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Clinical Trials/NCT07257718
NCT07257718
Not yet recruiting
Phase 2

The Combined Role of FAPI PET and Liquid Biopsy in the Staging and Clinical Management of Bladder Cancer

Chiti Arturo0 sites262 target enrollmentStarted: September 1, 2026Last updated:

Overview

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Chiti Arturo
Enrollment
262
Primary Endpoint
Sensitivity of FAPI PET/CT for the detection in the Staging of Bladder Cancer

Overview

Brief Summary

The study will be a prospective two arms diagnostic phase II single-center trial.

Patients referred for diagnosis and treatment with diagnosis of bladder cancer, age > 18 years, ECOG performance status < 2, ability to undergo an imaging study procedure will be considered for inclusion. For the study will be include 262 patients (118 and 144 in the arm 1 and 2, respectively).

Eligible patients will sign the inform consent to be included in the study. The participation to other clinical studies will be not, per se, an exclusion criterion. Before treatment, enrolled patients will be imaged by FAPI PET/CT and urine samples will be collected and analyzed by Epicheck® test and Xpert® Bladder Cancer Detection. Thereafter, patients will be managed and treated according to international guidelines and standard of care procedures in our institution. Safety will be recorded. Results of FAPI imaging, Epicheck® test, and Xpert® Bladder Cancer Detection will be compared to stage, risk assessment groups as defined by currentguidelines, and clinical outcome. Diagnostic and predictive performances of FAPI imaging and liquid biopsy will be assessed and compared by using machine learning approaches.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Investigator)

Eligibility Criteria

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

Inclusion Criteria

  • age \> 18 years
  • ECOG performance status \< 2
  • ability to undergo an imaging study procedure

Exclusion Criteria

  • pregnant or breast-feeding women
  • uncontrolled active infection.

Outcomes

Primary Outcomes

Sensitivity of FAPI PET/CT for the detection in the Staging of Bladder Cancer

Time Frame: from enrollment to 48 months

Sensitivity will be calculated as the proportion of true positive findings obtained with FAPI PET/CT compared with the reference standard (e.g., clinical follow-up).

Secondary Outcomes

  • PET Imaging(from month 12 to 60)

Investigators

Sponsor
Chiti Arturo
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Chiti Arturo

Professor

IRCCS San Raffaele

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