drugset / Trial / NCT02412475

Epigenetic Reprogramming in Relapse AML

NCT02412475

NaSingle-groupOpen-labelTreatment

Summary

Successful treatment for children and young adults with relapsed acute myeloid leukemia (AML) continues to be a significant challenge. Despite relative improvements in survival for patients with newly diagnosed AML, an estimated 40-60% will relapse with the majority eventually dying of their relapsed disease. Attaining a subsequent remission in patients who relapse is the initial critical step toward achieving a potential cure. As chemotherapy resistance is one of the primary drivers of poor treatment response and subsequent relapse in AML, identifying methods to reverse this resistance are desperately needed. This clinical trial is aimed at improving the remission re-Induction rates for children and adults with relapsed or refractory AML through epigenetic modifying agents that have the ability to reverse chemotherapy resistance. Decitabine, a DNA methyltransferase inhibitor (DNMTi) and Vorinostat, a histone deacetylase inhibitor (HDACi), are two epigenetic modifying drugs that act on the methylation of proximal promoter regions of genes and on proteins involved in the wrapping of DNA around histones, respectively. Both processes play a critical role in regulating gene expression, and frequently these genes are involved in chemotherapy resistance. These agents are FDA-approved for treatment in adult hematologic malignancies, making this an opportune time to begin testing these novel therapies in pediatric leukemia trials. This study will investigate chemotherapy priming of relapsed/refractory AML using Decitabine and Vorinostat given for 5 days prior to standard re-Induction with Fludarabine, Cytarabine and G-CSF for children and adults.

Timeline

Start
2015-02-21
Primary completion
2017-06-21
Completion
2017-06-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule 10 mg/m2 Intravenous
Subject Vorinostat Small molecule 180 mg/m2 Oral
Subject Vorinostat Small molecule 300 mg Oral
Background Cytarabine Small molecule 30 mg Intravenous
Background Cytarabine Small molecule 50 mg Intravenous
Background Cytarabine Small molecule 70 mg Intravenous
Background Cytarabine Small molecule 100 mg Intravenous
Background Cytarabine Small molecule 2000 mg/m2 Intravenous
Background Fludarabine Small molecule 30 mg/m2 Intravenous
Background Sorafenib Small molecule 150 mg/m2 Oral
Background filgrastim Protein / enzyme biologic 5 ug/kg Intravenous