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NCT Number: NCT07067749

Treatment Expedition With MRI Processing and Optimization for Muscle Invasive Bladder Cancer

The TEMPO-MIBC trial is a phase III, single-center, two-arm, randomized, controlled trial. Its primary objective is to evaluate the efficacy of a simplified diagnostic and treatment pathway for muscle-invasive bladder cancer (MIBC). This study investigates the role of multiparametric bladder MRI (mpMRI) in patients with biopsy proven cancer of the bladder with clinical features of detrusor muscle invasion. In the experimental arm, enrolled patients will receive a bladder mpMRI, if this exam will confirm the high suspicion of muscle invasion a conventional endoscopic transurethral resection of bladder tumour (TURBt) for staging purposes will be foregone and patients will immediately access the next step of their clinical management. Experimental arm outcomes will be compared to a control arm in which all enrolled patients will be receiving TURBt as part of the standard management of bladder cancer. The aim of this study is demonstrating a significant reduction of the time needed to offer patients the definitive treatment for their disease, possibly ensuring better long-term oncological outcomes.

A blood sample will be collected from each patient enrolled in the study at pre-planned time points to measure the levels of circulating tumour (ctDNA), a primer will be built from bladder cancer biopsies performed at enrolment. ctDNA has been shown to be a proxy measure of tumour burden and residual molecular disease after treatment. The ctDNA levels in the experimental arm will be compared to those of the control arm to investigate wether foregoing endoscopic resection of the tumour and reducing time to definitive cancer treatment might be associated to lower ctDNA levels.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Policlinico Tor Vergata

Rome, RM, 00133, Italy

Location status: Recruiting

Location contact

Emanuele Casciani, Associate Prof of Radiology

SUB_INVESTIGATOR

Luca Orecchia, Consultant Urologist

SUB_INVESTIGATOR

Simone Albisinni, Associate Professor of Urology

CONTACT

[email protected]

06020902977

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Clinical suspicion of muscle invasive bladder cancer at cystoscopy and pre-cystoscopy imaging

Exclusion criteria

  • Anticipated survival < 3 months due to comorbidities
  • Pregnant patients
  • Breastfeeding patients
  • Previous chemotherapy within 6 weeks
  • Previous radiotherapy withing 6 weeks
  • Previous TURBt within 6 weeks
  • Severe renal impairment (eGFR < 40 mL/min/1.73 m2)
  • non MRI-compatible metal implants
  • Claustrophobia
  • Denial of written consent to participate in the study

Treatment and study plan

multiparametric magnetic resonance imaging (mpMRI) of the bladder

Diagnostic Test

This study will investigate the role of bladder mpMRI as a tool to expedite treatment in patients with muscle invasive bladder cancer.

mpMRIs will be investigated as a possible replacement of standard TURBt, a planned surgical procedure for cancer local staging.

mpMRis will be reported according to the Vesical Imaging - Reporting and Data System Stanrdars (VI-RADS) to provide a score indicating probability of muscle invasion.

Transurethral resection of bladder tumour (TURBt)

Procedure

This is a planned endoscopic surgical procedure consisting in resection of the bladder tumour through a electrified loop manouvred with an endoscope. In muscle invasive bladder cancer, this procedure allows histological confirmation of presence of detrusor muscle invasion.

Circulating tumour DNA levels assessment

Genetic

Blood samples will be collected from each enrolled patient at pre-planned time points:

  • Cystoscopy, both arms
  • mpMRI (experimental arm) or TURBt (control arm)
  • Definite cancer treatment, both arms

ctDNA levels will be measured on the collected blood samples.

Primary outcomes

  1. Time to definitive treatment

    Time frame: From the day of enrollment at baseline until the day of the start of definitive treatment for muscle invasive bladder cancer. Expected timeframe between 45 and 180 days.

    Time in days needed to complete the diagnostic pathway, multidisciplinary board discussion and finally offer the appropriate definitive treatment for muscle invasive bladder cancer: surgery, drugs, radiation, palliative care

Secondary outcomes

  1. Concentration of ctDNA levels

    Time frame: Three specific time points: 1) Enrolment at baseline 2) During intervention (mpMRI or TURBt) 3) On the day of definitive treatment for muscle invasive cancer Expected timeframe 1 to 180 days

    ctDNA leves from blood samples collected at pre-planned time points in both arms

  2. Cancer Specific Survival

    Time frame: through study completion, an average of 2 years

    Length of time from enrolment to the date of death from the disease.

  3. Overall Survival

    Time frame: through study completion, an average of 2 years

    Length of time from enrolment to the date of death from any cause

  4. Time to cancer recurrence

    Time frame: "through study completion, an average of 2 years".

    Length of time from enrolment to the date of clinically proven cancer recurrence

  5. Number of procedure Related Complications

    Time frame: For 30 days following the procedure

    Monitoring of procedure related complications for TURBt and mpMRI

Study contacts

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

Luca Orecchia, MD

CONTACT

[email protected]

Simone Albisinni, MD, Phd, FEBU

CONTACT

[email protected]

+390620902977

Sponsors and collaborators

Lead sponsor

University of Rome Tor Vergata

Other

Registry information

Acronym: TEMPO-MIBC

Important dates

Study start
2025
Primary completion
2028
Study completion
2030
First posted
Jul 16, 2025
Registry last updated
Jul 24, 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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