EXTH-14. Endovascular Intra-arterial delivery of D24-RGD-loaded MSCs for diffuse midline glioma

Abstract INTRODUCTION Diffuse midline glioma (DMG)/diffuse intrinsic pontine glioma (DIPG) are deadly childhood gliomas with median survival less than 12 months. D24, a genetically engineered adenovirus specific for glioma, has anti-tumoral effect in a phase 1 study when given by direct intratumoral injection. Our preliminary work has shown endovascular super-selective intra-arterial delivery of D24 packaged in mesenchymal stem cells (MSC-D24) is feasible and safe in patients. OBJECTIVE We hypothesize that endovascular intra-arterial delivery of MSC-D24 will be safe and effective for treatment of DMG/DIPG. METHODS In vitro killing assays were used to assess the tumoricidal effects of MSC-D24 against DIPG using TP54, DIPG 36, and SF8628 cell lines (from 102 to 105 cells). Transwell migration assays were performed to test homing of MSC (105 cells) to the same cell lines. To assess safety of infusion in the vertebrobasilar circulation, a rabbit survival model (7 days) was used and 0.4 mL of 107 MSC-D24 cells were infused into the basilar artery. Clinical examination, histology, angiography, and MRI were used to assess stroke and other complications after infusion. The efficacy of MSC-D24 against will be tested in-vivo using a mice xenograft model of DIPG. RESULTS Transwell killing assays showed a dose dependent tumoricidal effects of MSC-D24 against all 3 DIPG cell lines. MSCs successfully homed to TP54 in the migration assay. Rabbits (n=3) did not exhibit neurologic deficits after the MSC-D24 intra-arterial infusion and MRI, histology, and angiography post-infusion did not show any strokes or other evidence of tissue injury. Bioluminescent imaging of DIPG bearing mice showed tumor reduction and improved survival. CONCLUSION Endovascular vertebrobasilar intra-arterial infusion of MSC-D24 is safe and the oncolytic virus appears effective against DIPG in both in vitro and in vivo models. The results support a phase 1 trial of MSC-D24 for patients with DMG/DIPG.

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Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.1348
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

EXTH-14. Endovascular Intra-arterial delivery of D24-RGD-loaded MSCs for diffuse midline glioma

Christopher J. Young, Frederick F. Lang, Peter Kan, Joy Gumin et al.
Neuro-Oncology
Glioma Diagnosis and Treatment
article

EXTH-14. Endovascular Intra-arterial delivery of D24-RGD-loaded MSCs for diffuse midline glioma

Christopher J. Young, Frederick F. Lang, Peter Kan, Joy Gumin, Stephen Chen, Daniel Ledbetter, Siresha Bathina
article en

Abstract

Abstract INTRODUCTION Diffuse midline glioma (DMG)/diffuse intrinsic pontine glioma (DIPG) are deadly childhood gliomas with median survival less than 12 months. D24, a genetically engineered adenovirus specific for glioma, has anti-tumoral effect in a phase 1 study when given by direct intratumoral injection. Our preliminary work has shown endovascular super-selective intra-arterial delivery of D24 packaged in mesenchymal stem cells (MSC-D24) is feasible and safe in patients. OBJECTIVE We hypothesize that endovascular intra-arterial delivery of MSC-D24 will be safe and effective for treatment of DMG/DIPG. METHODS In vitro killing assays were used to assess the tumoricidal effects of MSC-D24 against DIPG using TP54, DIPG 36, and SF8628 cell lines (from 102 to 105 cells). Transwell migration assays were performed to test homing of MSC (105 cells) to the same cell lines. To assess safety of infusion in the vertebrobasilar circulation, a rabbit survival model (7 days) was used and 0.4 mL of 107 MSC-D24 cells were infused into the basilar artery. Clinical examination, histology, angiography, and MRI were used to assess stroke and other complications after infusion. The efficacy of MSC-D24 against will be tested in-vivo using a mice xenograft model of DIPG. RESULTS Transwell killing assays showed a dose dependent tumoricidal effects of MSC-D24 against all 3 DIPG cell lines. MSCs successfully homed to TP54 in the migration assay. Rabbits (n=3) did not exhibit neurologic deficits after the MSC-D24 intra-arterial infusion and MRI, histology, and angiography post-infusion did not show any strokes or other evidence of tissue injury. Bioluminescent imaging of DIPG bearing mice showed tumor reduction and improved survival. CONCLUSION Endovascular vertebrobasilar intra-arterial infusion of MSC-D24 is safe and the oncolytic virus appears effective against DIPG in both in vitro and in vivo models. The results support a phase 1 trial of MSC-D24 for patients with DMG/DIPG.

Neuro-OncologyVol. 27(Supplement_5)
The University of Texas MD Anderson Cancer Center (US), The University of Texas Medical Branch at Galveston (US)
Openalex Percentile: Top 52%
Glioma Diagnosis and Treatment
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