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Tyrosine kinase inhibition: A therapeutic target for the management of chronic-phase chronic myeloid leukemia

  • Elias J. Jabbour(corresponding author)
    ,
  • ,
  • Hagop M. Kantarjian
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Abstract

Chronic myeloid leukemia (CML) is a hematologic neoplasm with a progressive, ultimately terminal, disease course. In most cases, CML arises owing to the aberrant formation of a chimeric gene for a constitutively active tyrosine kinase. Inhibition of the signaling activity of this kinase has proved to be a highly successful treatment target, transforming the prognosis of patients with CML. New tyrosine kinase inhibitors continue to improve the management of CML, offering alternative options for those resistant to or intolerant of standard tyrosine kinase inhibitors. Here we review the pathobiology of CML and explore emerging strategies to optimize the management of chronic-phase CML, particularly first-line treatment.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1433-1452 (20 pages)

Journal (Volume, Issue Number)

Expert Review of Anticancer Therapy (Volume 13, Issue 12)

Publication milestones

  • Published - 2013

Publication status

Published - 2013

ISSN

1473-7140

Publication IDs

  • Scopus: 84888263504
  • PubMed: 24236822

Publication metrics

Metrics

SciVal
citations
17
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
FWCI
0.24
SciVal
Author count
3
SciVal
Paper percentile
77
Scopus
citations

PlumX, opens in new tab

Citation count
25
Captures
34

Funding Details

Medical writing support was provided by T Lonergan and J Ponting of Anthemis Consulting Ltd and was funded by Teva Pharmaceutical Industries, Frazer, PA, USA. Teva provided a single medical accuracy review of the final draft. The authors were not compensated and retained full editorial control over the content of the paper.
FundersFunding number
NCI
P30CA016672
Teva Pharmaceutical Industries Ltd.
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