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Anthracycline-Free FLA-VEN with or Without Midostaurin in Newly Diagnosed Intermediate- and Adverse-Risk AML: A Single-Center Retrospective Study

Journal
Cancers (Q1)
Published
27 September 2026
Study design
Prospective / inception cohort
Evidence level
Level 4, Very Low (CEBM 4)
Authors
Sinem Namdaroglu, Merve Kakcı, Berrak Şenol, Osman Can Öztürk, Ömer Şeker, Mehmet Can Uğur, et al.
PMID
42882827
DOI
10.3390/cancers18193132

Why clinicians should know about it

  • Picked for Hematology (paper of the day, 20 October 2026): Anthracycline‑free FLA‑VEN regimen yields high CR in AML

Abstract

BACKGROUND: Anthracycline-containing intensive chemotherapy remains a standard frontline approach for medically fit patients with acute myeloid leukemia (AML). We retrospectively evaluated an exploratory anthracycline-sparing regimen combining fludarabine, cytarabine, and venetoclax (FLA-VEN), with midostaurin added in FLT3-mutated cases, in selected patients with intermediate- or adverse-risk AML. METHODS: This retrospective single-center study included 24 consecutive adults with newly diagnosed intermediate- or adverse-risk AML treated between March 2024 and March 2026. Patients with favorable-risk AML were excluded. The primary endpoints were complete remission (CR) and safety. Secondary endpoints included hematologic recovery, allogeneic hematopoietic stem cell transplantation (allo-HSCT) rate, relapse incidence, transplant-related mortality (TRM), and overall survival (OS). RESULTS: The median age was 49 years (range, 22-64), and 16.7% of patients were aged ≥60 years. FMS-like tyrosine kinase 3 internal tandem duplication (FLT3-ITD) mutations were present in 8 patients (33.3%). Following one induction cycle, 21 of 24 patients (87.5%) achieved CR. Among FLT3-ITD-mutated patients, 7 of 8 (87.5%) achieved CR, and FLT3-ITD became undetectable by the available polymerase chain reaction (PCR) fragment assay in all seven responders before transplantation. The 60-day mortality rate was 0/24 (0%). Median neutrophil and platelet recovery times were 17 and 21 days, respectively. Twenty-one patients (87.5%) underwent allo-HSCT in first remission. With a database cutoff of 30 August 2026, Kaplan-Meier estimated OS was 83.3% (95% CI, 61.5-93.4%) at 12 months. The longer-term 24-month OS estimate was 54.4% (95% CI, 25.5-76.3%); however, this estimate was imprecise because only five patients remained at risk at 24 months. Median OS was not reached. CONCLUSIONS: In this small exploratory cohort, anthracycline-free and G-CSF-free FLA-VEN, with or without midostaurin, was associated with high remission rates, no early mortality, and frequent bridging to allo-HSCT. These findings support prospective controlled evaluation of this anthracycline-sparing strategy.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.