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Ischaemic heart disease in patients with cancer
Pietro Ameri1,2, Edoardo Bertero2,3, Marco Lombardi2,4
1Cardiovascular Disease Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Insights
Cancer patients increasingly face ischaemic heart disease (IHD). Shared risk factors, cancer treatments, and social determinants contribute to this complex relationship, demanding tailored management strategies.
Area of Science:
- Cardio-oncology
- Cardiovascular disease
- Cancer survivorship
Background:
- Cardiovascular (CV) risk factors like hypercholesterolaemia and obesity contribute to both ischaemic heart disease (IHD) and cancer.
- Systemic inflammation, potentially fueled by clonal hematopoiesis, links IHD and cancer development.
- Anticancer therapies can cause cardiotoxicity, leading to IHD in cancer patients.
Observation:
- Cancer patients with IHD present unique management challenges, including atypical symptoms and increased risks.
- Decisions regarding coronary revascularization and antithrombotic therapy require careful consideration of individual patient factors.
- Social determinants of health significantly influence the interplay between IHD and cancer outcomes.
Findings:
- Established CV risk factors and systemic inflammation are key contributors to the IHD-cancer link.
- IHD and cancer can mutually promote each other's progression.
- Cancer therapies pose a risk for developing IHD.
Implications:
- There is a critical need for more clinical trial data to guide the management of IHD in cancer patients.
- Multidisciplinary collaboration between cardio-oncology, cardiology, and oncology is essential.
- Personalized treatment strategies are necessary due to limited evidence and complex patient profiles.
Abstract:
Cardiologists are encountering a growing number of cancer patients with ischaemic heart disease (IHD). Several factors account for the interrelationship between these two conditions, in addition to improving survival rates in the cancer population. Established cardiovascular (CV) risk factors, such as hypercholesterolaemia and obesity, predispose to both IHD and cancer, through specific mechanisms and via low-grade, systemic inflammation. This latter is also fuelled by clonal haematopoiesis of indeterminate potential. Furthermore, experimental work indicates that IHD and cancer can promote one another, and the CV or metabolic toxicity of anticancer therapies can lead to IHD. The connections between IHD and cancer are reinforced by social determinants of health, non-medical factors that modify health outcomes and comprise individual and societal domains, including economic stability, educational and healthcare access and quality, neighbourhood and built environment, and social and community context. Management of IHD in cancer patients is often challenging, due to atypical presentation, increased bleeding and ischaemic risk, and worse outcomes as compared to patients without cancer. The decision to proceed with coronary revascularization and the choice of antithrombotic therapy can be difficult, particularly in patients with chronic coronary syndromes, necessitating multidisciplinary discussion that considers both general guidelines and specific features on a case by case basis. Randomized controlled trial evidence in cancer patients is very limited and there is urgent need for more data to inform clinical practice. Therefore, coexistence of IHD and cancer raises important scientific and practical questions that call for collaborative efforts from the cardio-oncology, cardiology, and oncology communities.
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