Blood Cancer Journal· 2016Q1· Review
‘Acute myeloid leukemia: a comprehensive review and 2016 update’
- 1,351citations
- Q1SCImago
- 2016year
Short summary
Recurrent genetic mutations like FLT3-ITD, NMP1, and CEBPA refine prognosis and guide treatment for acute myeloid leukemia (AML), a heterogeneous disease affecting over 20,000 US cases annually.
AI-generated from the title and abstract; the full text is not read.
Key points
- AML is the most common acute leukemia in adults, with over 20,000 US cases yearly.
- Heterogeneity in AML is driven by chromosomal translocations and gene mutations.
- Recurrent mutations (FLT3-ITD, NMP1, CEBPA) improve individual prognosis and treatment decisions.
- Standard therapy involves cytarabine/anthracycline regimens and stem cell transplantation.
- Elderly patients have a poor prognosis and often cannot tolerate standard regimens.
AI-generated from the title and abstract; the full text is not read.
Abstract
Acute myeloid leukemia (AML) is the most common acute leukemia in adults, with an incidence of over 20 000 cases per year in the United States alone. Large chromosomal translocations as well as mutations in the genes involved in hematopoietic proliferation and differentiation result in the accumulation of poorly differentiated myeloid cells. AML is a highly heterogeneous disease; although cases can be stratified into favorable, intermediate and adverse-risk groups based on their cytogenetic profile, prognosis within these categories varies widely. The identification of recurrent genetic mutations, such as FLT3-ITD, NMP1 and CEBPA, has helped refine individual prognosis and guide management. Despite advances in supportive care, the backbone of therapy remains a combination of cytarabine- and anthracycline-based regimens with allogeneic stem cell transplantation for eligible candidates. Elderly patients are often unable to tolerate such regimens, and carry a particularly poor prognosis. Here, we review the major recent advances in the treatment of AML.
The authors' abstract, as published at the source. Blood Cancer Journal, 2016 · DOI ↗
Continue with a free account
Ask the paper: 3 free questions a day about this paper; save it, get its citation, new summaries every day for your field. Takeaways are Premium.
Continue free on the webSign in with Google or Apple; no card needed. You come back to this paper.
On your phone:
Field: Hematology
HematologyMedicine