Background: The addition of a FLT3 inhibitor (FLT3i) to standard chemotherapy to treat fit newly diagnosed (ND) patients with FLT3-mutated acute myeloid leukemia (AML) represents the standard of care resulting from clinical trial results. However, evidence regarding FLT3i adoption in routine clinical practice is still scarce. Methods: Clinical data are reported from 394 ND patients with FLT3-mutated AML enrolled in the retrospective observational Italian Cohort Study on FLT3-mutated patients with AML and treated with an upfront intensive regimen with (FLT3i group, n = 92) or without (CT group, n = 302) the addition of a FLT3i. Results: With a median follow-up time of 34.5 months, an effectiveness benefit obtained by FLT3i incorporation both in terms of overall survival (median, 34.9 in the FLT3i vs 12.7 months in the CT group, p <.01) and relapse-free survival (median, 18.9 in the FLT3i vs 7.6 months in the CT group, p =.01) was documented, with a higher composite complete remission rate (75.4% in the FLT3i vs 62.4% in the CT group, p =.052). FLT3i benefit seemed to be independent from the transplant rate. Conclusions: In conclusion, the benefit of FLT3i addition to upfront intensive treatment in newly diagnosed FLT3-mutated AML patients was confirmed in a large, real-life cohort study.

Nanni, J., Azzali, I., Papayannidis, C., Mule, A., Audisio, E., Martelli, M.P., et al. (2025). Upfront intensive treatment analysis of the Italian Cohort Study on FLT3-mutated AML patients (FLAM): The impact of a FLT3 inhibitor addition to standard chemotherapy in the real-life setting. CANCER, 131(7) [10.1002/cncr.35824].

Upfront intensive treatment analysis of the Italian Cohort Study on FLT3-mutated AML patients (FLAM): The impact of a FLT3 inhibitor addition to standard chemotherapy in the real-life setting

Bocchia M.;
2025-01-01

Abstract

Background: The addition of a FLT3 inhibitor (FLT3i) to standard chemotherapy to treat fit newly diagnosed (ND) patients with FLT3-mutated acute myeloid leukemia (AML) represents the standard of care resulting from clinical trial results. However, evidence regarding FLT3i adoption in routine clinical practice is still scarce. Methods: Clinical data are reported from 394 ND patients with FLT3-mutated AML enrolled in the retrospective observational Italian Cohort Study on FLT3-mutated patients with AML and treated with an upfront intensive regimen with (FLT3i group, n = 92) or without (CT group, n = 302) the addition of a FLT3i. Results: With a median follow-up time of 34.5 months, an effectiveness benefit obtained by FLT3i incorporation both in terms of overall survival (median, 34.9 in the FLT3i vs 12.7 months in the CT group, p <.01) and relapse-free survival (median, 18.9 in the FLT3i vs 7.6 months in the CT group, p =.01) was documented, with a higher composite complete remission rate (75.4% in the FLT3i vs 62.4% in the CT group, p =.052). FLT3i benefit seemed to be independent from the transplant rate. Conclusions: In conclusion, the benefit of FLT3i addition to upfront intensive treatment in newly diagnosed FLT3-mutated AML patients was confirmed in a large, real-life cohort study.
2025
Nanni, J., Azzali, I., Papayannidis, C., Mule, A., Audisio, E., Martelli, M.P., et al. (2025). Upfront intensive treatment analysis of the Italian Cohort Study on FLT3-mutated AML patients (FLAM): The impact of a FLT3 inhibitor addition to standard chemotherapy in the real-life setting. CANCER, 131(7) [10.1002/cncr.35824].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/1314174