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

Michele BaccaraniDepartment of Hematology “L. and A. Seràgnoli,” S.Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy;Michael DeiningerDivision of Hematology and Hematologic Malignancies, University of Utah Huntsman Cancer Institute, Salt Lake City, UT;Gianantonio RostiDepartment of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;Andreas HochhausHematology/Oncology, Universitätsklinikum Jena, Jena, Germany;Simona SoveriniDepartment of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;Jane F. ApperleyCentre for Hematology, Imperial College, London, United Kingdom;Francisco CervantesHospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain;Richard E. ClarkRoyal Liverpool University Hospital, Liverpool, United Kingdom;Jörge E. CortesDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX;François GuilhotInstitut National de la Santé et de la Recherche Médicale Centres d'investigation clinique 0802, CHU de Poitiers, Université de Poitiers, Poitiers, France;Henrik Hjorth‐HansenDepartment of Hematology, St. Olavs Hospital, and Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway;Timothy P. HughesSA Pathology and University of Adelaide, Adelaide, SA, Australia;Hagop M. KantarjianDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX;Dong‐Wook KimDepartment of Hematology, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seoul, South Korea;Richard A. LarsonThe University of Chicago, Chicago, IL;Jeffrey H. LiptonPrincess Margaret Hospital, University of Toronto, ON, Canada,François-Xavier MahonLaboratoire 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 MartinelliDepartment of Experimental, Diagnostic, and Specialty Medicine, University of Bologna and S.Orsola-Malpighi Hospital, Bologna, Italy;Jiřı́ MayerUniversity Hospital Brno and Central European Institute of Technology Masaryk University, Brno, Czech Republic;Martin MüllerIII Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;Dietger NiederwieserFabrizio PaneDipartimento di Medicina Clinica e Chirurgia, Università di Napoli Federico II, and CEINGE Biotecnologie Avanzate, Napoli, Italy;Jerald P. RadichClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;Philippe RousselotService d’ Hématologie et d’ Oncologie, Hôpital Mignot, Université Versailles Saint-Qentin-en-Yvelines, Versailles, France;Giuseppe SaglioDepartment of Oncology, University of Turin, Turin, Italy;Susanne SaußeleIII Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;Charles A. SchifferDivision of Medicine and Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI;Richard T. SilverWeill Cornell Medical College, New York, NY;Bengt SimonssonUniversity Hospital, Uppsala, Sweden;Juan-Luis SteegmannServicio de Hematologia, Hospital Universitario de la Princesa, IIS-IP, Madrid, Spain; andJohn M. GoldmanDepartment of Hematology, Imperial College, London, United KingdomRüdiger HehlmannIII Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;
2013en
ABI

Аннотация

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.

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