Kochar Arshneel Singh, Madhavan Maya, Manjila Sunil, Scoco Aleka, Belle Vaijayantee K, Geertman Robert T
Department of Medicine, Hospital of the University of Pennsylvania, PA, USA.
Department of Neurology, Weill Cornell Medical College, NY, USA.
Asian J Neurosurg. 2018 Jul-Sep;13(3):546-554. doi: 10.4103/ajns.AJNS_266_16.
Glioblastoma multiforme (GBM) has the highest rate of vascular proliferation among solid tumors. Angiogenesis is the central feature of rapid tumor growth in GBM and therefore remains an appealing therapeutic target in the treatment of these highly malignant tumors. Antiangiogenic therapy is emerging as an important adjuvant treatment. Multiple antiangiogenic agents targeting various sites in vascular endothelial growth factor (VEGF) and integrin pathways have been tested in clinical trials of newly diagnosed and recurrent GBMs. These include bevacizumab, enzastaurin, aflibercept, cediranib, and cilengitide. In this review, we discuss the current status and challenges facing clinical application of antiangiogenic treatment including anti-VEGF therapy and integrin pathway agents' therapy in glioblastoma. Here, we highlight a strong biologic rationale for this strategy, also focusing on integrin pathways. PubMed-indexed clinical trials published in English on antiangiogenic treatment of glioblastomas in the past 5 years were reviewed. The results of the current clinical trials of these agents are presented.
多形性胶质母细胞瘤(GBM)在实体瘤中具有最高的血管增殖率。血管生成是GBM肿瘤快速生长的核心特征,因此仍然是治疗这些高度恶性肿瘤的一个有吸引力的治疗靶点。抗血管生成疗法正在成为一种重要的辅助治疗方法。多种针对血管内皮生长因子(VEGF)和整合素途径中各个位点的抗血管生成药物已在新诊断和复发性GBM的临床试验中进行了测试。这些药物包括贝伐单抗、恩杂鲁胺、阿柏西普、西地尼布和西仑吉肽。在本综述中,我们讨论了抗血管生成治疗在胶质母细胞瘤临床应用中面临的现状和挑战,包括抗VEGF治疗和整合素途径药物治疗。在此,我们强调了这一策略强大的生物学原理,同时也聚焦于整合素途径。回顾了过去5年发表在PubMed上的关于胶质母细胞瘤抗血管生成治疗的英文索引临床试验。展示了这些药物当前临床试验的结果。