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Clinical Trials/NCT00025428
NCT00025428
Completed
Phase 3

Treatment Of Children Over The Age Of 1 Year With Unresectable Localized Neuroblastoma Without MYCN Amplification

Societe Internationale d'Oncologie Pediatrique12 sites in 12 countries100 target enrollmentDecember 2000

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Neuroblastoma
Sponsor
Societe Internationale d'Oncologie Pediatrique
Enrollment
100
Locations
12
Primary Endpoint
Event-free survival at 3 years
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving chemotherapy drugs before surgery may shrink the tumor so that it can be removed during surgery.

PURPOSE: Phase III trial to determine the effectiveness of combination chemotherapy given before surgery in treating children who have localized neuroblastoma.

Detailed Description

OBJECTIVES: * Determine the outcome, in terms of local control, event-free survival, and overall survival, of children with localized unresectable neuroblastoma without MYCN amplification treated with carboplatin, etoposide, cyclophosphamide, doxorubicin, and vincristine followed by surgery. OUTLINE: This is a multicenter study. Patients receive carboplatin IV over 1 hour and etoposide IV over 2 hours on days 1-3 (courses 1 and 3). Patients receive cyclophosphamide IV over 1 hour on days 1-5 (or orally on days 2 and 3), doxorubicin IV over 6 hours on days 4-5, and vincristine IV on days 1 and 5 (courses 2 and 4). Treatment repeats every 21 days for 4 courses. Patients then undergo surgical resection followed by 2 additional courses of chemotherapy. Patients are followed at months 8, 10, 12, 16, 20, 24, 30, 36, 42, 48, and 60. PROJECTED ACCRUAL: A total of 100 patients will be accrued for this study within 4 years.

Registry
clinicaltrials.gov
Start Date
December 2000
End Date
November 2013
Last Updated
12 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Societe Internationale d'Oncologie Pediatrique

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Event-free survival at 3 years

Study Sites (12)

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