Clinical Trial · NCT04703543

Evaluating the Role of Both PSMA and 64Cu-PET/CT Total Body in Patients With Locally Relapsed Prostate Cancer

Overview

The purpose of this study is to assess the detection rate of local relapse after radical prostatectomy with either PSMA or 64Cu-PET/CTs and whether the delineation of relapsed lesions using both methods can facilitate/change the therapeutic strategy of the radiation oncologist

Sponsor

National Cancer Institute

Phase

N/A

ClinicalTrials.gov

NCT04703543

Eligibility

Inclusion

  • Local relapse at mpMR
  • Performance Status 0-1 according to ECOG
  • Localized prostate adenocarcinoma (M0), any PSA value, any Gleason Score
  • Biochemical recurrence (two consecutive PSA values of at least 0.2 ng/ml)
  • Previous radical surgery with subsequent undetectable PSA (\<0.2 ng/ml)
  • M0 to 18F-choline PET/TC
  • Informed written consent

Exclusion

  • Presence of coxo-femoral implants
  • Contraindication to MRI (metal prostheses, pacemakers, claustrophobia, etc.)
  • Secondary bone lesions from prostate cancer or M1
  • Previous pelvic radiotherapy
  • Psychiatric diseases
  • Detectable PSA after surgery
  • Crohn's disease or ulcerative colitis (active phase)
  • Hormone therapy started before staging examinations