European LeukemiaNet recommendations for the management of chronic myeloid leukemia: 2013

  • Michele Baccarani
    Department of Hematology “L. and A. Seràgnoli,” S.Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy;
  • Michael W. Deininger
    Division of Hematology and Hematologic Malignancies, University of Utah Huntsman Cancer Institute, Salt Lake City, UT;
  • Gianantonio Rosti
    Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;
  • Andreas Hochhaus
    Hematology/Oncology, Universitätsklinikum Jena, Jena, Germany;
  • Simona Soverini
    Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;
  • Jane F. Apperley
    Centre for Hematology, Imperial College, London, United Kingdom;
  • Francisco Cervantes
    Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain;
  • Richard E. Clark
    Royal Liverpool University Hospital, Liverpool, United Kingdom;
  • Jorge E. Cortes
    Department of Leukemia, MD Anderson Cancer Center, Houston, TX;
  • François Guilhot
    Institut National de la Santé et de la Recherche Médicale Centres d'investigation clinique 0802, CHU de Poitiers, Université de Poitiers, Poitiers, France;
  • Henrik Hjorth-Hansen
    Department of Hematology, St. Olavs Hospital, and Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway;
  • Timothy P. Hughes
    SA Pathology and University of Adelaide, Adelaide, SA, Australia;
  • Hagop M. Kantarjian
    Department of Leukemia, MD Anderson Cancer Center, Houston, TX;
  • Dong-Wook Kim
    Department of Hematology, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seoul, South Korea;
  • Richard A. Larson
    The University of Chicago, Chicago, IL;
  • Jeffrey H. Lipton
    Princess Margaret Hospital, University of Toronto, ON, Canada,
  • François-Xavier Mahon
    Laboratoire d’ Hématologie CHU de Bordeaux et Laboratoire Hématopoïese Leucémique et Cible Therapeutique, Université Bordeaux Ségalen, Institut National de la Santé et de la Recherche Médicale 1035, Bordeaux, France;
  • Giovanni Martinelli
    Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;
  • Jiri Mayer
    University Hospital Brno and Central European Institute of Technology Masaryk University, Brno, Czech Republic;
  • Martin C. Müller
    III Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;
  • Dietger Niederwieser
    Department of Hematology and Oncology, University of Leipzig, Leipzig, Germany;
  • Fabrizio Pane
    Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli Federico II, and CEINGE Biotecnologie Avanzate, Napoli, Italy;
  • Jerald P. Radich
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Philippe Rousselot
    Service d’ Hématologie et d’ Oncologie, Hôpital Mignot, Université Versailles Saint-Qentin-en-Yvelines, Versailles, France;
  • Giuseppe Saglio
    Department of Oncology, University of Turin, Turin, Italy;
  • Susanne Saußele
    III Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;
  • Charles Schiffer
    Division of Medicine and Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI;
  • Richard Silver
    Weill Cornell Medical College, New York, NY;
  • Bengt Simonsson
    University Hospital, Uppsala, Sweden;
  • Juan-Luis Steegmann
    Servicio de Hematologia, Hospital Universitario de la Princesa, IIS-IP, Madrid, Spain; and
  • John M. Goldman
    Department of Hematology, Imperial College, London, United Kingdom
  • Rüdiger Hehlmann
    III Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;

Abstract

<jats:title>Abstract</jats:title><jats:p>Advances in chronic myeloid leukemia treatment, particularly regarding tyrosine kinase inhibitors, mandate regular updating of concepts and management. A European LeukemiaNet expert panel reviewed prior and new studies to update recommendations made in 2009. We recommend as initial treatment imatinib, nilotinib, or dasatinib. Response is assessed with standardized real quantitative polymerase chain reaction and/or cytogenetics at 3, 6, and 12 months. BCR-ABL1 transcript levels ≤10% at 3 months, <1% at 6 months, and ≤0.1% from 12 months onward define optimal response, whereas >10% at 6 months and >1% from 12 months onward define failure, mandating a change in treatment. Similarly, partial cytogenetic response (PCyR) at 3 months and complete cytogenetic response (CCyR) from 6 months onward define optimal response, whereas no CyR (Philadelphia chromosome–positive [Ph+] >95%) at 3 months, less than PCyR at 6 months, and less than CCyR from 12 months onward define failure. Between optimal and failure, there is an intermediate warning zone requiring more frequent monitoring. Similar definitions are provided for response to second-line therapy. Specific recommendations are made for patients in the accelerated and blastic phases, and for allogeneic stem cell transplantation. Optimal responders should continue therapy indefinitely, with careful surveillance, or they can be enrolled in controlled studies of treatment discontinuation once a deeper molecular response is achieved.</jats:p>

Journal

  • Blood

    Blood 122 (6), 872-884, 2013-08-08

    American Society of Hematology

Citations (52)*help

See more

Details 詳細情報について

Report a problem

Back to top