Sathornsumetee Sith, Rich Jeremy N, Reardon David A
Division of Neurology, The Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, DUMC 3624, Durham, NC 27710, USA.
Neurol Clin. 2007 Nov;25(4):1111-39, x. doi: 10.1016/j.ncl.2007.07.004.
High-grade astrocytomas include the most common adult central nervous system (CNS) tumor, glioblastoma multiforme, and anaplastic astrocytoma--a highly aggressive cancer with short median survival despite maximal multimodality therapy. Diagnosis is by clinical and radiographic findings confirmed by histopathology. Standard-of-care therapy includes surgical resection, radiotherapy, and temozolomide. Nearly all patients who have high-grade astrocytomas develop tumor recurrence or progression after this multimodality treatment. Two treatment challenges are molecular/genetic heterogeneity of tumors and limited CNS tumor delivery. It is probable that targeted therapies will be most effective in combination with one another or with cytotoxic therapies. This article discusses diagnosis and current treatment of high-grade astrocytomas.
高级别星形细胞瘤包括最常见的成人中枢神经系统(CNS)肿瘤——多形性胶质母细胞瘤,以及间变性星形细胞瘤,这是一种侵袭性很强的癌症,尽管采用了最大程度的多模式治疗,其平均生存期仍很短。诊断依据是经组织病理学证实的临床和影像学检查结果。标准治疗方案包括手术切除、放疗和替莫唑胺。几乎所有患有高级别星形细胞瘤的患者在这种多模式治疗后都会出现肿瘤复发或进展。两个治疗挑战是肿瘤的分子/基因异质性和中枢神经系统肿瘤递送受限。靶向治疗可能彼此联合或与细胞毒性治疗联合使用时最为有效。本文讨论了高级别星形细胞瘤的诊断和当前治疗方法。