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PSMA-PET: Deep Radiomic Biomarkers of Progression and Response Prediction in Prostate Cancer

StatusRecruiting
PhasePhase 3
Started2018-12-01
View on ClinicalTrials.gov ↗

Amendment history

2026-03-17
minor
2 amendments v9-v10
2 re-verifications since 2024-06-03, no change to tracked fields
2023-12-12
minor
Study Status, Outcome Measures v8
Primary completion date2023-12→2028-12
Completion date2024-12→2029-12
Secondary endpointsdetails revised at 1 of 1 entry
2023-06-12
minor
5 amendments v3-v7
5 re-verifications since 2020-07-13, no change to tracked fields
2019-01-29
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2023-11→2023-12
Completion date2024-11→2024-12
Start dateestimated 2018-11→confirmed 2018-12-01
Study sitesdetails revised at 1 of 1 site
2018-10-17
minor
Study Status v1
Re-verified, no change to tracked fields
2018-07-19
minor
Original filing
Prostate cancer (PCa) is the most common non-skin malignancy and the third leading cause of cancer death in North American men. The accurately mapped metastatic state is a necessary prerequisite to guiding treatment in practice and in clinical trials. Imaging biomarkers (BMs) can provide information on disease volume and distribution, prognosis, changes in biologic behavior, therapy-induced changes (both responders and non-responders), durations of response, emergence of treatment resistance, and the host reaction to the therapies. Of particular relevance to metastatic prostate cancer is the emergence of a promising imaging technique involving new prostate specific membrane antigen (PSMA) positron emission tomography (PET) tracers. This approach has demonstrated higher sensitivity in detecting metastases, prior to and during therapy, than current imaging standard of care (CT and bone scan), and is not widely clinically available outside of the research realm in North America. Positron emission tomography / computer tomography (PET/CT) is a nuclear medicine diagnostic imaging procedure based on the measurement of positron emission from radiolabeled tracer molecules in vivo. PSMA is a homodimeric type II membrane metalloenzyme that functions as a glutamate carboxypeptidase/folate hydrolase and is overexpressed in PCa. PSMA is expressed in the vast majority of PCa tissue specimens and its degree of expression correlates with a number of important metrics of PCa tumor aggressiveness including Gleason score, propensity to metastasize and the development of castration resistance. \[18F\]DCFPyL is a promising high-sensitivity second generation PSMA-targeted urea-based PET probe. Studies employing second-generation PSMA PET/CT imaging in men with biochemical progression after definitive therapy suggest detection of metastases in over 60% of men imaged. Deep learning is defined as a variant of artificial neural networks, using multiple layers of 'neurons'. Deep learning has been investigated in medical imaging in numerous applications across organ systems. In oncology, basic artificial neural networks to support decision-making have previously been developed retrospectively in breast cancer and prostate cancer, but have not been validated or integrated prospectively. Novel data-driven methods are needed to predict outcomes as early as possible in order to guide the duration and the aggressiveness of a particular therapy. They are also needed for optimal patient selection based on the patient's response to a given therapy. Here the investigators hypothesize that the combination of a highly performing prostate cancer imaging technique combined with machine learning has high potential. The main objective of this study is to acquire PSMA-PET data in patients with prostate cancer who receive treatment and follow-up in order to enable the discovery of predictive imaging biomarkers through deep learning techniques.
Trial Details
NCT Number NCT03594760
Lead Sponsor Centre hospitalier de l'Université de Montréal (CHUM)
Conditions Prostate Cancer
Enrollment 1,000 participants
Start Date 2018-12-01
Primary Completion 2028-12 (estimated)
Study Completion 2029-12 (estimated)
Updated on ClinicalTrials.gov 2026-03-19