Cardiac dysfunction induced by novel targeted anticancer therapy: an emerging issue

Curr Cardiol Rep. 2009 May;11(3):167-74. doi: 10.1007/s11886-009-0025-9.

Abstract

Increasing use of targeted anticancer agents that inhibit tyrosine kinase signaling (monoclonal antibodies or tyrosine kinase inhibitors) has dramatically improved the survival of patients with malignancies. However, cardiotoxicity, including heart failure, left ventricular dysfunction, hypertension, myocardial infarction, and thromboembolism, has occurred. Importantly, these cardiotoxicities are at least partially reversible and responsive to medical management. Early recognition of cardiovascular side effects is vital to allow long-term, continuous therapy with these life-prolonging agents. This article reviews potential cardiovascular side effects of frequently used inhibitors of tyrosine kinase activity (eg, trastuzumab, sunitinib) and discusses the diagnosis and management of cardiotoxicity associated with targeted therapy.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / adverse effects*
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / therapeutic use
  • Benzenesulfonates / adverse effects
  • Benzenesulfonates / therapeutic use
  • Dose-Response Relationship, Drug
  • Drug Delivery Systems
  • Female
  • Heart / drug effects
  • Heart Diseases / chemically induced*
  • Heart Diseases / mortality*
  • Heart Diseases / physiopathology
  • Heart Failure / chemically induced
  • Heart Failure / mortality
  • Heart Failure / physiopathology
  • Humans
  • Indoles / adverse effects
  • Indoles / therapeutic use
  • Male
  • Neoplasms / drug therapy
  • Neoplasms / pathology
  • Niacinamide / analogs & derivatives
  • Phenylurea Compounds
  • Prognosis
  • Protein Kinase Inhibitors / adverse effects*
  • Protein Kinase Inhibitors / therapeutic use
  • Pyridines / adverse effects
  • Pyridines / therapeutic use
  • Pyrroles / adverse effects
  • Pyrroles / therapeutic use
  • Risk Assessment
  • Sorafenib
  • Sunitinib
  • Survival Analysis
  • Trastuzumab

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Benzenesulfonates
  • Indoles
  • Phenylurea Compounds
  • Protein Kinase Inhibitors
  • Pyridines
  • Pyrroles
  • Niacinamide
  • Sorafenib
  • Trastuzumab
  • Sunitinib