Literature DB >> 26297284

Decitabine and Sorafenib Therapy in FLT-3 ITD-Mutant Acute Myeloid Leukemia.

Monica R Muppidi1, Scott Portwood2, Elizabeth A Griffiths2, James E Thompson2, Laurie A Ford2, Craig W Freyer3, Meir Wetzler2, Eunice S Wang2.   

Abstract

BACKGROUND: Acute myeloid leukemia (AML) characterized by Feline McDonough Sarcoma-like tyrosine kinase-3 (FLT-3) internal tandem duplication (ITD) mutations have poor outcomes. Treatment options are limited, because these mutations confer resistance to conventional chemotherapy. FLT-3 inhibitors such as sorafenib have been studied as a single agent and in combination with conventional chemotherapy or azacytidine with fair responses. PATIENTS AND METHODS: Here we describe our preclinical and clinical experience with the combination of the DNA hypomethylating agent, decitabine and sorafenib for the treatment of FLT-3 ITD-mutant AML.
RESULTS: In vitro treatment of the human FLT-3 ITD-mutant AML cell line, MV4-11, with both drugs significantly improved growth inhibition over single-agent therapy and resulted in synergistic antitumor effects (combination index < 1). A case series of 6 patients treated with off protocol combination of decitabine and sorafenib demonstrated overall responses in 5 patients (83%) with a median survival of 155 days. Four of the 5 patients (80%) with relapsed/refractory AML achieved complete responses with incomplete count recovery. The combination was also well tolerated.
CONCLUSION: Further investigation is warranted to confirm these responses.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Combination therapy; FLT-3 inhibitors; Hypomethylating agents; Targeted agents

Mesh:

Substances:

Year:  2015        PMID: 26297284     DOI: 10.1016/j.clml.2015.02.033

Source DB:  PubMed          Journal:  Clin Lymphoma Myeloma Leuk        ISSN: 2152-2669


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