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Clinical Trials/NCT05022914
NCT05022914
Recruiting
Not Applicable

Prostate-Specific Membrane Antigen (PSMA) Guided Approach for bIoCHEmical Relapse After Prostatectomy- A Prospective Observational Study-PSICHE

Azienda Ospedaliero-Universitaria Careggi1 site in 1 country180 target enrollmentJanuary 19, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Azienda Ospedaliero-Universitaria Careggi
Enrollment
180
Locations
1
Primary Endpoint
Progression free survival
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

This observational study was designed to evaluate progression free survival after PSMA-PET/CT based salvage approach for patients affected by biochemical relapse after radical prostatectomy.

Detailed Description

This is a prospective observational multicenter study including patients treated with upfront radical prostatectomy +/- postoperative prostate bed radiotherapy, with histological result of Prostate adenocarcinoma, affected by biochemical relapse (defined as PSA\>/= 0.2 ng/ml) with a PSA at recurrence \</=1 ng/ml. Patients will be staged with centralized 68 Ga- PSMA PET/CT and treated with a pre-defined approach based on 68 Ga-PSMA PET/CT findings. The predefined approach will consist in the following flowchart: 1. In negative 68Ga-PSMA PET/CT or positive findings within prostate bed: Prostate bed RT 2. In 68Ga-PSMA PET/CT detecting pelvic nodal recurrence amenable with stereotactic body radiation therapy (SBRT) on all sites of disease: SBRT to all positive nodal disease. 3. In abdominal nodal or bone oligometastatic disease amenable with stereotactic body radiation therapy (SBRT) on all sites of disease: SBRT on all sites of disease 4. In abdominal nodal or bone metastatic disease (\>3 lesions or non-amenable with SBRT) and/or visceral disease: ADT+/-other systemic therapies available for metastatic hormone sensitive pCa at physician discretion.

Registry
clinicaltrials.gov
Start Date
January 19, 2021
End Date
January 19, 2027
Last Updated
4 years ago
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lorenzo Livi

Full Professor

Azienda Ospedaliero-Universitaria Careggi

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent
  • Patient suitable for 68Ga-PSMA PET/CT re-staging according to clinical practice (Previous radical prostatectomy with histological result of Prostate adenocarcinoma +/- postoperative prostate bed radiotherapy (adjuvant or salvage setting), with a biochemical relapse defined as a PSA \> 0.2 and \<1

Exclusion Criteria

  • ADT administration within 6 months from study enrollment
  • Persistent elevation of PSA after RP measured within 16 weeks from surgery (\> 0.1 ng/ml)

Outcomes

Primary Outcomes

Progression free survival

Time Frame: 2 year

PFS is defined as time from end of salvage treatment performed at first relapse to documented biochemical progression or radiological progression (or both), death from any cause or censoring at date of last follow-up.

Secondary Outcomes

  • Cause-specific survival(2 years)
  • Overall Survival(2 years)
  • Radiological Progression Free Survival(2 years)
  • Management Change(2 years)
  • Association between PSMA PET/CT Detection Rate and specific miRNA panel(2 year)
  • Quality of Life(2 years)

Study Sites (1)

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