Abstract
Mutations of FLT3 in AML is an entity characterized by a significant poor prognosis and are described in about 30% of AML in adults. Usually patients with this subtype of AML carrying either internal tandem duplication (ITD) or mutation at codon 835 are referred for allogeneic stem cell transplantation (ASCT) but a proportion of them would eventually relapse. The introduction of targeted therapy against FLT3 + AML is yielding conflicting results and many trials are running with new molecules. We used sorafenib, a multi-targeted tyrosine kinase inhibitor FDA approved for the treatment of advanced renal cell and hepatocellular carcinoma, on a compassionate basis in two patients with FLT3 + AML relapsing after ASCT.
| Original language | English |
|---|---|
| Pages (from-to) | 422-423 |
| Number of pages | 2 |
| Journal | Leukemia Research |
| Volume | 35 |
| DOIs | |
| Publication status | Published - 2011 |
Keywords
- sorafenib
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