HER2 and response to anthracycline-based neoadjuvant chemotherapy in breast cancer.
HER2 and response to anthracycline-based neoadjuvant chemotherapy in breast cancer.
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DOI:
10.1093/annonc/mdq612
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发表时间:
2011-06
期刊:
影响因子:
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通讯作者:
L. Yao;Y. Liu;Z. Li;T. Ouyang;Jiuqiang Li;Tianmiao Wang;Z. Fan;T. Fan;B. Lin;Y. Xie
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文献类型:
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作者:
L. Yao;Y. Liu;Z. Li;T. Ouyang;Jiuqiang Li;Tianmiao Wang;Z. Fan;T. Fan;B. Lin;Y. Xie
BACKGROUND The predictive role of human epidermal growth factor receptor 2 (HER2) to adjuvant anthracycline-based chemotherapy remains controversial. Here, we investigated the association between HER2 status and pathological response in breast cancer patients who received neoadjuvant anthracycline-based regimens. PATIENTS AND METHODS Women (n = 538) with operable primary breast cancer received neoadjuvant anthracycline-based chemotherapy. Pathological complete response (pCR) was defined as no invasive breast tumor cells in breast after completion of neoadjuvant chemotherapy. HER2 status was determined by immunohistochemistry and/or by fluorescence in situ hybridization in core biopsy breast cancer tissue obtained before initiation of neoadjuvant chemotherapy. RESULTS In this cohort of 538 patients, 23.9% of patients achieved a pCR in their breast. HER2-positive tumors had a lower rate of pCR than did HER2-negative tumors (14.7% versus 25.7%, P = 0.013); negative HER2 status remained as an independent favorable predictor of pCR after adjusted for age, estrogen receptor, progesterone receptor, tumor size, chemotherapy cycles, and tumor grade in a multivariate analysis (odds ratio = 3.14; 95% confidence interval = 1.60-6.16, P = 0.001). Furthermore, patients with a pCR had a higher 3-year disease-free survival (DFS) rate than did patients without a pCR (P = 0.007). CONCLUSION Women with HER2-negative breast cancers rather than HER2-positive tumors benefit from anthracycline-based neoadjuvant chemotherapy.