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Anti-VEGF Therapy-Induced Accelerated Atherosclerosis: STEMI in a Young Adult
Stefano H Byer1, Aditya Ravindra2, Alex Cuskey3
1Department of Internal Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
JACC. Case Reports
|August 1, 2025
Summary
Long-term bevacizumab therapy can accelerate atherosclerosis in young patients by impairing endothelial function and causing hyperlipidemia. Vigilance for cardiovascular complications and proactive risk factor management are essential.
Area of Science:
- Cardiovascular Medicine
- Oncology
- Pharmacology
Background:
- Bevacizumab, an antiangiogenic monoclonal antibody, is used for central nervous system malignancies to manage cerebral edema.
- Long-term bevacizumab use is associated with potential cardiovascular risks, including endothelial dysfunction and hyperlipidemia.
Observation:
- A young patient with neurofibromatosis type 2 on long-term bevacizumab experienced ventricular fibrillation arrest due to myocardial infarction.
- Angiography revealed coronary artery disease, suggesting bevacizumab-induced endothelial injury and hyperlipidemia as contributing factors.
Findings:
- Bevacizumab therapy may accelerate the development of coronary atherosclerosis.
- Nitric oxide pathway disruption and proteinuria-induced dyslipidemia are key mechanisms involved.
Implications:
- This case highlights the critical need for monitoring cardiovascular health in patients receiving long-term bevacizumab.
- Early detection of atherosclerosis and aggressive management of lipid levels and blood pressure are crucial for mitigating risks.
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