Hyperthermia Treatment in Conjunction With Mitomycin C Versus Bacillus Calmette-Guérin Immunotherapy (BCG) for Superficial Bladder Cancer

Last updated: October 5, 2014
Sponsor: Medical Enterprises Europe B.V.
Overall Status: Terminated

Phase

3

Condition

Fever

Bladder Cancer

Urothelial Cancer

Treatment

N/A

Clinical Study ID

NCT00384891
102.1
  • Ages > 18
  • All Genders

Study Summary

The study is designed to compare the efficacy and safety of 2 treatment types for the prevention of tumor recurrence of superficial bladder cancer:

  1. A combination of bladder wall heating and local chemotherapy (Synergo)

  2. Bacillus Calmette-Guérin (BCG)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Superficial TCC: Any G3 or any T1 and/or CIS

  • Multifocal (>1) Ta lesions

  • Multiple recurrences (>2) of Ta lesions in the last 24 months

  • Complete tumor eradication must be confirmed

  • WHO performance status 0-2 (Appendix V)

  • Life expectancy of more than 24 months

  • Patients willing to sign informed consent

Exclusion

Exclusion Criteria:

  • Bladder tumors other than TCC

  • Coexistence of another primary malignant tumor other than BCC of the skin

  • TCC of the bladder involving the urethra or upper urinary tract

  • Previous history of TCC stage T2 or higher

  • Clinical presence or previous history of regional spreading or distant metastases

  • Intravesical MMC treatments during the last 12 months

  • Previous intravesical BCG therapy (Any intravesical BCG therapy in the last 24 months,or More than 6 BCG intravesical instillations in the last 48 months.

  • Previous pelvic radiotherapy or systemic chemotherapy

  • Partial cystectomy

  • Diverticle of bladder larger than 1cm in diameter

  • Residual urine > 100cc measured by uroflowmetry

  • Bladder volume < 150cc measured by ultrasound

  • Urinary incontinence (more than one wet pad a day)

  • Urethral stricture impeding 20F catheterization

  • Urethral bleeding or persistent hematuria

  • Active intractable or uncontrollable UTI

  • Active tuberculosis or BCG infection

  • Patients who experienced BCG life threatening sepsis

  • Known allergy to MMC or BCG

  • Known impaired immune response, positive HIV serology, patients receiving systemicsteroids or immunosuppressive therapy

  • Hematological disorders; leukocytes < 3500, platelets < 100,000

  • Kidney or liver function disorders (more than 1.5 times upper normal limit)

  • Pregnant or lactating women

  • Patients who cannot be followed up properly or are unable to collaborate

Study Design

Total Participants: 190
Study Start date:
February 01, 2002
Estimated Completion Date:
December 31, 2013

Study Description

The study is a randomized controlled study, designed to test the efficacy and safety of a new treatment modality for the prevention of tumor recurrence in superficial bladder cancer.

Patients must have their tumors surgically resected prior to study enrollment, and undergo a series of tests to prove their bladder is now free of tumor. Eligible patients will be randomly assigned to one of 2 treatment arms:

  1. A combination of bladder wall heating and local chemotherapy (Synergo)

  2. Bacillus Calmette-Guérin (BCG)

Patients will be treated during the first year of the study, and will be followed up for a total of 2 years. The follow up will include a visual evaluation of the patient's bladder by cystoscopy, a cytological examination of the urine (to look for malignant cells) and other additional exams. The patients' general welfare will be monitored through out the study.

The aim of this study is to compare the efficacy and safety of the novel treatment (Synergo) to that of the well-known BCG

Connect with a study center

  • University Hospital - AKH Vienna

    Vienna,
    Austria

    Site Not Available

  • Hospital Erasme

    Brussels,
    Belgium

    Site Not Available

  • Bnai Zion Medical Center

    Haifa,
    Israel

    Site Not Available

  • Wolfson Hospital

    Holon,
    Israel

    Site Not Available

  • Hadassah University Hospital

    Jerusalem,
    Israel

    Site Not Available

  • Galliera Hospital

    Genova,
    Italy

    Site Not Available

  • Istituto Europeo del Oncologia

    Milan,
    Italy

    Site Not Available

  • San Raffaele Hospital (HSR)

    Milan,
    Italy

    Site Not Available

  • Policlinico Gemelli, Universita Cattolica del Sacro Cuore

    Rome,
    Italy

    Site Not Available

  • Department of Urology, Radboud University Hospital

    Nijmegen,
    Netherlands

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.