Navigating cancer therapy induced cardiotoxicity: From pathophysiology to treatment innovations

[Display omitted] Every year, more than a million people in the United States undergo chemotherapy or radiation therapy for cancer, as estimated by the CDC. While chemotherapy has been an instrumental tool for treating cancer, it also causes severe adverse effects. The more commonly acknowledged adv...

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Veröffentlicht in:Advanced drug delivery reviews 2024-08, Vol.211, p.115361, Article 115361
Hauptverfasser: Tetterton-Kellner, Jessica, Jensen, Brian C., Nguyen, Juliane
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] Every year, more than a million people in the United States undergo chemotherapy or radiation therapy for cancer, as estimated by the CDC. While chemotherapy has been an instrumental tool for treating cancer, it also causes severe adverse effects. The more commonly acknowledged adverse effects include hair loss, fatigue, and nausea, but a more severe and longer lasting side effect is cardiotoxicity. Cardiotoxicity, or heart damage, is a common complication of cancer treatments. It can range from mild to severe, and it can affect some patients temporarily or others permanently, even after they are cured of cancer. Dexrazoxane is the only FDA-approved drug for treating anthracycline induced cardiotoxicity, but it also has drawbacks and adverse effects. There is no other type of chemotherapy induced cardiotoxicity that has an approved treatment option. In this review, we discuss the pathophysiology of chemotherapeutic-induced cardiotoxicity, methods and guidelines of diagnosis, methods of treatment and mitigation, and current drug delivery approaches in therapeutic development.
ISSN:0169-409X
1872-8294
1872-8294
DOI:10.1016/j.addr.2024.115361