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Phase I trial of convection-enhanced delivery of IL13RA2 and EPHA2 receptor targeted cytotoxins in dogs with spontaneous intracranial gliomas.

Authors :
Rossmeisl JH
Herpai D
Quigley M
Cecere TE
Robertson JL
D'Agostino RB
Hinckley J
Tatter SB
Dickinson PJ
Debinski W
Source :
Neuro-oncology [Neuro Oncol] 2021 Mar 25; Vol. 23 (3), pp. 422-434.
Publication Year :
2021

Abstract

Background: The interleukin-13 receptor alpha 2 (IL13RA2) and ephrin type A receptor 2 (EPHA2) are attractive therapeutic targets, being expressed in ~90% of canine and human gliomas, and absent in normal brain. Clinical trials using an earlier generation IL-13 based cytotoxin showed encouraging clinical effects in human glioma, but met with technical barriers associated with the convection-enhanced delivery (CED) method. In this study, IL-13 mutant and ephrin A1 (EFNA1)-based bacterial cytotoxins targeted to IL13RA2 and EPHA2 receptors, respectively, were administered locoregionally by CED to dogs with intracranial gliomas to evaluate their safety and preliminary efficacy.<br />Methods: In this phase I, 3 + 3 dose escalation trial, cytotoxins were infused by CED in 17 dogs with gliomas expressing IL13RA2 or EPHA2 receptors. CED was performed using a shape-fitting therapeutic planning algorithm, reflux-preventing catheters, and real-time intraoperative MRI monitoring. The primary endpoint was to determine the maximum tolerated dose of the cytotoxic cocktail in dogs with gliomas.<br />Results: Consistent intratumoral delivery of the cytotoxic cocktail was achieved, with a median target coverage of 70% (range, 40-94%). Cytotoxins were well tolerated over a dose range of 0.012-1.278 μg/mL delivered to the target volume (median, 0.099 μg/mL), with no dose limiting toxicities observed. Objective tumor responses, up to 94% tumor volume reduction, were observed in 50% (8/16) of dogs, including at least one dog in each dosing cohort >0.05 μg/mL.<br />Conclusions: This study provides preclinical data fundamental to the translation of this multireceptor targeted therapeutic approach to the human clinic.<br /> (© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.)

Details

Language :
English
ISSN :
1523-5866
Volume :
23
Issue :
3
Database :
MEDLINE
Journal :
Neuro-oncology
Publication Type :
Academic Journal
Accession number :
32812637
Full Text :
https://doi.org/10.1093/neuonc/noaa196