胶质母细胞瘤的治疗:现在该怎么办?

T. Ware, Hong-Jian Zhu
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引用次数: 1

摘要

胶质母细胞瘤(GBM)仍然是一种无法治愈的疾病,总生存率很低。尽管对临床试验进行了广泛的研究,替莫唑胺在过去的50年里仍然是唯一能提高患者生存率的治疗药物。尽管中位生存期只略微增加了2.5个月。由于其复杂和不确定的分子结构,对传统疗法的耐药性已成为GBM的标志。目前的研究表明,GBM是一种遗传亚型的疾病,需要量身定制的治疗方法。GBM治疗的进一步策略包括靶向肿瘤相关的新生血管。虽然早期尝试用抗vegf减弱肿瘤血管化尚未成功,但现在的研究正在寻找其他血管生成因子和尚未探索的新血管化新机制。向理解GBM发病机制的分子和生物学机制的转变代表了一种有希望的治疗新策略。在这里,我们强调一些主要的发展,遗传谱和抗新生血管治疗。
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Glioblastoma treatment: Where to now?
Glioblastoma (GBM) remains an incurable disease with a poor overall survival. Despite extensive research into clinical trials, temozolomide remains the only therapeutic agent to improve patient survival in the past 50 years. This is despite only providing a modest increase of 2.5 months to median survival. Resistance to traditional therapies has become a hallmark of GBM, owing to its complex and undetermined molecular landscape. Studies now suggest that GBM is a disease of genetic subtypes and require tailored approaches to therapeutic care. Further strategies for GBM treatment involve targeting tumour associated neovascularisation. While early attempts to attenuate the tumour vascularisation with anti-VEGF has not been successful, studies are now looking towards other angiogenic factors and novel mechanisms of neovascularisation that have yet to be explored. A shift towards understanding the molecular and biological mechanisms of GBM pathogenesis represents a promising new strategy for treatment. Here we highlight some of the major developments to genetic profiling and anti-neovascularisation therapy.
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