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首页> 外文期刊>Current Opinion in Oncology >Angiogenesis inhibition in non-small cell lung cancer: a critical appraisal, basic concepts and updates from American Society for Clinical Oncology 2019
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Angiogenesis inhibition in non-small cell lung cancer: a critical appraisal, basic concepts and updates from American Society for Clinical Oncology 2019

机译:非小细胞肺癌中的血管生成抑制作用:2019年美国临床肿瘤学会的重要评估,基本概念和更新

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Purpose of review Recently, the combination of antiangiogenic agents, chemotherapy and immunotherapy has shown synergistic anticancer effects in non-small cell lung cancer (NSCLC). The future for this approach appears bright in lung cancer treatment; however, many challenges remain to be overcome regarding its true potential, optimal sequence and timing of therapy, and safety profile. In this review, we will discuss the current status and future direction of antiangiogenic therapy for the treatment of NSCLC, and highlight emerging strategies, such as tumor vessel normalization (TVN). Recent findings Bevacizumab was the first antiangiogenic agent approved for the treatment of advanced NSCLC. Recently, the combination of chemotherapy/antiangiogenic therapy with immunotherapy showed high efficacy in first-line settings. A subgroup of patients with liver metastasis and driver mutation-addicted tumors benefited most, suggesting that the metastatic location, as well as the genetic background of the tumor, are key determinants for therapy responses. The efficacy of antiangiogenic therapies in unselected patients is rather limited. The tumor microenvironment has appeared to be more complex and heterogeneous than previously assumed. Only a contextual rather than a cell-specific approach might provide valuable insights towards the clinical validation of combinational therapies.
机译:目的近期审查,抗血管生成剂,化疗和免疫疗法的组合在非小细胞肺癌(NSCLC)中表明了协同抗癌作用。这种方法的未来在肺癌治疗中表现出明亮;然而,关于其真正潜在,最佳序列和治疗的定时以及安全性剖面,仍有许多挑战。在本文中,我们将讨论抗血管生成治疗的现状和未来方向,用于治疗NSCLC,突出新兴策略,如肿瘤血管标准化(TVN)。最近的发现是普蚊属的第一个批准用于治疗先进NSCLC的抗血管生成剂。最近,使用免疫疗法的化疗/抗血管生成治疗的组合在一线环境中显示出高效率。肝转移和司机突变的患者的亚群受益最多,这表明转移性位置以及肿瘤的遗传背景是治疗反应的关键决定因素。抗血管生成疗法在未选择患者中的疗效相当有限。肿瘤微环境似乎比以前假设更复杂和异质。只有一个语境而不是细胞特异性方法可能会对组合疗法的临床验证提供有价值的见解。

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