Cardiac toxicity of ErbB2-targeted therapies: what do we know?
1Division of Hematology/Oncology, Mayo Clinic, Jacksonville, FL 32224, USA. perez.edith@mayo.edu
Abstract:
The potential for cardiac toxicity in association with targeted biologic agents was first observed with trastuzumab, a monoclonal antibody that targets the ErbB2/HER2 receptor. In the pivotal trial of trastuzumab in ErbB2-positive metastatic cancer, an increased incidence of serious cardiac events was observed, particularly when trastuzumab was administered in combination with anthracyclines. The ErbB2 receptor is expressed on cardiomyocytes, in addition to tumor tissue, where it exerts a protective effect on cardiac function; thus, interference with ErbB2-signaling may block this protective effect. However, in contrast to anthracycline-induced cardiac toxicity, trastuzumab-related cardiac dysfunction does not appear to increase with cumulative dose or to be associated with ultrastructural changes in the myocardium and is generally reversible. When used in adjuvant regimens for the treatment of ErbB2-positive early-stage breast cancer, trastuzumab has been shown to significantly improve disease-free and overall survival. The incidence of class III/IV congestive heart failure (CHF) ranged from 0.4%-3.8% in the major adjuvant trastuzumab trials. More recently, small-molecule tyrosine kinase inhibitors such as lapatinib have been investigated for the treatment of ErbB2-positive metastatic breast cancer. In a comprehensive analysis of cardiac safety data from all lapatinib trials completed to date, which included 3558 healthy volunteers and patients with a variety of solid cancers on 43 trials, the overall incidence of left ventricular ejection fraction declines was 1.6%, with 0.2% of patients experiencing symptomatic CHF. Risk factors that might predict for cardiac dysfunction with ErbB2-targeted therapy are actively under investigation and will aid in the identification of at-risk populations and in the development of strategies for risk minimization in the future. It is important to note that, while careful cardiac monitoring is required for all patients receiving ErbB2-targeted therapy in any disease setting, the overall impact of these agents on the outcomes of patients with ErbB2-positive breast cancer has been dramatic and positive.
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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