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Current Immunotherapies for Sarcoma: Clinical Trials and Rationale
Sarcoma tumors are rare and heterogeneous, yet they possess many characteristics that may facilitate immunotherapeutic responses. Both active strategies including vaccines and passive strategies involving cellular adoptive immunotherapy have been applied clinically. Results of these clinical trials...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039267/ https://www.ncbi.nlm.nih.gov/pubmed/27703409 http://dx.doi.org/10.1155/2016/9757219 |
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author | Mitsis, Demytra Francescutti, Valerie Skitzki, Joseph |
author_facet | Mitsis, Demytra Francescutti, Valerie Skitzki, Joseph |
author_sort | Mitsis, Demytra |
collection | PubMed |
description | Sarcoma tumors are rare and heterogeneous, yet they possess many characteristics that may facilitate immunotherapeutic responses. Both active strategies including vaccines and passive strategies involving cellular adoptive immunotherapy have been applied clinically. Results of these clinical trials indicate a distinct benefit for select patients. The recent breakthrough of immunologic checkpoint inhibition is being rapidly introduced to a variety of tumor types including sarcoma. It is anticipated that these emerging immunotherapies will exhibit clinical efficacy for a variety of sarcomas. The increasing ability to tailor immunologic therapies to sarcoma patients will undoubtedly generate further enthusiasm and clinical research for this treatment modality. |
format | Online Article Text |
id | pubmed-5039267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50392672016-10-04 Current Immunotherapies for Sarcoma: Clinical Trials and Rationale Mitsis, Demytra Francescutti, Valerie Skitzki, Joseph Sarcoma Review Article Sarcoma tumors are rare and heterogeneous, yet they possess many characteristics that may facilitate immunotherapeutic responses. Both active strategies including vaccines and passive strategies involving cellular adoptive immunotherapy have been applied clinically. Results of these clinical trials indicate a distinct benefit for select patients. The recent breakthrough of immunologic checkpoint inhibition is being rapidly introduced to a variety of tumor types including sarcoma. It is anticipated that these emerging immunotherapies will exhibit clinical efficacy for a variety of sarcomas. The increasing ability to tailor immunologic therapies to sarcoma patients will undoubtedly generate further enthusiasm and clinical research for this treatment modality. Hindawi Publishing Corporation 2016 2016-09-14 /pmc/articles/PMC5039267/ /pubmed/27703409 http://dx.doi.org/10.1155/2016/9757219 Text en Copyright © 2016 Demytra Mitsis et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Mitsis, Demytra Francescutti, Valerie Skitzki, Joseph Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title | Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title_full | Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title_fullStr | Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title_full_unstemmed | Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title_short | Current Immunotherapies for Sarcoma: Clinical Trials and Rationale |
title_sort | current immunotherapies for sarcoma: clinical trials and rationale |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039267/ https://www.ncbi.nlm.nih.gov/pubmed/27703409 http://dx.doi.org/10.1155/2016/9757219 |
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