Which PET scan is better at spotting prostate cancer?
NCT ID NCT03604757
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested two different radioactive tracers (68Ga-RM2 and 68Ga-PSMA-617) used in PET/CT scans to see which one better detects prostate cancer in men scheduled for prostate removal surgery. Twenty-two men with low, intermediate, or high-risk prostate cancer received both scans. The goal was to compare how well each tracer highlights cancer cells, which could help doctors choose the best imaging method for planning treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 68Ga-PSMA-617 and 68Ga-RM2 (radioactive tracers for PET/CT imaging)
- What this could lead to
- If successful, this could help doctors choose the best imaging method to detect prostate cancer spread before surgery, improving treatment planning.
- What could go wrong
- This is a small, early-phase study with only 22 participants, so results may not apply to all patients. The tracers are used only for imaging, not treatment.
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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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
22 people
The number who actually took part.
- Started
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Apr 2018
- Finished
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Dec 2019
- Lead sponsor
-
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
-
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.
Inclusion criteria : 24 patients divided in : * 6 patients with low risk prostate cancer (Gleason score ≤ 6 and cT1-T2a and Prostate Specific Antigen (PSA) value \< 10 ng/mL) * 12 patients with intermediate risk prostate cancer (Gleason score 7 or cT2b or PSA value 10-20 ng/mL) divided in : 6 patients who are Gleason score 7(3+4) (favourable intermediate risk) 6 patients who are Gleason score 7(4+3) (unfavourable intermediate risk) * 6 patients with high risk prostate cancer (Gleason \> 7 or cT2c or PSA value \> 20 ng/mL) * Candidate for radical prostatectomy after discussion in multidisciplinary committee * Covered by the national health insurance system * Written informed consent willingly obtained Exclusion criteria : * any kind of previous treatment for prostate cancer (hormonal treatment, EBRT, brachytherapy, cryotherapy, etc…); * patient not candidate for radical prostatectomy and/or unable to benefit from surgery * freedom deprivated patient by judiciary or administrative decision * patient under legal protection or unable to express its own consent * patient within exclusion period from another clinical trial * known contraindication to radiopharmaceuticals and / or excipients
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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
-
Bordeaux University Hospital
Bordeaux, 33076, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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