Molecular Imaging, Prostate Cancer, PSMA PET/CT, RNA, Transcriptomics
Conditions
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
Study design
Eligibility
Inclusion criteria
* Signed informed consent * PCa diagnosis * Available samples * Performed both PSMA PET and MRI
Exclusion criteria
* Low quality samples availability
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of omic features in MRI-PSMA PET discordant versus concordant lesions | At the time of biopsy |
| Number of molecular features in MRI-PSMA PET discordant versus concordant lesions | At the time of biopsy |
Countries
Italy