ArticleFrontiers in oncology2025
Comprehensive risk profiling and long-term cardiovascular toxicity in HER2-positive breast cancer patients treated with trastuzumab.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Review
- The mechanisms and therapeutic advances of interactions between breast cancer and cardiovascular diseases.Frontiers in pharmacology · 2026Review
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11 authors.
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Abstract
Objective: Trastuzumab-based therapy is a cornerstone for HER2-positive breast cancer but carries a risk of significant cardiotoxicity. This study aims to investigate the long-term incidence of cardiovascular adverse events (CVDs), identify a comprehensive set of risk factors, and develop a robust predictive model for trastuzumab-induced cardiotoxicity (TIC) in a well-characterized, single-center patient cohort. Methods: We retrospectively analyzed 600 HER2-positive breast cancer patients on trastuzumab-based regimens from 2018-2023. Patients were divided into CVD (n=100) and non-CVD (n=500) groups based on cardiotoxicity occurrence during a median 3.6-year follow-up. We analyzed baseline characteristics, treatment protocols, and serial monitoring data including ECG, NT-proBNP, LVEF, left ventricular global longitudinal strain (LVGLS), and cardiac biomarkers (creatine kinase (CK), CK-MB, and hs-cTnI). Results: The cumulative incidence of CVDs was 16.7%. Cardiotoxicity events included symptomatic heart failure (n=11), asymptomatic LVEF decline (n=51), significant LVGLS reduction (n=29), and significant arrhythmias (n=9). Significant baseline predictors of cardiotoxicity included age >60 years, pre-existing hyperlipidemia, and elevated NT-proBNP levels (p<0.05). Treatment with anthracycline-based chemotherapy and chest radiotherapy were also strongly associated with increased CVD risk. During follow-up, the CVD group exhibited a significantly greater decline in LVEF (baseline vs. follow-up: 64.1% vs. 48.8%) and LVGLS (-20.9% vs. -15.3%) compared to the non-CVD group (p<0.001). In multivariate logistic regression analysis, the strongest independent predictors for CVDs were a post-treatment LVEF decline >10% (OR 5.75, 95% CI 3.95-8.41), a post-treatment relative LVGLS decline >15% from baseline (OR 4.42, 95% CI 3.10-6.22), and elevated hs-cTnI (OR 4.10, 95% CI 2.91-5.74). A predictive model incorporating both baseline and on-treatment factors showed excellent discrimination (AUC = 0.88). Conclusion: Cardiotoxicity remains a major concern in long-term trastuzumab therapy. This single-center study highlights the critical importance of integrating baseline risk stratification with serial monitoring of advanced echocardiographic parameters like LVGLS and sensitive biomarkers like hs-cTnI. Our comprehensive predictive model offers a powerful tool for early identification of at-risk patients, guiding personalized surveillance and facilitating timely implementation of cardioprotective strategies to mitigate the risk of irreversible cardiac damage in this patient population.
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