Predictors of complete pathological response after neoadjuvant systemic therapy for breast cancer

被引:68
|
作者
Tan, Marcus C. [1 ]
Al Mushawah, Fatema [1 ]
Gao, Feng [2 ]
Aft, Rebecca L. [1 ]
Gillanders, William E. [1 ]
Eberlein, Timothy J. [1 ]
Margenthaler, Julie A. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Surg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
来源
AMERICAN JOURNAL OF SURGERY | 2009年 / 198卷 / 04期
关键词
Breast cancer; Neoadjuvant therapy; Pathological response; SURGICAL ADJUVANT BREAST; ESTROGEN-RECEPTOR STATUS; PREOPERATIVE CHEMOTHERAPY; TUMOR RESPONSE; DOXORUBICIN; CYCLOPHOSPHAMIDE; DOCETAXEL; EXPRESSION; HER-2; CHEMOSENSITIVITY;
D O I
10.1016/j.amjsurg.2009.06.004
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: The aim of the current study was to identify predictors of pathologic complete response (pCR) following neoadjuvant therapy. METHODS: From 2000 to 2007, 518 breast cancer patients received neoadjuvant therapy. Data were compared using chi(2) and Fisher's exact tests and multivariate analysis of variance, as appropriate. RESULTS: Of 518 breast cancer patients receiving neoadjuvant therapy, 81 (16%) had pCR (77 of 456 [17%] with chemotherapy, 4 of 62 [6%] with endocrine therapy; P < .05). Four factors were associated with pCR: higher tumor grade (P = .015), lack of estrogen receptor (ER) and progesterone receptor (PR) expression (P < .0001), HER2/neu amplification (P = .025), and negative lymph node status (P < .0001). On multivariate analysis, ER and PR negativity, HER2/neu amplification, and negative lymph node status were found to significantly correlate with pCR. CONCLUSIONS: Patients with ER-negative and PR-negative and HER2/neu-amplified breast cancer phenotypes are more likely to experience pCR to neoadjuvant therapy. Although pCR is more frequently observed following neoadjuvant chemotherapy, it is rare following neoadjuvant endocrine therapy. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:520 / 525
页数:6
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