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Gilteritinib (Xospata®) for Relapsed/Refractory Acute Myeloid Leukemia

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Last Updated: October 2, 2023

By: Bryan J. Brinda, PharmD

About this PQI

This PQI will discuss proper patient selection and management of adverse events related to the administration of oral gilteritinib pharmacotherapy in patients with relapsed/refractory (R/R) acute myeloid leukemia (AML) that have an FMS-like tyrosine kinase 3 (FLT3) mutation as detected by an FDA-approved test. Optimal patient identification, dosing, and follow-up are essential to help patients fully benefit from this medication.

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