Trials / Unknown
UnknownNCT00003804
Chemotherapy Plus Surgery in Treating Children at Risk of or With Stage I Wilms' Tumor
Nephroblastoma Clinical Trial and Study
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 350 (estimated)
- Sponsor
- University of Leicester · Academic / Other
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Not accepted
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. It is not yet known which regimen of chemotherapy is more effective for stage I Wilms' tumor. PURPOSE: Randomized phase III trial to study the effectiveness of chemotherapy and surgery in treating children who are at risk of or who have stage I Wilms' tumor.
Detailed description
OBJECTIVES: I. Determine the initial extension of disease, surgical procedures, gross and histological morphology, treatments, clinical outcome, and late consequences of therapy after treatment with neoadjuvant chemotherapy, surgery, and adjuvant chemotherapy with or without maintenance chemotherapy in patients with intermediate risk or anaplastic stage I Wilms' tumor. II. Determine the safety and effectiveness of reduced chemotherapy in these patients. OUTLINE: This is a randomized, multicenter study. Patients receive dactinomycin IV on days 1-3 and 15-17 and vincristine IV on days 1, 8, 15, and 22. Patients then undergo surgery about a week after completion of chemotherapy. After surgery, patients receive vincristine IV on days 1, 8, 15, and 22 and dactinomycin IV on days 8-12. Patients are then randomized to one of two treatment arms after week 9. Arm I: Patients receive dactinomycin IV on days 1-5 of week 10 and vincristine IV on day 1 of both weeks 10 and 11. This course is repeated during weeks 17 and 18. Arm II: Patients receive no further treatment. Patients are followed every 3 months for 3 years, then annually thereafter. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 350 patients (175 per treatment arm) will be accrued for this study within 7-8 years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | dactinomycin | |
| DRUG | vincristine sulfate | |
| PROCEDURE | conventional surgery |
Timeline
- Start date
- 1993-07-01
- First posted
- 2004-07-16
- Last updated
- 2014-06-24
Locations
44 sites across 15 countries: Belgium, Croatia, Czechia, Denmark, France, Greece, Italy, Netherlands, Norway, Poland, Portugal, Slovenia, Spain, Sweden, United Arab Emirates
Source: ClinicalTrials.gov record NCT00003804. Inclusion in this directory is not an endorsement.