Key result
Cancer therapy-related cardiac dysfunction affects ~33% of treated breast cancer patients, with marked LVEF decline.
Why the study?
Cardiovascular toxicity related to cancer therapies is a major concern in breast cancer management, with limited data from North African populations and scarce access to structured cardio-oncology services in low- and middle-income countries.
Cohort (n=150)
No
In a North African cohort of breast cancer patients, one-third developed cancer therapy-related cardiac dysfunction, highlighting a critical need for structured cardio-oncology screening and management programs in the region.
Background Cardiovascular toxicity related to cancer therapies has become a major concern in breast cancer management, particularly in low- and middle-income countries where access to structured cardio-oncology services remains limited. Data from North African populations are scarce despite potential regional specificities in cardiovascular risk profiles, cancer characteristics, and treatment patterns. This study aimed to describe the cardio-oncological profile of breast cancer patients followed in a North African tertiary center. Methods We conducted a prospective descriptive study including breast cancer patients referred to a dedicated cardio-oncology clinic between January 1, 2023 and June 30, 2025. Clinical, oncological, and cardiovascular data were collected from medical records. Variables included demographic characteristics, cardiovascular risk factors, cancer stage, oncological treatments, baseline and follow-up cardiac function, and treatment-related cardiotoxicity. Cancer therapy–related cardiac dysfunction (CTRCD) was defined according to current international guidelines. Results A total of 150 patients were included, with a mean age of 58 ± 12.6 years; all patients were female. At baseline, the most prevalent cardiovascular risk factors were hypertension (47.3%), dyslipidemia (29.3%), and diabetes (26.7%). Regarding cancer characteristics, 26.7% of patients had locally advanced or metastatic disease. The main oncological treatments received were trastuzumab (58.6%), anthracyclines (44.6%), radiotherapy (43.3%), taxanes (17.3%), pertuzumab (14.6%), and alkylating agents (13.3%). Only two patients received immunotherapy and nine received hormone therapy. At baseline, mean left ventricular ejection fraction (LVEF) was 60.1% ± 7.8% and mean global longitudinal strain (GLS) was –19.2% ± 3.1%. During follow-up, CTRCD occurred in 33.3% of patients. Echocardiographic reassessment demonstrated a significant decline in systolic function, with mean LVEF decreasing to 52.9% ± 9.1% (p < 0.001) and mean GLS worsening to –17.3% ± 3.1% (p = 0.001). Cardio-protective therapy was prescribed in all cases of cardiotoxicity. Conclusion This study provides one of the first comprehensive descriptions of cardio-oncological profiles in breast cancer patients from North Africa. The high prevalence of cardiovascular risk factors and treatment-related cardiac dysfunction underscores the need for structured cardio-oncology programs in the region. Larger studies with longer follow-up are required to better characterize long-term cardiovascular outcomes and optimize preventive strategies.
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Elelmi et al. (2026) conducted a cohort in Breast cancer (n=150). Cancer therapies (including trastuzumab, anthracyclines, radiotherapy) was evaluated on Cancer therapy-related cardiac dysfunction (CTRCD). Among breast cancer patients receiving oncological therapies, cancer therapy-related cardiac dysfunction occurred in 33.3%, with mean LVEF significantly decreasing to 52.9% (p<0.001).
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