Key result
Higher Charlson comorbidity index is linked to ~20% greater CTRCD risk in breast cancer patients.
Why the study?
Increasing cardiovascular events in cancer patients highlight the importance of identifying preexisting risk factors as predictors of cancer therapy-related cardiac dysfunction during cardiotoxic treatment.
What are the predictive risk factors for cancer therapy-related cardiac dysfunction in female breast cancer patients treated with anthracyclines and/or anti-HER-2 therapies?
Cohort (n=161)
No
What are the predictive risk factors for cancer therapy-related cardiac dysfunction in female breast cancer patients treated with anthracyclines and/or anti-HER-2 therapies?
Hazard Ratio: 1.2 (95% CI 1–1.4)
In female breast cancer patients receiving anthracyclines or anti-HER2 therapies, baseline comorbidities and LVEF are independent predictors of cancer therapy-related cardiac dysfunction.
May inform risk stratification in breast cancer; leaves open prospective validation before guiding practice.
IntroductionThe increasing cardiovascular events in cancer patients underscore the importance of identifying preexisting risk factors as predictors of heart disease outcomes. This study aimed to assess the predictive risk factors associated with cancer therapy-related cardiac dysfunction (CTRCD) in female patients with breast cancer undergoing treatment with anthracyclines and/or anti-HER-2 therapies.MethodsA cohort study was conducted at a university hospital outpatient clinic from 2019 to 2024. CTRCD was defined according to the European Society of Cardiology criteria as an absolute LVEF reduction of >10 percentage points to <50% during treatment.ResultsA total of 161 female patients were analyzed (mean age: 51.2 ± 11.6 years), with most being white/Caucasian (83.8%). The most prevalent cardiovascular risk factors were hypertension (47.2%), obesity (31.7%), smoking (31.0%), dyslipidemia (14.3%), and type 2 diabetes mellitus (12.4%). CTRCD occurred in 18 patients (11.1%), with a markedly higher prevalence (27.3%) in those with four or more cardiovascular risk factors. The median time (IQR) from the initiation of chemotherapy to CTRCD was 395 (248-674) days. Multivariable analysis identified the Charlson comorbidity index (HR 1.2; 95% CI: 1.0-1.4), chemotherapy duration (HR 1.0; 95%CI: 1.0-1.0) and LVEF before (HR 0.8; 95%CI: 0.7-0.9) and after chemotherapy (HR 0.8; 95%CI: 0.8-0.9) as independent factors for CTRCD. Breast cancer patients had a 17.7% risk of developing CTRCD within the first two years of antineoplastic treatment.ConclusionHypertension, obesity, and smoking were the most prevalent cardiovascular risk factors. Independent predictors of CTRCD included the Charlson comorbidity index, chemotherapy duration, and LVEF before and after treatment.
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Machado et al. (2025) conducted a cohort in Breast cancer (n=161). Charlson comorbidity index was evaluated on Cancer therapy-related cardiac dysfunction (CTRCD) (HR 1.2, 95% CI 1.0-1.4). The Charlson comorbidity index (HR 1.2; 95% CI 1.0-1.4), chemotherapy duration, and LVEF were independent predictors of cancer therapy-related cardiac dysfunction in female breast cancer patients.
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