TY - JOUR
T1 - Evolving concepts in the management of chronic myeloid leukemia
T2 - Recommendations from an expert panel on behalf of the European LeukemiaNet
AU - Baccarani, Michele
AU - Saglio, Giuseppe
AU - Goldman, John
AU - Hochhaus, Andreas
AU - Simonsson, Bengt
AU - Appelbaum, Frederick
AU - Apperley, Jane
AU - Cervantes, Francisco
AU - Cortes, Jorge
AU - Deininger, Michael
AU - Gratwohl, Alois
AU - Guilhot, François
AU - Horowitz, Mary
AU - Hughes, Timothy
AU - Kantarjian, Hagop
AU - Larson, Richard
AU - Niederwieser, Dietger
AU - Silver, Richard
AU - Hehlmann, Rudiger
N1 - Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2006/9/15
Y1 - 2006/9/15
N2 - The introduction of imatinib mesylate (IM) has revolutionized the treatment of chronic myeloid leukemia (CML). Although experience is too limited to permit evidence-based evaluation of survival, the available data fully justify critical reassessment of CML management. The panel therefore reviewed treatment of CML since 1998. It confirmed the value of IM (400 mg/day) and of conventional allogeneic hematopoietic stem cell transplantation (alloHSCT). It recommended that the preferred initial treatment for most patients newly diagnosed in chronic phase should now be 400 mg IM daily. A dose increase of IM, alloHSCT, or investigational treatments were recommended in case of failure, and could be considered in case of suboptimal response. Failure was defined at 3 months (no hematologic response [HR]), 6 months (incomplete HR or no cytogenetic response [CgR]), 12 months (less than partial CgR [Philadelphia chromosome-positive (Ph+) > 35%]), 18 months (less than complete CgR), and in case of HR or CgR loss, or appearance of highly IM-resistant BCR-ABL mutations. Suboptimal response was defined at 3 months (incomplete HR), 6 months (less than partial CgR), 12 months (less than complete CgR), 18 months (less than major molecular response [MMolR]), and, in case of MMolR loss, other mutations or other chromosomal abnormalities. The importance of regular monitoring at experienced centers was highlighted.
AB - The introduction of imatinib mesylate (IM) has revolutionized the treatment of chronic myeloid leukemia (CML). Although experience is too limited to permit evidence-based evaluation of survival, the available data fully justify critical reassessment of CML management. The panel therefore reviewed treatment of CML since 1998. It confirmed the value of IM (400 mg/day) and of conventional allogeneic hematopoietic stem cell transplantation (alloHSCT). It recommended that the preferred initial treatment for most patients newly diagnosed in chronic phase should now be 400 mg IM daily. A dose increase of IM, alloHSCT, or investigational treatments were recommended in case of failure, and could be considered in case of suboptimal response. Failure was defined at 3 months (no hematologic response [HR]), 6 months (incomplete HR or no cytogenetic response [CgR]), 12 months (less than partial CgR [Philadelphia chromosome-positive (Ph+) > 35%]), 18 months (less than complete CgR), and in case of HR or CgR loss, or appearance of highly IM-resistant BCR-ABL mutations. Suboptimal response was defined at 3 months (incomplete HR), 6 months (less than partial CgR), 12 months (less than complete CgR), 18 months (less than major molecular response [MMolR]), and, in case of MMolR loss, other mutations or other chromosomal abnormalities. The importance of regular monitoring at experienced centers was highlighted.
UR - http://www.scopus.com/inward/record.url?scp=33747154547&partnerID=8YFLogxK
U2 - 10.1182/blood-2006-02-005686
DO - 10.1182/blood-2006-02-005686
M3 - Review article
C2 - 16709930
AN - SCOPUS:33747154547
SN - 0006-4971
VL - 108
SP - 1809
EP - 1820
JO - Blood
JF - Blood
IS - 6
ER -