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Tumor Treating Field Therapy in Combination with Bevacizumab for the Treatment of Recurrent Glioblastoma
Published on: October 27, 2014
Noninvasive therapy of brain cancer using a unique systemic delivery methodology with a cancer terminator virus
Praveen Bhoopathi1,2, Padmanabhan Mannangatti1,2, Anjan K Pradhan1,2
1Department of Human and Molecular Genetics, Virginia Commonwealth University, School of Medicine, Richmond, Virginia, USA.
Abstract:
Primary, glioblastoma, and secondary brain tumors, from metastases outside the brain, are among the most aggressive and therapeutically resistant cancers. A physiological barrier protecting the brain, the blood-brain barrier (BBB), functions as a deterrent to effective therapies. To enhance cancer therapy, we developed a cancer terminator virus (CTV), a unique tropism-modified adenovirus consisting of serotype 3 fiber knob on an otherwise Ad5 capsid that replicates in a cancer-selective manner and simultaneously produces a potent therapeutic cytokine, melanoma differentiation-associated gene-7/interleukin-24 (MDA-7/IL-24). A limitation of the CTV and most other viruses, including adenoviruses, is an inability to deliver systemically to treat brain tumors because of the BBB, nonspecific virus trapping, and immune clearance. These obstacles to effective viral therapy of brain cancer have now been overcome using focused ultrasound with a dual microbubble treatment, the focused ultrasound-double microbubble (FUS-DMB) approach. Proof-of-principle is now provided indicating that the BBB can be safely and transiently opened, and the CTV can then be administered in a second set of complement-treated microbubbles and released in the brain using focused ultrasound. Moreover, the FUS-DMB can be used to deliver the CTV multiple times in animals with glioblastoma growing in their brain thereby resulting in a further enhancement in survival. This strategy permits efficient therapy of primary and secondary brain tumors enhancing animal survival without promoting harmful toxic or behavioral side effects. Additionally, when combined with a standard of care therapy, Temozolomide, a further increase in survival is achieved. The FUS-DMB approach with the CTV highlights a noninvasive strategy to treat brain cancers without surgery. This innovative delivery scheme combined with the therapeutic efficacy of the CTV provides a novel potential translational therapeutic approach for brain cancers.
Insights
Focused ultrasound with microbubbles safely opens the blood-brain barrier, enabling targeted delivery of a cancer terminator virus (CTV) for brain tumors. This noninvasive approach enhances survival in glioblastoma models, even with standard therapies.
Area of Science:
- Oncolytic virotherapy
- Nanomedicine
- Neurosurgery
Background:
- Primary, glioblastoma, and secondary brain tumors are aggressive and resistant to therapy.
- The blood-brain barrier (BBB) limits effective treatment delivery for brain cancers.
- A cancer terminator virus (CTV) was developed for cancer-selective replication and cytokine production (MDA-7/IL-24).
Purpose of the Study:
- To overcome the BBB limitation for systemic viral delivery to brain tumors.
- To evaluate the efficacy of a focused ultrasound with dual microbubble (FUS-DMB) approach for CTV delivery.
- To assess the therapeutic potential of FUS-DMB mediated CTV delivery in brain cancer models.
Main Methods:
- Developed a cancer terminator virus (CTV) with Ad5 capsid and serotype 3 fiber knob.
- Utilized focused ultrasound with dual microbubble (FUS-DMB) treatment to transiently open the BBB.
- Administered CTV via complement-treated microbubbles after BBB opening, followed by focused ultrasound.
- Evaluated FUS-DMB mediated CTV delivery and therapeutic efficacy in animal models with glioblastoma.
Main Results:
- Demonstrated safe and transient opening of the BBB using the FUS-DMB approach.
- Successfully delivered CTV to the brain in animal models, enhancing survival.
- Multiple FUS-DMB treatments further improved survival in glioblastoma models.
- Combined FUS-DMB/CTV therapy with Temozolomide yielded increased survival benefits.
Conclusions:
- The FUS-DMB approach enables noninvasive, targeted delivery of CTV across the BBB for brain cancer therapy.
- This strategy enhances survival in glioblastoma models without significant toxic side effects.
- FUS-DMB mediated CTV delivery represents a promising translational therapeutic strategy for primary and secondary brain tumors.
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