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Spots Global Cancer Trial Database for Combination Chemotherapy in Treating Children With Relapsed or Refractory Acute Lymphocytic Leukemia

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Trial Identification

Brief Title: Combination Chemotherapy in Treating Children With Relapsed or Refractory Acute Lymphocytic Leukemia

Official Title: Phase II Study of Fludarabine + Idarubicin + Aracytine in Refractory or Relapsed ALL in Children

Study ID: NCT00003729

Conditions

Leukemia

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating children who have relapsed or refractory acute lymphocytic leukemia.

Detailed Description: OBJECTIVES: I. Evaluate the complete response rate to combination fludarabine, idarubicin, and cytarabine in children with relapsed or refractory acute lymphocytic leukemia. II. Evaluate the safety and tolerance of this treatment in these patients. III. Evaluate the time to progression, disease free survival, and overall survival of these patients. OUTLINE: This is an open label, multicenter study. Patients receive idarubicin IV over 1 hour on days 1-3. Fludarabine IV is administered over 30 minutes on days 1-5. Cytarabine IV is administered over 4 hours on days 1-5. If partial response is obtained, patients receive a second course of treatment. Patients receive a consolidation course in the absence of disease progression and unacceptable toxicity. Idarubicin IV is administered over 1 hour on days 1 and 2. Fludarabine IV is administered over 30 minutes, followed by cytarabine IV over 4 hours on days 1-5. Patients are followed every 3 months for 2 years or until death. PROJECTED ACCRUAL: A total of 24-45 patients will be accrued for this study within 27 months.

Eligibility

Minimum Age:

Eligible Ages: CHILD

Sex: ALL

Healthy Volunteers: No

Locations

Algemeen Ziekenhuis Middelheim, Antwerp, , Belgium

Hopital Universitaire Des Enfants Reine Fabiola, Brussels (Bruxelles), , Belgium

Academisch Ziekenhuis der Vrije Universiteit Brussel, Brussels (Bruxelles), , Belgium

Universitair Ziekenhuis Gent, Ghent (Gent), , Belgium

U.Z. Gasthuisberg, Leuven, , Belgium

Centre Hospitalier Regional de la Citadelle, Liege (Luik), , Belgium

Clinique de l'Esperance, Montegnee, , Belgium

Centre Hospitalier Regional et Universitaire d'Angers, Angers, , France

CHR de Besancon - Hopital Saint-Jacques, Besancon, , France

CHU de Caen, Caen, , France

CHR de Grenoble - La Tronche, Grenoble, , France

Centre Hospitalier Regional de Lille, Lille, , France

Hopital Debrousse, Lyon, , France

Hopital Arnaud de Villeneuve, Montpellier, , France

CHR Hotel Dieu, Nantes, , France

Centre Antoine Lacassagne, Nice, , France

Hopital Robert Debre, Paris, , France

Institut Curie - Section Medicale, Paris, , France

Hopital Jean Bernard, Poitiers, , France

Hopital Americain, Reims, , France

Hopital Universitaire Hautepierre, Strasbourg, , France

Hopital des Enfants (Purpan Enfants), Toulouse, , France

Hospital Escolar San Joao, Porto, , Portugal

Contact Details

Name: Antoine Thyss, MD

Affiliation: Centre Antoine Lacassagne

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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