Evolving paradigms in targeting FLT3 for acute myeloid leukemia therapy
Abstract
FLT3 mutations drive acute myeloid leukemia (AML) progression through aberrant signaling, making FLT3 inhibition a key therapeutic strategy. Current inhibitors show efficacy, yet resistance and toxicity remain challenges. Emerging approaches, including selective inhibitors, proteolysis-targeting chimeras, and protein degraders, offer enhanced potency, sustained suppression, and combinatorial potential, representing a precision-based advancement in AML treatment.
Fields of Study & Subjects
Acute Myeloid Leukemia Research
Protein Degradation and Inhibitors
Nuclear Structure and Function
Publication details
- Journal / source
- Trends in Pharmacological Sciences
- Publisher
- Elsevier BV
- Volume
- 47
- Issue
- 3
- Pages
- 244–247
- Publication date
- 23 February 2026
- Language
- EN