TY - JOUR
T1 - European LeukemiaNet recommendations for the management of chronic myeloid leukemia
T2 - 2013
AU - Baccarani, Michele
AU - Deininger, Michael W.
AU - Rosti, Gianantonio
AU - Hochhaus, Andreas
AU - Soverini, Simona
AU - Apperley, Jane F.
AU - Cervantes, Francisco
AU - Clark, Richard E.
AU - Cortes, Jorge E.
AU - Guilhot, François
AU - Hjorth-Hansen, Henrik
AU - Hughes, Timothy P.
AU - Kantarjian, Hagop M.
AU - Kim, Dong Wook
AU - Larson, Richard A.
AU - Lipton, Jeffrey H.
AU - Mahon, François Xavier
AU - Martinelli, Giovanni
AU - Mayer, Jiri
AU - Müller, Martin C.
AU - Niederwieser, Dietger
AU - Pane, Fabrizio
AU - Radich, Jerald P.
AU - Rousselot, Philippe
AU - Saglio, Giuseppe
AU - Saußele, Susanne
AU - Schiffer, Charles
AU - Silver, Richard
AU - Simonsson, Bengt
AU - Steegmann, Juan Luis
AU - Goldman, John M.
AU - Hehlmann, Rüdiger
PY - 2013/8/8
Y1 - 2013/8/8
N2 - Advances in chronic myeloid leukemia treatment, particularly regarding tyro-sine 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, nilo-tinib, or dasatinib. Response is assessed with standardized real quantitative poly-merase 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.
AB - Advances in chronic myeloid leukemia treatment, particularly regarding tyro-sine 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, nilo-tinib, or dasatinib. Response is assessed with standardized real quantitative poly-merase 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.
UR - http://www.scopus.com/inward/record.url?scp=84881298446&partnerID=8YFLogxK
U2 - 10.1182/blood-2013-05-501569
DO - 10.1182/blood-2013-05-501569
M3 - Review article
C2 - 23803709
AN - SCOPUS:84881298446
SN - 0006-4971
VL - 122
SP - 872
EP - 884
JO - Blood
JF - Blood
IS - 6
ER -