Journal article
Gain and Loss of FLT3 Mutations in Patients with Acute Myeloid Leukemia: A Noninterventional Cohort Study (CLEVO)
- Abstract:
- INTRODUCTION: FMS-like tyrosine kinase 3 (FLT3) mutations show variable detectability in relapse/refractory acute myeloid leukemia (AML) with unclear clonal evolution dynamics. METHODS: This prospective noninterventional study examined clonal evolution and outcomes from AML diagnosis to relapse/refractory disease occurrences. RESULTS: Of 650 patients included, 172 were FLT3-positive (FLT3pos) and 472 were FLT3-negative (FLT3neg; 99.1% testing rate; unknown FLT3 status, six patients). At first occurrence, the FLT3 testing rate decreased (57.0% [166/291]). Among tested patients, 45 had FLT3pos and 121 had FLT3neg AML. A gain or loss of mutations was seen in 15.6% (7/45) of patients with FLT3pos AML and 14.9% (18/121) of patients with FLT3neg AML. Median (95% confidence interval [CI]) overall survival was 22.8 (19.6, not estimable [NE]) months across patients (FLT3pos, NE;FLT3neg, 20.3 [15.2-23.7] months; hazard ratio [HR] [95% CI] 0.6 [0.5-0.8]). Median (95% CI) disease-free survival across patients was NE (26.3-NE) (FLT3pos, NE;FLT3neg, NE; HR [95% CI] 0.8 [0.6-1.1]). Median event-free survival (95% CI) was 11.8 (10.0-15.5) months in all patients (FLT3pos, 17.2 [11.0-NE] months;FLT3neg, 10.4 [8.4-13.2] months; HR [95% CI] 0.8 [0.6-1.0]). CONCLUSIONS: Dynamic changes in FLT3 mutation status were observed during these patients' disease course. FLT3pos status at baseline, but not at first occurrence, was associated with improved outcomes; other confounders should be considered. Timelier FLT3 mutation retesting may aid in personalizing treatment. Graphical abstract available for this article.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.7MB, Terms of use)
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- Publisher copy:
- 10.1007/s40487-026-00427-w
Authors
- Publisher:
- Springer
- Journal:
- Oncology and Therapy More from this journal
- Publication date:
- 2026-03-11
- Acceptance date:
- 2026-02-17
- DOI:
- EISSN:
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2366-1089
- ISSN:
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2366-1070
- Language:
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English
- Keywords:
- Pubs id:
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2389313
- Local pid:
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pubs:2389313
- Source identifiers:
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W7134901300
- Deposit date:
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2026-03-15
- ARK identifier:
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- Copyright date:
- 2026
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