Skip to search boxSkip to navigationSkip to main content

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

  • Elias Jabbour(corresponding author)
    ,
  • Hagop M. Kantarjian
    ,
  • Dan Jones
    ,
  • Jenny Shan
    ,
  • Susan O'Brien
    ,
  • Neeli Reddy
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

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.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2154-2160 (7 pages)

Journal (Volume, Issue Number)

Blood (Volume 113, Issue 10)

Publication milestones

  • Published - 03/05/2009

Publication status

Published - 03/05/2009

ISSN

0006-4971

Publication IDs

  • Scopus: 64049099666
  • PubMed: 19060245
  • ORCID: /0000-0002-8636-1071/work/68811387

Publication metrics

Metrics

Fractional count
1
Fractional count
0.08
Fractional count
11
Fractional count
0.92
Fractional count
1
Fractional count
1
SciVal
FWCI
5.48
SciVal
Author count
12
SciVal
citations
115
SciVal
Paper percentile
96
SciVal
Top percentile
5
Scopus
citations

PlumX, opens in new tab

Captures
56
Citation count
131

Funding Details

FunderFunding number
NCI
P30CA016672