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Ki67 expression and docetaxel efficacy in patients with estrogen receptor–positive breast cancer
Journal of Clinical Oncology, 06/10/09
Penault-Llorca F et al. - In a study to analyze the predictive value of Ki67, HER2, and progesterone receptor (PR) expression for the efficacy of docetaxel in pts with ER-positive, node-positive breast cancer, it was concluded that Ki67 expression identifies a subset of pts with ER-positive breast cancer who could be sensitive to docetaxel treatment in the adjuvant setting.
Methods- Expression of Ki67, HER2, and PR was measured by immunohistochemistry in tumor samples from 798 pts with ER-positive breast cancer.
- Risk reduction was evaluated using a Cox model adjusted for age, tumor size, nodal involvement, treatment arm, and biomarkers.
- Predictive value of biomarkers was assessed by an interaction test.
- Disease-free survival (DFS) was the primary endpoint.
- Ki67, HER2, and PR were expressed in 21%, 9%, and 62% of samples, respectively.
- Hazard ratios for relapse associated with docetaxel were 0.51 in ER-positive/Ki67-positive tumors and 1.03 in ER-positive/Ki67-negative tumors.
- 5-yr DFS rates were 81% and 84% in pts with ER-positive/Ki67-negative and ER-positive/Ki67-positive tumors treated with docetaxel and 81% and 62% in pts with ER-positive/Ki67-negative and ER-positive/Ki67-positive tumors treated with fluorouracil, epirubicin, and cisplatin.
- No trend for interaction was observed between docetaxel and HER2, nor between docetaxel and PR.
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