Real-time, Image-Guided, Convection-Enhanced Delivery of Interleukin 13 Bound to Pseudomonas Exotoxin
GJA Murad, S Walbridge, PF Morrison… - Clinical cancer …, 2006 - AACR
GJA Murad, S Walbridge, PF Morrison, K Garmestani, JW Degen, MW Brechbiel, EH Oldfield…
Clinical cancer research, 2006•AACRPurpose: To determine if the tumor-targeted cytotoxin interleukin 13 bound to Pseudomonas
exotoxin (IL13-PE) could be delivered to the brainstem safely at therapeutic doses while
monitoring its distribution in real-time using a surrogate magnetic resonance imaging tracer,
we used convection-enhanced delivery to perfuse rat and primate brainstems with IL13-PE
and gadolinium-bound albumin (Gd-albumin). Experimental Design: Thirty rats underwent
convective brainstem perfusion of IL13-PE (0.25, 0.5, or 10 μg/mL) or vehicle. Twelve …
exotoxin (IL13-PE) could be delivered to the brainstem safely at therapeutic doses while
monitoring its distribution in real-time using a surrogate magnetic resonance imaging tracer,
we used convection-enhanced delivery to perfuse rat and primate brainstems with IL13-PE
and gadolinium-bound albumin (Gd-albumin). Experimental Design: Thirty rats underwent
convective brainstem perfusion of IL13-PE (0.25, 0.5, or 10 μg/mL) or vehicle. Twelve …
Abstract
Purpose: To determine if the tumor-targeted cytotoxin interleukin 13 bound to Pseudomonas exotoxin (IL13-PE) could be delivered to the brainstem safely at therapeutic doses while monitoring its distribution in real-time using a surrogate magnetic resonance imaging tracer, we used convection-enhanced delivery to perfuse rat and primate brainstems with IL13-PE and gadolinium-bound albumin (Gd-albumin).
Experimental Design: Thirty rats underwent convective brainstem perfusion of IL13-PE (0.25, 0.5, or 10 μg/mL) or vehicle. Twelve primates underwent convective brainstem perfusion of either IL13-PE (0.25, 0.5, or 10 μg/mL; n = 8), co-infusion of 125I-IL13-PE and Gd-albumin (n = 2), or co-infusion of IL13-PE (0.5 μg/mL) and Gd-albumin (n = 2). The animals were permitted to survive for up to 28 days before sacrifice and histologic assessment.
Results: Rats showed no evidence of toxicity at all doses. Primates showed no toxicity at 0.25 or 0.5 μg/mL but showed clinical and histologic toxicity at 10 μg/mL. Quantitative autoradiography confirmed that Gd-albumin precisely tracked IL13-PE anatomic distribution and accurately showed the volume of distribution.
Conclusions: IL13-PE can be delivered safely and effectively to the primate brainstem at therapeutic concentrations and over clinically relevant volumes using convection-enhanced delivery. Moreover, the distribution of IL13-PE can be accurately tracked by co-infusion of Gd-albumin using real-time magnetic resonance imaging.
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