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Cardioprotection of High-Risk Individuals
Jenica N Upshaw1, Sharanya Mohanty1, Akash Rastogi1
1Division of Cardiology, Tufts Medical Center, 800 Washington St, Boston, MA 02111, USA.
Insights
Identifying high-risk patients is key for effective cardioprotective strategies. Dexrazoxane and other therapies may protect anthracycline-treated patients from heart failure, while managing cardiovascular disease is crucial for all cancer patients.
Area of Science:
- Cardiology and Oncology
- Cancer Therapeutics
- Cardiovascular Risk Management
Background:
- Cardiotoxicity is a significant concern with cancer therapies.
- Identifying patients at high risk for cardiac events is crucial for effective intervention.
- Pre-existing cardiovascular disease (CVD) is a known risk factor for cardiotoxicity.
Purpose of the Study:
- To review cardioprotective strategies for cancer patients.
- To identify specific therapies beneficial for high-risk populations.
- To discuss the role of managing cardiovascular disease in mitigating cardiotoxicity.
Main Methods:
- Literature review of cardioprotective strategies.
- Analysis of risk factors for cardiac events in cancer patients.
- Evaluation of specific drug classes and treatment modalities.
Main Results:
- Dexrazoxane, liposomal formulations, continuous infusions, and neurohormonal antagonists show promise for cardioprotection in anthracycline-treated patients.
- Prevalent CVD is a risk factor for cardiac events with anthracyclines, anti-HER2 therapy, radiation, and BCR-Abl inhibitors.
- Evidence for cardioprotection in non-anthracycline therapies is limited, but risk factor optimization is recommended.
Conclusions:
- Targeted cardioprotective strategies can maximize benefits for high-risk cancer patients.
- Proactive management of cardiovascular disease and risk factors is essential for all cancer patients undergoing therapy.
- Further research is needed to establish cardioprotective guidelines for non-anthracycline cancer treatments.
Abstract:
Targeting cardioprotective strategies to patients at the highest risk for cardiac events can help maximize therapeutic benefits. Dexrazoxane, liposomal formulations, continuous infusions, and neurohormonal antagonists may be useful for cardioprotection for anthracycline-treated patients at the highest risk for heart failure. Prevalent cardiovascular disease is a risk factor for cardiac events with many cancer therapies, including anthracyclines, anti-human-epidermal growth factor receptor-2 therapy, radiation, and BCR-Abl tyrosine kinase inhibitors, and may be a risk factor for cardiac events with other therapies. Although evidence for cardioprotective strategies is sparse for nonanthracycline therapies, optimizing cardiac risk factors and prevalent cardiovascular disease may improve outcomes.
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