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Intra-arterial chemotherapy for malignant gliomas: a critical analysis
J-K Burkhardt1, H A Riina, B J Shin
1Department of Neurological Surgery, Weill Cornell Brain Tumor Center, Weill Cornell Medical College, New York, [corrected] USA.
Intra-arterial (IA) chemotherapy for malignant gliomas is reviewed for safety and efficacy compared to other methods. This approach may offer targeted delivery to cancer stem cells in the perivascular niche.
Area of Science:
- Neuro-oncology
- Chemotherapy delivery systems
- Cancer stem cell research
Background:
- Malignant gliomas, including glioblastoma multiforme, have historically been treated with various chemotherapy methods.
- Intra-arterial (IA) chemotherapy delivery for these tumors has been explored for decades.
- Advances in endovascular techniques have refined IA delivery, but its superiority remains debated.
Purpose of the Study:
- To review the existing literature on IA chemotherapy for malignant gliomas.
- To assess the advantages and disadvantages of IA chemotherapy compared to intravenous (IV) and oral routes.
- To propose a hypothesis for utilizing IA delivery to target cancer stem cells in their niche.
Main Methods:
- Comprehensive literature review of preclinical and clinical studies on IA chemotherapy for malignant gliomas.
- Analysis of safety and efficacy data for IA versus IV and oral chemotherapy.
- Exploration of endovascular devices and techniques in IA therapy.
Main Results:
- The review synthesizes data on the safety and comparative effectiveness of IA chemotherapy.
- Identifies benefits and drawbacks of IA drug delivery for malignant gliomas.
- Highlights the potential for IA delivery to target specific tumor cell populations.
Conclusions:
- IA chemotherapy presents a potential treatment modality for malignant gliomas, with ongoing debate regarding its superiority.
- Targeted IA delivery may offer advantages in reaching specific tumor microenvironments.
- Further research is warranted to validate the hypothesis of targeting cancer stem cells via IA delivery.
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