首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Synergies of Targeting Tumor Angiogenesis and Immune Checkpoints in Non-Small Cell Lung Cancer and Renal Cell Cancer: From Basic Concepts to Clinical Reality
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Synergies of Targeting Tumor Angiogenesis and Immune Checkpoints in Non-Small Cell Lung Cancer and Renal Cell Cancer: From Basic Concepts to Clinical Reality

机译:针对非小细胞肺癌和肾细胞癌的靶向肿瘤血管生成和免疫检查点的协同作用:从基本概念到临床现实

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摘要

In recent years, considerable advances concerning therapeutic strategies in patients with metastatic cancer have been achieved. Particularly in renal cell cancer (RCC) and advanced stage non-small cell lung cancer (NSCLC), immune-activating and antiangiogenic (AA) drugs (i.e., checkpoint antibodies and vascular endothelial growth factor (VEGF)/VEGF receptors (VEGFR) targeting compounds, respectively) have been successfully developed. As immune-effector cells have to enter the tumor, it is tempting to speculate that the combination of immunotherapy with AA treatment may induce synergistic effects. In this short review, we explore the theoretical background and the therapeutic potential of this novel treatment option for patients with advanced RCC or NSCLC. We discuss the growing body of evidence that pro-angiogenic factors negatively modulate the T-cell-mediated immune response and examine the preclinical evidence for testing combined immune-activating and AA therapy concepts in clinical practice. Particular attention will also be paid to potential novel treatment-related adverse events induced by combination treatment.
机译:近年来,关于转移性癌症患者的治疗策略已经取得了相当大的进步。特别是在肾细胞癌(RCC)和晚期非小细胞肺癌(NSCLC)中,以免疫激活和抗血管生成(AA)药物(即检查点抗体和血管内皮生长因子(VEGF)/ VEGF受体(VEGFR))为靶标化合物)已成功开发。由于免疫效应细胞必须进入肿瘤,因此很容易推测免疫疗法与AA治疗相结合可能会产生协同效应。在这篇简短的评论中,我们探讨了这种新型治疗方案对晚期RCC或NSCLC患者的理论背景和治疗潜力。我们讨论越来越多的证据,即促血管生成因子会对T细胞介导的免疫反应产生负调节作用,并检验临床前证据以在临床实践中测试联合免疫激活和AA疗法的概念。还将特别注意联合治疗引起的潜在的新型治疗相关不良事件。

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