Herrlinger U, Platten M
Schwerpunkt Klinische Neuroonkologie, Neurologische Universitätsklinik Bonn, Bonn, Deutschland.
Nervenarzt. 2015 Jun;86(6):684, 686-8, 690-1. doi: 10.1007/s00115-014-4225-1.
Therapeutic concepts for malignant gliomas increasingly target the genetically non-transformed tumor stroma rather than the tumor cells themselves. There are two particular compartments of the tumor stroma which are currently tackled: the vascular compartment by using antiangiogenic treatment with the aim of vascular normalization and the immune compartment with the aim of enhancing or inducing anti-tumor immunity. Although the vascular endothelial growth factor (VEGF) A antibody bevacizumab has not been approved for the treatment of malignant glioma in European countries, there is evidence from smaller trials of biological efficacy particularly in recurrent disease and the results of a large European phase III study testing the clinical efficacy are currently expected. Immunotherapies are on the verge of entering the clinical arena with the first randomized phase III clinical trials having already been completed. In these studies, active vaccination and checkpoint inhibitors which are approved for other tumor entities are being tested. This article provides an overview on the current antiangiogenic and immunological therapies for gliomas, summarizes the results of clinical trials and discusses further developments.
恶性胶质瘤的治疗理念越来越多地针对基因未转化的肿瘤基质,而非肿瘤细胞本身。目前正在攻克肿瘤基质的两个特定部分:通过采用旨在实现血管正常化的抗血管生成治疗来针对血管部分,以及旨在增强或诱导抗肿瘤免疫的免疫部分。尽管血管内皮生长因子(VEGF)A抗体贝伐单抗在欧洲国家尚未被批准用于治疗恶性胶质瘤,但小型试验中有关于其生物学疗效的证据,尤其是在复发性疾病中,目前正在期待一项大型欧洲III期研究测试其临床疗效的结果。免疫疗法即将进入临床领域,首个随机III期临床试验已经完成。在这些研究中,正在测试已被批准用于其他肿瘤实体的主动疫苗接种和检查点抑制剂。本文概述了目前针对胶质瘤的抗血管生成和免疫疗法,总结了临床试验结果并讨论了进一步的发展。