Proteasome Inhibitors as a Potential Cause of Heart Failure

Heart Fail Clin. 2017 Apr;13(2):289-295. doi: 10.1016/j.hfc.2016.12.001.

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.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / therapeutic use
  • Boron Compounds / adverse effects
  • Boron Compounds / therapeutic use
  • Bortezomib / adverse effects
  • Bortezomib / therapeutic use
  • Clinical Trials as Topic
  • Drug Approval
  • Early Diagnosis
  • Glycine / adverse effects
  • Glycine / analogs & derivatives
  • Glycine / therapeutic use
  • Heart Failure / chemically induced*
  • Heart Failure / diagnosis
  • Humans
  • Meta-Analysis as Topic
  • Multiple Myeloma / complications
  • Multiple Myeloma / drug therapy*
  • Oligopeptides / adverse effects
  • Oligopeptides / therapeutic use
  • Proteasome Inhibitors / adverse effects*
  • Proteasome Inhibitors / therapeutic use

Substances

  • Antineoplastic Agents
  • Boron Compounds
  • Oligopeptides
  • Proteasome Inhibitors
  • Bortezomib
  • ixazomib
  • carfilzomib
  • Glycine