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

Primary Purpose

Bladder Cancer

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
BCG vaccine
mitomycin C
radiation therapy
Sponsored by
Medical Research Council
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Cancer focused on measuring stage I bladder cancer, transitional cell carcinoma of the bladder

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Diagnosis of transitional cell carcinoma of the bladder Stage T1 Nx M0, grade 3 disease No muscle invasion at base of tumor Diagnosis of this stage made within the past 6 months Earlier diagnosis of tumors with lower stage or grade allowed No history of higher stage urothelial tumors Presence of partial involvement of bladder with carcinoma in situ (CIS) or asymptomatic widespread CIS allowed No widespread CIS causing severe symptoms Prior complete transurethral resection of tumor with deep biopsy of underlying bladder wall required Disease currently amenable to adjuvant radiotherapy, followed by cystoscopy with biopsies PATIENT CHARACTERISTICS: Age: Any age Performance status: WHO 0-2 Life expectancy: Not specified Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No other prior or concurrent malignancy except nonmelanomatous skin cancer or cervical intraepithelial neoplasia 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

Sites / Locations

  • Middlesex Hospital- Meyerstein Institute

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 1, 1999
Last Updated
December 17, 2013
Sponsor
Medical Research Council
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1. Study Identification

Unique Protocol Identification Number
NCT00002490
Brief Title
Radiation Therapy, Chemotherapy, or Observation in Treating Patients With Bladder Cancer
Official Title
A RANDOMIZED TRIAL OF RADICAL RADIOTHERAPY IN pT1G3 NXM0 BLADDER CANCER
Study Type
Interventional

2. Study Status

Record Verification Date
June 2001
Overall Recruitment Status
Completed
Study Start Date
September 1991 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Medical Research Council

4. Oversight

5. Study Description

Brief Summary
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.
Detailed Description
OBJECTIVES: Compare the efficacy of adjuvant radical radiotherapy vs intravesical BCG or mitomycin vs observation alone after endoscopic resection in terms of the progression rate and survival of patients with stage I, grade 3 transitional cell carcinoma of the bladder. Determine the toxicity of radical radiotherapy in these patients. Determine the incidence of carcinoma in situ elsewhere in the bladder and its correlation with the subsequent clinical outcome of these patients. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
stage I bladder cancer, transitional cell carcinoma of the bladder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
BCG vaccine
Intervention Type
Drug
Intervention Name(s)
mitomycin C
Intervention Type
Radiation
Intervention Name(s)
radiation therapy

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of transitional cell carcinoma of the bladder Stage T1 Nx M0, grade 3 disease No muscle invasion at base of tumor Diagnosis of this stage made within the past 6 months Earlier diagnosis of tumors with lower stage or grade allowed No history of higher stage urothelial tumors Presence of partial involvement of bladder with carcinoma in situ (CIS) or asymptomatic widespread CIS allowed No widespread CIS causing severe symptoms Prior complete transurethral resection of tumor with deep biopsy of underlying bladder wall required Disease currently amenable to adjuvant radiotherapy, followed by cystoscopy with biopsies PATIENT CHARACTERISTICS: Age: Any age Performance status: WHO 0-2 Life expectancy: Not specified Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No other prior or concurrent malignancy except nonmelanomatous skin cancer or cervical intraepithelial neoplasia 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen J. Harland, MD
Organizational Affiliation
University College London Hospitals
Official's Role
Study Chair
Facility Information:
Facility Name
Middlesex Hospital- Meyerstein Institute
City
London
State/Province
England
ZIP/Postal Code
WIT 3AA
Country
United Kingdom

12. IPD Sharing Statement

Citations:
Citation
Harland SJ: A randomised trial of radical radiotherapy in pT1G3 NXM0 bladder cancer (MRC BS06). [Abstract] J Clin Oncol 23 (Suppl 16): A-4505, 379s, 2005.
Results Reference
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Radiation Therapy, Chemotherapy, or Observation in Treating Patients With Bladder Cancer

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