Abstract
Background: Acute myeloid leukemia (AML) cases with t(8;21) or inv(16) have a favorable outcome, but the associated prognoses are heterogeneous and complicated by additional molecular aberrations. Patients and Methods: Between January 2000 to December 2010, 67 patients were diagnosed with t(8;21) or inv(16) AML. We collected cytogenetic variables and analyzed treatment outcomes. Results: Among 67 patients, 51 (7.8%) had t(8;21) AML and 16 (2.4%) had inv(16) AML. Thrombocytopenia, and a high percentage of blasts in the peripheral blood and bone marrow were associated with poor overall survival. Twenty-five (49.0%) patients with t(8;21) had an additional chromosomal abnormality, while only six (37.5%) patients with inv(16) AML had a secondary chromosomal abnormality. The most common chromosomal abnormalities were deletion of the Y or X sex chromosomes. Conclusion: Deletion of the Y chromosome may be a favorable prognostic factor in patients with core binding factor-positive AML.
| Original language | English |
|---|---|
| Pages (from-to) | 1037-1046 |
| Number of pages | 10 |
| Journal | Anticancer Research |
| Volume | 34 |
| Issue number | 2 |
| State | Published - 1 Feb 2014 |
Bibliographical note
Publisher Copyright:© 2014, International Institute of Anticancer Research. All rights reserved.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Core-binding factor-positive AML
- Prognostic factor
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