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Anti-angiogenesis therapies: their potential in cancer management

机译:抗血管生成疗法:其在癌症治疗中的潜力

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摘要

Angiogenesis plays an important role in normal animal growth and development. This process is also vital for the growth of tumors. Angiogenesis inhibitors have a different mechanism of action to traditional chemotherapy agents and radiation therapy. The angiogenesis inhibitors can act synergistically with conventional treatments and tend to have non-overlapping toxicities. There are four drugs which have a proven role in treating cancer patients. Bevacizumab is a humanized monoclonal antibody that binds to and neutralizes vascular endothelial growth factor (VEGF). Sunitinib and sorafenib inhibit multiple tyrosine kinase receptors that are important for angiogenesis. Thalidomide inhibits the activity of basic fibroblast growth factor-2 (bFGF). The licensed indications and the supporting evidence are discussed. Other drugs are currently being tested in clinical trials and the most promising of these drugs are discussed. Aflibercept, also known as VEGF-trap, is a recombinant fusion protein that binds to circulating VEGF. The vascular disrupting agents act by targeting established blood vessels. These exciting new treatments have the potential to transform the management of cancer.
机译:血管生成在正常动物的生长发育中起重要作用。这个过程对于肿瘤的生长也至关重要。血管生成抑制剂对传统化学疗法和放射疗法具有不同的作用机制。血管生成抑制剂可以与常规治疗协同作用,并且倾向于具有不重叠的毒性。有四种药物在治疗癌症患者中具有公认的作用。贝伐单抗是一种人源化单克隆抗体,可结合并中和血管内皮生长因子(VEGF)。舒尼替尼和索拉非尼抑制多种酪氨酸激酶受体,这些受体对血管新生很重要。沙利度胺抑制碱性成纤维细胞生长因子2(bFGF)的活性。讨论了许可的适应症和支持证据。目前正在临床试验中测试其他药物,并讨论了这些药物中最有希望的药物。 Aflibercept,也称为VEGF-trap,是与循环VEGF结合的重组融合蛋白。血管破坏剂通过靶向已建立的血管而起作用。这些令人兴奋的新疗法具有改变癌症治疗的潜力。

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