Prostate Cancer
Conditions
Brief summary
This study assess the Diagnostic Performance of \[18F\]PSMA-1007 PET/CT Imaging in Patients with Newly-Diagnosed High-Risk or Very-High-Risk Prostate Cancer
Interventions
DRUG[18F]PSMA-1007
Diagnostic radiopharmaceutical for PET scan
Sponsors
ABX advanced biochemical compounds GmbH
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. The patient (male) is aged 18 years or above. 2. The patient is able to understand the information presented to him concerning the nature, scope, and consequences of the trial as set out in the information provided to the patient AND has provided written informed consent to participate. 3. The patient has newly diagnosed, biopsy-proven, clinically localized prostate adenocarcinoma, and curative prostatectomy with extended pelvic lymph node dissection is his preferred course of treatment. 4. The patient has at least high-risk disease as defined by the NCCN guidelines (version 1.2023). That is, the presence of any one or more of the following: * Overall ISUP grade group 4 or 5, * Clinical category T3a or greater, * Serum PSA level greater than 20 ng/ml. 5. The patient has undergone conventional imaging (CT or MRI, and bone scan if clinically indicated) to detect the presence of pelvic nodal involvement and bone or visceral metastases within 60 days of the planned PET-CT procedure.
Exclusion criteria
1. Patients for whom radical prostatectomy is not clinically appropriate or the patient is otherwise unlikely to undergo radical prostatectomy with extensive pelvic lymph node dissection. 2. The patient has received any therapy - be it radiation, surgical or drug therapy - for his prostate cancer. 3. The patient has any contraindication(s) for and/or known hypersensitivity to any constituent(s) of \[18F\]PSMA-1007. 4. The patient is not able to have PET-CT scans (for example, because of weight, claustrophobia, or inability to lie still for the duration of the scan). 5. The patient is closely affiliated to the investigation site; e.g. is a first-degree relative of the investigator. 6. At the time of screening, the patient is receiving any other investigational agent(s), or he has received any such agent(s) within the previous 30 days, or he is scheduled to receive any such agent(s) in the period up to the planned date for the last study visit. 7. The patient has previously been enrolled in this trial. 8. The patient has previously undergone PET imaging with any PSMA-avid product. 9. The patient has histological evidence of small-cell carcinoma of the prostate. 10. The patient is clinically unstable or requires emergency treatment. 11. The patient has any mental condition rendering him incapable of understanding the nature, scope, and consequences of the trial as set out in the information given to the patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sensitivity and specificity of [18F]PSMA-1007 PET/CT for the detection of pelvic nodal disease (N1) compared to histology as the standard of reference | 6 to 8 weeks post-surgery |
Countries
France, Germany, Italy, Japan, Netherlands, Spain
Contacts
CONTACTAlexander Hoepping, Dr.
Outcome results
None listed