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Radiation Therapy, Chemotherapy, or Observation in Treating Patients With Bladder Cancer - Article


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Cancer Radiation Therapy


Clinical Trial: Radiation Therapy, Chemotherapy, or Observation in Treating Patients With Bladder Cancer

This study is no longer recruiting patients.

Sponsored by: Medical Research Council
Information provided by: National Cancer Institute (NCI)

Purpose

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with radiation therapy may kill more tumor cells. It is not known whether receiving either radiation therapy, chemotherapy, or observation is more effective for cancer of the bladder.

PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy, chemotherapy, or observation following tumor surgery in treating patients who have bladder cancer.

Condition Treatment or Intervention Phase
stage I bladder cancer
transitional cell carcinoma of the bladder
 Drug: BCG
 Drug: mitomycin
 Procedure: biological response modifier therapy
 Procedure: chemotherapy
 Procedure: non-specific immune-modulator therapy
 Procedure: radiation therapy
Phase III

MedlinePlus related topics:  Bladder Cancer;   Cancer
Genetics Home Reference related topics:  bladder cancer

Study Type: Interventional
Study Design: Treatment

Official Title: Phase III Randomized Study of Adjuvant Radical Radiotherapy Versus Intravesical BCG or Mitomycin Versus Observation Alone After Endoscopic Resection in Patients With Stage I, Grade 3 Transitional Cell Carcinoma of the Bladder

Further Study Details: 

OBJECTIVES:

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to center, extent of tumor (single tumor without carcinoma in situ (CIS) vs multiple tumors or CIS), and WHO performance status. Patients with a single tumor and no CIS are randomized to arm I or II. Patients with multiple tumors or CIS are randomized to arm II or III.

  • Arm I: Patients undergo observation only.
  • Arm II: Patients undergo radical radiotherapy 5 days a week for 6 weeks. Patients found to be node positive on CT scan may undergo pelvic irradiation and remain on study.
  • Arm III: Patients receive intravesical BCG or mitomycin (at the discretion of the physician) weekly for 6-12 weeks. Patients on arms I and III are followed at 3 months after randomization. All patients are followed at 6, 9, and 12 months and then annually thereafter.

PROJECTED ACCRUAL: A total of 200 patients will be accrued for this study.

Eligibility

Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

PATIENT CHARACTERISTICS: Age:

  • Any age

Performance status:

  • WHO 0-2

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • Not specified

Other:

PRIOR CONCURRENT THERAPY: Biologic therapy:

  • No more than 1 prior adjuvant treatment with intravesical BCG

Chemotherapy:

  • No more than 1 prior adjuvant treatment with intravesical chemotherapy

Endocrine therapy:

  • Not specified

Radiotherapy:

  • See Disease Characteristics

Surgery:

  • See Disease Characteristics
  • Diathermic removal of associated small papillary growths allowed

Location Information


United Kingdom, England
      Middlesex Hospital- Meyerstein Institute, London,  England,  WIT 3AA,  United Kingdom

Study chairs or principal investigators

Stephen John Harland, MD,  Study Chair,  Middlesex Hospital - Meyerstein Institute   

More Information

Clinical trial summary from the National Cancer Institute's PDQ® database

Study ID Numbers:  CDR0000077404; MRC-BS06; EU-91019
Record last reviewed:  May 2003
Last Updated:  October 13, 2004
Record first received:  November 1, 1999
ClinicalTrials.gov Identifier:  NCT00002490
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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September 7, 2008



Page Updated: September 6, 2005
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