming innate mechanisms of immunosuppression that favor tumorigenesis. Molecular Diversity Preservation International (MDPI) 2011-11-10 /pmc/articles/PMC3763415/ /pubmed/24213130 http://dx.doi.org/10.3390/cancers3044139 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Gouw, Launce G.
Jones, Kevin B.
Sharma, Sunil
Randall, R. Lor
Sarcoma Immunotherapy
title Sarcoma Immunotherapy
title_full Sarcoma Immunotherapy
title_fullStr Sarcoma Immunotherapy
title_full_unstemmed Sarcoma Immunotherapy
title_short Sarcoma Immunotherapy
title_sort sarcoma immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763415/
https://www.ncbi.nlm.nih.gov/pubmed/24213130
http://dx.doi.org/10.3390/cancers3044139
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