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- W1684140257 endingPage "133" @default.
- W1684140257 startingPage "133" @default.
- W1684140257 abstract "Recognition and management of treatment-related cardiovascular toxicity, defined as either an acute cardiac event or a chronic condition, has been tightly integrated into routine cancer care and has become an important component in treatment selection. Several chemotherapeutic agents, such as anthracyclines, are traditionally characterized as cardiotoxic, but cardiovascular adverse events are also associated with commonly used molecular targeted therapies. In the past decade, bevacizumab, a monoclonal humanized antibody against vascular endothelial growth factor, has been introduced in the treatment of a variety of metastatic malignancies. Despite its efficacy, bevacizumab has been associated with significant risk of cardiovascular complications, such as hypertension, cardiac ischemia, and congestive heart failure. This review will focus on the cardiovascular toxicity of bevacizumab, providing the latest evidence on the incidence, clinical spectrum, risk factors, and responsible mechanisms." @default.
- W1684140257 created "2016-06-24" @default.
- W1684140257 creator A5003736175 @default.
- W1684140257 creator A5014087122 @default.
- W1684140257 creator A5060243325 @default.
- W1684140257 creator A5087963010 @default.
- W1684140257 date "2015-06-01" @default.
- W1684140257 modified "2023-10-09" @default.
- W1684140257 title "Cancer therapy and cardiovascular risk: focus on bevacizumab" @default.
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