Advances in Immunotherapy for Adult Glioblastoma
Despite aggressive multimodal therapy, glioblastoma (GBM) remains the most common malignant primary brain tumor in adults. With the advent of therapies that revitalize the anti-tumor immune response, several immunotherapeutic modalities have been developed for treatment of GBM. In this review, we su...
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Veröffentlicht in: | Cancers 2021-07, Vol.13 (14), p.3400 |
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description | Despite aggressive multimodal therapy, glioblastoma (GBM) remains the most common malignant primary brain tumor in adults. With the advent of therapies that revitalize the anti-tumor immune response, several immunotherapeutic modalities have been developed for treatment of GBM. In this review, we summarize recent clinical and preclinical efforts to evaluate vaccination strategies, immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR) T cells. Although these modalities have shown long-term tumor regression in subsets of treated patients, the underlying biology that may predict efficacy and inform therapy development is being actively investigated. Common to all therapeutic modalities are fundamental mechanisms of therapy evasion by tumor cells, including immense intratumoral heterogeneity, suppression of the tumor immune microenvironment and low mutational burden. These insights have led efforts to design rational combinatorial therapies that can reignite the anti-tumor immune response, effectively and specifically target tumor cells and reliably decrease tumor burden for GBM patients. |
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With the advent of therapies that revitalize the anti-tumor immune response, several immunotherapeutic modalities have been developed for treatment of GBM. In this review, we summarize recent clinical and preclinical efforts to evaluate vaccination strategies, immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR) T cells. Although these modalities have shown long-term tumor regression in subsets of treated patients, the underlying biology that may predict efficacy and inform therapy development is being actively investigated. Common to all therapeutic modalities are fundamental mechanisms of therapy evasion by tumor cells, including immense intratumoral heterogeneity, suppression of the tumor immune microenvironment and low mutational burden. These insights have led efforts to design rational combinatorial therapies that can reignite the anti-tumor immune response, effectively and specifically target tumor cells and reliably decrease tumor burden for GBM patients.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13143400</identifier><identifier>PMID: 34298615</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antigens ; Brain cancer ; Brain tumors ; Chimeric antigen receptors ; Clinical trials ; Cytomegalovirus ; Glioblastoma ; Immune checkpoint inhibitors ; Immunotherapy ; Lymphatic system ; Lymphocytes ; Lymphocytes T ; Microenvironments ; Monoclonal antibodies ; Patients ; Peptides ; Proteins ; Review ; Tumor cells ; Tumors ; Vaccines ; Vascular endothelial growth factor</subject><ispartof>Cancers, 2021-07, Vol.13 (14), p.3400</ispartof><rights>2021 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 (https://creativecommons.org/licenses/by/4.0/). 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subjects | Antigens Brain cancer Brain tumors Chimeric antigen receptors Clinical trials Cytomegalovirus Glioblastoma Immune checkpoint inhibitors Immunotherapy Lymphatic system Lymphocytes Lymphocytes T Microenvironments Monoclonal antibodies Patients Peptides Proteins Review Tumor cells Tumors Vaccines Vascular endothelial growth factor |
title | Advances in Immunotherapy for Adult Glioblastoma |
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