drugset / Trial / NCT07232134

The Efficacy of Therapy in Patients With Acute Myeloid Leukemia and Down Syndrome in Russia

NCT07232134

NaSingle-groupOpen-labelTreatment

Summary

This prospective non-randomized multicenter trial created based on protocol ML DS 2006 and aimed at standardization of current therapy approaches and creating a national network for diagnostic, treatment and monitoring of children (0-18 years) with AML and Down syndrome in Russia. Based on the results the investigators expect to increase long-term overall and event-free survival in children with AML and DS and reduce the immediate and remote toxicity of chemotherapy by reducing the dose load of chemotherapeutic drugs. The study protocol therapy for all patients includes four chemotherapy blocks: Course 1 AIE (cytarabine/idarubicin/etoposide) Course 2 AI (cytarabine/idarubicin) Course 3 HAD (high -dose cytarabine (1g)/daunorubicin) Course 4 HA (high-dose cytarabine) Safety to be monitored based on CTCAE v5.0

Timeline

Start
2025-07-24
Primary completion
2030-07-24
Completion
2032-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytarabine Small molecule 1 g
Subject Daunorubicin Small molecule
Subject Etoposide Small molecule
Subject Idarubicin Small molecule