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Evolution of Cytogenetically Normal Acute Myeloid Leukemia During Therapy and Relapse: An Exome Sequencing Study of 50 Patients.
Greif, Philipp A; Hartmann, Luise; Vosberg, Sebastian; Stief, Sophie M; Mattes, Raphael; Hellmann, Ines; Metzeler, Klaus H; Herold, Tobias; Bamopoulos, Stefanos A; Kerbs, Paul; Jurinovic, Vindi; Schumacher, Daniela; Pastore, Friederike; Bräundl, Kathrin; Zellmeier, Evelyn; Ksienzyk, Bianka; Konstandin, Nikola P; Schneider, Stephanie; Graf, Alexander; Krebs, Stefan; Blum, Helmut; Neumann, Martin; Baldus, Claudia D; Bohlander, Stefan K; Wolf, Stephan; Görlich, Dennis; Berdel, Wolfgang E; Wörmann, Bernhard J; Hiddemann, Wolfgang; Spiekermann, Karsten.
Afiliación
  • Greif PA; Department of Medicine III, University Hospital, LMU Munich, München, Germany. pgreif@med.uni-muenchen.de.
  • Hartmann L; German Cancer Consortium (DKTK), and.
  • Vosberg S; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Stief SM; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Mattes R; German Cancer Consortium (DKTK), and.
  • Hellmann I; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Metzeler KH; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Herold T; German Cancer Consortium (DKTK), and.
  • Bamopoulos SA; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Kerbs P; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Jurinovic V; German Cancer Consortium (DKTK), and.
  • Schumacher D; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Pastore F; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Bräundl K; German Cancer Consortium (DKTK), and.
  • Zellmeier E; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Ksienzyk B; Anthropology and Human Genomics, Department Biology II, LMU Munich, Martinsried, Germany.
  • Konstandin NP; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Schneider S; German Cancer Consortium (DKTK), and.
  • Graf A; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Krebs S; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Blum H; German Cancer Consortium (DKTK), and.
  • Neumann M; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Baldus CD; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Bohlander SK; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Wolf S; German Cancer Consortium (DKTK), and.
  • Görlich D; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Berdel WE; Institute for Medical Information Procesing, Biometry and Epidemiology (IBE), LMU Munich, München, Germany.
  • Wörmann BJ; Department of Medicine III, University Hospital, LMU Munich, München, Germany.
  • Hiddemann W; German Cancer Consortium (DKTK), and.
  • Spiekermann K; German Cancer Research Center (DKFZ), Heidelberg, Germany.
Clin Cancer Res ; 24(7): 1716-1726, 2018 04 01.
Article en En | MEDLINE | ID: mdl-29330206
ABSTRACT

Purpose:

To study mechanisms of therapy resistance and disease progression, we analyzed the evolution of cytogenetically normal acute myeloid leukemia (CN-AML) based on somatic alterations.Experimental

Design:

We performed exome sequencing of matched diagnosis, remission, and relapse samples from 50 CN-AML patients treated with intensive chemotherapy. Mutation patterns were correlated with clinical parameters.

Results:

Evolutionary patterns correlated with clinical outcome. Gain of mutations was associated with late relapse. Alterations of epigenetic regulators were frequently gained at relapse with recurring alterations of KDM6A constituting a mechanism of cytarabine resistance. Low KDM6A expression correlated with adverse clinical outcome, particularly in male patients. At complete remission, persistent mutations representing preleukemic lesions were observed in 48% of patients. The persistence of DNMT3A mutations correlated with shorter time to relapse.

Conclusions:

Chemotherapy resistance might be acquired through gain of mutations. Insights into the evolution during therapy and disease progression lay the foundation for tailored approaches to treat or prevent relapse of CN-AML. Clin Cancer Res; 24(7); 1716-26. ©2018 AACR.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Exoma Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Exoma Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article