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Updated: Jul 17, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
PSMA-targeted therapy for non-prostate cancers
1Department of Radiation Oncology and Molecular Radiation Sciences, School of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Abstract:
Radioligand therapy (RLT) agents are demonstrating a crucial role in the clinical approach to aggressive malignancies such as metastatic castrate-resistant prostate cancer (m-CRPC). With the recent FDA approval of prostate-specific membrane antigen (PSMA)-targeted RLT for m-CRPC, the field has broadened its gaze to explore other cancers that express PSMA in the tumor parenchyma or tumor neovasculature. In this review article, we discuss current progress in the clinical use of PSMA RLTs in non-prostate cancers such salivary gland cancers, renal cell carcinoma, high grade glioma, and soft tissue sarcoma. We highlight early reports in small case series and clinical trials indicating promise for PSMA-targeted RLT and highlighting the importance of identifying patient cohorts who may most benefit from these interventions. Further study is indicated in non-prostate cancers investigating PSMA RLT dosimetry, PSMA PET/CT imaging as a biomarker, and assessing PSMA RLT safety and efficacy in these cancers.
Insights
Prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) shows promise beyond prostate cancer. Research is exploring its use in salivary gland cancers, renal cell carcinoma, glioma, and sarcoma, with further studies needed for optimal application.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiopharmaceutical Therapy
Background:
- Radioligand therapy (RLT) is vital for aggressive cancers like metastatic castrate-resistant prostate cancer (m-CRPC).
- Prostate-specific membrane antigen (PSMA)-targeted RLT is now FDA-approved for m-CRPC.
- PSMA expression in non-prostate tumors suggests potential therapeutic applications.
Purpose of the Study:
- To review the current clinical progress of PSMA-targeted RLT in non-prostate cancers.
- To highlight early findings and potential benefits in various malignancies.
- To identify areas for future research in PSMA RLT for new indications.
Main Methods:
- Literature review of clinical studies and case series involving PSMA RLT in non-prostate cancers.
- Analysis of reported efficacy, safety, and patient selection criteria.
- Identification of key research questions for advancing PSMA RLT in new cancer types.
Main Results:
- Early data from small cohorts suggest promise for PSMA RLT in salivary gland cancers, renal cell carcinoma, high-grade glioma, and soft tissue sarcoma.
- PSMA expression in tumor parenchyma and neovasculature is a key factor for targeting.
- Patient selection and understanding PSMA expression levels are critical for treatment success.
Conclusions:
- PSMA-targeted RLT is a promising therapeutic strategy for select non-prostate cancers.
- Further research is essential to optimize dosimetry, utilize PSMA PET/CT imaging as a biomarker, and establish safety and efficacy profiles.
- Identifying specific patient populations who will benefit most from PSMA RLT is crucial for clinical implementation.
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