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The evolving role of VEGF-targeted therapies in the treatment of metastatic colorectal cancer.

机译:靶向VEGF的疗法在转移性结直肠癌治疗中的作用不断演变。

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摘要

Therapies that target angiogenesis and the VEGF pathway are a component of treatment for patients with metastatic colorectal cancer (mCRC). Bevacizumab is a humanized monoclonal antibody that binds to VEGFA. Chemotherapy plus bevacizumab has led to improved outcomes for mCRC patients. Despite these benefits, progressive disease invariably ensues. Multiple members of the VEGF family can potentially contribute to tumor angiogenesis and/or evasion of antiangiogenic therapy if one pathway should be inhibited. Aflibercept, a new biological agent, is a multiple angiogenic factor trap that prevents not only VEGFA, but also VEGFB and PlGF from activating their native receptors. Key clinical data for bevacizumab and aflibercept for treatment of mCRC, clinical evidence for use of these agents beyond progression, and the search for angiogenic biomarkers to better define patients most likely to benefit from these interventions will be reviewed.
机译:靶向血管生成和VEGF途径的疗法是转移性结直肠癌(mCRC)患者治疗的组成部分。贝伐单抗是与VEGFA结合的人源化单克隆抗体。化疗加贝伐单抗已使mCRC患者的预后得到改善。尽管有这些好处,仍会不断发生疾病。如果应抑制一种途径,则VEGF家族的多个成员可以潜在地促进肿瘤血管生成和/或逃避抗血管生成疗法。 Aflibercept是一种新的生物制剂,是一种多重血管生成因子陷阱,不仅可以阻止VEGFA,而且可以阻止VEGFB和PlGF激活其天然受体。将审查贝伐单抗和aflibercept治疗mCRC的关键临床数据,这些药物超过进展使用的临床证据以及寻找血管生成生物标记物以更好地定义最有可能从这些干预措施中受益的患者的机会。

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