Abstract

Purpose
The main purpose of this study is to explore the predictive value of HER3 expression level and PIK3CA mutation for the efficacy of neoadjuvant therapy in HER2 positive breast cancer patients. Material and Methods The clinicopathological data of HER2 positive non-specific invasive breast cancer patients who received neoadjuvant treatment in the Second Affiliated Hospital of Anhui Medical University from June 2017 to June 2024 were retrospectively analyzed. The correlation between HER3 expression level detected by immunohistochemistry and PIK3CA gene mutation detected by ARMS-PCR and pathological complete response rate (pCR) was analyzed.
Results
Among 51 patients, 29 (56.86%) had positive HER3 expression, 15 (29.41%) had PIK3CA mutation, and 19 (37.25%) had pCR. The expression level of HER3 was correlated with the pCR rate (χ2=7.905, p=0.019). The PIK3CA mutation status was not correlated with the pCR rate (χ2=0.140, p=0.708). The HER3 expression level combined with PIK3CA mutation status affected the pCR rate (p=0.036). Multivariable regression further identified HER3 positivity as an independent negative predictor of pCR (OR=0.08, 95% CI: 0.01–0.50, p=0.008), underscoring its role in therapeutic resistance.
Conclusion
HER3 expression may serve as a critical biomarker for guiding therapeutic strategies in HER2-positive breast cancer patients. The combinatorial effect of HER3 overexpression and PIK3CA mutations may exacerbate therapeutic resistance, while dual-targeted strategies against the HER3/PI3K pathway could potentially improve clinical outcomes in treatment-resistant populations.

• Keywords: Breast neoplasms, HER3, PIK3CA, Neoadjuvant therapy, Therapeutic uses, Pathological Complete Response