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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doaj-4712cf49ea534c0fa091d4d5248372cd2021-07-23T13:33:15ZengMDPI AGCancers2072-66942021-07-01133400340010.3390/cancers13143400Advances in Immunotherapy for Adult GlioblastomaChirayu R. Chokshi0Benjamin A. Brakel1Nazanin Tatari2Neil Savage3Sabra K. Salim4Chitra Venugopal5Sheila K. Singh6Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Surgery, Faculty of Health Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8N 3Z5, CanadaDespite 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.https://www.mdpi.com/2072-6694/13/14/3400glioblastomaimmunotherapyvaccineimmune checkpoint inhibitorschimeric antigen receptor (CAR) T cells |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chirayu R. Chokshi Benjamin A. Brakel Nazanin Tatari Neil Savage Sabra K. Salim Chitra Venugopal Sheila K. Singh |
spellingShingle |
Chirayu R. Chokshi Benjamin A. Brakel Nazanin Tatari Neil Savage Sabra K. Salim Chitra Venugopal Sheila K. Singh Advances in Immunotherapy for Adult Glioblastoma Cancers glioblastoma immunotherapy vaccine immune checkpoint inhibitors chimeric antigen receptor (CAR) T cells |
author_facet |
Chirayu R. Chokshi Benjamin A. Brakel Nazanin Tatari Neil Savage Sabra K. Salim Chitra Venugopal Sheila K. Singh |
author_sort |
Chirayu R. Chokshi |
title |
Advances in Immunotherapy for Adult Glioblastoma |
title_short |
Advances in Immunotherapy for Adult Glioblastoma |
title_full |
Advances in Immunotherapy for Adult Glioblastoma |
title_fullStr |
Advances in Immunotherapy for Adult Glioblastoma |
title_full_unstemmed |
Advances in Immunotherapy for Adult Glioblastoma |
title_sort |
advances in immunotherapy for adult glioblastoma |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2021-07-01 |
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. |
topic |
glioblastoma immunotherapy vaccine immune checkpoint inhibitors chimeric antigen receptor (CAR) T cells |
url |
https://www.mdpi.com/2072-6694/13/14/3400 |
work_keys_str_mv |
AT chirayurchokshi advancesinimmunotherapyforadultglioblastoma AT benjaminabrakel advancesinimmunotherapyforadultglioblastoma AT nazanintatari advancesinimmunotherapyforadultglioblastoma AT neilsavage advancesinimmunotherapyforadultglioblastoma AT sabraksalim advancesinimmunotherapyforadultglioblastoma AT chitravenugopal advancesinimmunotherapyforadultglioblastoma AT sheilaksingh advancesinimmunotherapyforadultglioblastoma |
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