Affiliation:
1. From the Department of Hematology/Oncology, L. and A. Seràgnolì, University of Bologna; Division of Hematology, University Federico II, Naples; and Department of Clinical and Biological Sciences, University of Turin at Orbassano, Turin, Italy; Department of Haematology, Hammersmith Hospital; and Department of Haematology, Imperial College, London, United Kingdom; Hematology Department, Hospital Clinic, lnstitut d'lnvestigations Biomédiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain;...
Abstract
PurposeTo review and update the European LeukemiaNet (ELN) recommendations for the management of chronic myeloid leukemia with imatinib and second-generation tyrosine kinase inhibitors (TKIs), including monitoring, response definition, and first- and second-line therapy.MethodsThese recommendations are based on a critical and comprehensive review of the relevant papers up to February 2009 and the results of four consensus conferences held by the panel of experts appointed by ELN in 2008.ResultsCytogenetic monitoring was required at 3, 6, 12, and 18 months. Molecular monitoring was required every 3 months. On the basis of the degree and the timing of hematologic, cytogenetic, and molecular results, the response to first-line imatinib was defined as optimal, suboptimal, or failure, and the response to second-generation TKIs was defined as suboptimal or failure.ConclusionInitial treatment was confirmed as imatinib 400 mg daily. Imatinib should be continued indefinitely in optimal responders. Suboptimal responders may continue on imatinb, at the same or higher dose, or may be eligible for investigational therapy with second-generation TKIs. In instances of imatinib failure, second-generation TKIs are recommended, followed by allogeneic hematopoietic stem-cell transplantation only in instances of failure and, sometimes, suboptimal response, depending on transplantation risk.
Publisher
American Society of Clinical Oncology (ASCO)
Cited by
1068 articles.
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