Outcomes with single-agent gilteritinib for relapsed or refractory FLT3-mutant AML after contemporary induction therapy.

Othman, J.; Hwang, A.; Brodermann, M.; Abdallah, I.; McCloskey, K.; Gallipoli, P.; Clarke, G.; Dang, R.; Vidler, J.; Krishnamurthy, P.; Basheer, F.; Latif, AL.; Palanicawandar, R.; Taylor, T.; Khan, A.; Campbell, V.; Hogan, F.; Kanellopoulos, A.; Fleming, K.; Collins, A.; Dalley, C.; Loke, J.; Marshall, S.; Taussig, D.; Munisamy, S.; Loizou, E.; Yassin, H.; Dennis, M.; Zhao, R.; Belsham, E.; Murray, D.; Fowler, N.; O'Nions, J.; Sellar, R.; Dillon, R.

Outcomes with single-agent gilteritinib for relapsed or refractory FLT3-mutant AML after contemporary induction therapy.

All Authors

Othman, J.

Hwang, A.

Brodermann, M.

Abdallah, I.

McCloskey, K.

Gallipoli, P.

Clarke, G.

Dang, R.

Vidler, J.

Krishnamurthy, P.

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LTHT Author

Abdallah, Islam
Khan, Anjum

LTHT Department

Haematology

Publication Date

2024

Item Type

Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't

Abstract

ABSTRACT: Gilteritinib is the current standard of care for relapsed or refractory fms related receptor tyrosine kinase 3 (FLT3)-mutated acute myeloid leukemia in many countries, however outcomes for patients relapsing after contemporary first-line therapies (intensive chemotherapy with midostaurin, or nonintensive chemotherapy with venetoclax) are uncertain. Moreover, reported data on toxicity and health care resource use is limited. Here, we describe a large real-world cohort of 152 patients receiving single-agent gilteritinib in 38 UK hospitals. Median age was 61 years, and 36% had received >=2 prior lines of therapy, including a FLT3 inhibitor in 41% and venetoclax in 24%. A median of 4 cycles of gilteritinib were administered, with 56% of patients requiring hospitalization in the first cycle (median, 10 days). Over half of patients required transfusion in each of the first 4 cycles. Complete remission (CR) was achieved in 21%, and CR with incomplete recovery (CRi) in a further 9%. Remission rates were lower for patients with FLT3-tyrosine kinase domain or adverse karyotype. Day-30 and day-60 mortality were 1% and 10.6%, respectively, and median overall survival was 9.5 months. On multivariable analysis, increasing age, KMT2A rearrangement, and complex karyotype were associated with worse survival whereas RUNX1 mutations were associated with improved survival. Twenty patients received gilteritinib as first salvage having progressed after first-line therapy with venetoclax, with CR/CRi achieved in 25% and median survival 4.5 months. Real-world results with gilteritinib mirror those seen in the clinical trials, but outcomes remain suboptimal, with more effective strategies needed.