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New treatment for acute myelogenous leukemia

*Corresponding author for this work
  • University of Texas MD Anderson Cancer Center
Scholary Output:
Contribution to journal
Review article
Peer-review

Abstract

Introduction: Acute myelogenous leukemia (AML) is a genetically heterogeneous disease. Yet current therapy has changed little over the decades and includes the nucleoside analog cytarabine in combination with an anthracycline as primary therapy. With this approach, durable cures occur in the minority of patients. With the recent improved scientific understanding of the underlying genetic and epigenetic aberrations in AML, there is now the potential of individualized and targeted therapeutic approaches for the curative treatment of AML.

Areas covered: The focus of this article is to review the therapeutic potential of many of the novel agents currently under investigation in the treatment of acute myeloid leukemia. The results of pivotal Phase III studies, as well as ongoing Phase II and III studies and selected Phase I studies with impact on the field of AML therapy will be discussed.

Expert opinion: Advances in the scientific knowledge of the various genetic and epigenetic alterations in AML, in conjunction with more effective, rationally designed and/or novel targeted therapeutics, offers a real hope and expectation of improved AML outcomes in the future.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 95-106 (12 pages)

Journal (Volume, Issue Number)

Expert Opinion on Pharmacotherapy (Volume 16, Issue 1)

Publication milestones

  • Published - 01/01/2015

Publication status

Published - 01/01/2015

ISSN

1465-6566

Publication IDs

  • Scopus: 84917708460
  • PubMed: 25480777

Publication metrics

Metrics

SciVal
citations
23
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
1.21
SciVal
Author count
2
SciVal
Paper percentile
85

PlumX, opens in new tab

Captures
35
Citation count
28

Funding Details

FunderFunding number
NCI
P30CA016672