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Updated: May 16, 2025

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PSMA-targeted PET imaging for brain metastases from non-prostatic solid tumors: a systematic review
Sara Dall' Armellina1, Gayane Aghakhanyan2, Alessio Rizzo3
1Nuclear Medicine Unit, Service Area Department, Azienda Socio-Sanitaria Territoriale (ASST)-Rhodense P.O. Bollate, Milan, Italy.
Prostate-Specific Membrane Antigen (PSMA) PET imaging shows superior detection of brain metastases from non-prostatic cancers compared to conventional methods. This review highlights its diagnostic accuracy and potential for theranostic applications in neuro-oncology.
Area of Science:
- Oncology
- Radiology
- Nuclear Medicine
Background:
- Prostate-Specific Membrane Antigen (PSMA) is expressed in various solid tumors' neovasculature.
- PSMA PET imaging is emerging as a promising tool for detecting brain metastases (BMs) from non-prostatic cancers.
- Conventional imaging modalities have limitations in diagnosing BMs from non-prostatic origins.
Purpose of the Study:
- To systematically review the diagnostic performance of PSMA-targeted radiopharmaceuticals in imaging BMs from non-prostatic cancers.
- To compare PSMA PET's efficacy against conventional imaging techniques.
- To explore the potential theranostic applications of PSMA PET in neuro-oncology.
Main Methods:
- Systematic literature review following PRISMA guidelines.
- Inclusion of studies evaluating diagnostic accuracy of PSMA PET for BMs from non-prostatic solid tumors.
- Assessment of methodological quality using QUADAS-2 tool and qualitative data synthesis.
Main Results:
- 23 studies analyzed 77 BMs from diverse primary malignancies.
- PSMA PET demonstrated superior detection of BMs with high tumor-to-background ratios compared to MRI and [18F]FDG PET.
- PSMA PET effectively differentiated radionecrosis from tumor recurrence and showed higher sensitivity for thyroid metastases.
Conclusions:
- PSMA PET imaging holds significant promise for improved diagnosis and management of BMs from non-prostatic cancers.
- Theranostic applications of PSMA PET are underexplored but suggest potential for personalized neuro-oncology.
- Future research should standardize protocols, explore diverse tumor subtypes, and validate clinical utility.
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