drugset / Trial / NCT00428558

Timed-Sequential Induction in CBF-AML

NCT00428558

RandomizedParallel-groupOpen-labelTreatment

Summary

Core binding factor (CBF) acute myeloid leukemias (AML) include AMLs carrying the t(8;21) translocation as well as AMLs carrying either the inversion of chromosome 16 or translocation t(16;16). CBF-AMLs are characterized by their high sensitivity to standard chemotherapeutical agents, especially to cytarabine when administered as high-dose bolus infusions, and thus by a relative good prognosis. However, relapse rates are still comprised between 30 and 50% in these patients, even if overall survival may reach approximately 65% due to the potential salvage of late relapses. The primary purpose of the protocol is to compare two modalities of timed-sequential induction in order to improve the results of the treatment of CBF-AML patients. This protocol also includes the biological characterization of the heterogeneity of these diseases (gene mutation and transcription profiles), as well as a centralized minimal residual disease monitoring and centralized evaluation of pharmacogenetic polymorphisms.

Timeline

Start
2007-07
Primary completion
2011-06
Completion
2011-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytarabine Small molecule 200 mg/m2 Intravenous
Subject Cytarabine Small molecule 500 mg/m2 Intravenous
Subject Cytarabine Small molecule 1000 mg/m2 Intravenous
Subject Cytarabine Small molecule 3000 mg/m2 Intravenous
Subject Daunorubicin Small molecule 35 mg/m2 Intravenous
Subject Daunorubicin Small molecule 60 mg/m2 Intravenous