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Clinical Trials/NCT01304485
NCT01304485
Completed
Phase 2

Phase 2 Study: PET Imaging Characteristics of C11-Acetate in Patients With Prostate Carcinoma, Detection of Recurrent Disease With PSA Relapse

Phoenix Molecular Imaging1 site in 1 country2,000 target enrollmentApril 2011

Overview

Phase
Phase 2
Intervention
Sodium Acetate C11
Conditions
Prostate Cancer
Sponsor
Phoenix Molecular Imaging
Enrollment
2000
Locations
1
Primary Endpoint
SUV (Standardized Uptake Value)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Positron emission tomography (PET) imaging evaluation in men with recurrent prostate cancer to select patients who may benefit from directed therapy

Detailed Description

The goal of this project is improved imaging of prostate cancer by positron emission tomography (PET) with use of the radiopharmaceutical C-11 Acetate, utilizing state-of-the-art PET/CT camera technology and processing algorithms. A successful effort will lead to more accurate diagnosis of recurrence in patients with prostate cancer to allow for early directed therapy. This study is designed to generate data to add to the understanding of the effectiveness of C-11 Acetate, focusing on patients with recurrent or persistent disease after prostatectomy or radiation therapy. The study is designed to expand on the database of C11-Acetate PET imaging in patients with prior definitive therapy for prostate cancer and evidence of biochemical recurrence (post therapy rise in PSA), and to evaluate the relationship between detection on C11-Acetate PET imaging, PSA (Trigger, Velocity and Doubling Time) and FDG PET imaging. Specific questions to be addressed: 1. What is the yield of current state-of-the-art PET/CT with C-11 Acetate in detecting recurrent disease in this patient population? 2. How does the performance of PET with C-11 Acetate compare with that of PET using F-18 fluorodeoxyglucose (FDG-PET), Sodium F18 PET bone scans and with that of CT? 3. What is the optimal imaging protocol in terms of imaging time after injection?

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
January 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fabio Almeida MD

Fabio Almeida MD, Medical Director

Phoenix Molecular Imaging

Eligibility Criteria

Inclusion Criteria

  • recurrent prostate cancer (detectable PSA following radical prostatectomy or rising PSA in patients with radiation therapy as the primary treatment)

Exclusion Criteria

  • \< 18 years old
  • claustrophobic patients

Arms & Interventions

Sodium Acetate C11 PET Imaging

Intervention: Sodium Acetate C11

Outcomes

Primary Outcomes

SUV (Standardized Uptake Value)

Time Frame: Day1 - Assessed at time of PET imaging - i.e. at the time of primary investigation/PET agent administration

Imaging studies will be evaluated both qualitatively and quantitatively using SUV (standardized uptake values): a measure of metabolism based on injected dose, patient weight and region of interest.

Secondary Outcomes

  • PSA (prostate specific antigen)(Every 3 - 6 months for 24 months after PET imaging)

Study Sites (1)

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