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Clinical Trials/NCT00384891
NCT00384891
Terminated
Phase 3

A Randomized Controlled Study Comparing Adjuvant Hyperthermia Treatment in Conjunction With Mitomycin C Versus BCG Immunotherapy (BCG) Adjuvant Treatment in Patients With Superficial Transitional Cell Carcinoma of the Bladder (STCCB)

Medical Enterprises Europe B.V.8 sites in 4 countries190 target enrollmentFebruary 2002

Overview

Phase
Phase 3
Intervention
Synergo + MMC
Conditions
Urinary Bladder Diseases
Sponsor
Medical Enterprises Europe B.V.
Enrollment
190
Locations
8
Primary Endpoint
Recurrence free survival
Status
Terminated
Last Updated
11 years ago

Overview

Brief 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)

Detailed 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

Registry
clinicaltrials.gov
Start Date
February 2002
End Date
December 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medical Enterprises Europe B.V.
Responsible Party
Sponsor

Eligibility Criteria

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 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

Arms & Interventions

Synergo + MMC

Combined bladder wall hyperthermia and intravesical instillation with cooled Mitomycin-C

Intervention: Synergo + MMC

Bacillus Calmette-Guérin

Intravesical instillation with BCG (Bacillus Calmette-Guérin)

Intervention: Bacillus Calmette-Guérin

Outcomes

Primary Outcomes

Recurrence free survival

Time Frame: 2 years

Recurrence free survival probability of STCCB in patients with pure (non-CIS) papillary tumor

Secondary Outcomes

  • Proportion of complete response in CIS patients(3 months)
  • Progression rate (to disease stage>T1) and/or metastatic disease(2 years)
  • Local and systemic side effects, both subjective and objective(2 years)

Study Sites (8)

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