Key result
Anthracyclines linked to a ~4% drop in left atrial reservoir strain, predicting early subclinical cardiotoxicity.
Why the study?
Anthracycline-based breast cancer chemotherapy can cause acute, subacute, or chronic cardiac complications, with most cardiotoxicity signs being subclinical.
Does anthracycline-based chemotherapy reduce left atrial strain in patients with breast cancer, and does ACEI pretreatment offer protection?
Cohort (n=94)
Blinded offline analysis
No
Does anthracycline-based chemotherapy reduce left atrial strain in patients with breast cancer, and does ACEI pretreatment offer protection?
Left atrial strain is significantly reduced early after anthracycline therapy in breast cancer patients, and ACE inhibitor use may attenuate this subclinical cardiotoxicity.
Answers are grounded in this paper and cite their sources.
Supports left atrial strain monitoring for early anthracycline cardiotoxicity detection; leaves open ACE inhibitor protection pending prospective trials.
Background Cancer breast is the most common malignancy worldwide in females and is commonly treated using regimens based on anthracycline therapy. Cardiac complications related to breast cancer treatment using chemotherapy can manifest as either acute, subacute, or chronic dysfunction of the heart. Most of the signs of cardiotoxicity are subclinical. Our study aimed to evaluate left atrial strain (LAS) changes before and after anthracycline-based therapy in patients with breast cancer. One hundred and twenty patients with invasive breast cancer stages I–III eligible to receive anthracycline-based chemotherapy were enrolled in the study. We used doxorubicin 60 mg/m 2 plus cyclophosphamide 600 mg/m 2 every three weeks for 3–4 cycles. Every patient completed at least two echocardiograms: baseline and after each chemotherapy cycle. Results We initially enrolled 120 patients in this observational cohort prospective study. Twenty-six patients were excluded. All LAS measures were significantly reduced at follow-up with a significant positive correlation with left ventricular global longitudinal strain. 56.4% of our patients were hypertensive, and 81% of hypertensive patients received angiotensin-converting enzyme inhibitors (ACEI). The subgroup of patients who received ACEI for treatment of HTN had a lower rate of left atrial strain changes following anthracycline therapy compared with non-ACEI-treated patients, either hypertensive or not. Conclusion We concluded that LAS deteriorated usually after anthracycline treatment, and it predicted early chemotherapy-induced cardiotoxicity.
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Mokadem et al. (2025) conducted a cohort in Breast cancer (n=94). Anthracycline-based chemotherapy vs. Baseline (pre-chemotherapy) was evaluated on Left atrial reservoir strain (LASr) (p=<0.001). Anthracycline-based chemotherapy significantly reduced left atrial reservoir strain from 39.31% to 37.59% in patients with breast cancer, serving as an early predictor of subclinical cardiotoxicity.
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