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Is immunotherapy in the future of therapeutic management of sarcomas?
Sarcomas are rare, ubiquitous and heterogeneous tumors usually treated with surgery, chemotherapy, target therapy, and radiotherapy. However, 25–50% of patients experience local relapses and/or distant metastases after chemotherapy with an overall survival about 12–18 months. Recently, immuno-therap...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077947/ https://www.ncbi.nlm.nih.gov/pubmed/33902630 http://dx.doi.org/10.1186/s12967-021-02829-y |
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author | Clemente, Ottavia Ottaiano, Alessandro Di Lorenzo, Giuseppe Bracigliano, Alessandra Lamia, Sabrina Cannella, Lucia Pizzolorusso, Antonio Di Marzo, Massimiliano Santorsola, Mariachiara De Chiara, Annarosaria Fazioli, Flavio Tafuto, Salvatore |
author_facet | Clemente, Ottavia Ottaiano, Alessandro Di Lorenzo, Giuseppe Bracigliano, Alessandra Lamia, Sabrina Cannella, Lucia Pizzolorusso, Antonio Di Marzo, Massimiliano Santorsola, Mariachiara De Chiara, Annarosaria Fazioli, Flavio Tafuto, Salvatore |
author_sort | Clemente, Ottavia |
collection | PubMed |
description | Sarcomas are rare, ubiquitous and heterogeneous tumors usually treated with surgery, chemotherapy, target therapy, and radiotherapy. However, 25–50% of patients experience local relapses and/or distant metastases after chemotherapy with an overall survival about 12–18 months. Recently, immuno-therapy has revolutionized the cancer treatments with initial indications for non-small cell lung cancer (NSCLC) and melanoma (immune-checkpoint inhibitors).Here, we provide a narrative review on the topic as well as a critical description of the currently available trials on immunotherapy treatments in patients with sarcoma. Given the promising results obtained with anti-PD-1 monoclonal antibodies (pembrolizumab and nivolumab) and CAR-T cells, we strongly believe that these new immunotherapeutic approaches, along with an innovative characterization of tumor genetics, will provide an exciting opportunity to ameliorate the therapeutic management of sarcomas. |
format | Online Article Text |
id | pubmed-8077947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80779472021-04-29 Is immunotherapy in the future of therapeutic management of sarcomas? Clemente, Ottavia Ottaiano, Alessandro Di Lorenzo, Giuseppe Bracigliano, Alessandra Lamia, Sabrina Cannella, Lucia Pizzolorusso, Antonio Di Marzo, Massimiliano Santorsola, Mariachiara De Chiara, Annarosaria Fazioli, Flavio Tafuto, Salvatore J Transl Med Review Sarcomas are rare, ubiquitous and heterogeneous tumors usually treated with surgery, chemotherapy, target therapy, and radiotherapy. However, 25–50% of patients experience local relapses and/or distant metastases after chemotherapy with an overall survival about 12–18 months. Recently, immuno-therapy has revolutionized the cancer treatments with initial indications for non-small cell lung cancer (NSCLC) and melanoma (immune-checkpoint inhibitors).Here, we provide a narrative review on the topic as well as a critical description of the currently available trials on immunotherapy treatments in patients with sarcoma. Given the promising results obtained with anti-PD-1 monoclonal antibodies (pembrolizumab and nivolumab) and CAR-T cells, we strongly believe that these new immunotherapeutic approaches, along with an innovative characterization of tumor genetics, will provide an exciting opportunity to ameliorate the therapeutic management of sarcomas. BioMed Central 2021-04-26 /pmc/articles/PMC8077947/ /pubmed/33902630 http://dx.doi.org/10.1186/s12967-021-02829-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Clemente, Ottavia Ottaiano, Alessandro Di Lorenzo, Giuseppe Bracigliano, Alessandra Lamia, Sabrina Cannella, Lucia Pizzolorusso, Antonio Di Marzo, Massimiliano Santorsola, Mariachiara De Chiara, Annarosaria Fazioli, Flavio Tafuto, Salvatore Is immunotherapy in the future of therapeutic management of sarcomas? |
title | Is immunotherapy in the future of therapeutic management of sarcomas? |
title_full | Is immunotherapy in the future of therapeutic management of sarcomas? |
title_fullStr | Is immunotherapy in the future of therapeutic management of sarcomas? |
title_full_unstemmed | Is immunotherapy in the future of therapeutic management of sarcomas? |
title_short | Is immunotherapy in the future of therapeutic management of sarcomas? |
title_sort | is immunotherapy in the future of therapeutic management of sarcomas? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077947/ https://www.ncbi.nlm.nih.gov/pubmed/33902630 http://dx.doi.org/10.1186/s12967-021-02829-y |
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