Screening for Coronary Artery Disease in Cancer Survivors: JACC: CardioOncology State-of-the-Art Review
- PMID: 36875910
- PMCID: PMC9982229
- DOI: 10.1016/j.jaccao.2022.12.007
Screening for Coronary Artery Disease in Cancer Survivors: JACC: CardioOncology State-of-the-Art Review
Abstract
Coronary artery disease (CAD) is an important contributor to the cardiovascular burden in cancer survivors. This review identifies features that could help guide decisions about the benefit of screening to assess the risk or presence of subclinical CAD. Screening may be appropriate in selected survivors based on risk factors and inflammatory burden. In cancer survivors who have undergone genetic testing, polygenic risk scores and clonal hematopoiesis markers may become useful CAD risk prediction tools in the future. The type of cancer (especially breast, hematological, gastrointestinal, and genitourinary) and the nature of treatment (radiotherapy, platinum agents, fluorouracil, hormonal therapy, tyrosine kinase inhibitors, endothelial growth factor inhibitors, and immune checkpoint inhibitors) are also important in determining risk. Therapeutic implications of positive screening include lifestyle and atherosclerosis interventions, and in specific instances, revascularization may be indicated.
Keywords: ACS, acute coronary syndrome; AYA, adolescent and young adult; CAC, coronary artery calcium; CAD, coronary artery disease; CHIP, clonal hematopoiesis of indeterminate potential; CMR, cardiac magnetic resonance; CTA, computed tomography angiography; CVD, cardiovascular disease; IGF, insulin-like growth factor; LDL, low-density lipoprotein; PCE, pooled cohort equations; PCI, percutaneous coronary intervention; PRS, polygenic risk score; ROS, reactive oxygen species; TKI, tyrosine kinase inhibitor; VEGF, vascular endothelial growth factor; calcification; coronary artery calcium; coronary artery disease; prevention; risk factor; risk prediction.
© 2023 Published by Elsevier on behalf of the American College of Cardiology Foundation.
Conflict of interest statement
Dr Marwick was supported by an Investigator grant from the National Health and Medical Research Council, Canberra, Australia (No. 2008129). Dr Thavendiranathan was supported by the Canadian Institutes of Health Research New Investigator Award (No. 147814), the Ontario Early Research Award, and a Canada Research Chair in Cardio-Oncology. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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