Marty Michel, Pivot Xavier
Centre for Therapeutic Innovations in Oncology and Haematology, Saint Louis University Hospital, 1 Avenue Claude Vellefaux, 75010 Paris, France.
Eur J Cancer. 2008 May;44(7):912-20. doi: 10.1016/j.ejca.2008.01.005. Epub 2008 Apr 7.
The importance of angiogenesis in tumour growth and development is well known. Overexpression of vascular endothelial growth factor (VEGF), the key mediator of angiogenesis, is associated with poor prognosis in breast cancer. As a result, several therapeutic agents that inhibit the actions of VEGF or its receptors are currently in development for use in metastatic breast cancer (MBC). This review describes the function of VEGF in normal and tumour angiogenesis, explores the rationale behind the use of anti-VEGF therapy in MBC and details the therapeutic impact of such agents on tumour vasculature. Clinical data from trials of anti-VEGF agents in MBC are discussed, with a particular focus on the efficacy and safety of bevacizumab, the anti-VEGF agent at the most advanced stage of development in this tumour type. Future potential uses of bevacizumab in breast cancer are introduced.
血管生成在肿瘤生长和发展中的重要性已广为人知。血管内皮生长因子(VEGF)作为血管生成的关键介质,其过表达与乳腺癌的不良预后相关。因此,目前有几种抑制VEGF或其受体作用的治疗药物正在研发中,用于转移性乳腺癌(MBC)的治疗。本综述描述了VEGF在正常和肿瘤血管生成中的功能,探讨了在MBC中使用抗VEGF治疗的理论依据,并详细阐述了此类药物对肿瘤血管系统的治疗作用。讨论了抗VEGF药物在MBC试验中的临床数据,特别关注贝伐单抗的疗效和安全性,贝伐单抗是在该肿瘤类型中处于最先进研发阶段的抗VEGF药物。还介绍了贝伐单抗在乳腺癌中的未来潜在用途。