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乳腺癌新辅助化疗结局的预测因素——单中心经验

Predictive factors determining neoadjuvant chemotherapy outcomes in breast cancer - a single center experience.

作者信息

Yu Yang, Xiang Hua, He Xiang-Ming, Yang Hong-Jian, Zong Xiang-Yun

机构信息

Department of Breast Surgery, Zhejiang Cancer Hospital, China.

出版信息

Asian Pac J Cancer Prev. 2013;14(4):2401-6. doi: 10.7314/apjcp.2013.14.4.2401.

DOI:10.7314/apjcp.2013.14.4.2401
PMID:23725148
Abstract

From January 1, 2008 to March 31, 2010, 101 patients with stage II-III breast cancer were enrolled in this study and subjected to an anthracycline-based neoadjuvant chemotherapy regimen with or without docetaxel. Surgery was performed after 2-6 cycles of chemotherapy, and the clinical response was determined by pathological and histochemical assessments. The clinical response rate, as indicated by complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD), were 6.9, 52.5, 36.6, and 4.0%, respectively. A multivariable correlation analysis indicated that the overall clinical response rate correlated with the number of metastatic lymph nodes, number of chemotherapy cycles, and vessel invasion status. Importantly, the CR rate was only associated with the number of chemotherapy cycles. Nonparametric tests failed to detect a correlation between HER2 or Topo IIα status and clinical response to neoadjuvant chemotherapy in these patients. When they were stratified by HER2 or HR status, for HER2-positive patients the CR rate was associated with vessel invasion and Topo IIα status. Based on our findings, we propose that HR, HER-2 and Topo IIα are not putative predictive biomarkers of chemotherapy outcome for breast cancer patients. Topo IIα expression level was only inversely correlated with CR rate among HR-positive patients. Importantly, the achievement of CR was largely related to the number of chemotherapy cycles.

摘要

2008年1月1日至2010年3月31日,101例II - III期乳腺癌患者入组本研究,接受含蒽环类药物的新辅助化疗方案,部分患者联合多西他赛。化疗2 - 6个周期后进行手术,通过病理和组织化学评估确定临床反应。以完全缓解(CR)、部分缓解(PR)、疾病稳定(SD)和疾病进展(PD)表示的临床缓解率分别为6.9%、52.5%、36.6%和4.0%。多变量相关性分析表明,总体临床缓解率与转移淋巴结数量、化疗周期数和血管侵犯状态相关。重要的是,CR率仅与化疗周期数有关。非参数检验未能检测到这些患者中HER2或拓扑异构酶IIα状态与新辅助化疗临床反应之间的相关性。当根据HER2或HR状态进行分层时,对于HER2阳性患者,CR率与血管侵犯和拓扑异构酶IIα状态相关。基于我们的研究结果,我们提出HR、HER-2和拓扑异构酶IIα不是乳腺癌患者化疗结果的假定预测生物标志物。拓扑异构酶IIα表达水平仅在HR阳性患者中与CR率呈负相关。重要的是,CR的实现很大程度上与化疗周期数有关。

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