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Clinical Trials/NCT07168616
NCT07168616RecruitingNot Applicable

Prospective Evaluation of Istanbul PSMA PET/CT Criteria for Selecting Candidates for Active Surveillance in Low-Risk Prostate Cancer

Istanbul University - Cerrahpasa10 sites in 1 country201 target enrollmentStarted: September 1, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
201
Locations
10
Primary Endpoint
1. Diagnostic Accuracy of the Istanbul PSMA PET/CT Criteria (IPPC) for Detecting Clinically Significant Prostate Cancer (csPCa)

Study Overview

Brief Summary

This is a multicenter, prospective diagnostic accuracy study evaluating the Istanbul PSMA PET/CT Criteria (IPPC) for selecting patients with biopsy-confirmed low-risk prostate cancer (ISUP Grade 1) for active surveillance (AS). The study integrates delayed Ga-68 PSMA PET/CT imaging into the diagnostic pathway to refine patient stratification, minimize overtreatment and potentially reduce unnecessary biopsies and MRI, or exposing high-risk individuals to the danger of cancer progression if left untreated scans.

Detailed Description

Prostate cancer is the most common malignancy in men and demonstrates heterogeneous clinical behavior. While many low-risk patients have indolent disease, a subset harbors clinically significant prostate cancer (csPCa) requiring early intervention. Active Surveillance (AS) is widely used to avoid overtreatment; however, current selection criteria-PSA, DRE, biopsy Gleason score, number of positive cores, PSA density, and mpMRI-lack sufficient predictive accuracy. Studies indicate that up to 30% of patients classified as low-risk by biopsy are found to have higher-grade disease at radical prostatectomy. The Istanbul PSMA PET/CT Criteria (IPPC) were developed by a multidisciplinary expert panel in Turkey to classify intraprostatic lesions on delayed (120-minute) Ga-68 PSMA PET/CT imaging into three risk categories:

  • IPPC 1 No or homogeneous low uptake - safe for monitoring.
  • IPPC 2: Indeterminate uptake - AS with close follow-up.
  • IPPC 3: Focal, lentiform, high SUVmax ≥12 uptake in peripheral zone - definitive treatment recommended.

This study will evaluate the diagnostic performance of IPPC compared to standard mpMRI and biopsy findings, using radical prostatectomy pathology or long-term clinical follow-up as the reference standard.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •mpMRI performed within 3 months prior to enrollment
  • •Systematic or MRI-targeted prostate biopsy performed
  • •Biopsy-confirmed ISUP Grade 1 low-risk PCa
  • •Prostate biopsy report specifying tumor localization and number of positive cores
  • •Meets AS criteria: ISUP 1, PSA ≤10 ng/mL, PSAd >0.15 ng/mL², clinical stage cT1c-T2a, ≤3 positive cores
  • •Life expectancy ≥10 years
  • •No prior PSMA PET imaging
  • •No evidence of extra-prostatic disease on mpMRI
  • •Signed informed consent for study procedures

Exclusion Criteria

  • •High-risk or unfavorable intermediate-risk PCa, or adverse histologies (neuroendocrine, ductal adenocarcinoma, basal cell carcinoma, TP53 or BRCA1/2 mutations if available)
  • •Prior prostate cancer treatment or prostate surgery
  • •MRI evidence of extracapsular extension, seminal vesicle invasion, or nodal metastasis
  • •History of pelvic radiotherapy
  • •Life expectancy <10 years
  • •Severe renal impairment
  • •Inability to comply with follow-up schedule

Outcomes

Primary Outcomes

1. Diagnostic Accuracy of the Istanbul PSMA PET/CT Criteria (IPPC) for Detecting Clinically Significant Prostate Cancer (csPCa)

Time Frame: Baseline imaging; confirmed at prostatectomy or through 2-year follow-up.

Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and area under the ROC curve (AUC) for IPPC classification in identifying csPCa, defined as ISUP Grade Group ≥2 on radical prostatectomy pathology or disease progression on long-term follow-up.

Secondary Outcomes

  • Reduction in Repeat Biopsy Rate(Assessed over 2 years.)

Investigators

Sponsor
Istanbul University - Cerrahpasa
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Levent Kabasakal

Professor of Nuclear Medicine, Medical Doctor

Istanbul University - Cerrahpasa

Study Sites (10)

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