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Molecular Profiling of MRI-PSMA PET Discordance in Prostate Cancer

Molecular Profiling of Prostate Cancer Lesions With MRI-PSMA PET Discordance

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07485257
Acronym
MP-PET-MRI
Enrollment
30
Registered
2026-03-20
Start date
2023-12-04
Completion date
2025-12-09
Last updated
2026-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Molecular Imaging, Prostate Cancer, PSMA PET/CT, RNA, Transcriptomics

Brief summary

MRI and PSMA-PET are highly sensitive imaging tools for prostate cancer, yet they often detect different lesions. These discordant findings pose clinical uncertainty because their biological significance is unclear. This project aims to molecularly characterize MRI-PSMA PET discordant lesions using high-quality biobanked samples from patients enrolled in an institutional study (NCT06187870). By integrating imaging and molecular data, the study will clarify whether these lesions represent indolent disease, aggressive subclones, or biologically distinct entities, and will assess their clinical implications.

Detailed description

Magnetic Resonance Imaging and PSMA-PET are currently the most sensitive imaging modalities for prostate cancer, yet they do not always provide concordant results. Discordant lesions, those detected by one modality but not the other, represent a significant clinical challenge, as their biological nature and implications remain poorly understood. A molecular characterization of these lesions may clarify whether they correspond to indolent clones missed due to imaging limitations, aggressive subclones with distinct molecular features, or biologically different disease entities. We aim to investigate prostate cancer lesions that are discordant between MRI and PSMA-PET, with the specific objective of elucidating their molecular characteristics and clinical implications. Molecular omic analyses will be performed on existing biobank samples from patients enrolled at our institution who have already provided informed consent for research use. This resource provides access to high-quality biospecimens linked with imaging data, enabling a comprehensive evaluation of MRI-PSMA PET discordant prostate cancer lesions.

Interventions

None listed

Sponsors

IRCCS San Raffaele
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum

Inclusion criteria

* Signed informed consent * PCa diagnosis * Available samples * Performed both PSMA PET and MRI

Exclusion criteria

* Low quality samples availability

Design outcomes

Primary

MeasureTime frame
Number of omic features in MRI-PSMA PET discordant versus concordant lesionsAt the time of biopsy
Number of molecular features in MRI-PSMA PET discordant versus concordant lesionsAt the time of biopsy

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 16, 2026