Durgical
EN
Open the app

FLT3 inhibitors

Oral kinase inhibitors for acute myeloid leukaemia with FLT3 mutations: added to first-line chemotherapy or used alone at relapse.

Updated

What they are

FLT3 carries activating mutations in many cases of AML, as internal tandem duplications (ITD) or point mutations. Midostaurin is added to induction chemotherapy in newly diagnosed disease; gilteritinib is used alone at relapse; quizartinib is another FLT3 inhibitor.

Mechanism of action

FLT3 is a receptor tyrosine kinase on blood progenitors. Activating mutations keep it switched on, driving blast growth and survival. FLT3 inhibitors bind the ATP pocket and cut off this signal; blasts stop growing and some differentiate.

Target: FLT3 receptor tyrosine kinase

Drugs in this class

Others in the class

  • Quizartinib

Test yourself

Think of the answer, then tap the question to see it.

What are the two main types of FLT3 mutation in AML?

Internal tandem duplications (ITD) and point mutations.

Which FLT3 inhibitor is added to induction chemotherapy?

Midostaurin.

Which FLT3 inhibitor carries a differentiation syndrome warning and is used at relapse?

Gilteritinib.

Add to my cards (3)

More Pharmacology questions →

← All of pharmacology

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026); Midostaurin: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2017); Gilteritinib: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2019); RCSB PDB - 6JQR: Crystal structure of FLT3 in complex with gilteritinib (RCSB Protein Data Bank, 2026).

Spotted a mistake?We are always improving for the community. Tell us what is wrong and our team will review it.Report a mistake

Representative model, for educational purposes only.