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[Ga]Ga-PSMA PET/MRI, histological PSMA expression and preliminary experience with [Lu]Lu-PSMA therapy in relapsing high-grade glioma. | LitMetric

[Ga]Ga-PSMA PET/MRI, histological PSMA expression and preliminary experience with [Lu]Lu-PSMA therapy in relapsing high-grade glioma.

Front Oncol

Department of Neurosurgery, Berlin Institute of Health, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.

Published: September 2022

AI Article Synopsis

  • The study investigates the use of prostate specific membrane antigen (PSMA) as a target for treating high-grade gliomas (HGG) with radioligand therapy, specifically [Lu]Lu-PSMA RLT.
  • Researchers assessed patients' eligibility by performing [Ga]Ga-PSMA PET/MRI scans and comparing tumor PSMA expression to treatment outcomes.
  • Results showed that only 15% of patients qualified for [Lu]Lu-PSMA RLT, and the correlation between PSMA expression in blood vessels and PET/MRI uptake suggests potential for using this as a patient screening method in future studies.

Article Abstract

Purpose: High-grade gliomas (HGG) are still associated with a dismal prognosis. Prostate specific membrane antigen (PSMA) is discussed as a theranostic target for PSMA-directed radioligand therapy ([Lu]Lu-PSMA RLT). Here, we report on the correlation of [Ga]Ga-PSMA uptake with histological PSMA expression and on our preliminary experience with [Lu]Lu-PSMA RLT in relapsing HGG.

Methods: Patients with relapsing HGG underwent [Ga]Ga-PSMA PET/MRI to evaluate eligibility for an individualized treatment approach with [Lu]Lu-PSMA. Standard uptake values (SUV) for tumor and liver and respective tumor-to-background ratios (compared to the liver) (TBR) on [Ga]Ga-PSMA PET/MRI were assessed. Eligibility criteria for [Lu]Lu-PSMA therapy were exhaustion of all standard treatment options available and TBR>1.0. In 11 samples, immunohistochemical PSMA expression was determined, quantified using the H-score and correlated with uptake on [Ga]Ga-PSMA PET/MRI.

Results: We included 20 patients with a median age of 53 years (IQR 42-57). The median SUV on [Ga]Ga-PSMA PET/MRI was 4.5 (3.7-6.2) for SUV and 1.4 (1.1-1.7) for SUV. The respective TBR was maximum 0.6 (0.4-0.8) and mean 0.3 (0.2-0.4). High TBR correlated with increased endothelial PSMA expression [H-score of 65 (62.5-77.5)]. Three patients (15%) presented a TBR>1.0 and qualified for [Lu]Lu-PSMA RLT. No treatment related toxicity was observed.

Conclusion: Only a minority of patients with relapsing HGG qualified for [Lu]Lu-PSMA RLT. Our data demonstrates that PSMA expression in the neo-vasculature corresponds to PSMA uptake on [Ga]Ga-PSMA PET/MRI and might be used as a screening tool for patient selection. Future prospective studies need to focus the debate on TBR thresholds as inclusion criteria for PSMA RLT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478729PMC
http://dx.doi.org/10.3389/fonc.2022.980058DOI Listing

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