Abstract

Simple SummaryGlioblastoma is the most frequent and the most aggressive brain tumor. Even with the most current treatment, its prognosis remains dismal. Immunotherapies, novel cancer therapies using the patient’s own immune system to fight cancer, have revolutionized the treatment of numerous cancer types and generate great hope for glioblastoma. In this review, we analyze the challenges immunotherapy is facing in glioblastoma, present the different immunotherapy approaches with corresponding key clinical trial findings, and finally discuss limitations and how they might be overcome. Proof of efficacy for immunotherapies remains to be demonstrated in glioblastoma, but novel combinatorial approaches remain promising.Glioblastoma is the most frequent and the most aggressive brain tumor. It is notoriously resistant to current treatments, and the prognosis remains dismal. Immunotherapies have revolutionized the treatment of numerous cancer types and generate great hope for glioblastoma, alas without success until now. In this review, the rationale underlying immune targeting of glioblastoma, as well as the challenges faced when targeting these highly immunosuppressive tumors, are discussed. Innovative immune-targeting strategies including cancer vaccines, oncolytic viruses, checkpoint blockade inhibitors, adoptive cell transfer, and CAR T cells that have been investigated in glioblastoma are reviewed. From a clinical perspective, key clinical trial findings and ongoing trials are discussed for each approach. Finally, limitations, either biological or arising from trial designs are analyzed, and strategies to overcome them are presented. Proof of efficacy for immunotherapy approaches remains to be demonstrated in glioblastoma, but our rapidly expanding understanding of its biology, its immune microenvironment, and the emergence of novel promising combinatorial approaches might allow researchers to finally fulfill the medical need for GBM patients.

Highlights

  • Glioblastoma multiforme (GBM) is the most frequent malignant primary central nervous system (CNS) tumor in adults [1]

  • Three main approaches have been considered in GBM: (1) peptide/DNA vaccines involve the injection of tumor-specific antigens or nucleic acids, often with immune stimulatory molecules to improve the adaptative immune response; (2) in cell-based therapies, peripheral blood mononuclear cells (PBMCs) can be differentiated into mature dendritic cells that are primed and loaded with tumor antigens prior to being reinfused to the patient; and (3) alternatively, viral vectors loaded with mRNA coding for key tumor antigens can be used as vaccination platform triggering potent immune responses

  • We look forward to seeing this approach being tested in GBM clinical trials, hopefully unleashing Tumor infiltrating lymphocytes (TILs) against GBM tumors

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Summary

Introduction

Glioblastoma multiforme (GBM) is the most frequent malignant primary central nervous system (CNS) tumor in adults [1] It is highly aggressive, notoriously resistant to all current standard of care treatments, and shows a very poor outcome, with a 6.8% 5-year overall survival [1]. Immunotherapy has demonstrated its efficacy against a wide range of solid tumors, including melanoma, non-small-cell lung cancer, and renal cell carcinoma, establishing the 5th pillar of anticancer treatment [2]. This progress has not yet translated to improved outcome for glioblastoma patients. We will take a look at future outlooks and provide elements to optimize clinical trials in immunotherapy

Standard of Care
Immune Privilege of the CNS
Significant Results
H-1 PV in recurrent HGG
Oncolytic Viruses
Checkpoint Inhibitors
Adoptive Cell Transfer and CAR T Cells
Identified Limits and How to Overcome Them
Conclusions

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