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Panobinostat for the treatment of multiple myeloma: the evidence to date

Authors Bailey H, Stenehjem DD, Sharma S

Received 21 June 2015

Accepted for publication 17 August 2015

Published 8 October 2015 Volume 2015:6 Pages 269—276

DOI https://doi.org/10.2147/JBM.S69140

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Marek Witold Radomski

Peer reviewer comments 3

Editor who approved publication: Dr Martin H. Bluth

Hanna Bailey,1 David D Stenehjem,1,2 Sunil Sharma1

1Huntsman Cancer Institute, 2Department of Pharmacotherapy, Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, UT, USA

Abstract: Multiple myeloma is a malignancy involving plasma cell proliferation within the bone marrow. Survival of patients diagnosed with myeloma has significantly improved in the last decade, following the approval of novel agents. Despite great strides achieved in the management of multiple myeloma, it is still considered an incurable disease as the majority of patients relapse after initiation of therapy. Additionally, the duration of response generally decreases with an increasing number of therapy lines. The need to overcome resistance to therapy dictates research into more potent agents and those with novel mechanisms of action. A therapeutic option for relapsed/refractory myeloma includes histone deacetylase inhibition. Various histone deacetylase inhibitors, including the newly approved panobinostat, are currently under evaluation in this setting. Panobinostat for multiple myeloma is used in combination with other potent therapeutic agents, such as proteasome inhibitors and steroids. Ongoing research evaluating other panobinostat-containing regimens will provide additional insight into its place in myeloma management.

Keywords: panobinostat, LBH589, multiple myeloma, relapsed, HDAC inhibitor

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