UBTF tandem duplications are rare but recurrent alterations in adult AML and associated with younger age, myelodysplasia, and inferior outcome

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Julia-Annabell Georgi - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Sebastian Stasik - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Jan-Niklas Eckardt - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Sven Zukunft - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Marita Hartwig - , University Hospital Carl Gustav Carus Dresden (Author)
  • Christoph Röllig - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Jan Moritz Middeke - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Uta Oelschlägel - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Utz Krug - , Klinikum Leverkusen (Author)
  • Tim Sauer - , Heidelberg University  (Author)
  • Sebastian Scholl - , Klinik für Innere Medizin und Kardiologie (Author)
  • Andreas Hochhaus - , Klinik für Innere Medizin und Kardiologie (Author)
  • Tim H Brümmendorf - , Medizinische Klinik (Author)
  • Ralph Naumann - , Medizinische Klinik und Poliklinik III, Bereich Allgemeinmedizin (Author)
  • Björn Steffen - , Abteilung Hämatologie/Onkologie (Author)
  • Hermann Einsele - , Medizinische Klinik und Poliklinik III, Bereich Allgemeinmedizin (Author)
  • Markus Schaich - , Klinik für Hämatologie (Author)
  • Andreas Burchert - , Klinik für Innere Medizin und Kardiologie (Author)
  • Andreas Neubauer - , Klinik für Innere Medizin und Kardiologie (Author)
  • Kerstin Schäfer-Eckart - , Klinikum Nurnberg (Author)
  • Christoph Schliemann - , Medizinische Klinik (Author)
  • Stefan W Krause - , State Vocational Colleges at the University Hospital Erlangen (Author)
  • Mathias Hänel - , Klinikum Chemnitz gGmbH (Author)
  • Richard Noppeney - , Klinik für Hämatologie (Author)
  • Ulrich Kaiser - , Medizinische Klinik (Author)
  • Claudia D Baldus - , Klinik für Innere Medizin und Kardiologie (Author)
  • Martin Kaufmann - , Abteilung für Hämatologie (Author)
  • Carsten Müller-Tidow - , Heidelberg University  (Author)
  • Uwe Platzbecker - , University Hospital Leipzig (Author)
  • Wolfgang E Berdel - , Medizinische Klinik (Author)
  • Hubert Serve - , Abteilung Hämatologie/Onkologie (Author)
  • Gerhard Ehninger - , AvenCell Europe GmbH (Author)
  • Martin Bornhäuser - , University Cancer Centre, National Center for Tumor Diseases (Partners: UKD, MFD, HZDR, DKFZ), Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Johannes Schetelig - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden, DKMS Clinical Trials Unit (Author)
  • Frank Kroschinsky - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Christian Thiede - , Department of internal Medicine I, University Hospital Carl Gustav Carus Dresden, AgenDix GmbH (Author)

Abstract

Tandem-duplication mutations of the UBTF gene (UBTF-TDs) coding for the upstream binding transcription factor have recently been described in pediatric patients with acute myeloid leukemia (AML) and were found to be associated with particular genetics (trisomy 8 (+8), FLT3-internal tandem duplications (FLT3-ITD), WT1-mutations) and inferior outcome. Due to limited knowledge on UBTF-TDs in adult AML, we screened 4247 newly diagnosed adult AML and higher-risk myelodysplastic syndrome (MDS) patients using high-resolution fragment analysis. UBTF-TDs were overall rare (n = 52/4247; 1.2%), but significantly enriched in younger patients (median age 41 years) and associated with MDS-related morphology as well as significantly lower hemoglobin and platelet levels. Patients with UBTF-TDs had significantly higher rates of +8 (34% vs. 9%), WT1 (52% vs. 7%) and FLT3-ITD (50% vs. 20.8%) co-mutations, whereas UBTF-TDs were mutually exclusive with several class-defining lesions such as mutant NPM1, in-frame CEBPAbZIP mutations as well as t(8;21). Based on the high-variant allele frequency found and the fact that all relapsed patients analyzed (n = 5) retained the UBTF-TD mutation, UBTF-TDs represent early clonal events and are stable over the disease course. In univariate analysis, UBTF-TDs did not represent a significant factor for overall or relapse-free survival in the entire cohort. However, in patients under 50 years of age, who represent the majority of UBTF-mutant patients, UBTF-TDs were an independent prognostic factor for inferior event-free (EFS), relapse-free (RFS) and overall survival (OS), which was confirmed by multivariable analyses including established risk factors such as age and ELN2022 genetic risk groups (EFS [HR: 2.20; 95% CI 1.52-3.17, p < 0.001], RFS [HR: 1.59; 95% CI 1.02-2.46, p = 0.039] and OS [HR: 1.64; 95% CI 1.08-2.49, p = 0.020]). In summary, UBTF-TDs appear to represent a novel class-defining lesion not only in pediatric AML but also younger adults and are associated with myelodysplasia and inferior outcome in these patients.

Details

Original languageEnglish
Article number88
JournalBlood cancer journal
Volume13
Issue number1
Publication statusPublished - 26 May 2023
Peer-reviewedYes

External IDs

PubMedCentral PMC10220021
Scopus 85160375206

Keywords

Keywords

  • Adult, Humans, Child, Nuclear Proteins/genetics, Nucleophosmin, Leukemia, Myeloid, Acute/genetics, Mutation, Myelodysplastic Syndromes/genetics, Prognosis, fms-Like Tyrosine Kinase 3/genetics

Library keywords