Case Report: Pazopanib-induced acute coronary syndrome.

Front Cardiovasc Med

Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States.

Published: September 2024

AI Article Synopsis

  • Pazopanib, a medication used for certain cancers, may pose a risk of acute coronary syndrome (ACS), but its direct link to heart issues hasn't been definitively established.
  • A 65-year-old woman with metastatic leiomyosarcoma experienced ACS after being on pazopanib for 8 months, and prior tests showed only mild coronary artery disease.
  • This case emphasizes the need for careful heart risk assessments for patients taking pazopanib, considering the potential for serious cardiovascular complications.

Article Abstract

Introduction: Pazopanib is a tyrosine kinase inhibitor approved for the treatment of metastatic renal cell carcinoma and advanced soft-tissue sarcoma that functions by inhibiting vascular endothelial growth factor receptors. Although the package insert and current cardio-oncology guidelines indicate a risk of acute coronary syndrome (ACS) associated with pazopanib, the causative role of pazopanib in arterial thrombosis is unclear due to a lack of focused coronary disease evaluation in oncological clinical trials prior to pazopanib initiation. Herein we present an antecedent ischemic evaluation of a patient who was prescribed pazopanib to demonstrate the first reported case of ACS directly attributable to pazopanib.

Case Description: A 65-year-old woman with metastatic leiomyosarcoma presented to the hospital with ACS. Pazopanib had been initiated 8 months prior, and an ischemic evaluation 6 weeks prior to hospitalization indicated mild coronary artery disease (CAD). Emergent cardiac catheterization revealed a large thrombotic occlusion of the mid-left anterior descending coronary artery involving the secondary diagonal artery, which was treated with manual aspiration thrombectomy. Pazopanib was discontinued, and the patient was discharged from the hospital 12 days later.

Discussion: Although pazopanib is associated with ACS, there is a lack of definitive data supporting this association. This case-based demonstration of pazopanib-induced ACS provides a discrete clinical example of this phenomenon. The patient's minimal atherosclerotic burden 6 weeks prior to her presentation for ACS strongly suggests causality attributable to pazopanib. Given the increased risk for ischemic heart disease, careful attention and an individualized risk assessment for CAD should be provided to patients who are prescribed pazopanib.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11458525PMC
http://dx.doi.org/10.3389/fcvm.2024.1466395DOI Listing

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