New PET scan technique could map hidden prostate cancer recurrences
NCT ID NCT03718260
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This large registry study is testing whether a special type of PET scan, called PSMA-PET, can better detect where prostate cancer has returned after initial treatment. Thousands of men with suspected recurrent prostate cancer across Ontario will receive this scan. The goal is to see how often the scan finds cancer that standard imaging misses, and whether this information helps doctors choose more personalized treatments like targeted radiation or surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PSMA-PET scan using [18F]-DCFPyL or [18F]PSMA-1007
- What this could lead to
- If successful, this registry could show that PSMA-PET scans find recurrent prostate cancer more accurately than standard imaging, helping doctors tailor treatments like targeted radiation or surgery to each person's specific pattern of spread.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove that using PSMA-PET improves outcomes like survival. The scans may also detect lesions that are not clinically significant, leading to unnecessary procedures.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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9,684 people
The number who actually took part.
- Started
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Sep 2018
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Phase 2 Inclusion Criteria: 1. Written informed consent obtained 2. Male, Age ≥ 18 years 3. Prior primary treatment for prostate cancer with curative intent such as radical prostatectomy or radiotherapy for localized prostate cancer. Unless PET/CT requested as part of Cohort 7. 4. Suspected persistent or recurrent disease defined as one of the following (unless PET/CT requested as part of Cohort 7): 1. High risk disease at the time of radical prostatectomy characterized by pathologically involved node(s) or persistently detectable PSA (\>0.1ng/ml) within 3 months post-surgery 2. Primary treatment for prostate cancer and biochemical failure (BF) with current management according to the following: i. Following primary radical prostatectomy, BF is defined as rising PSA on at least 2 occasions measured at least 1 month apart and with the most recent PSA measured at \>0.1 ng/ml ii. Following primary radiotherapy for localized disease, BF is defined according to the Phoenix Definition, which is rising PSA on at least 2 occasions measured at least 1 month apart and with the most recent PSA measured greater than the nadir PSA + 2.0 ng/ml 5. Patient scenario falls into one of the 7 pre-defined cohorts. When patient scenario falls outside cohorts 1-6 participation in the Registry must be approved through the established CCO adjudication process for Cohort 7. 6. Karnofsky performance status 70 or better (ECOG 0, 1). 7. If PSA \>10 mg/mL, conventional imaging consisting of bone scan and abdo-pelvic CT scan within 3 months of registration that is either equivocal, negative (no lesions) or positive for oligometastatic disease (4 or fewer unequivocal lesions identified). Exclusion Criteria: 1. Prostate cancer with significant sarcomatoid or spindle cell or neuroendocrine small cell components. 2. Prior PSMA PET scan within 6 months of enrollment. 3. Patient cannot lie still for at least 60 minutes or comply with imaging. 4. Patients falling outside of Cohorts 1-6 where independent adjudication by CCO does not support participation in the Registry. Phase 3 Inclusion Criteria: 1. Written informed consent obtained 2. Male, Age ≥ 18 years 3. Biopsy proven, clinically high risk (cT3, PSA ≥20, biopsy Gleason Grade Group 4-5) prostate cancer undergoing initial staging prior to primary treatment with surgery or radiotherapy OR Biochemical failure (BF) with current management defined as at least two consecutive rises in PSA measured at least 1 month apart with the most recent PSA level \>0.1 ng/ml (post radical prostatectomy or post PSMA Directed therapy, Cohorts 1-5) or PSA level \> nadir PSA + 2.0 ng/ml (Phoenix definition post radiotherapy failure, Cohorts 5, 6) OR Men with rising PSA and/or progression on conventional imaging despite prior second line hormone therapy or chemotherapy for castrate resistant prostate cancer (Cohort 8). OR PET/CT requested as part of Cohort 7. 4. Patient scenario falls into one of the 8 pre-defined cohorts. When patient scenario falls outside cohorts 0-6 and 8, participation in the Registry must be approved through the established CCO adjudication process for Cohort 7. 5. Karnofsky performance status 70 or better (ECOG 0, 1) 6. If recurrent disease suspected and PSA prior to PSMA PET/CT is \>10 ng/ml, conventional imaging consisting of bone scan and abdominal-pelvic CT scan performed within 3 months of registration that is either equivocal, negative (no lesions) or positive for oligometastatic disease (4 or fewer unequivocal lesions identified). Registration is defined as Form A: Eligibility is complete. 7. If patient is enrolled in Cohort 8, conventional imaging consisting of at least bone scan and abdominal-pelvic CT scan completed within 3 months of registration. Registration is defined as Form A: Eligibility is complete. Exclusion Criteria: 1. Prostate cancer with significant sarcomatoid or spindle cell or neuroendocrine small cell components 2. Prior PSMA PET scan within 6 months of enrollment 3. Institution of or change in systemic therapy within 6 weeks prior to PSMA PET/CT request 4. Patient cannot lie still for at least 60 minutes or comply with imaging 5. Patients falling outside of Cohorts 0-6 and 8 where independent adjudication by CCO does not support participation in the Registry
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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London Health Sciences Centre
London, Ontario, N6A 5W9, Canada
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Princess Margaret Cancer Centre, University Health Network
Toronto, Ontario, M5G 2M9, Canada
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St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8N 4A6, Canada
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The Ottawa Hospital, General Campus
Ottawa, Ontario, K1H 8L6, Canada
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Thunder Bay Regional Health Sciences Centre
Thunder Bay, Ontario, P7B 6V4, Canada
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Toronto Sunnybrook Cancer Centre
Toronto, Ontario, M4N 3M5, Canada
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Windsor Regional Hospital
Windsor, Ontario, Canada
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