Prognostic impact of t(16;21)(p11;q22) and t(16;21)(q24;q22) in pediatric AML: a retrospective study by the I-BFM Study Group

  • Sanne Noort
    Pediatric Oncology/Hematology, Erasmus MC–Sophia Children’s Hospital Rotterdam, Rotterdam, The Netherlands;
  • Martin Zimmermann
    Department of Pediatric Hematology/Oncology, Medical School Hannover, Hannover, Germany;
  • Dirk Reinhardt
    Acute Myeloid Leukemia-Berlin-Frankfurt-Münster Study Group, Pediatric Hematology and Oncology, Essen, Germany;
  • Wendy Cuccuini
    Department of Cytogenetics, Saint Louis Hospital, Paris, France;
  • Martina Pigazzi
    Women and Children’s Health, Hematology-Oncology Laboratory, University of Padova, Padova, Italy;
  • Jenny Smith
    Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Rhonda E. Ries
    Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Todd A. Alonzo
    Children's Oncology Group, Monrovia, CA;
  • Betsy Hirsch
    Children's Oncology Group, Monrovia, CA;
  • Daisuke Tomizawa
    Division of Leukemia and Lymphoma, Children’s Cancer Center, National Center for Child Health and Development, Tokyo, Japan;
  • Franco Locatelli
    Department of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico, Ospedale Pediatrico Bambino Gesù, Rome, Italy;
  • Tanja A. Gruber
    Department of Oncology and
  • Susana Raimondi
    Department of Pathology, St. Jude Children’s Research Hospital, Memphis, TN;
  • Edwin Sonneveld
    Dutch Childhood Oncology Group, The Hague, The Netherlands;
  • Daniel K. Cheuk
    Department of Pediatrics and Adolescent Medicine, Queen Mary Hospital, University of Hong Kong, Hong Kong;
  • Michael Dworzak
    Department of Pediatrics, Children’s Cancer Research Institute and St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria;
  • Jan Stary
    Czech Pediatric Hematology/Oncology, University Hospital Motol and Charles University, Prague, Czech Republic;
  • Jonas Abrahamsson
    Nordic Society for Pediatric Hematology and Oncology, Department of Pediatrics, Institution for Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;
  • Nira Arad-Cohen
    Pediatric Hemato-Oncology Department, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, Haifa, Israel;
  • Malgorzata Czogala
    Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland;
  • Barbara De Moerloose
    Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium;
  • Henrik Hasle
    Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark;
  • Soheil Meshinchi
    Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Marry van den Heuvel-Eibrink
    Pediatric Oncology/Hematology, Erasmus MC–Sophia Children’s Hospital Rotterdam, Rotterdam, The Netherlands;
  • C. Michel Zwaan
    Pediatric Oncology/Hematology, Erasmus MC–Sophia Children’s Hospital Rotterdam, Rotterdam, The Netherlands;

抄録

<jats:title>Key Points</jats:title> <jats:p>t(16;21) translocations in AML comprise t(16;21)(p11;q22) (FUS-ERG) as well as t(16;21)(q24;q22) (RUNX1-CBFA2T3). Survival in pediatric AML with FUS-ERG is poor, whereas survival in RUNX1-CBFA2T3 is similar to other core-binding factor leukemias.</jats:p>

収録刊行物

  • Blood

    Blood 132 (15), 1584-1592, 2018-10-11

    American Society of Hematology

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