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Comprehensive analysis of FLT3-mutated patients with acute myeloid leukemia with updated 2022 European LeukemiaNet recommendations: Insights from the Turkish AML registry project

dc.contributor.authorPinar, Ibrahim Ethem
dc.contributor.authorCelik, Serhat
dc.contributor.authorPolat, Merve Gokcen
dc.contributor.authorKaratas, Aylin Fatma
dc.contributor.authorDogan, Ali
dc.contributor.authorIltar, Utku
dc.contributor.authorSeval, Guldane Cengiz
dc.contributor.authorMalkan, Umit Yavuz
dc.contributor.authorInce, Idris
dc.contributor.authorYenihayat, Emel Merve
dc.contributor.authorAkdeniz, Aydan
dc.contributor.authorKacmaz, Murat
dc.contributor.authorErdem, Ramazan
dc.contributor.authorOzturk, Hacer Berna Afacan
dc.contributor.authorKirkizlar, Hakki Onur
dc.contributor.authorKorkmaz, Gulten
dc.contributor.authorAykas, Fatma
dc.contributor.authorMehtap, Ozgur
dc.contributor.authorDeveci, Burak
dc.contributor.authorSevindik, Omur Gokmen
dc.contributor.authorCan, Ferda
dc.contributor.authorOzbalci, Demircan
dc.contributor.authorBulbul, Hale
dc.contributor.authorDurusoy, Salih Sertac
dc.contributor.authorAtas, Unal
dc.contributor.authorKeklik, Muzaffer
dc.contributor.authorToprak, Selami Kocak
dc.contributor.authorGoker, Hakan
dc.contributor.authorDemirkan, Fatih
dc.contributor.authorOzkalemkas, Fahir
dc.contributor.authorAlacacioglu, Inci
dc.contributor.authorKarakus, Volkan
dc.contributor.buuauthorPINAR, İBRAHİM ETHEM
dc.contributor.buuauthorÖZKALEMKAŞ, FAHİR
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.researcheridJGM-6601-2023
dc.contributor.researcheridDLR-8474-2022
dc.date.accessioned2025-11-06T17:03:33Z
dc.date.issued2025-10-10
dc.description.abstractBackground This study aimed to evaluate the prognostic significance and clinical impact of the revised 2022 European LeukemiaNet (ELN) classification for acute myeloid leukemia (AML), focusing particularly on patients harboring fms-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) mutations. Methods A retrospective, multicenter observational study was conducted by the Turkish Society of Hematology-Acute Leukemias Working Group, analyzing 312 adult patients newly diagnosed with AML from January 2012 to December 2022. Patients with acute promyelocytic leukemia were excluded. FLT3-ITD mutations were detected using polymerase chain reaction and, when available, next-generation sequencing. Patients were classified according to the 2017 ELN risk stratification, and FLT3-ITD-positive cases were reclassified based on the updated 2022 ELN criteria. Endpoints were complete remission (CR), disease-free survival (DFS), and overall survival (OS). Results FLT3-ITD mutations were identified in 54 (17.3%) patients. According to the 2022 ELN classification, 29 patients previously categorized as the favorable (n = 6) or adverse-risk (n = 23) groups were reclassified into the intermediate-risk group, highlighting the substantial impact of removing the FLT3-ITD allelic ratio from risk stratification. With a median follow-up of 31.8 months, OS significantly differed among the 2017 ELN favorable-, intermediate-, and adverse-risk categories (not reached, 21.6 months, and 9.5 months, respectively, p < 0.001). FLT3-ITD-positive patients demonstrated significantly inferior DFS (p = 0.038) and OS (p = 0.009) compared to FLT3-ITD-negative patients. In patients achieving first CR, allogeneic hematopoietic stem cell transplantation (HSCT) improved OS in intermediate-risk (p = 0.003), showed a trend in adverse-risk (p = 0.098), and no benefit in favorable-risk (p = 0.351). Among reclassified FLT3-ITD-positive patients, survival outcomes aligned closely with the original intermediate-risk group defined by the 2017 ELN, supporting the rationale behind the ELN revision. Conclusions Our findings validate the prognostic utility of the revised 2022 ELN guidelines, especially regarding FLT3-ITD-positive AML, emphasizing that the exclusion of the FLT3-ITD allelic ratio yields a more biologically consistent risk categorization. Furthermore, the data support tailored ELN-based risk stratification for older AML patients. Given the modest benefit of HSCT in adverse-risk patients, future refinements should further stratify this group to address their unmet therapeutic needs and enhance survival outcomes. Trial registration The study was registered at ClinicalTrials.gov (NCT05979675).
dc.identifier.doi10.1186/s12885-025-14987-z
dc.identifier.issue1
dc.identifier.scopus2-s2.0-105018398183
dc.identifier.urihttps://doi.org/10.1186/s12885-025-14987-z
dc.identifier.urihttps://hdl.handle.net/11452/56759
dc.identifier.volume25
dc.identifier.wos001591855500002
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherBMC
dc.relation.journalBMC Cancer
dc.subjectAcute myeloid leukemia
dc.subjectEuropean LeukemiaNet
dc.subjectFLT3-ITD mutation
dc.subjectRisk stratification
dc.subjectOncology
dc.subjectPrognostic value
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.titleComprehensive analysis of FLT3-mutated patients with acute myeloid leukemia with updated 2022 European LeukemiaNet recommendations: Insights from the Turkish AML registry project
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus
relation.isAuthorOfPublication780690ec-9c57-47ed-a462-d5d676cd36e3
relation.isAuthorOfPublication6d4676a2-f825-4560-bfa8-c7eb6daf748d
relation.isAuthorOfPublication.latestForDiscovery780690ec-9c57-47ed-a462-d5d676cd36e3

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