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Updated: Oct 1, 2025

Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Prevention of chemotherapy-induced left ventricular dysfunction
Irma Bisceglia1, Maria Laura Canale2, Domenico Cartoni1
1UOSD Servizi Cardiologici Integrati (SCI), A.O. S. Camillo-Forlanini, Roma, Italy.
Preventing heart dysfunction from cancer drugs like anthracyclines and trastuzumab is crucial. Early risk assessment and managing heart health factors are key to effective cardioprotection strategies.
Area of Science:
- Cardio-oncology
- Cardiovascular Medicine
- Cancer Therapeutics
Background:
- Left ventricular dysfunction is a significant challenge in cardio-oncology, often induced by anthracyclines and/or trastuzumab.
- This cardiotoxicity can limit the survival benefits gained from cancer treatments.
- Current preventive strategies require refinement to effectively manage this risk.
Purpose of the Study:
- To review current strategies for preventing anthracycline and/or trastuzumab-induced left ventricular dysfunction.
- To emphasize the importance of baseline cardiovascular risk assessment and management.
- To highlight the need for identifying high-risk populations and genetically predisposed individuals for targeted cardioprotection.
Main Methods:
- Review of existing oncology strategies for mitigating cardiotoxicity, including dose limitation and specific drug formulations.
- Evaluation of the evidence for preventive use of medications such as ACE inhibitors, sartans, and beta-blockers.
- Discussion of baseline cardiovascular risk assessment and management of modifiable risk factors.
Main Results:
- Certain oncology strategies (dose limitation, dexrazoxane, liposomal formulations) can reduce anthracycline cardiotoxicity.
- Preventive use of ACE inhibitors, sartans, and beta-blockers has shown limited clinical relevance for left ventricular ejection fraction decline.
- Baseline cardiovascular risk assessment and control of modifiable factors are essential primary prevention steps.
Conclusions:
- Effective prevention of cancer therapy-induced cardiotoxicity requires a multi-faceted approach.
- Identifying high-risk and genetically susceptible patients is crucial for implementing timely and appropriate cardioprotective therapies.
- Further research is needed to optimize preventive strategies in cardio-oncology.
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