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乳腺癌新辅助化疗的当前方法。

Current approaches for neoadjuvant chemotherapy in breast cancer.

作者信息

Connolly Roisin M, Stearns Vered

机构信息

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, 1650 Orleans Street, CRB I, Room 153, Baltimore, MD 21287-0013, United States.

出版信息

Eur J Pharmacol. 2013 Oct 5;717(1-3):58-66. doi: 10.1016/j.ejphar.2013.02.057. Epub 2013 Mar 29.

DOI:10.1016/j.ejphar.2013.02.057
PMID:23545358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3758450/
Abstract

Compared to adjuvant chemotherapy, the administration of the same regimen in the neoadjuvant setting provides women with identical improvements in disease free and overall survival. Neoadjuvant chemotherapy may offer benefits to properly selected women such as broadening surgical options and enhancing the likelihood of breast conservation. Assessment of response to neoadjuvant chemotherapy provides women with an individualized estimate of prognosis. For example, a woman who achieves a complete pathological response following neoadjuvant chemotherapy has a very low risk of recurrence compared to a woman with similar tumor characteristics and a large residual disease. In this review we will provide a historical perspective and discuss the aims of neoadjuvant chemotherapy in primary operable breast cancer; as well as appropriate patient selection, treatment strategies, response monitoring, and postoperative care. We will also discuss the attractiveness of this approach to study the mechanism of action of standard and novel agents, and the role of predictive biomarkers of response to treatment and outcomes.

摘要

与辅助化疗相比,在新辅助治疗中使用相同的方案可为女性带来无病生存期和总生存期方面相同的改善。新辅助化疗可能会为经过适当选择的女性带来益处,例如拓宽手术选择范围并提高保乳的可能性。评估对新辅助化疗的反应可为女性提供个性化的预后估计。例如,与具有相似肿瘤特征但有大量残留病灶的女性相比,在新辅助化疗后实现完全病理缓解的女性复发风险非常低。在本综述中,我们将提供历史视角并讨论原发性可手术乳腺癌新辅助化疗的目的;以及合适的患者选择、治疗策略、反应监测和术后护理。我们还将讨论这种方法在研究标准药物和新型药物作用机制方面的吸引力,以及治疗反应和结果预测生物标志物的作用。

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本文引用的文献

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Multicenter phase II study of neoadjuvant lapatinib and trastuzumab with hormonal therapy and without chemotherapy in patients with human epidermal growth factor receptor 2-overexpressing breast cancer: TBCRC 006.多中心 II 期研究:曲妥珠单抗和拉帕替尼联合激素治疗且不联合化疗治疗人表皮生长因子受体 2 过表达乳腺癌患者:TBCRC 006。
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The role for sentinel lymph node dissection after neoadjuvant chemotherapy in patients who present with node-positive breast cancer.新辅助化疗后前哨淋巴结活检在淋巴结阳性乳腺癌患者中的作用。
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A common language in neoadjuvant breast cancer clinical trials: proposals for standard definitions and endpoints.新辅助乳腺癌临床试验中的通用语言:标准定义和终点建议。
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Pathological complete response and accelerated drug approval in early breast cancer.早期乳腺癌的病理完全缓解与加速药物批准
N Engl J Med. 2012 Jun 28;366(26):2438-41. doi: 10.1056/NEJMp1205737. Epub 2012 May 30.
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Gene modules and response to neoadjuvant chemotherapy in breast cancer subtypes: a pooled analysis.基因模块与乳腺癌亚型新辅助化疗反应:汇总分析。
J Clin Oncol. 2012 Jun 1;30(16):1996-2004. doi: 10.1200/JCO.2011.39.5624. Epub 2012 Apr 16.
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J Clin Oncol. 2012 Jun 1;30(16):1989-95. doi: 10.1200/JCO.2011.39.0823. Epub 2012 Apr 9.
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Bevacizumab added to neoadjuvant chemotherapy for breast cancer.贝伐珠单抗联合新辅助化疗治疗乳腺癌。
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Neoadjuvant chemotherapy and bevacizumab for HER2-negative breast cancer.新辅助化疗联合贝伐珠单抗治疗人表皮生长因子受体 2 阴性乳腺癌。
N Engl J Med. 2012 Jan 26;366(4):299-309. doi: 10.1056/NEJMoa1111065.
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Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial.拉帕替尼联合曲妥珠单抗治疗人表皮生长因子受体 2 阳性早期乳腺癌(NeoALTTO):一项随机、开放标签、多中心、III 期临床试验。
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Lapatinib versus trastuzumab in combination with neoadjuvant anthracycline-taxane-based chemotherapy (GeparQuinto, GBG 44): a randomised phase 3 trial.拉帕替尼对比曲妥珠单抗联合新辅助蒽环类紫杉类化疗(GeparQuinto,GBG 44):一项随机 3 期临床试验。
Lancet Oncol. 2012 Feb;13(2):135-44. doi: 10.1016/S1470-2045(11)70397-7. Epub 2012 Jan 17.