Consolidation Therapy for Acute Myeloid Leukemia Guided by Leukemia Stem Cell Behavior
- Conditions
- Acute Myeloid Leukemia
- Interventions
- Drug: Allogeneic transplant
- Registration Number
- NCT01588951
- Brief Summary
The primary objective of the trial is to compare the two-year relapse-free survival (RFS) of patients with acute myeloid leukemia (AML), presumed to be at high risk for relapse due to the presence of leukemia stem cells (LSCs) in their bone marrow at first complete remission (CR1), who receive either standard cytarabine-based chemotherapy or allogeneic stem cell transplantation (SCT).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 10
- Age greater than or equal to 18 years
- Able to give informed consent
- New diagnosis of AML, other than APL or poor-risk AML, as defined in section 3.2
Exclusion criteria:
- Has already had a bone marrow biopsy and aspirate to assess remission status after induction therapy
- Any debilitating medical or psychiatric illness that would preclude ability to give informed consent or receive optimal treatment and follow-up
- Pregnancy: Women of childbearing potential who are β- HCG+
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description No Leukemia Stem Cells - Consolidation Cytarabine consolidation Without LSC, standard cytarabine consolidation Leukemia Stem Cells - Consolidation Cytarabine consolidation LSC present, randomized to cytarabine consolidation Leukemia Stem Cells - Transplant Allogeneic transplant LSC present, randomized to allogeneic transplant
- Primary Outcome Measures
Name Time Method Relapse Free Survival 2 years Percentage of participants alive and without relapsed disease at two years.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
🇺🇸Baltimore, Maryland, United States