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Published on: May 16, 2020
Cardiotoxicity of molecular-targeted drug therapy
Duong L Le1, Huynh Cao1, Li-Xi Yang2
1St. Mary's Medical Center, San Francisco, CA, U.S.A.
Abstract:
Cardiotoxicity is a well-known side-effect described in patients receiving various antineoplastic agents. With the abundance of clinical research and a heavy focus on drug development over the past decade, there has been a major shift in the use of non-specific cytotoxic drugs to molecular-targeted drug therapy. However, as a result, it has become clear that these drugs have numerous adverse effects, both on-target and off-target. Small-molecule tyrosine kinase inhibitors and other molecular-targeted agents, including monoclonal antibodies, have been the primary agents associated with cardiotoxicity. As more molecular-targeted therapies are developed, early recognition and management of drug-related cardiotoxicity will be extremely important in order to reduce morbidity and mortality. Pre-treatment evaluation with a surface electrocardiogram, echocardiography, cardiac history, and comprehensive review of concomitant medications are the current mainstay of treatment. However, much is still unknown about the potential cardiotoxic side-effects of these drug and optimal management. In the present article, we aim to review the cardiovascular implications and related cardiotoxicities associated with molecular target-based chemotherapeutic agents, with special emphasis on hypertension, cardiac dysfunction, and QT prolongation. Their implication, mechanism, and management are discussed where possible.
Insights
Molecular-targeted cancer therapies can cause cardiotoxicity, affecting blood pressure and heart function. Early detection and management of these cardiovascular side effects are crucial for patient outcomes.
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- Antineoplastic agents are associated with cardiotoxicity.
- A shift from cytotoxic drugs to molecular-targeted therapies has revealed new adverse effects.
- Molecular-targeted agents, including tyrosine kinase inhibitors and monoclonal antibodies, are linked to cardiotoxicity.
Purpose of the Study:
- To review the cardiovascular implications of molecular target-based chemotherapeutic agents.
- To focus on hypertension, cardiac dysfunction, and QT prolongation.
- To discuss the implications, mechanisms, and management of drug-related cardiotoxicity.
Main Methods:
- Review of clinical research and drug development.
- Analysis of adverse effects of molecular-targeted therapies.
- Discussion of cardiovascular implications, mechanisms, and management.
Main Results:
- Molecular-targeted therapies present unique cardiotoxic risks.
- Hypertension, cardiac dysfunction, and QT prolongation are key concerns.
- Current management involves pre-treatment evaluation, but optimal strategies are still evolving.
Conclusions:
- Early recognition and management of cardiotoxicity are vital.
- Understanding the cardiovascular effects of novel therapies is essential.
- Further research is needed to optimize the management of drug-induced cardiotoxicity.
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