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Updated: Nov 1, 2025

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Published on: October 27, 2014
Current progress in chimeric antigen receptor T cell therapy for glioblastoma multiforme
Hany E Marei1, Asmaa Althani2, Nahla Afifi3
1Department of Cytology and Histology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Chimeric antigen receptor T-cell (CAR-T) therapy shows promise for glioblastoma multiforme (GBM), a deadly brain cancer. Overcoming challenges like tumor heterogeneity and the brain microenvironment is key to successful clinical application.
Area of Science:
- Oncology
- Immunotherapy
- Neuro-oncology
Background:
- Glioblastoma multiforme (GBM) is an aggressive brain tumor with poor prognosis and limited treatment options.
- Current treatments including surgery, chemotherapy, and radiotherapy are largely ineffective for GBM.
- CAR-T cell therapy, successful in blood cancers, offers potential for treating solid tumors like GBM.
Purpose of the Study:
- To review the rationale for using CAR-T cell therapy in GBM.
- To identify GBM-associated antigens for CAR-T targeting.
- To discuss challenges and potential solutions for CAR-T therapy in GBM.
Main Methods:
- Review of scientific literature on CAR-T cell therapy and GBM.
- Analysis of CAR-T cell mechanisms, including FcγRs.
- Examination of GBM-specific challenges and antigen escape.
- Enumeration of ongoing and completed clinical trials.
Main Results:
- CAR-T therapy involves genetically engineering patient T cells to target tumor antigens.
- CAR-T cells eliminate tumor cells via cytotoxicity and cytokine release.
- Significant challenges impede CAR-T therapy for GBM, including tumor heterogeneity, immunosuppressive microenvironment, and the blood-brain barrier.
Conclusions:
- CAR-T cell therapy holds significant promise for treating glioblastoma multiforme.
- Addressing challenges such as antigen heterogeneity, the tumor microenvironment, and immune escape is crucial.
- Further research and clinical trials are necessary to optimize CAR-T therapy for GBM and improve patient outcomes.
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