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探索贝伐单抗对乳腺癌影响的随机试验临床结果及“真实世界”数据:临床实践机遇与研究展望

Clinical results of randomized trials and 'real-world' data exploring the impact of Bevacizumab for breast cancer: opportunities for clinical practice and perspectives for research.

作者信息

Zambonin Valentina, De Toma Alessandro, Carbognin Luisa, Nortilli Rolando, Fiorio Elena, Parolin Veronica, Pilotto Sara, Cuppone Federica, Pellini Francesca, Lombardi Davide, Pollini Giovanni Paolo, Tortora Giampaolo, Bria Emilio

机构信息

a U.O. Oncology, University of Verona, Azienda Ospedaliera Universitaria Integrata , Verona , Italy.

b Breast Unit, Azienda Ospedaliera Universitaria Integrata , Verona , Italy.

出版信息

Expert Opin Biol Ther. 2017 Apr;17(4):497-506. doi: 10.1080/14712598.2017.1289171. Epub 2017 Feb 13.

DOI:10.1080/14712598.2017.1289171
PMID:28133971
Abstract

Angiogenesis plays a fundamental role in breast cancer (BC) growth, progression and metastatic spread. After the promising introduction of bevacizumab for the treatment of advanced BC, the initial enthusiasm decreased when the FDA withdrew its approval in 2011. Nevertheless, several clinical studies exploring the role of bevacizumab have been subsequently published. Areas covered: The aim of this study is to review the available clinical trials exploring the potential effectiveness of bevacizumab in BC, regardless of the disease setting. Expert opinion: Even if the evidence suggests that bevacizumab must be ruled out from the HER2-positive and adjuvant setting, bevacizumab's benefit remains uncertain in the neoadjuvant setting and in the advanced treatment of HER2-negative patients. In the first setting, the addition of bevacizumab to chemotherapy increased the pathological complete response (pCR) rate in most clinical trials. However, the current absence of evidence that pCR is a trial-level surrogate for survival requires waiting for long-term results. In the advanced setting, all trials showed a benefit in progression-free survival, but not in overall survival, highlighting an increase of adverse events. The lack of predictors of response represents the main unmet need in which future clinical research will undoubtedly invest.

摘要

血管生成在乳腺癌(BC)的生长、进展和转移扩散中起着至关重要的作用。在贝伐单抗被引入用于治疗晚期BC且前景看好之后,当美国食品药品监督管理局(FDA)在2011年撤回其批准时,最初的热情有所下降。尽管如此,随后还是发表了几项探索贝伐单抗作用的临床研究。涵盖领域:本研究的目的是回顾现有的临床试验,探讨贝伐单抗在BC中的潜在疗效,无论疾病处于何种阶段。专家意见:即使有证据表明在HER2阳性和辅助治疗中必须排除使用贝伐单抗,但在新辅助治疗以及HER2阴性患者的晚期治疗中,贝伐单抗的益处仍不确定。在第一种情况下,在大多数临床试验中,将贝伐单抗添加到化疗中可提高病理完全缓解(pCR)率。然而,目前缺乏证据表明pCR是生存的试验水平替代指标,这需要等待长期结果。在晚期治疗中,所有试验均显示在无进展生存期有获益,但在总生存期无获益,这突出了不良事件的增加。缺乏反应预测指标是未来临床研究无疑将投入精力的主要未满足需求。

相似文献

1
Clinical results of randomized trials and 'real-world' data exploring the impact of Bevacizumab for breast cancer: opportunities for clinical practice and perspectives for research.探索贝伐单抗对乳腺癌影响的随机试验临床结果及“真实世界”数据:临床实践机遇与研究展望
Expert Opin Biol Ther. 2017 Apr;17(4):497-506. doi: 10.1080/14712598.2017.1289171. Epub 2017 Feb 13.
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Neoadjuvant Bevacizumab plus Chemotherapy versus Chemotherapy Alone to Treat Non-Metastatic Breast Cancer: A Meta-Analysis of Randomised Controlled Trials.新辅助贝伐单抗联合化疗与单纯化疗治疗非转移性乳腺癌:一项随机对照试验的荟萃分析
PLoS One. 2015 Dec 30;10(12):e0145442. doi: 10.1371/journal.pone.0145442. eCollection 2015.
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A systematic review of bevacizumab efficacy in breast cancer.贝伐珠单抗治疗乳腺癌的系统评价
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Phase II open-label study of bevacizumab combined with neoadjuvant anthracycline and taxane therapy for locally advanced breast cancer.贝伐珠单抗联合新辅助蒽环类和紫杉类治疗局部晚期乳腺癌的 II 期开放标签研究。
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[Systemic treatments of inflammatory breast cancer: an overview].[炎性乳腺癌的全身治疗:综述]
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The role of angiogenesis inhibition in the treatment of breast cancer.血管生成抑制在乳腺癌治疗中的作用。
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Cancer Treat Rev. 2017 Feb;53:98-110. doi: 10.1016/j.ctrv.2016.12.009. Epub 2017 Jan 3.

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Guillain-Barré syndrome in a cancer patient treated with bevacizumab.一名接受贝伐单抗治疗的癌症患者发生格林-巴利综合征。
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Neoadjuvant Therapy for Breast Cancer: Established Concepts and Emerging Strategies.
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Drugs. 2017 Aug;77(12):1313-1336. doi: 10.1007/s40265-017-0774-5.