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Clinical Trial Summary

The purpose of the study is to observe the outcomes of patients with acute myeloid leukemia who do not receive an immediate second round of chemotherapy after undergoing a standard mid-induction bone marrow biopsy.


Clinical Trial Description

This will be a pilot study that will include patients with AML receiving intensive induction therapy with 7+3 +/- a third agent (for any actionable cytogenetics or mutations). All patients will have a planned mid-induction bone marrow assessment as standard of care. All patients will subsequently be observed for count recovery, regardless of bone marrow results and in the absence of peripheral blood disease proliferation, and an end of induction bone marrow biopsy will be performed either at count recovery or between days 28 and 42 in the absence of count recovery. Patients with complete remission (CR) will proceed to consolidation chemotherapy as determined by the treating investigator. Patients with refractory disease will proceed to further therapy as determined by the treating investigator. All patients will be followed for long-term outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06323590
Study type Observational
Source University of Alabama at Birmingham
Contact Omer Jamy, MD
Phone 2059342721
Email omerjamy@uabmc.edu
Status Recruiting
Phase
Start date May 2, 2024
Completion date May 2028

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