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    PURPOSE Gilteritinib is a type 1 FLT3 inhibitor active as monotherapy for relapsed or refractory FLT3-mutated AML. We investigated the safety, tolerability, and efficacy of gilteritinib incorporated into intensive induction and consolidation chemotherapy, and as maintenance therapy for adult patients with newly diagnosed, non–favorable-risk AML. METHODS In this phase IB study (2215-CL-0103; ClinicalTrials.gov identifier: NCT02236013), 103 participants were screened and 80 were allocated to treatment. The study was divided into four parts: dose escalation, dose expansion, investigation of alternate anthracycline and gilteritinib schedule, and continuous gilteritinib during consolidation. RESULTS After dose escalation, 120 mg gilteritinib once daily was chosen for further study. There were 58 participants evaluable for response at this dose, 36 of whom harbored FLT3 mutations. For participants with FLT3-mutated AML, the composite complete response (CRc) rate was 89% (83% were conventiona

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    • 🧐 Gilteritinib in combination with induction and consolidation chemotherapy and as maintenance therapy was tolerable in patients with newly-diagnosed #AcuteMyeloidLeukemia ➡️ https://t.co/x6w5kyNKdn #AML #leusm https://t.co/Vs3hzdTJLm

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    #ASCO23 - 10 month(s) ago

    Catch up with our live Twitter coverage from the American Society of Clinical Oncology (#ASCO23) Annual Congress.

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    • 📢 #ASCO23 | In case you missed our live coverage from ASCO 2023, you can catch up below. 👉 https://t.co/fHKkT8DOIy #AMLHub #AMLsm #acutemyeloidleukemia @ASCO https://t.co/fIdH1YJRMV