Biomarker conversion from primary breast cancer to synchronous axillary lymph node metastasis and neoadjuvant therapy response: a single-center analysis
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Summary
This summary is machine-generated.Biomarker profiles (ER, PR, HER2, Ki67) differ between primary breast cancer and lymph node metastases. This receptor discordance impacts neoadjuvant therapy response, particularly for hormone receptor-positive cases.
Area Of Science
- Oncology
- Breast Cancer Research
- Biomarker Discovery
Background
- Biomarker characteristics like estrogen receptor (ER), progesterone receptor (PR), HER2, and Ki67 are crucial for predicting breast cancer treatment sensitivity.
- Understanding receptor status in both primary tumors and metastatic sites is essential for tailoring neoadjuvant therapy.
Purpose Of The Study
- To compare immunohistochemical profiles (ER, PR, HER2, Ki67) between primary breast tumors and synchronous axillary lymph node metastases.
- To investigate the impact of receptor discordance on response to neoadjuvant therapy in breast cancer patients.
Main Methods
- Retrospective study of 358 breast cancer patients with synchronous axillary lymph node metastasis treated with neoadjuvant therapy.
- Analysis of clinicopathologic data, focusing on receptor status (ER, PR, HER2, Ki67) in primary and metastatic lesions.
Main Results
- Discordance in ER, PR, HER2, and Ki67 expression was observed in 5.9%, 8.7%, 12.6%, and 17.3% of patients, respectively.
- Hormone receptor (HR) discordance was more frequent with negative primary ER/PR status; HER2 discordance was more frequent with HER2-0/low primary status.
- Loss of HR-positivity correlated with better neoadjuvant chemotherapy response, while unstable HER2 status decreased pCR rates.
Conclusions
- Receptor discordance between primary breast tumors and axillary lymph node metastases exists before therapy.
- Current receptor instability has limited impact on neoadjuvant therapy choices but warrants further study with new treatments like ADCs.

