In the
context of modern cancer chemotherapeutics, cancer survivors are living longer
and being exposed to potential comorbidities related to non-cancer side effects
of such treatments. With close monitoring of cancer patients receiving
potentially cardiotoxic medical therapies, oncologists, and cardiologists alike
are identifying patients in both clinical and subclinical phases of
cardiovascular disease related to such chemotherapies. Specifically,
cardiotoxicity at the level of the myocardium and potential for the development
of heart failure are becoming a growing concern with increasing survival of
cancer patients. Traditional chemotherapeutic agents used commonly in the
treatment of breast cancer and hematologic malignancies, such as anthracyclines
and HER-2 antagonists, are well known to be associated with cardiovascular
sequelae. Patients often present without symptoms and an abnormal cardiac
imaging study performed as part of routine evaluation of patients receiving
cardiotoxic therapies. Additionally, patients can present with signs and
symptoms of cardiovascular disease months to years after receiving the
chemotherapies. As the understanding of the physiology underlying the various
cancers has grown, therapies have been developed that target specific molecules
that represent key aspects of physiologic pathways responsible for cancer
growth. Inhibition of these pathways, such as those involving tyrosine kinases,
has lead to the potential for cardiotoxicity as well. In view of the potential
cardiotoxicity of specific chemotherapies, there is a growing interest in
identifying patients who are at risk of cardiotoxicity prior to becoming
symptomatic or developing cardiotoxicity that may limit the use of potentially
life-saving chemotherapy agents. Serological markers and novel cardiac imaging
techniques have become the source of many investigations with the goal of
screening patients for pre-clinical cardiotoxicity. Additionally, studies have
been performed.
Source :
Cardiotoxicity of cancer
therapeutics: current issues in screening, prevention, and therapy. Sheppard RJ
(richard.sheppard@mcgill.ca),
Berger J, Sebag IA. Front Pharmacol. 2013;4:19.
Free
paper available at:
http://www.frontiersin.org/Pharmacology_of_Anti-Cancer_Drugs/10.3389/fphar.2013.00019/full
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