O13 First-in-human experience with NeoCast™ a solvent-free, non-adhesive, and distal penetrating embolic material in pre-surgical embolization of hypervascular tumors

<h3>Introduction</h3> NeoCast™ is a next-generation (solvent-free and non-adhesive) embolic material that is designed specifically for procedures where deep distal penetration is desired. <h3>Aim of Study</h3> Safety and feasibility assessment of NeoCast in pre-surgical middle meningeal artery embolization of hypervascular brain tumors. <h3>Methods</h3> The EMBO-01 study was an open-label, multicenter, prospective first-in-human clinical trial. The primary safety endpoint was freedom from device related disabling stroke or neurological death within 30 days of the embolization procedure. The primary feasibility endpoint was defined as the successful injection of NeoCast into targeted vessel(s) supplying the tumor, resulting in complete occlusion at or distal to the point of embolysate injection. <h3>Results</h3> Five subjects were enrolled with an average tumor size of 5.0 ± 1.2 cm. All subjects were successfully embolized with NeoCast achieving complete occlusion of targeted vessels. There were no adverse events or device deficiencies during the embolization procedure. Post-procedure CT showed exceptional penetration into the tumor vasculature with minimal artifact. An independent core lab determined there was no non-target embolization and measured the average percent tumor devascularization as 88 ± 7%. No significant differences were noted between Modified Rankin scores pre-embolization and pre-surgery. Tumor resection was successful and considered complete (Simpson Grade 1 or 2) with minimal estimated blood loss for all subjects. All subjects successfully met both the primary feasibility and safety endpoints. <h3>Conclusion</h3> Our first-in-human clinical experience has demonstrated the potential of NeoCast, a next-generation embolic material, to provide safe and effective embolization where deep distal penetration is desired. <h3>Disclosure of Interest</h3> no.

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Abstracts
Published
2024-09-01
DOI
https://doi.org/10.1136/jnis-2024-esmint.13
Primary Topic
Medical Imaging and Pathology Studies
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article
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article

O13 First-in-human experience with NeoCast™ a solvent-free, non-adhesive, and distal penetrating embolic material in pre-surgical embolization of hypervascular tumors

Laetitia de Villiers, Jeffrey Groom, Adam S Arthur, Lee‐Anne Slater et al.
Abstracts
Medical Imaging and Pathology Studies
article

O13 First-in-human experience with NeoCast™ a solvent-free, non-adhesive, and distal penetrating embolic material in pre-surgical embolization of hypervascular tumors

Laetitia de Villiers, Jeffrey Groom, Adam S Arthur, Lee‐Anne Slater, David Fiorella
article en

Abstract

<h3>Introduction</h3> NeoCast™ is a next-generation (solvent-free and non-adhesive) embolic material that is designed specifically for procedures where deep distal penetration is desired. <h3>Aim of Study</h3> Safety and feasibility assessment of NeoCast in pre-surgical middle meningeal artery embolization of hypervascular brain tumors. <h3>Methods</h3> The EMBO-01 study was an open-label, multicenter, prospective first-in-human clinical trial. The primary safety endpoint was freedom from device related disabling stroke or neurological death within 30 days of the embolization procedure. The primary feasibility endpoint was defined as the successful injection of NeoCast into targeted vessel(s) supplying the tumor, resulting in complete occlusion at or distal to the point of embolysate injection. <h3>Results</h3> Five subjects were enrolled with an average tumor size of 5.0 ± 1.2 cm. All subjects were successfully embolized with NeoCast achieving complete occlusion of targeted vessels. There were no adverse events or device deficiencies during the embolization procedure. Post-procedure CT showed exceptional penetration into the tumor vasculature with minimal artifact. An independent core lab determined there was no non-target embolization and measured the average percent tumor devascularization as 88 ± 7%. No significant differences were noted between Modified Rankin scores pre-embolization and pre-surgery. Tumor resection was successful and considered complete (Simpson Grade 1 or 2) with minimal estimated blood loss for all subjects. All subjects successfully met both the primary feasibility and safety endpoints. <h3>Conclusion</h3> Our first-in-human clinical experience has demonstrated the potential of NeoCast, a next-generation embolic material, to provide safe and effective embolization where deep distal penetration is desired. <h3>Disclosure of Interest</h3> no.

Abstracts
Gold Coast Hospital (AU), Arsenal Medical (United States) (US), Semmes Murphey Foundation (US), Monash Health (AU), Stony Brook University (US), University of Tennessee at Knoxville (US)
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Medical Imaging and Pathology Studies
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