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Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence

Despite recent advances in cancer therapeutics, glioblastoma (GBM) remains one of the most difficult cancers to treat in both the primary and recurrent settings. GBM presents a unique therapeutic challenge given the immune-privileged environment of the brain and the aggressive nature of the disease....

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Autores principales: Kreatsoulas, Daniel, Bolyard, Chelsea, Wu, Bill X., Cam, Hakan, Giglio, Pierre, Li, Zihai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188021/
https://www.ncbi.nlm.nih.gov/pubmed/35690784
http://dx.doi.org/10.1186/s13045-022-01298-0
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author Kreatsoulas, Daniel
Bolyard, Chelsea
Wu, Bill X.
Cam, Hakan
Giglio, Pierre
Li, Zihai
author_facet Kreatsoulas, Daniel
Bolyard, Chelsea
Wu, Bill X.
Cam, Hakan
Giglio, Pierre
Li, Zihai
author_sort Kreatsoulas, Daniel
collection PubMed
description Despite recent advances in cancer therapeutics, glioblastoma (GBM) remains one of the most difficult cancers to treat in both the primary and recurrent settings. GBM presents a unique therapeutic challenge given the immune-privileged environment of the brain and the aggressive nature of the disease. Furthermore, it can change phenotypes throughout the course of disease—switching between mesenchymal, neural, and classic gene signatures, each with specific markers and mechanisms of resistance. Recent advancements in the field of immunotherapy—which utilizes strategies to reenergize or alter the immune system to target cancer—have shown striking results in patients with many types of malignancy. Immune checkpoint inhibitors, adoptive cellular therapy, cellular and peptide vaccines, and other technologies provide clinicians with a vast array of tools to design highly individualized treatment and potential for combination strategies. There are currently over 80 active clinical trials evaluating immunotherapies for GBM, often in combination with standard secondary treatment options including re-resection and anti-angiogenic agents, such as bevacizumab. This review will provide a clinically focused overview of the immune environment present in GBM, which is frequently immunosuppressive and characterized by M2 macrophages, T cell exhaustion, enhanced transforming growth factor-β signaling, and others. We will also outline existing immunotherapeutic strategies, with a special focus on immune checkpoint inhibitors, chimeric antigen receptor therapy, and dendritic cell vaccines. Finally, we will summarize key discoveries in the field and discuss currently active clinical trials, including combination strategies, burgeoning technology like nucleic acid and nanoparticle therapy, and novel anticancer vaccines. This review aims to provide the most updated summary of the field of immunotherapy for GBM and offer both historical perspective and future directions to help inform clinical practice.
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spelling pubmed-91880212022-06-13 Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence Kreatsoulas, Daniel Bolyard, Chelsea Wu, Bill X. Cam, Hakan Giglio, Pierre Li, Zihai J Hematol Oncol Review Despite recent advances in cancer therapeutics, glioblastoma (GBM) remains one of the most difficult cancers to treat in both the primary and recurrent settings. GBM presents a unique therapeutic challenge given the immune-privileged environment of the brain and the aggressive nature of the disease. Furthermore, it can change phenotypes throughout the course of disease—switching between mesenchymal, neural, and classic gene signatures, each with specific markers and mechanisms of resistance. Recent advancements in the field of immunotherapy—which utilizes strategies to reenergize or alter the immune system to target cancer—have shown striking results in patients with many types of malignancy. Immune checkpoint inhibitors, adoptive cellular therapy, cellular and peptide vaccines, and other technologies provide clinicians with a vast array of tools to design highly individualized treatment and potential for combination strategies. There are currently over 80 active clinical trials evaluating immunotherapies for GBM, often in combination with standard secondary treatment options including re-resection and anti-angiogenic agents, such as bevacizumab. This review will provide a clinically focused overview of the immune environment present in GBM, which is frequently immunosuppressive and characterized by M2 macrophages, T cell exhaustion, enhanced transforming growth factor-β signaling, and others. We will also outline existing immunotherapeutic strategies, with a special focus on immune checkpoint inhibitors, chimeric antigen receptor therapy, and dendritic cell vaccines. Finally, we will summarize key discoveries in the field and discuss currently active clinical trials, including combination strategies, burgeoning technology like nucleic acid and nanoparticle therapy, and novel anticancer vaccines. This review aims to provide the most updated summary of the field of immunotherapy for GBM and offer both historical perspective and future directions to help inform clinical practice. BioMed Central 2022-06-11 /pmc/articles/PMC9188021/ /pubmed/35690784 http://dx.doi.org/10.1186/s13045-022-01298-0 Text en © The Author(s) 2022 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
Kreatsoulas, Daniel
Bolyard, Chelsea
Wu, Bill X.
Cam, Hakan
Giglio, Pierre
Li, Zihai
Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title_full Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title_fullStr Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title_full_unstemmed Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title_short Translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
title_sort translational landscape of glioblastoma immunotherapy for physicians: guiding clinical practice with basic scientific evidence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188021/
https://www.ncbi.nlm.nih.gov/pubmed/35690784
http://dx.doi.org/10.1186/s13045-022-01298-0
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