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Updated: Jun 1, 2026

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Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Sorafenib-associated multivessel coronary artery vasospasm
T Naib1, R M Steingart, C L Chen
1Division of Cardiology, Memorial Sloan-Kettering Cancer Center, New York, USA.
Herz
|May 18, 2011
Summary
Vascular endothelial growth factor pathway inhibitors (VSP) can cause cardiotoxicity. This study reports the first case of sorafenib-induced multivessel coronary vasospasm, a reversible side effect.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Cancer therapies increasingly utilize VEGF signaling pathway inhibitors (VSP).
- These inhibitors target VEGFRs and other kinases crucial for vascular and myocardial homeostasis.
- Hypertension is a common side effect, but VSP-related myocardial ischemia is poorly understood.
Observation:
- A 57-year-old patient with hepatocellular carcinoma developed multivessel coronary vasospasm.
- The patient was undergoing treatment with sorafenib, a tyrosine kinase inhibitor.
- Coronary vasospasm resolved upon administration of nitroglycerin.
Findings:
- This is the first reported case of sorafenib-associated multivessel coronary vasospasm.
- Sorafenib, a VSP inhibitor, can induce coronary artery vasospasm.
- The vasospastic event was reversible with medical intervention.
Implications:
- Highlights a potential mechanism for cardiotoxicity with VSP inhibitors.
- Suggests the need for vigilance regarding coronary vasospasm in patients receiving sorafenib.
- Warrants further investigation into the mechanisms of VSP inhibitor-induced cardiovascular events.
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