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PMID: 19060245 Published · ppublish English Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Imatinib mesylate dose escalation is associated with durable responses in patients with chronic myeloid leukemia after cytogenetic failure on standard-dose imatinib therapy.

Blood ·Vol. 113 ·No. 10 ·2009-03-05 ·Pages 2154-60

Jabbour E, Kantarjian HM, Jones D, Shan J, O'Brien S, Reddy N, Wierda WG, Faderl S, Garcia-Manero G, Verstovsek S, Rios MB, Cortes J

Abstract

We assessed the long-term efficacy of imatinib dose escalation in 84 patients with chronic myeloid leukemia in chronic phase who met the criteria of failure to standard-dose imatinib. Twenty-one patients with hematologic failure and 63 with cytogenetic failure had their imatinib dose escalated from 400 to 800 mg daily (n = 72) or from 300 to 600 mg daily (n = 12). After a median follow-up of 61 months from dose escalation, 69% remained alive. Complete cytogenetic responses were achieved in 40%; including 52% of patients with cytogenetic failure and 5% of those with hematologic failure. The estimated 2- and 3-year event-free survival and overall survival rates were 57% and 47%, and 84% and 76%, respectively. Responses were long-lasting; 88% of patients with major cytogenetic response sustained their response beyond 2 years. Treatment was well tolerated, with 76% of patients, at 12 months, continuing to receive imatinib at 100% of the intended dose. In conclusion, imatinib dose escalation can induce sustained responses in a subset of patients with cytogenetic failure and a previous cytogenetic response to standard-dose imatinib.

MeSH Terms
Adolescent Adult Aged Antineoplastic Agents/administration & dosage,adverse effects Benzamides DNA Mutational Analysis Disease-Free Survival Female Fusion Proteins, bcr-abl/genetics Humans Imatinib Mesylate In Situ Hybridization, Fluorescence Kaplan-Meier Estimate Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy,genetics,mortality Male Middle Aged Neoplasm Recurrence, Local/drug therapy,genetics,mortality Piperazines/administration & dosage,adverse effects Prognosis Pyrimidines/administration & dosage,adverse effects Reverse Transcriptase Polymerase Chain Reaction Treatment Outcome
Chemicals
Antineoplastic Agents Benzamides Piperazines Pyrimidines Imatinib Mesylate Fusion Proteins, bcr-abl
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Jabbour Elias
Department of Leukemia, University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.
Kantarjian Hagop M
Jones Dan
Shan Jenny
O'Brien Susan
Reddy Neeli
Wierda William G
Faderl Stefan
Garcia-Manero Guillermo
Verstovsek Srdan
Rios Mary Beth
Cortes Jorge
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Article Info
Journal
Blood
Abbr.
Blood
ISSN
1528-0020
Published
2009-03-05
Epub
2008-00-05
Pages
2154-60
Language
English
Region
United States
NLM ID
7603509
PMCID
PMC4081392
Subset
IM
Grants
NCI NIH HHS · P30 CA016672 · United States
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