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Noninvasive therapy of brain cancer using a unique systemic delivery methodology with a cancer terminator virus.

Authors: Bhoopathi P, Mannangatti P, Pradhan AK, Kumar A, Maji S, Lang FF, Klibanov AL, Madan E, Cavenee WK, Keoprasert T, Sun D, Bjerkvig R, Thorsen F, Gogna R, Das SK, Emdad L, Fisher PB

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.

Introduction

Purpose Drug delivery with BBB opening
Animal model / Human subject C57BL/6 mice
Disease model Glioblastoma
Cargo name and characteristics Cancer terminator virus (CTV), a unique tropism-modified adenovirus consisting of serotype 3 fiber knob on an otherwise Ad5 capsid
Route of administration intravenous

Outcomes and Safety

Summary of Outcomes Focused ultrasound–double microbubble (FUS-DMB) enabled safe, transient BBB opening and repeated intracranial delivery of a cancer terminator virus (CTV) expressing MDA-7/IL-24 in glioblastoma-bearing animals. This approach significantly improved survival in models of primary and metastatic brain tumors without inducing detectable toxicity or behavioral deficits. Combining FUS-DMB-mediated CTV delivery with temozolomide further prolonged survival, demonstrating enhanced therapeutic efficacy over either treatment alone.
Duration of biological effect Information unavailable due to restricted access to the full paper.
Safety-related matter Information unavailable due to restricted access to the full paper.

Brain Region

Targeted brain region(s) Not specified

Ultrasound Parameters

Treatment frequency single session

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