Canine model of convection-enhanced delivery of liposomes containing CPT-11 monitored with real-time magnetic resonance imaging

Author:

Dickinson Peter J.1,Lecouteur Richard A.1,Higgins Robert J.2,Bringas John R.3,Roberts Byron1,Larson Richard F.1,Yamashita Yoji3,Krauze Michal3,Noble Charles O.4,Drummond Daryl4,Kirpotin Dmitri B.4,Park John W.5,Berger Mitchel S.3,Bankiewicz Krystof S.3

Affiliation:

1. Departments of Surgical and Radiological Sciences, and

2. Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis;

3. Department of Neurosurgery, Brain Tumor Research Center, University of California, San Francisco;

4. Hermes Biosciences, Inc., San Francisco; and

5. University of California at San Francisco Comprehensive Cancer Center, San Francisco, California

Abstract

Object Many factors relating to the safety and efficacy of convection-enhanced delivery (CED) into intracranial tumors are poorly understood. To investigate these factors further and establish a more clinically relevant large animal model, with the potential to investigate CED in large, spontaneous tumors, the authors developed a magnetic resonance (MR) imaging–compatible system for CED of liposomal nanoparticles into the canine brain, incorporating real-time MR imaging. Additionally any possible toxicity of liposomes containing Gd and the chemotherapeutic agent irinotecan (CPT-11) was assessed following direct intraparenchymal delivery. Methods Four healthy laboratory dogs were infused with liposomes containing Gd, rhodamine, or CPT-11. Convection-enhanced delivery was monitored in real time by sequential MR imaging, and the volumes of distribution were calculated from MR images and histological sections. Assessment of any toxicity was based on clinical and histopathological evaluation. Convection-enhanced delivery resulted in robust volumes of distribution in both gray and white matter, and real-time MR imaging allowed accurate calculation of volumes and pathways of distribution. Results Infusion variability was greatest in the gray matter, and was associated with leakage into ventricular or subarachnoid spaces. Complications were minimal and included mild transient proprioceptive deficits, focal hemorrhage in 1 dog, and focal, mild perivascular, nonsuppurative encephalitis in 1 dog. Conclusions Convection-enhanced delivery of liposomal Gd/CPT-11 is associated with minimal adverse effects in a large animal model, and further assessment for use in clinical patients is warranted. Future studies investigating real-time monitored CED in spontaneous gliomas in canines are feasible and will provide a unique, clinically relevant large animal translational model for testing this and other therapeutic strategies.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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