Abstract
Proteasome inhibitors have become an important drug class in the treatment of multiple myeloma. In addition to its role in myeloma cells, the proteasome plays a critical role in the myocardium, particularly in the context of cardiac stress. The growing awareness of the cardiovascular toxicity of proteasome inhibitors is emerging following the phase 3 trials and the transition into real-world practice. This article reviews the background to this problem and the incidence of the problem in phase 3 trials and subsequent phase 2 trials in new patient cohorts and discusses the strategy to detect and manage this emerging problem.
Keywords:
Heart failure; Multiple myeloma; Myocardium; Proteasome inhibitors.
Copyright © 2016 Elsevier Inc. All rights reserved.
MeSH terms
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Antineoplastic Agents / adverse effects*
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Antineoplastic Agents / therapeutic use
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Boron Compounds / adverse effects
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Boron Compounds / therapeutic use
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Bortezomib / adverse effects
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Bortezomib / therapeutic use
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Clinical Trials as Topic
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Drug Approval
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Early Diagnosis
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Glycine / adverse effects
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Glycine / analogs & derivatives
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Glycine / therapeutic use
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Heart Failure / chemically induced*
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Heart Failure / diagnosis
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Humans
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Meta-Analysis as Topic
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Multiple Myeloma / complications
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Multiple Myeloma / drug therapy*
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Oligopeptides / adverse effects
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Oligopeptides / therapeutic use
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Proteasome Inhibitors / adverse effects*
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Proteasome Inhibitors / therapeutic use
Substances
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Antineoplastic Agents
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Boron Compounds
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Oligopeptides
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Proteasome Inhibitors
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Bortezomib
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ixazomib
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carfilzomib
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Glycine