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FLT3 is a receptor tyrosine kinase that is mutated in approximately 10%-15% of new-onset acute myeloid leukemia (AML) pediatric
leukemia childhood stem cells
The COG AAML1031 study evaluated the efficacy and feasibility of adding the multikinase tyrosine kinase inhibitor sorafenib to standard chemotherapy regimens and maintaining sorafenib monotherapy in this patient population
The test patients were divided into three cohorts
The measured plasma concentrations are sufficient to inhibit phosphorylated FLT3
HAR FLT3/ITD+ patients not treated with sorafenib had approximately twice the risk of certain endpoint events than patients receiving sorafenib HAR FLT3/ITD+ patients not treated with sorafenib had certain endpoints The risk of events was approximately twice as high as in patients treated with sorafenib
In conclusion, this study shows that the addition of sorafenib to the conventional chemotherapy regimen in children with HAR FLT3/ITD positive acute myeloid leukemia is feasible and safe, and is expected to improve the clinical prognosis of the children
It is feasible and safe to add sorafenib to routine chemotherapy in children with HAR FLT3/ITD positive acute myeloid leukemia, and it is expected to improve the clinical prognosis of children
Original source:
Original source:Jessica A.
Jessica A.
Pollard, et al.
Sorafenib in Combination With Standard Chemotherapy for Children With High Allelic Ratio FLT3/ITD+ Acute Myeloid Leukemia: A Report From the Children's Oncology Group Protocol AAML1031.
Journal of Clinical Oncology.
March 29, 2022.
https:/ /ascopubs.
org/doi/full/10.
1200/JCO.
21.
01612
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