Correlation between Androgen Receptor Expression in Luminal B (HER-2 Negative) Breast Cancer and Disease Outcomes.
Fan YangJiayi LiHong ZhangShuang ZhangJingming YeYuanjia ChengQian LiuLing XinHongyu XiangYinhua LiuXuening DuanLing XuPublished in: Journal of personalized medicine (2022)
(1) Background: Hormone receptor positive breast cancer is a subtype of breast cancer with relatively good prognosis, but luminal B (HER-2 negative) breast cancer has a higher risk of recurrence and metastasis. Patients with endocrine therapy resistance and chemotherapy insensitivity have poor prognosis. Androgen receptor (AR) is widely expressed in breast cancer, but there is no clear conclusion about its function and correlation with prognosis in luminal B breast cancer. Further research is needed to reveal the role of AR in luminal B (HER-2 negative) breast cancer. (2) Methods: Retrospectively analyzed patients with early-stage luminal B breast cancer. The correlation between AR and its associated indexes with long-term survival was determined. (3) Results: A total of 985 patients were included with 143 treated by neoadjuvant therapy. Of these, 83.5% of the patients had AR expression ≥65%. High AR expression was associated with good disease-free survival (DFS) and overall survival (OS). In the neoadjuvant population, AR/estrogen receptor (ER) > 1.06 and residual tumor Ki67 > 23% had significantly worse DFS. (4) Conclusion: Low AR (<65%) expression is associated with poor prognosis in luminal B (HER-2 negative) breast cancer patients. High AR/ER and residual tumor Ki67 were associated with poor DFS in neoadjuvant group with a cutoff value of AR/ER > 1.06 and residual tumor Ki67 > 23%.
Keyphrases
- poor prognosis
- long non coding rna
- estrogen receptor
- free survival
- early stage
- end stage renal disease
- newly diagnosed
- rectal cancer
- locally advanced
- ejection fraction
- lymph node
- chronic kidney disease
- positive breast cancer
- squamous cell carcinoma
- peritoneal dialysis
- stem cells
- patient reported outcomes
- adipose tissue
- metabolic syndrome
- binding protein
- bone marrow
- breast cancer risk
- cell therapy
- insulin resistance
- endoplasmic reticulum
- weight loss
- patient reported