A Prospective Study on 18F-DCFPyL PET/CT Imaging in Biochemical Recurrence of Prostate Cancer (Python)
Primary Purpose
Prostate Cancer Recurrent
Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
DCFPyL
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Cancer Recurrent
Eligibility Criteria
Inclusion Criteria:
- Male.
- Age min 18 years.
- Histopathological proven prostate adenocarcinoma per original diagnosis.
- First suspected recurrence of prostate cancer based on rising prostate-specific antigen (PSA) after initial curative therapy with radical prostatectomy of PSA ≥ 0.2 ng/mL confirmed by a subsequent PSA value of ≥0.2 ng/mL or with radiation therapy (external beam or brachytherapy) of PSA > 2 ng/mL above the nadir after therapy regardless of the serum concentration of the nadir.
- Able and willing to provide informed consent and comply with protocol requirements
- Patient who can undergo all study procedures per Investigator's point of view
- Patient with social insurance cover.
Exclusion Criteria:
Patients displaying any of the following criteria will not be included:
- ECOG > 2
- History of previous salvage therapies (including salvage radiotherapy or salvage lymph node dissection)
- History of adjuvant radiotherapy
- History of cryotherapy, high-intensity focused ultrasound (HIFU)
- Other active malignant tumour
- Treatment with Androgen Deprivation Therapy (ADT) in the past 30 days or ongoing
- Treatment with colchicine in the past 8 days or ongoing
- Treatment with hematopoietic colony stimulating factors (CSF) in the past 5 days or ongoing
- Unable to lie supine for imaging
- Known allergy to investigational or reference products or to any excipients
- Unable to provide written consent (linguistic or psychological inability)
- Participation in another clinical study within one month prior to inclusion
- Uncooperative, in the Investigator's opinion.
- Subjects deprived of their freedom by administrative or legal decision or who are under guardianship
Sites / Locations
- CURIUM PET France
Outcomes
Primary Outcome Measures
to compare per-patient detection rate of 18F-DCFPyL PET/CT versus that of 18F-FCH PET/CT.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04734184
Brief Title
A Prospective Study on 18F-DCFPyL PET/CT Imaging in Biochemical Recurrence of Prostate Cancer
Acronym
Python
Official Title
Title A Prospective Study on 18F-DCFPyL PET/CT Imaging in Biochemical Recurrence of Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 7, 2020 (Actual)
Primary Completion Date
May 2021 (Anticipated)
Study Completion Date
February 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Curium PET France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
PYTHON is designed to establish the efficacy and safety of 18F-DCFPyL in comparison with that of 18F-fluorocholine, in patients with first biochemical recurrence (BCR) after initial definitive therapy (prostatectomy, external beam radiotherapy or brachytherapy) for histopathologically confirmed prostate adenocarcinoma per original diagnosis. PET/CT scans will be each interpreted by three independent masked experts who are not otherwise involved in the trial.
Detailed Description
The primary objective is the per-patient detection rate of 18F-DCFPyL in comparison with 18F-Fluorocholine. Secondary objectives include the assessment of the impact on patient treatment management, the per-region detection rate, the sensitivity and specificity on a per-patient and per-region basis, the concordance rate between both tracers, and the safety. The study was initiated in July 2020, and the recruitment of the planned 217 patients has been completed in October 2020. The follow-up phase is ongoing. Typically, as part of the routine care practice, these patients receive appropriate treatment and follow-up. The investigating sites are therefore requested for the period of 7 months after the second tracer injection, to provide any results of subsequent biopsies, imaging studies, clinical findings, PSA measurements, and disease management, if performed in routine practice. Treatment decisions are locally made at the discretion of the referring physician based on all available clinical information, including the non-masked local reports of both PET/CT and any other imaging results. After completion of the study, a consensus will be obtained from a multidisciplinary independent board (truth panel), based on the surrogate standard of reference which will include all the above-mentioned available results. Assessments will be made on a per-region and per-patient basis. The truth panel will consist in 3 independent experts not otherwise involved in the trial. All above information will be sequentially presented to the truth panel experts. The order of presentation of 18F-FCH PET/CT and 18F-DCFPyl PET/CT results will be randomized. The truth panel will have to assess the impact of each PET/CT examination on disease restaging and change in treatment intent, by filling in a patient management questionnaire after review of each PET/CT examination report.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer Recurrent
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
217 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Diagnostic Test
Intervention Name(s)
DCFPyL
Intervention Description
Single dose injection
Primary Outcome Measure Information:
Title
to compare per-patient detection rate of 18F-DCFPyL PET/CT versus that of 18F-FCH PET/CT.
Time Frame
10 weeks
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male.
Age min 18 years.
Histopathological proven prostate adenocarcinoma per original diagnosis.
First suspected recurrence of prostate cancer based on rising prostate-specific antigen (PSA) after initial curative therapy with radical prostatectomy of PSA ≥ 0.2 ng/mL confirmed by a subsequent PSA value of ≥0.2 ng/mL or with radiation therapy (external beam or brachytherapy) of PSA > 2 ng/mL above the nadir after therapy regardless of the serum concentration of the nadir.
Able and willing to provide informed consent and comply with protocol requirements
Patient who can undergo all study procedures per Investigator's point of view
Patient with social insurance cover.
Exclusion Criteria:
Patients displaying any of the following criteria will not be included:
ECOG > 2
History of previous salvage therapies (including salvage radiotherapy or salvage lymph node dissection)
History of adjuvant radiotherapy
History of cryotherapy, high-intensity focused ultrasound (HIFU)
Other active malignant tumour
Treatment with Androgen Deprivation Therapy (ADT) in the past 30 days or ongoing
Treatment with colchicine in the past 8 days or ongoing
Treatment with hematopoietic colony stimulating factors (CSF) in the past 5 days or ongoing
Unable to lie supine for imaging
Known allergy to investigational or reference products or to any excipients
Unable to provide written consent (linguistic or psychological inability)
Participation in another clinical study within one month prior to inclusion
Uncooperative, in the Investigator's opinion.
Subjects deprived of their freedom by administrative or legal decision or who are under guardianship
Facility Information:
Facility Name
CURIUM PET France
City
Saint-Beauzire
ZIP/Postal Code
63360
Country
France
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
A Prospective Study on 18F-DCFPyL PET/CT Imaging in Biochemical Recurrence of Prostate Cancer
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