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本文引用的文献

1
Selection of chemotherapy for glioblastoma expressing O(6)-methylguanine-DNA methyltransferase.针对表达O(6)-甲基鸟嘌呤-DNA甲基转移酶的胶质母细胞瘤的化疗药物选择
Exp Ther Med. 2010 Jan;1(1):53-57. doi: 10.3892/etm_00000009. Epub 2010 Jan 1.
2
Comprehensive analysis of MGMT promoter methylation: correlation with MGMT expression and clinical response in GBM.全面分析 MGMT 启动子甲基化:与 GBM 中 MGMT 表达和临床反应的相关性。
PLoS One. 2011 Jan 7;6(1):e16146. doi: 10.1371/journal.pone.0016146.
3
New treatment options in the management of glioblastoma multiforme: a focus on bevacizumab.多形性胶质母细胞瘤治疗新选择:聚焦贝伐珠单抗。
Onco Targets Ther. 2010 Jun 24;3:27-38. doi: 10.2147/ott.s5307.
4
Exciting new advances in neuro-oncology: the avenue to a cure for malignant glioma.神经肿瘤学的激动人心新进展:攻克恶性脑胶质瘤的途径。
CA Cancer J Clin. 2010 May-Jun;60(3):166-93. doi: 10.3322/caac.20069.
5
Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma.鉴定出一种 CpG 岛甲基化表型,它定义了神经胶质瘤的一个独特亚群。
Cancer Cell. 2010 May 18;17(5):510-22. doi: 10.1016/j.ccr.2010.03.017. Epub 2010 Apr 15.
6
Interstitial infusion of glioma-targeted recombinant immunotoxin 8H9scFv-PE38.胶质瘤靶向重组免疫毒素 8H9scFv-PE38 间质内灌注。
Mol Cancer Ther. 2010 Apr;9(4):1039-46. doi: 10.1158/1535-7163.MCT-09-0996. Epub 2010 Apr 6.
7
Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival.LIG4、BTBD2、HMGA2 和 RTEL1 基因的多态性与双链断裂修复途径有关,可预测胶质母细胞瘤的生存。
J Clin Oncol. 2010 May 10;28(14):2467-74. doi: 10.1200/JCO.2009.26.6213. Epub 2010 Apr 5.
8
Therapy for recurrent high-grade gliomas: does continuous dose-intense temozolomide have a role?复发性高级别胶质瘤的治疗:持续高剂量替莫唑胺是否起作用?
J Clin Oncol. 2010 Apr 20;28(12):1977-9. doi: 10.1200/JCO.2009.27.6014. Epub 2010 Mar 22.
9
Recent advances in therapy for glioblastoma.胶质母细胞瘤治疗的最新进展
Arch Neurol. 2010 Mar;67(3):279-83. doi: 10.1001/archneurol.2010.5.
10
Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1.整合基因组分析确定了具有 PDGFRA、IDH1、EGFR 和 NF1 异常的胶质母细胞瘤的临床相关亚型。
Cancer Cell. 2010 Jan 19;17(1):98-110. doi: 10.1016/j.ccr.2009.12.020.

多形性胶质母细胞瘤:分子特征与当前治疗策略(综述)

Glioblastoma multiforme: Molecular characterization and current treatment strategy (Review).

作者信息

Zhang Xiang, Zhang Wei, Cao Wei-Dong, Cheng Gang, Zhang Yong-Qiang

机构信息

Institute of Neurosurgery, and.

出版信息

Exp Ther Med. 2012 Jan;3(1):9-14. doi: 10.3892/etm.2011.367. Epub 2011 Oct 18.

DOI:10.3892/etm.2011.367
PMID:22969836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3438851/
Abstract

Glioblastoma multiforme (GBM) is the most common and lethal malignant primary brain tumor. It is classified by the World Health Organization (WHO) in the group of diffusely infiltrating astrocytomas, representing up to 50% of all primary brain gliomas, and carries the poorest prognosis. Aberrant genetic events and signaling pathways have clearly demonstrated that GBM is highly anaplastic and a morphologically highly heterogeneous tumor. Understanding the genetic alterations, specific molecular biomarkers and proliferative pathways may promote therapeutic development for the management of GBM. Age, Karnofsky performance score, histology, position and the extent of tumor resection have been identified as potential prognostic factors for patients with GBM. In this study, we review the molecular characterization of tumor cells, the current standard of care for patients diagnosed with GBM, including gross or near-total resection of the tumor, followed by radiotherapy, stereotactic brachytherapy, chemotherapy and new targeted therapies. Thus, we conclude that multimodal approaches for the treatment of patients with GBM may significantly improve their prognoses.

摘要

多形性胶质母细胞瘤(GBM)是最常见且致命的原发性恶性脑肿瘤。它被世界卫生组织(WHO)归类为弥漫性浸润性星形细胞瘤,占所有原发性脑胶质瘤的50%,预后最差。异常的基因事件和信号通路已清楚表明GBM具有高度间变性且是形态学上高度异质性的肿瘤。了解基因改变、特定分子生物标志物和增殖途径可能会促进GBM治疗方法的发展。年龄、卡诺夫斯基功能状态评分、组织学、肿瘤位置和切除范围已被确定为GBM患者的潜在预后因素。在本研究中,我们回顾了肿瘤细胞的分子特征、目前诊断为GBM患者的标准治疗方法,包括肿瘤的大体或近全切除,随后进行放疗、立体定向近距离放疗、化疗和新的靶向治疗。因此,我们得出结论,多模式治疗方法可能会显著改善GBM患者的预后。