Ishikawa Eiichi, Miyazaki Tsubasa
Department of Neurosurgery, University of Tsukuba.
No Shinkei Geka. 2021 May;49(3):597-607. doi: 10.11477/mf.1436204433.
Elucidation of the ecological characteristics of malignant tumors has shown that angiogenesis and an immunosuppressive status in the tumor microenvironment are important for resolving treatment resistance and poor prognosis. Vascular endothelial growth factor(VEGF) and components of related signaling pathway can be targeted by anti-angiogenic therapy. Suppression of abundant angiogenesis using anti-angiogenic agents in high-grade gliomas inhibits rapid neurological deterioration in patients. Additionally, as VEGF promotes the formation of an immunosuppressive tumor microenvironment, anti-angiogenic therapy is expected to contribute to improving the immune status in the tumor microenvironment. In this review, we discuss the role of VEGF-targeted therapy and immunotherapy targeting immune checkpoint inhibitors and macrophages in high-grade gliomas. The authors also discuss the possibility of using these as combination therapies.
对恶性肿瘤生态特征的阐明表明,肿瘤微环境中的血管生成和免疫抑制状态对于解决治疗耐药性和不良预后至关重要。血管内皮生长因子(VEGF)及相关信号通路的成分可成为抗血管生成治疗的靶点。在高级别胶质瘤中使用抗血管生成药物抑制丰富的血管生成可抑制患者快速的神经功能恶化。此外,由于VEGF促进免疫抑制性肿瘤微环境的形成,抗血管生成治疗有望有助于改善肿瘤微环境中的免疫状态。在本综述中,我们讨论了VEGF靶向治疗以及针对免疫检查点抑制剂和巨噬细胞的免疫治疗在高级别胶质瘤中的作用。作者还讨论了将这些作为联合治疗方法的可能性。