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Review
. 2024 Sep;30(9):e70013.
doi: 10.1111/cns.70013.

Immunotherapeutic advances in glioma management: The rise of vaccine-based approaches

Affiliations
Review

Immunotherapeutic advances in glioma management: The rise of vaccine-based approaches

Wireko Andrew Awuah et al. CNS Neurosci Ther. 2024 Sep.

Abstract

Background: Gliomas, particularly glioblastoma multiforme (GBM), are highly aggressive brain tumors that present significant challenges in oncology due to their rapid progression and resistance to conventional therapies. Despite advancements in treatment, the prognosis for patients with GBM remains poor, necessitating the exploration of novel therapeutic approaches. One such emerging strategy is the development of glioma vaccines, which aim to stimulate the immune system to target and destroy tumor cells.

Aims: This review aims to provide a comprehensive evaluation of the current landscape of glioma vaccine development, analyzing the types of vaccines under investigation, the outcomes of clinical trials, and the challenges and opportunities associated with their implementation. The goal is to highlight the potential of glioma vaccines in advancing more effective and personalized treatments for glioma patients.

Materials and methods: This narrative review systematically assessed the role of glioma vaccines by including full-text articles published between 2000 and 2024 in English. Databases such as PubMed/MEDLINE, EMBASE, the Cochrane Library, and Scopus were searched using key terms like "glioma," "brain tumor," "glioblastoma," "vaccine," and "immunotherapy." The review incorporated both pre-clinical and clinical studies, including descriptive studies, animal-model studies, cohort studies, and observational studies. Exclusion criteria were applied to omit abstracts, case reports, posters, and non-peer-reviewed studies, ensuring the inclusion of high-quality evidence.

Results: Clinical trials investigating various glioma vaccines, including peptide-based, DNA/RNA-based, whole-cell, and dendritic-cell vaccines, have shown promising results. These vaccines demonstrated potential in extending survival rates and managing adverse events in glioma patients. However, significant challenges remain, such as therapeutic resistance due to tumor heterogeneity and immune evasion mechanisms. Moreover, the lack of standardized guidelines for evaluating vaccine responses and issues related to ethical considerations, regulatory hurdles, and vaccine acceptance among patients further complicate the implementation of glioma vaccines.

Discussion: Addressing the challenges associated with glioma vaccines involves exploring combination therapies, targeted approaches, and personalized medicine. Combining vaccines with traditional therapies like radiotherapy or chemotherapy may enhance efficacy by boosting the immune system's ability to fight tumor cells. Personalized vaccines tailored to individual patient profiles present an opportunity for improved outcomes. Furthermore, global collaboration and equitable distribution are critical for ensuring access to glioma vaccines, especially in low- and middle-income countries with limited healthcare resources CONCLUSION: Glioma vaccines represent a promising avenue in the fight against gliomas, offering hope for improving patient outcomes in a disease that is notoriously difficult to treat. Despite the challenges, continued research and the development of innovative strategies, including combination therapies and personalized approaches, are essential for overcoming current barriers and transforming the treatment landscape for glioma patients.

Keywords: glioma; glioma vaccines; immunotherapy; neuro‐oncology.

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Conflict of interest statement

The authors have no relevant financial or non‐financial interests to disclose.

Figures

FIGURE 1
FIGURE 1
Comprehensive framework for the rationale behind glioma vaccine development. Image was created with Biorender.com. APVAC, Actively personalized vaccines; GBM, Glioblastoma Multiforme; IDH, Isocitrate Dehydrogenase.
FIGURE 2
FIGURE 2
Overview of the tumor microenvironment and immunosuppressive foundations in glioma immunology. Created with Biorender.com. CCL22, CC Motif Chemokine Ligand 22; GAMs, Glioma‐associated microglia and macrophages; MDSC, Myeloid‐derived suppressor cells; PDL1, Programmed death‐ligand 1.
FIGURE 3
FIGURE 3
Mechanism of action of glioma vaccines. Image was created with Biorender.com. APCs, Antigen‐Presenting Cells; DMG, Diffuse midline gliomas; Poly‐ICLC, Polyinosinic‐polycytidylic acid; RIG‐1, Retinoic acid‐inducible gene I.

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