Key result
Adjuvant pegylated liposomal doxorubicin linked to ~25% better overall survival versus epirubicin.
Why the study?
Anthracycline-based regimens are standard adjuvant therapy for early-stage breast cancer but cause cumulative cardiotoxicity, prompting comparison of pegylated liposomal doxorubicin and epirubicin.
Does pegylated liposomal doxorubicin improve overall survival compared to epirubicin in women with early-stage, HER2-negative breast cancer?
Cohort (n=1,050)
Yes
Does pegylated liposomal doxorubicin improve overall survival compared to epirubicin in women with early-stage, HER2-negative breast cancer?
Hazard Ratio: 0.754 (95% CI 0.632–0.899)
p-value: p=<0.001
Adjuvant pegylated liposomal doxorubicin is associated with improved overall survival without increased cardiotoxicity compared to epirubicin in early-stage HER2-negative breast cancer.
May support liposomal doxorubicin in early HER2-negative breast cancer; leaves open randomized confirmation of survival benefit.
Purpose: Anthracycline-based regimens are a cornerstone of adjuvant therapy for early-stage breast cancer but are limited by cumulative cardiotoxicity. This study compared the effectiveness and cardiotoxicity of pegylated liposomal doxorubicin (Lipo-Dox) and epirubicin in women with early-stage, HER2-negative breast cancer using nationwide real-world data from Taiwan. Patients and Methods: This population-based retrospective cohort study used Taiwan’s National Health Insurance Research Database to identify adult women with stage I–III, HER2-negative breast cancer treated with adjuvant anthracycline-based chemotherapy between 2006 and 2018. Propensity score matching (1:1) was performed to balance baseline characteristics, resulting in 1050 matched patients with a median follow-up of 6.05 years. Overall survival (OS), disease-free survival (DFS), and cardiotoxicity were analyzed using Cox proportional hazards models and Kaplan–Meier methods. Results: Compared with epirubicin, Lipo-Dox was associated with significantly improved overall survival (adjusted hazard ratio 0.754, 95% CI 0.632– 0.899; P < 0.001). Survival benefits were consistent across 3-year, 5-year, and full follow-up analyses and demonstrated a dose-dependent relationship. Kaplan–Meier curves confirmed superior overall survival in the Lipo-Dox group (log-rank P < 0.001). No significant differences were observed between the two groups in disease-free survival or clinically diagnosed cardiac events. Conclusion: In this nationwide propensity score–matched cohort, adjuvant Lipo-Dox was associated with sustained overall survival benefits without increased cardiotoxic risk compared with epirubicin. Lipo-Dox may represent a favorable anthracycline alternative, particularly for patients with cardiovascular comorbidities or elevated cardiotoxicity risk.
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Chen et al. (2026) conducted a cohort in Early-stage, HER2-negative breast cancer (n=1,050). Pegylated liposomal doxorubicin (Lipo-Dox) vs. Epirubicin was evaluated on Overall survival (HR 0.754, 95% CI 0.632-0.899, p=<0.001). Adjuvant pegylated liposomal doxorubicin was associated with significantly improved overall survival compared with epirubicin (HR 0.754; 95% CI 0.632-0.899; P<0.001).
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