Combination of anti-angiogenic therapy Apatinib and immune therapy potentiate tumor microenvironment

Chunyi Gao, T. Hu
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引用次数: 0

Abstract

Tumor immune therapy, especially anti-programmed cell death ligand-1/programmed cell death-1 (PD-L1/PD-1) treatment, is currently the focus of substantial attention. However, despite its enormous successes, the overall response rate of cancer immunotherapy remains suboptimal. There is an increased interest in combining PD-L1/PD-1 treatment with anti-angiogenic drug Apatinib to enhance antitumor effect. Presently available data seem to suggest that Apatinib may exert immune suppressive effects to make the PD-L1/PD-1 treatment works. Here, we review the extensive tumor microenvironment immune modulatory effects from antiangiogenic agents Apatinib in order to supporting VEGFR2 targettherapies in clinical trials are existing.
抗血管生成药物阿帕替尼联合免疫治疗增强肿瘤微环境
肿瘤免疫治疗,特别是抗程序性细胞死亡配体-1/程序性细胞死亡-1 (PD-L1/PD-1)治疗,是目前备受关注的焦点。然而,尽管取得了巨大的成功,癌症免疫疗法的总体反应率仍然不理想。PD-L1/PD-1联合抗血管生成药物阿帕替尼以增强抗肿瘤效果的研究日益增加。目前可用的数据似乎表明,阿帕替尼可能发挥免疫抑制作用,使PD-L1/PD-1治疗有效。在这里,我们回顾了抗血管生成药物阿帕替尼广泛的肿瘤微环境免疫调节作用,以支持临床试验中存在的VEGFR2靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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