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Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?

SIMPLE SUMMARY: Treatment modalities for sarcoma have not changed significantly for the past few years despite 25–50% of patients experiencing relapse or progressing to metastatic diseases that become resistant to standard of care therapy, indicating an unmet need for better treatment strategies. Wh...

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Autores principales: Chew, Hui Yi, Chan, Victor, Simpson, Fiona, Dolcetti, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697818/
https://www.ncbi.nlm.nih.gov/pubmed/33207697
http://dx.doi.org/10.3390/cancers12113392
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author Chew, Hui Yi
Chan, Victor
Simpson, Fiona
Dolcetti, Riccardo
author_facet Chew, Hui Yi
Chan, Victor
Simpson, Fiona
Dolcetti, Riccardo
author_sort Chew, Hui Yi
collection PubMed
description SIMPLE SUMMARY: Treatment modalities for sarcoma have not changed significantly for the past few years despite 25–50% of patients experiencing relapse or progressing to metastatic diseases that become resistant to standard of care therapy, indicating an unmet need for better treatment strategies. While immunotherapy has shown promising results in other types of cancer such as melanoma, first generation immunotherapy trials in sarcomas patients showed unsatisfactory results. Nevertheless, the progressive deepening of our knowledge about the immune landscape of sarcomas and the consequent ability to dissect the heterogeneity of these tumours are leading to a more accurate stratification of patients to be treated with immunotherapy. In addition, new targets are being exploited by a variety of promising immunotherapeutic treatments, which are expected to considerably improve the clinical management of sarcoma patients. ABSTRACT: Sarcomas are a rare type of a heterogeneous group of tumours arising from mesenchymal cells that form connective tissues. Surgery is the most common treatment for these tumours, but additional neoadjuvant or adjuvant chemotherapy or radiation therapies may be necessary. Unfortunately, a significant proportion of patients treated with conventional therapies will develop metastatic disease that is resistant to therapies. Currently, there is an urgent need to develop more effective and durable therapies for the treatment of sarcomas. In recent years immunotherapies have revolutionised the treatment of a variety of cancers by restoring patient anti-tumour immune responses or through the adoptive infusion of immune effectors able to kill and eliminate malignant cells. The clinicopathologic and genetic heterogeneity of sarcomas, together with the generally low burden of somatic mutations potentially generating neoantigens, are currently limited to broad application of immunotherapy for patients with sarcomas. Nevertheless, a better understanding of the microenvironmental factors hampering the efficacy of immunotherapy and the identification of new and suitable therapeutic targets may help to overcome current limitations. Moreover, the recent advances in the development of immunotherapies based on the direct exploitation or targeting of T cells and/or NK cells may offer new opportunities to improve the treatment of sarcomas, particularly those showing recurrence or resistance to standard of care treatments.
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spelling pubmed-76978182020-11-29 Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit? Chew, Hui Yi Chan, Victor Simpson, Fiona Dolcetti, Riccardo Cancers (Basel) Review SIMPLE SUMMARY: Treatment modalities for sarcoma have not changed significantly for the past few years despite 25–50% of patients experiencing relapse or progressing to metastatic diseases that become resistant to standard of care therapy, indicating an unmet need for better treatment strategies. While immunotherapy has shown promising results in other types of cancer such as melanoma, first generation immunotherapy trials in sarcomas patients showed unsatisfactory results. Nevertheless, the progressive deepening of our knowledge about the immune landscape of sarcomas and the consequent ability to dissect the heterogeneity of these tumours are leading to a more accurate stratification of patients to be treated with immunotherapy. In addition, new targets are being exploited by a variety of promising immunotherapeutic treatments, which are expected to considerably improve the clinical management of sarcoma patients. ABSTRACT: Sarcomas are a rare type of a heterogeneous group of tumours arising from mesenchymal cells that form connective tissues. Surgery is the most common treatment for these tumours, but additional neoadjuvant or adjuvant chemotherapy or radiation therapies may be necessary. Unfortunately, a significant proportion of patients treated with conventional therapies will develop metastatic disease that is resistant to therapies. Currently, there is an urgent need to develop more effective and durable therapies for the treatment of sarcomas. In recent years immunotherapies have revolutionised the treatment of a variety of cancers by restoring patient anti-tumour immune responses or through the adoptive infusion of immune effectors able to kill and eliminate malignant cells. The clinicopathologic and genetic heterogeneity of sarcomas, together with the generally low burden of somatic mutations potentially generating neoantigens, are currently limited to broad application of immunotherapy for patients with sarcomas. Nevertheless, a better understanding of the microenvironmental factors hampering the efficacy of immunotherapy and the identification of new and suitable therapeutic targets may help to overcome current limitations. Moreover, the recent advances in the development of immunotherapies based on the direct exploitation or targeting of T cells and/or NK cells may offer new opportunities to improve the treatment of sarcomas, particularly those showing recurrence or resistance to standard of care treatments. MDPI 2020-11-16 /pmc/articles/PMC7697818/ /pubmed/33207697 http://dx.doi.org/10.3390/cancers12113392 Text en © 2020 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chew, Hui Yi
Chan, Victor
Simpson, Fiona
Dolcetti, Riccardo
Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title_full Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title_fullStr Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title_full_unstemmed Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title_short Will Next-Generation Immunotherapy Overcome the Intrinsic Diversity and Low Immunogenicity of Sarcomas to Improve Clinical Benefit?
title_sort will next-generation immunotherapy overcome the intrinsic diversity and low immunogenicity of sarcomas to improve clinical benefit?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697818/
https://www.ncbi.nlm.nih.gov/pubmed/33207697
http://dx.doi.org/10.3390/cancers12113392
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