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Delivery of Antibodies into the Murine Brain via Convection-enhanced Delivery
Published on: July 18, 2019
Convection-enhanced delivery of targeted toxins for malignant glioma
Walter A Hall1, Gregory T Sherr
1Department of Neurosurgery, University of Minnesota Medical School, MMC 96, 420 Delaware Street SE, Minneapolis, MN 55455, USA. hallx003@umn.edu
Abstract:
Malignant gliomas represent a difficult treatment challenge for the neuro-oncologist and the neurosurgeon. These tumours continue to be refractory to standard therapies, such as surgery, radiotherapy and conventional chemotherapy, and new therapeutic options are clearly needed. Therefore, investigators have recently taken a new direction and started to engineer compounds such as recombinant cytotoxins, antiangiogenesis factors and genetic delivery vectors. However, these promising new agents are all dependent on an effective distribution method in order to bypass the blood-brain barrier. Convection-enhanced delivery (CED) allows for the administration of targeted toxins and other agents directly into the brain at the site of a tumour via catheters placed with the aid of stereotactic or image-guided surgery. The use of this technique is gaining momentum as a newly accepted treatment modality where little else has produced durable results in the fight against gliomas. Direct intratumoural infusion was first performed in nude mouse flank tumour models of human malignant glioma. After significant testing in preclinical animal studies, this method of delivery was followed by the successful demonstration of in vivo efficacy in Phase I and II clinical trials. Currently, this technique is being used in the investigational setting at academic medical centres where investigators are starting to define the best practice for CED. Fundamental issues in this method of delivery such as rate of infusion, cannula size, infusate concentration and tissue-cannula sealing time shape the current discussion in the literature. Targeted toxin therapy represents one of the newest and most promising treatments for this unfortunate patient population, with proven clinical efficacy administered through CED, which is a novel approach to drug delivery.
Insights
Convection-enhanced delivery (CED) offers a novel method for directly administering targeted therapies to malignant gliomas, bypassing the blood-brain barrier. This technique shows promise for treating these challenging brain tumors where traditional methods have failed.
Area of Science:
- Neurosurgery
- Oncology
- Drug Delivery Systems
Background:
- Malignant gliomas are notoriously difficult to treat with standard therapies.
- Existing treatments like surgery, radiotherapy, and chemotherapy often prove ineffective.
- Novel therapeutic strategies are urgently needed to combat these aggressive brain tumors.
Purpose of the Study:
- To introduce and evaluate Convection-Enhanced Delivery (CED) as a method for treating malignant gliomas.
- To highlight the potential of CED in delivering novel therapeutic agents directly to brain tumors.
- To discuss the ongoing research and optimization of CED techniques.
Main Methods:
- Convection-Enhanced Delivery (CED) involves direct administration of therapeutic agents into the brain via catheters.
- Catheters are placed using stereotactic or image-guided surgical techniques.
- The method was initially tested in preclinical models and subsequently evaluated in Phase I and II clinical trials.
Main Results:
- CED enables direct intratumoral infusion, bypassing the blood-brain barrier.
- Preclinical studies demonstrated efficacy, followed by successful clinical trials.
- The technique is gaining acceptance as a viable treatment modality for gliomas.
Conclusions:
- Convection-Enhanced Delivery (CED) is a promising approach for delivering targeted therapies, including recombinant cytotoxins and genetic vectors, directly into malignant gliomas.
- This method has shown clinical efficacy and is being refined in academic centers.
- CED represents a significant advancement in the treatment of challenging brain tumors.

