Oncology Unit, Second Department of Surgery, "Aretaieion" University Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
Oncology Unit, Second Department of Surgery, "Aretaieion" University Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece
Anticancer Res. 2021 Feb;41(2):567-582. doi: 10.21873/anticanres.14809.
The progress of metastatic colorectal cancer (mCRC) depends essentially on two signaling pathways: the first mediated by vascular endothelial growth factor (VEGF) and the second by epidermal growth factor receptor (EGFR). In colorectal cancer (CRC), the balance between pro-angiogenic and anti-angiogenic factors is disturbed in favor of a pro-angiogenic outcome (angiogenic switch) early in the neoplastic progression of adenomas, thus, resulting in neovascularization and eventually in malignant tumor progression. Furthermore, angiogenesis plays an important role in tumor growth and the formation of metastases. Several angiogenic growth factors have been identified to be highly expressed during the progression and metastatic spread of CRC, but VEGFA is the predominant angiogenic cytokine and the most consistently expressed factor during the metastatic process. Agents targeting VEGF/VEGFR signaling have shown efficacy in the treatment of mCRC and are currently approved in this setting. In this review, we summarize the role of antiangiogenic tyrosine kinase inhibitors (TKIs) in the treatment of mCRC, focusing on regorafenib.
转移性结直肠癌(mCRC)的进展主要取决于两条信号通路:第一条由血管内皮生长因子(VEGF)介导,第二条由表皮生长因子受体(EGFR)介导。在结直肠癌(CRC)中,促血管生成和抗血管生成因子之间的平衡被打破,有利于早期腺瘤癌变过程中的促血管生成结果(血管生成开关),从而导致新血管生成,最终导致恶性肿瘤进展。此外,血管生成在肿瘤生长和转移形成中发挥重要作用。已经确定了几种在 CRC 的进展和转移扩散过程中高度表达的血管生成生长因子,但 VEGFA 是主要的血管生成细胞因子,也是转移过程中表达最一致的因子。针对 VEGF/VEGFR 信号的药物在 mCRC 的治疗中显示出疗效,目前在该领域已获得批准。在这篇综述中,我们总结了抗血管生成酪氨酸激酶抑制剂(TKIs)在 mCRC 治疗中的作用,重点介绍regorafenib。