Key result
In a contemporary cohort of women with breast cancer, 53% had multiple cardiovascular risk factors, and over 2.5 years, 3% developed left ventricular dysfunction and 2% experienced other cardiovascular events.
Why the study?
Women with breast cancer face heightened cardiovascular disease risk, but cardiologic assessment is mostly limited to detecting left ventricular dysfunction cardiotoxicity from anticancer therapies.
Cohort (n=508)
No
Women with breast cancer exhibit a high burden of cardiovascular risk factors and experience cardiovascular events beyond just treatment-induced left ventricular dysfunction, highlighting the importance of baseline cardio-oncology evaluation.
Broader CV assessment in BC patients may be warranted; leaves open optimal management strategies pending prospective data.
Background: Women with breast cancer (BC) represent a special population particularly exposed to cardiovascular disease (CVD) risk. However, cardiologic assessment in BC is mostly limited to detection of left ventricular dysfunction cardiotoxicity (LVD-CTX) due to anticancer treatments. Our aim was to comprehensively investigate CV profile and events in a contemporary BC cohort. Methods and Results: Records of BC patients referred for a Cardio-Oncologic evaluation before starting anticancer treatments, between 2016 and 2019, were retrospectively reviewed (n = 508). Information regarding prevalence and control of CV risk factors, and novel CVD diagnoses were extracted. Occurrence of LVD-CTX, CV events other than LVD-CTX and mortality was assessed. Mean age of study population was 64 ± 13 years; 287 patients were scheduled to receive anthracycline and 165 anti-HER2 therapy. Overall, 53% of BC women had ≥2 CV risk factors, and 67% had at least one of arterial hypertension, dyslipidaemia or diabetes mellitus not adequately controlled. Eighteen (4%) patients were diagnosed a previously unknown CVD. Over a mean follow-up of 2.5 ± 1 years, 3% of BC patients developed LVD-CTX, 2% suffered from other CV events and 11% died. CV risk factors were not associated with LVD-CTX, except for family history of CAD. On the contrary, patients with other CV events exhibited a worse CV profile. Those who died more commonly experienced CV events other than LVD-CTX (p = 0.02). Conclusions: BC women show a suboptimal CV risk profile and are at risk of CV events not limited to LVD-CTX. A baseline Cardio-Oncologic evaluation was instrumental to implement CV prevention and to optimize CV therapies.
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Tini et al. (2021) conducted a cohort in Breast cancer (n=508). Baseline cardiovascular risk profile and anticancer treatments was evaluated on Incidence of left ventricular dysfunction (LVD) cardiotoxicity. In a contemporary cohort of women with breast cancer, 53% had multiple cardiovascular risk factors, and over 2.5 years, 3% developed left ventricular dysfunction and 2% experienced other cardiovascular events.
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