Journal Article DKFZ-2026-00288

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Relapse following FLT3 inhibitor cessation in FLT3-ITD-positive AML: lessons from two clinical cases.

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2026
Springer New York

Annals of hematology 105(3), 82 () [10.1007/s00277-026-06776-w]
 GO

Abstract: The clinical success of FLT3 inhibitors has led to their steadily increasing use in the treatment of acute myeloid leukemia (AML), both in the relapsed/refractory setting and as post-transplant maintenance. Despite their expanding application, there is currently no guidance on the optimal duration of therapy or the feasibility of discontinuation. In the maintenance context, current practice is largely based on trial protocols with predefined treatment periods, yet relapses after cessation have been documented. Similarly, in the relapsed/refractory setting, the management of long-term responders to FLT3-directed monotherapy lacks evidence-based guidance.We report two cases of FLT3-ITD AML patients with relapse after discontinuation of prolonged FLT3 inhibitor therapy, despite sustained remission prior to withdrawal. As such scenarios remain insufficiently characterized in the literature, these case vignettes are presented to highlight the unresolved challenge of defining the appropriate duration of FLT3 inhibitor therapy and to underscore the need for systematic evaluation to establish evidence-based strategies for safe discontinuation or extended administration.

Keyword(s): Humans (MeSH) ; fms-Like Tyrosine Kinase 3: antagonists & inhibitors (MeSH) ; fms-Like Tyrosine Kinase 3: genetics (MeSH) ; Leukemia, Myeloid, Acute: drug therapy (MeSH) ; Leukemia, Myeloid, Acute: genetics (MeSH) ; Male (MeSH) ; Middle Aged (MeSH) ; Protein Kinase Inhibitors: administration & dosage (MeSH) ; Protein Kinase Inhibitors: therapeutic use (MeSH) ; Recurrence (MeSH) ; Female (MeSH) ; Adult (MeSH) ; FLT3 inhibitor ; FLT3-ITD AML ; Gilteritinib ; Measurable residual disease (MRD) ; Post-transplant maintenance ; Relapse ; fms-Like Tyrosine Kinase 3 ; FLT3 protein, human ; Protein Kinase Inhibitors

Classification:

Note: #NCTZFB9#

Contributing Institute(s):
  1. Koordinierungsstelle NCT Dresden (DD04)
Research Program(s):
  1. 899 - ohne Topic (POF4-899) (POF4-899)

Appears in the scientific report 2026
Database coverage:
Medline ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; DEAL Springer ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF < 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2026-02-05, last modified 2026-02-05



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