Cardio-Oncology: mechanisms of cardiovascular toxicity
- PMID: 29399333
- PMCID: PMC5785712
- DOI: 10.12688/f1000research.12598.1
Cardio-Oncology: mechanisms of cardiovascular toxicity
Abstract
The therapeutic options available to treat a wide range of malignancies are rapidly increasing. At the same time, the population being treated is aging with more cardiovascular risk factors, comorbid conditions, and associated poor cardiac reserve. Both traditional chemotherapeutic agents (for example, anthracyclines) and newer therapies (for example, targeted tyrosine kinase inhibitors and immune checkpoint inhibitors) have demonstrated profound cardiovascular toxicities. It is important to understand the mechanisms of these toxicities to establish strategies for the prevention and management of complications-arrhythmias, heart failure, and even death. In the first of this two-part review series, we focus on what is known and hypothesized about the mechanisms of cardiovascular toxicity from anthracyclines, HER2/ErbB2 inhibitors, immune checkpoint inhibitors, and vascular endothelial growth factor inhibitors.
Keywords: HER2/ErbB2 inhibitors; anthracyclines; cardio-oncology; cardiovascular toxicity; immune checkpoint inhibitors.
Conflict of interest statement
No competing interests were disclosed.No competing interests were disclosed.No competing interests were disclosed.
References
-
- Murphy SL, Xu J, Kochanek KD: Deaths: final data for 2010. Natl Vital Stat Rep. 2013;61(4):1–117. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous