Key result
Anthracyclines and HER2-targeted therapies define distinct treatment patterns in breast cancer-related cardiac dysfunction.
Why the study?
Data on the incidence of cancer therapy-related cardiac dysfunction (CTRCD) in contemporary breast cancer populations treated with anthracycline and HER2-targeted therapy remain limited, and the cardiovascular risk associated with HFA-ICOS risk categories is uncertain.
Does the HFA-ICOS risk assessment tool accurately stratify the risk of subsequent cancer therapy-related cardiac dysfunction (CTRCD) in women undergoing anthracycline or HER2-targeted therapy for breast cancer?
Observational (n=515)
Does the HFA-ICOS risk assessment tool accurately stratify the risk of subsequent cancer therapy-related cardiac dysfunction (CTRCD) in women undergoing anthracycline or HER2-targeted therapy for breast cancer?
The CARE study is a large prospective registry designed to systematically evaluate the real-world incidence of CTRCD and validate the HFA-ICOS cardio-oncology risk stratification tool in contemporary breast cancer patients.
Therapy patterns and low baseline risks described in breast cancer; leaves open HFA-ICOS tool performance for CTRCD prediction.
Background Anthracycline and Human Epidermal Growth Factor Receptor 2 (HER2) targeted therapy may induce cancer therapy-related cardiac dysfunction (CTRCD). Current guidelines recommend risk stratification using the Heart Failure Association–International Cardio-Oncology Society (HFA-ICOS) risk assessment tool. However, data on the incidence of CTRCD in contemporary breast cancer populations treated according to current standard-of-care regimens remain limited. Moreover, the actual cardiovascular risk associated with the HFA-ICOS risk categories in breast cancer treatment remains uncertain. Real-world evaluation of whether this consensus-based stratification appropriately separates patients according to subsequent CTRCD risk has been highlighted as a key research priority. Purpose Overall, the study aims to determine the incidence of CTRCD and to evaluate cardiovascular risk stratification using the HFA-ICOS tool and its association with subsequent CTRCD. Methods CARE is a prospective observational study including women scheduled for (neo)adjuvant anthracycline therapy and/or HER2-targeted therapy. Echocardiography, using standard and novel echocardiographic parameters, and circulating cardiac biomarkers were assessed at baseline (visit 1), after completion of scheduled therapy (visit 2), and 12 months after completion of scheduled therapy (visit 3). Participants were categorized into three treatment regimen groups: 1) Anthracycline therapy only, 2) HER2-targeted therapy only, and 3) HER2-targeted therapy sequentially to anthracyclines (Figure 1). The primary outcome is incidence of CTRCD. Secondary outcomes include HFA-ICOS risk stratification in relation to subsequent CTRCD. Results In total, 515 women (median age (Q1,Q3): 53 (45,64) years) were included. Overall, 335 (63%) participants received anthracycline therapy only, 100 (15%) received HER2-targeted therapy only, and 80 (19%) received anthracycline therapy followed by HER2-targeted therapy. Baseline cardiovascular risk factors included hypertension in 20%, current smoking in 13%, diabetes in 7%, and a history of heart disease in 7.6%, while 3.5% had received previous anti-cancer treatment (Table 1). Conclusion The CARE study is a large prospective observational cardio-oncology study evaluating the incidence of CTRCD after contemporary breast cancer therapy regimens. With systematic echocardiographic and biomarker assessment, the study will provide important insights into the incidence of CTRCD, the performance of the HFA-ICOS risk stratification tool and follow-up strategies in routine cardio-oncology care.
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Vinje et al. (2026) conducted an observational in Breast cancer (n=515). Anthracycline and/or HER2-targeted therapy was evaluated on Incidence of cancer therapy-related cardiac dysfunction (CTRCD). Among 515 women enrolled to evaluate cancer therapy-related cardiac dysfunction, 63% were scheduled for anthracyclines only, 15% HER2-targeted therapy only, and 19% received both.
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