European LeukemiaNet 2020 recommendations for treating chronic myeloid leukemia

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Hochhaus, Andreas | Baccarani, Michele | Silver, Richard T. | Schiffer, Charles A. | Apperley, J. | Cervantes, Francisco | Clark, Richard E. | Cortes, Jorge E. | Deininger, Michael Werner Nikolaus | Guilhot, François | Hjorth-Hansen, Henrik | Hughes, Timothy P. | Janssen, Jeroen J.W.M. | Kantarjian, Hagop M. | Kim, Dong-Wook | Larson, Richard A. | Lipton, Jeffrey Howard | Mahon, François Xavier | Mayer, Jir̂í | Nicolini, Franck Emmanuel | Niederwieser, Dietger Walter | Pane, F. | Radich, Jerald P. | Rea, Delphine | Richter, Johan | Rosti, Gianantonio A. | Rousselot, Philippe | Saglio, G. | Saussele, Susanne | Soverini, Simona | Steegmann, Juan Luis | Turkina, Anna G. | Zaritskey, Andrey Yu | Hehlmann, Rüediger

Edité par CCSD ; Springer Nature -

International audience. The therapeutic landscape of chronic myeloid leukemia (CML) has profoundly changed over the past 7 years. Most patients with chronic phase (CP) now have a normal life expectancy. Another goal is achieving a stable deep molecular response (DMR) and discontinuing medication for treatment-free remission (TFR). The European LeukemiaNet convened an expert panel to critically evaluate and update the evidence to achieve these goals since its previous recommendations. First-line treatment is a tyrosine kinase inhibitor (TKI; imatinib brand or generic, dasatinib, nilotinib, and bosutinib are available first-line). Generic imatinib is the cost-effective initial treatment in CP. Various contraindications and side-effects of all TKIs should be considered. Patient risk status at diagnosis should be assessed with the new EUTOS long-term survival (ELTS)-score. Monitoring of response should be done by quantitative polymerase chain reaction whenever possible. A change of treatment is recommended when intolerance cannot be ameliorated or when molecular milestones are not reached. Greater than 10% BCR-ABL1 at 3 months indicates treatment failure when confirmed. Allogeneic transplantation continues to be a therapeutic option particularly for advanced phase CML. TKI treatment should be withheld during pregnancy. Treatment discontinuation may be considered in patients with durable DMR with the goal of achieving TFR.

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