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Updated: Jul 16, 2025

Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Disparities in cardio-oncology: Implication of angiogenesis, inflammation, and chemotherapy
Carlos D Vera1, Agustín Rodríguez López2, Alex S Ewaneewane3
1Stanford Cardiovascular Institute, Stanford School of Medicine, Stanford, CA, USA.
Abstract:
Cancers and cardiovascular diseases are the top two causes of death in the United States. Over the past decades, novel therapies have slowed the cancer mortality rate, yet cardiac failures have risen due to the toxicity of cancer treatments. The mechanisms behind this relationship are poorly understood and it is crucial that we properly treat patients at risk of developing cardiac failure in response to cancer treatments. Currently, we rely on early-stage biomarkers of inflammation and angiogenesis to detect cardiotoxicity before it becomes irreversible. Identification of such biomarkers allows healthcare professionals to decrease the adverse effects of cancer therapies. Angiogenesis and inflammation have a systemic influence on the heart and vasculature following cancer therapy. In the field of cardio-oncology, there has been a recent emphasis on gender and racial disparities in cardiotoxicity and the impact of these disparities on disease outcomes, but there is a scarcity of data on how cardiotoxicity varies across diverse populations. Here, we will discuss how current markers of angiogenesis and inflammation induced by cancer therapy are related to disparities in cardiovascular health.
Insights
Cancer treatments can cause heart failure, a serious side effect. New research explores how inflammation and angiogenesis markers relate to cardiovascular health disparities in patients undergoing cancer therapy.
Area of Science:
- Cardio-oncology
- Cardiovascular disease
- Cancer therapy
Background:
- Cancer and cardiovascular diseases are leading causes of death in the US.
- Cancer treatments, while improving survival, increase cardiac failure risk.
- Mechanisms linking cancer treatments to cardiotoxicity are poorly understood.
Purpose of the Study:
- To discuss how current biomarkers of inflammation and angiogenesis relate to cardiovascular health disparities.
- To highlight the need for better understanding of cardiotoxicity in diverse populations.
- To address the impact of gender and racial disparities in cardio-oncology.
Main Methods:
- Review of current literature on cardiotoxicity biomarkers.
- Analysis of the role of inflammation and angiogenesis in cancer treatment-related cardiac dysfunction.
- Examination of existing data on gender and racial disparities in cardiotoxicity.
Main Results:
- Biomarkers of inflammation and angiogenesis are used to detect cardiotoxicity early.
- Cancer therapies can induce systemic effects on the heart and vasculature.
- There is a significant gap in data regarding cardiotoxicity variations across diverse populations.
Conclusions:
- Early detection of cardiotoxicity through biomarkers like inflammation and angiogenesis is crucial.
- Addressing gender and racial disparities in cardiotoxicity is an emerging focus in cardio-oncology.
- Further research is needed to understand and mitigate cardiotoxicity in diverse patient groups.
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