Iqbal Syma, Lenz Heinz-Josef
Norris Comprehensive Cancer Center, University of Southern California, 1441 Eastlake Avenue, Los Angeles, CA 90033, USA.
Semin Oncol. 2004 Dec;31(6 Suppl 17):10-6. doi: 10.1053/j.seminoncol.2004.11.029.
Angiogenesis is critical for normal and pathologic processes in new blood vessel formation. A recent significant advance in the treatment of metastatic colorectal cancer has occurred by the development of agents targeting key regulatory molecules involved in this process, specifically vascular endothelial growth factor (VEGF). These angiogenesis inhibitors, include bevacizumab (Avastin, Genentech, Inc, South San Francisco, CA), which binds free VEGF. Recently, a phase III, multicenter, double-blind, randomized, placebo-controlled trial was designed to determine whether or not the addition of bevacizumab to first-line irinotecan, 5-fluorouracil, and leucovorin chemotherapy was completed in patients with metastatic colorectal cancer. The trial showed a higher response rate, longer time to tumor progression, and prolonged overall survival in patients with metastatic colorectal cancer. Of note, this was the first large, randomized, phase III study to show the importance of targeting VEGF and tumor angiogenesis for the treatment of human cancer. Other potential targets of angiogenesis, such as the VEGF receptor and multi-targeted agents, are undergoing evaluation in clinical trials.
血管生成对于新血管形成的正常和病理过程至关重要。通过开发针对这一过程中关键调节分子的药物,尤其是血管内皮生长因子(VEGF),转移性结直肠癌的治疗最近取得了重大进展。这些血管生成抑制剂包括贝伐单抗(阿瓦斯汀,基因泰克公司,加利福尼亚州南旧金山),它能结合游离的VEGF。最近,一项III期、多中心、双盲、随机、安慰剂对照试验旨在确定在转移性结直肠癌患者中,将贝伐单抗添加到一线伊立替康、5-氟尿嘧啶和亚叶酸化疗中是否可行。该试验显示,转移性结直肠癌患者的缓解率更高、肿瘤进展时间更长、总生存期延长。值得注意的是,这是第一项大型、随机、III期研究,表明靶向VEGF和肿瘤血管生成对人类癌症治疗的重要性。血管生成的其他潜在靶点,如VEGF受体和多靶点药物,正在临床试验中进行评估。