Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors Journal Article


Authors: Steingart, R. M.; Bakris, G. L.; Chen, H. X.; Chen, M. H.; Force, T.; Ivy, S. P.; Leier, C. V.; Liu, G.; Lenihan, D.; Lindenfeld, J.; Maitland, M. L.; Remick, S. C.; Tang, W. H. W.
Article Title: Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors
Abstract: Background: Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarction. As the use of vascular endothelial growth factor signaling pathway (VSP) inhibitors broadens to include older patients and those with existing cardiovascular disease, the adverse effects are likely to be more frequent, and cardiologists will increasingly be enlisted to help oncologists manage patients who develop adverse cardiovascular effects. Methods: The Cardiovascular Toxicities Panel of the National Cancer Institute reviewed the published literature and abstracts from major meetings, shared experience gained during clinical development of VSP inhibitors, and contributed extensive clinical experience in evaluating and treating patients with cancer with cardiovascular disease. This report was edited and approved by the National Cancer Institute Investigational Drug Steering Committee. It presents the panel's expert opinion on the current clinical use and future investigation for safer, more expansive use of these drugs. Results and Conclusions: The panel recommends that physicians (1) conduct and document a formal risk assessment for existing cardiovascular disease and potential cardiovascular complications before VSP inhibitor treatment recognizing that preexisting hypertension and cardiovascular disease are common in patients with cancer, (2) actively monitor for blood pressure elevations and cardiac toxicity with more frequent assessments during the first treatment cycle, and (3) aggressively manage blood pressure elevations and early symptoms and signs of cardiac toxicity to prevent clinically limiting complications of VSP inhibitor therapy. © 2012 Mosby, Inc. All rights reserved.
Keywords: signal transduction; epidermal growth factor; sorafenib; bevacizumab; sunitinib; drug withdrawal; heart left ventricle failure; hypertension; nonhuman; side effect; antineoplastic agents; neoplasms; incidence; qt prolongation; risk factors; practice guideline; vasculotropin inhibitor; cancer therapy; risk assessment; drug mechanism; cardiovascular disease; cerebrovascular disease; heart failure; heart infarction; thromboembolism; cardiovascular diseases; cardiotoxicity; cardiovascular system; pazopanib; vandetanib; disease management; heart arrhythmia; hyperthyroidism; hypothyroidism; brain ischemia; rifampicin; congestive heart failure; heart muscle ischemia; world health; torsade des pointes; blood pressure monitoring; heart ejection fraction; acute coronary syndrome
Journal Title: American Heart Journal
Volume: 163
Issue: 2
ISSN: 0002-8703
Publisher: Mosby Elsevier  
Date Published: 2012-02-01
Start Page: 156
End Page: 163
Language: English
DOI: 10.1016/j.ahj.2011.10.018
PROVIDER: scopus
PUBMED: 22305831
DOI/URL:
Notes: --- - "Export Date: 1 March 2012" - "CODEN: AHJOA" - "Source: Scopus"
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  1. Richard M Steingart
    174 Steingart