Abstract

Cancer therapies have been evolving from conventional chemotherapeutics to targeted agents. This has fulfilled the hope of greater efficacy but unfortunatelynot ofgreater safety. In fact, a broad spectrum of toxicities can be seenwith targeted therapies, including cardiovascular toxicities. Among these, cardiomyopathy and heart failure have received greatest attention, given their profound implications for continuation of cancer therapies and cardiovascular morbidity and mortality. Prediction of risk has always posed a challengeand even more so with the newer targeted agents. The merits ofaccurate risk prediction, however, are very evident, e.g. facilitating treatmentdecisions even before the first dose is given. This is important for agents with a long half-life and high potential to induced life-threatening cardiac complications, such as myocarditis with immune checkpoint inhibitors. An opportunity to address these needs in the field of cardio-oncology is provided by the expanding repertoire of "-omics" and other tools in precision medicineand their integration in a systems biology approach. This may allow fornew insights into patho-mechanisms and the creation of more precise and cost-effective risk prediction toolswith the ultimate goals of improved therapy decisions and prevention of cardiovascular complications. Herein, we explore this topic as a future approach to translating the complexity of cardio-oncology to the reality of patient care.

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