Radiation Therapy With or Without Chemotherapy in Treating Patients With Stage II or Stage III Bladder Cancer

Last updated: December 17, 2013
Sponsor: University Hospital Birmingham
Overall Status: Completed

Phase

3

Condition

Bladder Cancer

Urothelial Cancer

Urothelial Carcinoma

Treatment

N/A

Clinical Study ID

NCT00024349
CDR0000068921
ISRCTN68324339
CRC-BC2001
EU-20052
  • Ages > 18
  • All Genders

Study Summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy such as fluorouracil and mitomycin use different ways to stop tumor cells from dividing so they stop growing or die. Fluorouracil and mitomycin may make the tumor cells more sensitive to radiation therapy. It is not yet known if radiation therapy is more effective with or without chemotherapy in treating bladder cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy to all or part of the bladder with or without chemotherapy in treating patients who have stage II or stage III bladder cancer.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS:

  • Histologically confirmed invasive bladder cancer (T2-4a, N0, M0)

  • Adenocarcinoma

  • Transitional cell carcinoma

  • Squamous cell carcinoma

  • Localized muscle invasion by surgery or imaging

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • WHO 0-2

Life expectancy:

  • Not specified

Hematopoietic:

  • WBC greater than 4,000/mm^3

  • Platelet count greater than 100,000/mm^3

Hepatic:

  • Bilirubin less than 1.5 times upper limit of normal (ULN)

  • ALT or AST less than 1.5 times ULN

Renal:

  • Glomerular filtration rate greater than 25 mL/min

Other:

  • Not pregnant

  • Negative pregnancy test

  • Fertile patients must use effective contraception

  • No inflammatory bowel disease

  • No other prior malignancy within the past 2 years except adequately treated basal cell skin cancer or carcinoma in situ of the cervix

  • No other prior malignancy or uncontrolled systemic disease that would preclude study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Not specified

Endocrine therapy:

  • Not specified

Radiotherapy:

  • No prior radiotherapy to the pelvis

Surgery:

  • See Disease Characteristics

  • No bilateral hip replacements

Other:

  • No concurrent metronidazole during fluorouracil administration

Study Design

Total Participants: 350
Study Start date:
June 01, 2001
Estimated Completion Date:
April 30, 2012

Study Description

OBJECTIVES:

  • Compare the efficacy of standard volume radiotherapy vs reduced volume radiotherapy with or without synchronous fluorouracil and mitomycin in patients with stage II or III (muscle invasive) bladder cancer.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center, prior neoadjuvant chemotherapy (yes vs no), and intent to enter only 1 of the possible 2 randomizations on study (yes vs no). Patients are randomized to one of two treatment arms.

  • Arm I: Patients undergo standard radiotherapy once daily 5 days a week for 4 or 6.5 weeks. Patients also receive synchronous chemotherapy comprising mitomycin IV on day 1 and fluorouracil IV continuously over days 1-5 and 16-20 during radiotherapy.

  • Arm II: Patients undergo standard radiotherapy as in arm I (without chemotherapy).

If standard radiotherapy is clearly indicated (e.g., patients with multiple tumors) patients may be randomized to standard radiotherapy with or without chemotherapy (arms I or III above). If chemotherapy is clearly contraindicated, patients are randomized to standard or reduced volume radiotherapy without chemotherapy (arms III or IV above).

Quality of life is assessed at baseline, at the end of therapy, at 6 and 12 months post-randomization, and then annually for at least 5 years.

Patients are followed at 6, 9, and 12 months post-randomization and then at least annually thereafter.

Peer Reviewed and Funded or Endorsed by Cancer Research UK

PROJECTED ACCRUAL: A total of 350 patients will be accrued for this study.

Connect with a study center

  • Royal United Hospital

    Bath, England BA1 3NG
    United Kingdom

    Site Not Available

  • Queen Elizabeth Hospital at University Hospital of Birmingham NHS Trust

    Birmingham, England B15 2TH
    United Kingdom

    Site Not Available

  • Royal Bournemouth Hospital NHS Trust

    Bournemouth, England BH7 7DW
    United Kingdom

    Site Not Available

  • Sussex Cancer Centre at Royal Sussex County Hospital

    Brighton, England BN2 5BF
    United Kingdom

    Site Not Available

  • Bristol Haematology and Oncology Centre

    Bristol, England BS2 8ED
    United Kingdom

    Site Not Available

  • Addenbrooke's Hospital

    Cambridge, England CB2 2QQ
    United Kingdom

    Site Not Available

  • Cheltenham General Hospital

    Cheltenham, England GL53 7AN
    United Kingdom

    Site Not Available

  • Essex County Hospital

    Colchester, England C03 3NB
    United Kingdom

    Site Not Available

  • Walsgrave Hospital

    Coventry, England CV2 2DX
    United Kingdom

    Site Not Available

  • Derbyshire Royal Infirmary

    Derby, England DE1 2QY
    United Kingdom

    Site Not Available

  • Royal Devon and Exeter Hospital

    Exeter, England EX2 5DW
    United Kingdom

    Site Not Available

  • St. Luke's Cancer Centre at Royal Surrey County Hospital

    Guildford, England GU2 7XX
    United Kingdom

    Site Not Available

  • Princess Royal Hospital at Hull and East Yorkshire NHS Trust

    Hull, England HU8 9HE
    United Kingdom

    Site Not Available

  • St. Thomas' Hospital

    London, England SE1 9RT
    United Kingdom

    Site Not Available

  • Maidstone Hospital

    Maidstone, England ME16 9QQ
    United Kingdom

    Site Not Available

  • Clatterbridge Centre for Oncology

    Merseyside, England CH63 4JY
    United Kingdom

    Site Not Available

  • James Cook University Hospital

    Middlesbrough, England TS4 3BW
    United Kingdom

    Site Not Available

  • Northern Centre for Cancer Treatment at Newcastle General Hospital

    Newcastle-Upon-Tyne, England NE4 6BE
    United Kingdom

    Site Not Available

  • Northampton General Hospital NHS Trust

    Northampton, England NN1 5BD
    United Kingdom

    Site Not Available

  • Royal Shrewsbury Hospital

    Shrewsbury, England SY3 8XQ
    United Kingdom

    Site Not Available

  • Royal Marsden NHS Foundation Trust - Surrey

    Sutton, England SM2 5PT
    United Kingdom

    Site Not Available

  • Torbay Hospital

    Torquay, England TQ2 7AA
    United Kingdom

    Site Not Available

  • Good Hope Hospital Trust

    West Midlands, England B75 7RR
    United Kingdom

    Site Not Available

  • Southend University Hospital NHS Foundation Trust

    Westcliff-On-Sea, England SS0 0RY
    United Kingdom

    Site Not Available

  • Worthing Hospital

    Worthing, England BN11 2DH
    United Kingdom

    Site Not Available

  • Yeovil District Hospital

    Yeovil, England BA21 4AT
    United Kingdom

    Site Not Available

  • Glan Clwyd Hospital

    Rhyl, Wales LL18 5UG
    United Kingdom

    Site Not Available

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