Laboratory of Pharmacology, Medical School, University of Athens, Athens, Greece.
Laboratory of Pharmacology, Medical School, University of Athens, Athens, Greece.
Pharmacol Ther. 2015 Aug;152:63-82. doi: 10.1016/j.pharmthera.2015.05.005. Epub 2015 May 2.
Each year, about 5-6 cases out of 100,000 people are diagnosed with primary malignant brain tumors, of which about 80% are malignant gliomas (MGs). Glioblastoma multiforme (GBM) accounts for more than half of MG cases. They are associated with high morbidity and mortality. Despite current multimodality treatment efforts including maximal surgical resection if feasible, followed by a combination of radiotherapy and/or chemotherapy, the median survival is short: only about 15months. A deeper understanding of the pathogenesis of these tumors has presented opportunities for newer therapies to evolve and an expectation of better control of this disease. Lately, efforts have been made to investigate tumor resistance, which results from complex alternate signaling pathways, the existence of glioma stem-cells, the influence of the blood-brain barrier as well as the expression of 0(6)-methylguanine-DNA methyltransferase. In this paper, we review up-to-date information on MGs treatment including current approaches, novel drug-delivering strategies, molecular targeted agents and immunomodulative treatments, and discuss future treatment perspectives.
每年,每 10 万人中约有 5-6 人被诊断出患有原发性恶性脑肿瘤,其中约 80%为恶性神经胶质瘤(MGs)。多形性胶质母细胞瘤(GBM)占 MG 病例的一半以上。它们与高发病率和死亡率相关。尽管目前采用了多种治疗方法,包括尽可能进行最大程度的手术切除,然后联合放疗和/或化疗,但中位生存期仍然很短:只有约 15 个月。对这些肿瘤发病机制的深入了解为新的治疗方法提供了发展机会,并期望更好地控制这种疾病。最近,人们一直在努力研究肿瘤耐药性,这是由于复杂的替代信号通路、胶质瘤干细胞的存在、血脑屏障的影响以及 O(6)-甲基鸟嘌呤-DNA 甲基转移酶的表达所致。在本文中,我们综述了 MGs 治疗的最新信息,包括目前的治疗方法、新型药物输送策略、分子靶向药物和免疫调节治疗,并讨论了未来的治疗前景。