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
a U.O. Oncology, University of Verona, Azienda Ospedaliera Universitaria Integrata , Verona , Italy.
b Breast Unit, Azienda Ospedaliera Universitaria Integrata , Verona , Italy.
Expert Opin Biol Ther. 2017 Apr;17(4):497-506. doi: 10.1080/14712598.2017.1289171. Epub 2017 Feb 13.
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.
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。