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J. Clin. Med. 2014, 3(4), 1466-1489; doi:10.3390/jcm3041466

Targeted Therapy of FLT3 in Treatment of AML—Current Status and Future Directions

1
Center for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Bergen N-5020, Norway
2
Department of Internal Medicine, Hematology Section, Haukeland University Hospital, Bergen N-5021, Norway
*
Author to whom correspondence should be addressed.
Received: 21 September 2014 / Revised: 27 November 2014 / Accepted: 28 November 2014 / Published: 15 December 2014
(This article belongs to the Special Issue AML in the Molecular Age: From Biology to Clinical Management)
View Full-Text   |   Download PDF [203 KB, uploaded 15 December 2014]

Abstract

Internal tandem duplications (ITDs) of the gene encoding the Fms-Like Tyrosine kinase-3 (FLT3) receptor are present in approximately 25% of patients with acute myeloid leukemia (AML). The mutation is associated with poor prognosis, and the aberrant protein product has been hypothesized as an attractive therapeutic target. Various tyrosine kinase inhibitors (TKIs) have been developed targeting FLT3, but in spite of initial optimism the first generation TKIs tested in clinical studies generally induce only partial and transient hematological responses. The limited treatment efficacy generally observed may be explained by numerous factors; extensively pretreated and high risk cohorts, suboptimal pharmacodynamic and pharmacokinetic properties of the compounds, acquired TKI resistance, or the possible fact that inhibition of mutated FLT3 alone is not sufficient to avoid disease progression. The second-generation agent quizartinb is showing promising outcomes and seems better tolerated and with less toxic effects than traditional chemotherapeutic agents. Therefore, new generations of TKIs might be feasible for use in combination therapy or in a salvage setting in selected patients. Here, we sum up experiences so far, and we discuss the future outlook of targeting dysregulated FLT3 signaling in the treatment of AML. View Full-Text
Keywords: acute myeloid leukemia; FLT3; tyrosine kinase inhibitors; clinical trials acute myeloid leukemia; FLT3; tyrosine kinase inhibitors; clinical trials
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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MDPI and ACS Style

Engen, C.B.N.; Wergeland, L.; Skavland, J.; Gjertsen, B.T. Targeted Therapy of FLT3 in Treatment of AML—Current Status and Future Directions. J. Clin. Med. 2014, 3, 1466-1489.

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