FLT3 Inhibitors in Acute Myeloid Leukemia: Challenges and Recent Developments in Overcoming Resistance.
Zhijie WangJiongheng CaiJie ChengWenqianzi YangYifan ZhuHongmei LiTao LuYa-Dong ChenShuai LuPublished in: Journal of medicinal chemistry (2021)
Mutations in the FMS-like tyrosine kinase 3 (FLT3) gene are often present in newly diagnosed acute myeloid leukemia (AML) patients with an incidence rate of approximately 30%. Recently, many FLT3 inhibitors have been developed and exhibit positive preclinical and clinical effects against AML. However, patients develop resistance soon after undergoing FLT3 inhibitor treatment, resulting in short durable responses and poor clinical effects. This review will discuss the main mechanisms of resistance to clinical FLT3 inhibitors and summarize the emerging strategies that are utilized to overcome drug resistance. Basically, medicinal chemistry efforts to develop new small-molecule FLT3 inhibitors offer a direct solution to this problem. Other potential strategies include the combination of FLT3 inhibitors with other therapies and the development of multitarget inhibitors. It is hoped that this review will provide inspiring insights into the discovery of new AML therapies that can eventually overcome the resistance to current FLT3 inhibitors.
Keyphrases
- acute myeloid leukemia
- tyrosine kinase
- allogeneic hematopoietic stem cell transplantation
- newly diagnosed
- small molecule
- epidermal growth factor receptor
- end stage renal disease
- ejection fraction
- stem cells
- chronic kidney disease
- genome wide
- mesenchymal stem cells
- prognostic factors
- dna methylation
- peritoneal dialysis
- risk assessment
- quality improvement
- copy number
- genome wide analysis