Evaluating the role of HER2-low versus HER2-0 status in predicting response to neoadjuvant chemotherapy in hormone receptor-positive breast cancer
Abstract
Objectives: The classification of human epidermal growth factor receptor 2 (HER2)-low breast cancer has gained clinical relevance following the success of antibody-drug conjugates in this subgroup. However, its prognostic and predictive role, particularly in hormone receptor-positive (HR+) early breast cancer treated with neoadjuvant chemotherapy (NACT), remains unclear. This study aimed to evaluate the impact of HER2-low versus HER2-0 status on pathological complete response (pCR) and disease-free survival (DFS) in HR+ breast cancer patients undergoing NACT.
Methods: A total of 216 HR+ and HER2-negative early breast cancer patients treated with NACT at Tokat Gaziosmanpasa University Hospital between January 2014 and January 2024 were retrospectively analyzed. HER2-low was defined as IHC 1+ or 2+ without gene amplification by FISH. pCR was assessed via the Miller-Payne grading system. Survival analyses were conducted using the Kaplan-Meier method; multivariate analyses were performed using Cox regression.
Results: Of the 216 patients, 30 (13.9%) achieved pCR. There was no statistically significant difference in pCR (P=0.83) or DFS (P=0.12) between HER2-0 and HER2-low groups. However, patients with ER <10% had significantly higher pCR rates (P=0.005). Achieving pCR was associated with longer DFS (P=0.045).
Conclusions: HER2-0 and HER2-low subgroups exhibited similar responses to NACT in HR+ breast cancer. Low ER expression was independently associated with higher pCR. Larger prospective studies are warranted to further define the biological and clinical implications of HER2 expression levels in early-stage HR+ breast cancer.
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Ethical Statement
References
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Details
Primary Language
English
Subjects
Chemotherapy
Journal Section
Research Article
Early Pub Date
August 6, 2025
Publication Date
September 4, 2025
Submission Date
May 22, 2025
Acceptance Date
August 1, 2025
Published in Issue
Year 2025 Volume: 11 Number: 5