CTNI-76. UNLOCKING THE POWER OF LDL- RECEPTORS IN GLIOBLASTOMA

Abstract BACKGROUND Low-density lipoprotein receptors (LDLR) are overexpressed in a variety of solid tumors, including glioblastoma (GBM), and are known to play a key role in tumor proliferation and metabolic regulation.-LDLRs are also expressed on the blood-brain barrier (BBB), offering a unique gateway for receptor-mediated delivery of radiopharmaceuticals to intracranial tumors. In this study, we present initial data from eIND on the use of a novel LDLR-targeted imaging agent, ⁶⁸Ga-RMX-VH, in patients with newly diagnosed or recurrent GBM, We will also discuss the selection of the second-generation RMX_VH_PKM, which features modified blood circulation times and improved tumor-targeting properties. METHODS We initiated an open-label, single-dose, eIND-study (#155880) using 68Ga-RMX-VH PET/CT in newly diagnosed or recurrent patients with GBM. The primary objective was to assess the biodistribution and dosimetry of 68Ga-RMX-VH. The secondary objective was to correlate the extent of GBM visualized by contrast-enhanced MRI of the brain with the distribution of 68Ga-RMX-VH PET/CT in the brain, in each subject. A total of 10 GBM subjects have been scheduled for enrollment, with 5 of them enrolled in the dosimetry group. RESULTS We enrolled four patients with glioblastoma (GBM) (3 males, 1 female, aged 58–68 years) who had undergone craniotomy, adjuvant chemotherapy, and/or radiation therapy (XRT) and exhibited disease progression on MRI/CT scans. Pathological evaluation confirmed GBM with MGMT promoter methylation, IDH wild-type status, and EGFR mutation (Ki-67 = 25–60%). PET/CT imaging with ⁶⁸Ga-RMX-VH demonstrated effective targeting of the solid portion of the residual tumor, correlating well with contrast-enhanced regions on MRI or FLAIR. Activity was primarily cleared via the kidneys. These results stimulated our work on the selection of the second-generation RMX-VH-PKM, which has a longer blood circulation time and improved tumor–specific retention, as confirmed in vivo studies. CONCLUSIONS RMX-VH agents effectively target LDLR-overexpressing glioblastoma (GBM), with ⁶⁸Ga- or 203Pb-labeled radiotracer uptake closely aligning with enhanced and FLAIR regions on brain MRI.

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Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0571
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

CTNI-76. UNLOCKING THE POWER OF LDL- RECEPTORS IN GLIOBLASTOMA

Rouzbeh Esfandiari, Izabela Tworowska, K.K.H. Siddiqui, Vinay K. Puduvalli et al.
Neuro-Oncology
Glioma Diagnosis and Treatment
article

CTNI-76. UNLOCKING THE POWER OF LDL- RECEPTORS IN GLIOBLASTOMA

Rouzbeh Esfandiari, Izabela Tworowska, K.K.H. Siddiqui, Vinay K. Puduvalli, Jamal Temsamani, Pascaline Lécorché, Pawan Singh, Ebrahim S. Delpassand, Afshin Shafie, Cedric Malicek
article en

Abstract

Abstract BACKGROUND Low-density lipoprotein receptors (LDLR) are overexpressed in a variety of solid tumors, including glioblastoma (GBM), and are known to play a key role in tumor proliferation and metabolic regulation.-LDLRs are also expressed on the blood-brain barrier (BBB), offering a unique gateway for receptor-mediated delivery of radiopharmaceuticals to intracranial tumors. In this study, we present initial data from eIND on the use of a novel LDLR-targeted imaging agent, ⁶⁸Ga-RMX-VH, in patients with newly diagnosed or recurrent GBM, We will also discuss the selection of the second-generation RMX_VH_PKM, which features modified blood circulation times and improved tumor-targeting properties. METHODS We initiated an open-label, single-dose, eIND-study (#155880) using 68Ga-RMX-VH PET/CT in newly diagnosed or recurrent patients with GBM. The primary objective was to assess the biodistribution and dosimetry of 68Ga-RMX-VH. The secondary objective was to correlate the extent of GBM visualized by contrast-enhanced MRI of the brain with the distribution of 68Ga-RMX-VH PET/CT in the brain, in each subject. A total of 10 GBM subjects have been scheduled for enrollment, with 5 of them enrolled in the dosimetry group. RESULTS We enrolled four patients with glioblastoma (GBM) (3 males, 1 female, aged 58–68 years) who had undergone craniotomy, adjuvant chemotherapy, and/or radiation therapy (XRT) and exhibited disease progression on MRI/CT scans. Pathological evaluation confirmed GBM with MGMT promoter methylation, IDH wild-type status, and EGFR mutation (Ki-67 = 25–60%). PET/CT imaging with ⁶⁸Ga-RMX-VH demonstrated effective targeting of the solid portion of the residual tumor, correlating well with contrast-enhanced regions on MRI or FLAIR. Activity was primarily cleared via the kidneys. These results stimulated our work on the selection of the second-generation RMX-VH-PKM, which has a longer blood circulation time and improved tumor–specific retention, as confirmed in vivo studies. CONCLUSIONS RMX-VH agents effectively target LDLR-overexpressing glioblastoma (GBM), with ⁶⁸Ga- or 203Pb-labeled radiotracer uptake closely aligning with enhanced and FLAIR regions on brain MRI.

Neuro-OncologyVol. 27(Supplement_5)
The University of Texas MD Anderson Cancer Center (US), RadioMedix (United States) (US), Excel Diagnostics Imaging (US), Horse Hospital (GB), The Ohio State University (US)
Openalex Percentile: Top 51%
Glioma Diagnosis and Treatment
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