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Type: Journal article
Title: Dasatinib-associated major molecular responses in patients with chronic myeloid leukemia in chronic phase following imatinib failure: response dynamics and predictive value
Author: Hochhaus, A.
Muller, M.
Radich, J.
Branford, S.
Kantarjian, H.
Hanfstein, B.
Rousselot, P.
Kim, D.
Lipton, J.
Bleickhardt, E.
Lambert, A.
Hughes, T.
Citation: Leukemia, 2009; 23(9):1628-1633
Publisher: Nature Publishing Group
Issue Date: 2009
ISSN: 0887-6924
Statement of
A Hochhaus, MC Müller, J Radich, S Branford, HM Kantarjian, B Hanfstein, P Rousselot, D-W Kim, JH Lipton, E Bleickardt, A Lambert and TP Hughes
Abstract: Dasatinib is a highly potent BCR–ABL inhibitor that has shown durable efficacy in patients with chronic phase (CP) chronic myeloid leukemia (CML) after resistance, suboptimal response, or intolerance to prior imatinib. In patients with CML, BCR–ABL transcript measurement is the most sensitive method for assessing minimal residual disease. Here, molecular responses were analyzed in 1067 patients with CML-CP treated with dasatinib during phase II/III trials. After 3, 6, 12, and 24 months of follow-up, a major molecular response (MMR) was achieved by 12, 22, 35, and 40% of patients, respectively. The 24-month MMR rate was 34% in patients with resistance or suboptimal response to imatinib (n=829) and 63% in imatinib-intolerant patients (n=238). Among patients who had achieved a complete cytogenetic response (CCyR), 72% also achieved MMR. Responses with dasatinib 100 mg once daily were similar to other doses. In landmark analyses, 24-month progression-free survival was higher in patients who had achieved MMR or CCyR at 12 months than in those without MMR or CCyR at 12 months. MMR at 12 months was associated with a longer duration of CCyR. Overall, this analysis shows that dasatinib treatment results in high MMR rates in patients with CML-CP after imatinib failure.
Keywords: chronic myeloid leukemia; dasatinib; BCR–ABL; treatment outcome; progression-free survival
Rights: © 2009 Macmillan Publishers Limited. All rights reserved.
RMID: 0020091533
DOI: 10.1038/leu.2009.156
Appears in Collections:Medicine publications

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