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Published on: June 18, 2013
Cardiotoxicity of HER2-targeted therapies
Robert S Copeland-Halperin1, Jennifer E Liu2,3, Anthony F Yu2,3
1Mount Sinai Heart, Mount Sinai Medical Center.
Purpose Of Review:
Cardiotoxicity is a well recognized adverse effect of human epidermal growth factor receptor 2 (HER2)-targeted therapies. The goal of this review is to highlight recent studies that have advanced our knowledge of the diagnosis, prevention, and management of cardiotoxicity associated with HER2-targeted agents.
Recent Findings:
Several clinical risk factors for cardiotoxicity associated with HER2-targeted therapies have been identified including age, low-baseline left ventricular ejection fraction, and treatment with anthracyclines; however, these remain insufficient to identify all patients at risk for cardiotoxicity. Routine cardiac monitoring remains the standard for cardiotoxicity surveillance, although the optimal frequency and modality of monitoring remains uncertain. Global longitudinal strain, T1/T2 weighted CMR imaging protocols, and circulating biomarkers can detect early signs of cardiotoxicity, but studies are needed to investigate whether use of these markers in clinical practice improves patient outcomes. Cardioprotective medications (e.g. beta-blockers or ACE-inhibitors) may be of benefit to patients at increased risk for cardiotoxicity from HER2-taregeted therapies, particularly those who are treated with an anthracycline-containing regimen.
Summary:
Improved risk stratification of patients during HER2-targeted therapy and effective prevention and management strategies for cardiotoxicity are needed to enhance the value of longitudinal cardiac monitoring and increase cardiac safety so that optimal breast cancer treatment can be delivered.
Insights
Cardiotoxicity from human epidermal growth factor receptor 2 (HER2)-targeted therapies requires better risk assessment. Recent studies explore improved diagnosis, prevention, and management strategies for cardiac safety during HER2-targeted cancer treatment.
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- Cardiotoxicity is a known adverse effect of HER2-targeted therapies.
- Identifying all at-risk patients using current clinical factors remains challenging.
Purpose of the Study:
- To review recent advancements in diagnosing, preventing, and managing cardiotoxicity from HER2-targeted agents.
- To highlight the need for improved risk stratification and cardiac safety measures.
Main Methods:
- Review of recent clinical studies and research.
- Analysis of risk factors, cardiac monitoring techniques, and cardioprotective strategies.
Main Results:
- Clinical risk factors (age, low ejection fraction, anthracyclines) are insufficient for comprehensive risk identification.
- Novel monitoring tools like strain imaging and biomarkers show promise but require outcome-based validation.
- Cardioprotective medications may benefit high-risk patients, especially those on anthracyclines.
Conclusions:
- Enhanced risk stratification is crucial for optimizing HER2-targeted therapy.
- Further research is needed to integrate new monitoring tools and confirm the efficacy of cardioprotective strategies.
- Improving cardiac safety ensures the delivery of optimal breast cancer treatment.
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