Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/86381
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Type: Journal article
Title: Dynamics of chronic myeloid leukemia response to long-term targeted therapy reveal treatment effects on leukemic stem cells
Author: Tang, M.
Gonen, M.
Quintas-Cardama, A.
Cortes, J.
Kantarjian, H.
Field, C.
Hughes, T.
Branford, S.
Michor, F.
Citation: Blood, 2011; 118(6):1622-1631
Publisher: American Society of Hematology
Issue Date: 2011
ISSN: 0006-4971
1528-0020
Statement of
Responsibility: 
Min Tang, Mithat Gonen, Alfonso Quintas-Cardama, Jorge Cortes, Hagop Kantarjian, Chani Field, Timothy P. Hughes, Susan Branford, and Franziska Michor
Abstract: Treatment of chronic myeloid leukemia (CML) with the tyrosine kinase inhibitors (TKIs) imatinib mesylate and nilotinib represents a successful application of molecularly targeted anticancer therapy. However, the effect of TKIs on leukemic stem cells remains incompletely understood. On the basis of a statistical modeling approach that used the 10-year imatinib mesylate treatment response of patients with CML and a patient cohort receiving first-line nilotinib therapy, we found that successful long-term therapy results in a triphasic exponential decline of BCR-ABL1 transcripts in many patients. Within our framework, the first slope of −0.052 ± 0.018 (imatinib mesylate) and −0.042 ± 0.015 (nilotinib) per day represents the turnover rate of leukemic differentiated cells, whereas the second slope of −0.0057 ± 0.0038 (imatinib mesylate) and −0.0019 ± 0.0013 (nilotinib) per day represents the turnover rate of leukemic progenitor cells. The third slope allows an inference of the behavior of immature leukemic cells, potentially stem cells. This third slope is negative in most patients, positive in others, and not observable in some patients. This variability in response may be because of insufficient follow-up, missing data, disease heterogeneity, inconsistent compliance to drug, or acquired resistance. Our approach suggests that long-term TKI therapy may reduce the abundance of leukemic stem cells in some patients.
Keywords: Humans; Benzamides; Piperazines; Pyrimidines; Fusion Proteins, bcr-abl; Protein Kinase Inhibitors; Treatment Outcome; Reverse Transcriptase Polymerase Chain Reaction; Transcription, Genetic; Algorithms; Models, Biological; Time Factors; Neoplastic Stem Cells; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Molecular Targeted Therapy; Imatinib Mesylate
Rights: © 2011 by The American Society of Hematology
RMID: 0020112357
DOI: 10.1182/blood-2011-02-339267
Appears in Collections:Medicine publications

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