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Retrospective analysis identifies risk factors for trastuzumab-induced cardiotoxicity in HER2-positive breast cancer patients

Retrospective analysis identifies risk factors for trastuzumab-induced cardiotoxicity in HER2-positi…
Photo by Dmytro Vynohradov / Unsplash
Key Takeaway
Recognize age, hypertension, anthracycline, NT-proBNP, and LVEF as risk factors for trastuzumab-induced cardiotoxicity.

This retrospective analysis evaluated 298 patients with HER2-positive breast cancer receiving trastuzumab therapy. The study aimed to identify predictors of trastuzumab-induced cardiotoxicity within this specific patient cohort. The investigation focused on clinical and baseline characteristics associated with the primary outcome.

Five independent risk factors were identified in the analysis. Age ≥60 years was an independent risk factor with an odds ratio of 1.97 (95%CI: 1.21–3.22). History of hypertension was an independent risk factor with an odds ratio of 2.10 (95%CI: 1.24–3.56). Combined anthracycline therapy was an independent risk factor with an odds ratio of 3.06 (95%CI: 1.67–5.62). Baseline NT-proBNP ≥200 pg/ml was an independent risk factor with an odds ratio of 2.34 (95%CI: 1.35–4.05). Baseline LVEF ≤55% was an independent risk factor with an odds ratio of 2.51 (95%CI: 1.42–4.43). These associations highlight specific patient subgroups at higher risk.

The primary adverse event monitored was cardiotoxicity. Follow-up duration was not reported in the provided data. No limitations were listed in the source data. The practice relevance suggests these findings may enable risk stratification before trastuzumab initiation. Clinicians should interpret these associations cautiously given the retrospective design and lack of reported limitations. Further prospective data may clarify these relationships.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
To analyze the risk factors for cardiotoxicity induced by trastuzumab in human epidermal growth factor receptor 2 (HER2) -positive breast cancer patients and provide a basis for early clinical intervention. A retrospective analysis was conducted on 298 HER2-positive breast cancer patients treated with trastuzumab. Clinical data including age, history of cardiovascular disease, combined chemotherapy regimens, N-terminal pro-brain natriuretic peptide (NT-proBNP) levels, and baseline left ventricular ejection fraction (LVEF) were collected. Multivariate logistic regression was used to identify independent risk factors for cardiotoxicity. A total of 65 patients (21.8%) developed cardiotoxicity. Multivariate analysis showed that age ≥60 years (OR = 1.97, 95%CI: 1.21–3.22), history of hypertension (OR = 2.10, 95%CI: 1.24–3.56), combined anthracycline therapy (OR = 3.06, 95%CI: 1.67–5.62), baseline NT-proBNP ≥200 pg/ml (OR = 2.34, 95%CI: 1.35–4.05), and baseline LVEF ≤55% (OR = 2.51, 95%CI: 1.42–4.43) were independent risk factors for trastuzumab-induced cardiotoxicity (all P < 0.05). These findings enable risk stratification before trastuzumab initiation. Future research should validate a predictive model incorporating these factors and assess cardioprotective strategies, thereby translating risk assessment into actionable protocols to optimize cardiac safety without compromising oncologic outcomes.
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