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NCT Number: NCT07257718

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

FAPI PET/CT and liquid biopsy in patients eligible for radical cystectomy

Procedure

We hypothesise that FAPI PET improves clinical staging, and that baseline FAPI PET metrics and ctDNA/utDNA profiles correlate with tumour aggressiveness and patient outcomes

FAPI PET/CT and liquid biopsy in patients eligible for conservative treatment

Procedure

We hypothesise that FAPI PET improves clinical staging, and that baseline FAPI PET metrics and ctDNA/utDNA profiles correlate with tumour aggressiveness and patient outcomes

Primary outcomes

  1. 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

  1. PET Imaging

    Time frame: from month 12 to 60

    secondary outcome aims to image patients

Study contacts

Contact information is provided by the study sponsor or research team.

Chiara Catalano

CONTACT

[email protected]

Martina Sollini

CONTACT

[email protected]

0226436319

Sponsors and collaborators

Lead sponsor

Chiti Arturo

Other

Registry information

Official study title

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

Acronym: FUTURE

Important dates

Study start
2026
Primary completion
2027
Study completion
2031
First posted
Dec 2, 2025
Registry last updated
Dec 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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