Cardiac toxicity of ErbB2-targeted therapies: what do we know?

Edith A Perez1

  • 1Division of Hematology/Oncology, Mayo Clinic, Jacksonville, FL 32224, USA. perez.edith@mayo.edu

Clinical Breast Cancer
|September 10, 2008
PubMed

Insights

Trastuzumab and lapatinib, ErbB2-targeted therapies, show significant benefits in ErbB2-positive cancers but carry risks of cardiac toxicity. Careful monitoring is crucial for managing potential heart problems in patients.

Area of Science:

  • Cardiology
  • Oncology
  • Pharmacology

Background:

  • Trastuzumab, an ErbB2-targeted monoclonal antibody, was the first biologic agent associated with cardiac toxicity, particularly when combined with anthracyclines.
  • The ErbB2 receptor's presence on cardiomyocytes suggests a role in cardiac function, and its blockade may impair this protective effect.
  • While anthracycline toxicity is dose-dependent and causes myocardial changes, trastuzumab-induced cardiac dysfunction is generally reversible and not cumulative.

Purpose of the Study:

  • To review the cardiac toxicity associated with ErbB2-targeted therapies, including trastuzumab and lapatinib.
  • To assess the incidence and characteristics of cardiac events in patients receiving these agents.
  • To highlight the importance of cardiac monitoring and risk management strategies for ErbB2-targeted treatments.

Main Methods:

  • Analysis of pivotal trials and comprehensive safety data from clinical trials involving trastuzumab and lapatinib.
  • Review of incidence rates for serious cardiac events, congestive heart failure (CHF), and left ventricular ejection fraction (LVEF) declines.
  • Examination of the relationship between ErbB2-targeted therapy and cardiac dysfunction.

Main Results:

  • Trastuzumab, used in adjuvant settings for ErbB2-positive breast cancer, significantly improves survival, with CHF incidence ranging from 0.4%-3.8%.
  • In lapatinib trials (3558 participants), LVEF declines occurred in 1.6% of patients, and symptomatic CHF in 0.2%.
  • Risk factors for cardiac dysfunction with ErbB2-targeted therapy are under investigation.

Conclusions:

  • ErbB2-targeted therapies like trastuzumab and lapatinib offer substantial benefits in ErbB2-positive cancers but require careful cardiac monitoring.
  • Understanding and mitigating cardiac risks are essential for optimizing patient outcomes.
  • Despite potential cardiac toxicity, the overall impact of ErbB2-targeted agents on patient survival has been dramatically positive.

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