Quizartinib in Combination With FLAG-IDA for Relapsed or Refractory Acute Myeloid Leukemia (FLAG-QUIDA): A PETHEMA Phase I-II Trial.
Teresa Bernal, Javier Zambrano Márquez, Rebeca Rodríguez-Veiga et al.
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In 30 seconds
The FLAG-QUIDA trial, a multicenter phase I/II study, evaluated quizartinib combined with FLAG-IDA in adults with relapsed or refractory acute myeloid leukemia (AML). Among 61 patients, the overall complete remission (CR) and CR with incomplete hematologic recovery (CRi) rate was 56%. The median relapse-free survival was significantly improved at 17 months compared to 7.6 months in a matched cohort (p=0.028).
Key findings
- The recommended phase 2 dose of quizartinib was established at 60 mg/day for 14 days.
- The overall CR/CRi rate was 56% among patients treated.
- Median relapse-free survival was 17 months compared to 7.6 months in the matched cohort (p=0.028).
- Measurable residual disease negativity was achieved in 38% of CR/CRi patients.
Why it matters
This study highlights the potential of quizartinib in combination with FLAG-IDA to improve outcomes in patients with relapsed or refractory AML, particularly in enhancing remission rates and prolonging relapse-free survival.