Foundation Medicine, Inc., Cambridge, MA, United States; Department of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY, United States.
Department of Radiology, Stanford University School of Medicine, Stanford, CA, United States.
Handb Clin Neurol. 2023;192:131-140. doi: 10.1016/B978-0-323-85538-9.00011-0.
Glioblastoma (GBM) is the most common and aggressive malignant adult brain tumor. Significant effort has been directed to achieve a molecular subtyping of GBM to impact treatment. The discovery of new unique molecular alterations has resulted in a more effective classification of tumors and has opened the door to subtype-specific therapeutic targets. Morphologically identical GBM may have different genetic, epigenetic, and transcriptomic alterations and therefore different progression trajectories and response to treatments. With a transition to molecularly guided diagnosis, there is now a potential to personalize and successfully manage this tumor type to improve outcomes. The steps to achieve subtype-specific molecular signatures can be extrapolated to other neuroproliferative as well as neurodegenerative disorders.
胶质母细胞瘤(GBM)是最常见和最具侵袭性的成人脑肿瘤。为了影响治疗效果,人们已经做出了巨大努力来实现 GBM 的分子亚型分类。新的独特分子改变的发现导致了肿瘤更有效的分类,并为特定于亚型的治疗靶点开辟了道路。形态上相同的 GBM 可能具有不同的遗传、表观遗传和转录组改变,因此具有不同的进展轨迹和对治疗的反应。随着向分子指导诊断的转变,现在有可能对这种肿瘤类型进行个性化治疗,以改善治疗效果。实现特定于亚型的分子特征的步骤可以外推到其他神经增殖性和神经退行性疾病。