Interactions between cardiology and oncology drugs in precision cardio-oncology

Author:

Kamaraju Sailaja1,Mohan Meera1,Zaharova Svetlana2,Wallace Brianna3,McGraw Joseph4,Lokken James4,Tierney John3,Weil Elizabeth5,Fatunde Olubadewa6,Brown Sherry-Ann2

Affiliation:

1. Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, WI, U.S.A.

2. Cardio-Oncology Program, Division of Cardiovascular Medicine, Medical College of Wisconsin, Milwaukee, WI, U.S.A.

3. School of Pharmacy, Medical College of Wisconsin, WI, U.S.A.

4. Department of Pharmacy, Concordia University, Milwaukee, WI, U.S.A.

5. Department of Pharmacy, Medical College of Wisconsin, WI, U.S.A.

6. Division of Cardiology, Department of Medicine, Mayo Clinic Arizona, Scottsdale, AZ, U.S.A.

Abstract

Abstract Recent advances in treatment have transformed the management of cancer. Despite these advances, cardiovascular disease remains a leading cause of death in cancer survivors. Cardio-oncology has recently evolved as a subspecialty to prevent, diagnose, and manage cardiovascular side effects of antineoplastic therapy. An emphasis on optimal management of comorbidities and close attention to drug interactions are important in cardio-oncologic care. With interdisciplinary collaboration among oncologists, cardiologists, and pharmacists, there is potential to prevent and reduce drug-related toxicities of treatments. The cytochrome P450 (CYP450) family of enzymes and the P-glycoprotein (P-g) transporter play a crucial role in drug metabolism and drug resistance. Here we discuss the role of CYP450 and P-g in drug interactions in the field of cardio-oncology, provide an overview of the cardiotoxicity of a spectrum of cancer agents, highlight the role of precision medicine, and encourage a multidisciplinary treatment approach for patients with cancer.

Publisher

Portland Press Ltd.

Subject

General Medicine

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