quizartinib (Vanflyta)

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Indications

*FDA-approved

Contraindications

Mechanism of action

  • targets internal tandem duplication (ITD) in mutated FLT3*

* this FLT3 mutation is associated with a higher relapse risk shorter survival

* median overall survival among patients on standard chemotherapy + quizartinib is 32 months vs 15 months with standard chemotherapy + placebo

More general terms

References

  1. 1.0 1.1 Otto MA FDA Approves Quizartinib for Newly Diagnosed AML. Medscape. July 20, 2023 https://www.medscape.com/viewarticle/994618