18F-DCFPyL PET-CT Scan and Prostate Cancer

• Status: Unknown status
• Trial end date: 2020-06-30
• Target enrollment: 0
• Participant gender: Male

Summary

Primary Objective:

The primary objective of this study is to assess the efficacy of 18F-DCFPyL PET-CT for initial staging of prostate cancer in Veterans compared to conventional imaging (99mTc-MDP bone scan and Diagnostic CT or MRI). The primary clinical endpoint of our study is the percent of Veterans with prostate cancer in which the 18F-DCFPyL PET-CT identifies M1 disease at initial staging.

Secondary Objectives:

Frequency of the change in primary treatment plan after initial staging.

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Lida Jafari
• Collaborator: University of California, Los Angeles

Criteria

Inclusion Criteria:

1. Age ≥ 18 years and male.

2. Ability to understand the study and the willingness to sign a written informed consent document.

3. Histologically confirmed adenocarcinoma of the prostate.

4. PSA greater than 10, or Gleason ≥4+3, or clinical stage greater than or equal toT2c.

5. Plan to undergo (or have already undergone) routine care initial systemic staging with conventional imaging for prostate cancer.

6. Eastern Cooperative Oncology Group (ECOG) Performance score of 0 to 2.

7. No prior local therapy for prostate cancer (i.e., prostatectomy, radiotherapy, etc.).

8. Willing to comply with the procedural requirements of this protocol.

Exclusion Criteria:

1. Serious or uncontrolled co-existent non-malignant disease, including active and uncontrolled infection.

2. The subject has a condition or situation that, in the investigator's opinion, may put the subject at significant risk, may confound the study results, or may interfere significantly with subject's participation in the study.

3. Primary small cell carcinoma of the prostate.

4. Participation in this study significantly delay the scheduled standard of care therapy.

5. Weighs greater than 350 lbs., or unable to fit within the imaging gantry.

6. The subject undergone prior local therapy for prostate cancer (i.e. prostatectomy, radiotherapy, etc.).

7. Currently receiving androgen deprivation therapy (ADT) or anti-androgen? Previous use of ADT is allowed IF the subject has been off ADT or anti-androgen for 3 months or more.