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恶性胶质瘤的基因治疗

Gene therapy for malignant glioma.

作者信息

Lesniak Maciej S

机构信息

Division of Neurological Surgery, The University of Chicago, Pritzker School of Medicine, 5841 S. Maryland Avenue, MC3026, Chicago, IL 60637, USA.

出版信息

Expert Rev Neurother. 2006 Apr;6(4):479-88. doi: 10.1586/14737175.6.4.479.

Abstract

Glioblastoma multiforme represents the most common primary malignant tumor of the adult CNS. Unfortunately, the median survival after surgical intervention alone is less than 6 months and the addition of radiotherapy can extend this time to only 9 months. Consequently, efforts aimed at developing new therapies have focused on new treatment strategies that specifically target tumor cells and spare normal cells. One such modality, gene therapy, has shown promise in the spectrum of agents utilized against brain tumors. This review highlights the principles of gene therapy and discusses the results of recent clinical trials in which gene therapy has been employed against malignant brain tumors.

摘要

多形性胶质母细胞瘤是成人中枢神经系统最常见的原发性恶性肿瘤。不幸的是,仅手术干预后的中位生存期不到6个月,而加用放疗也只能将生存期延长至9个月。因此,旨在开发新疗法的努力集中在专门针对肿瘤细胞且不损伤正常细胞的新治疗策略上。基因治疗就是这样一种治疗方式,在用于对抗脑肿瘤的药物范围内已显示出前景。本综述重点介绍了基因治疗的原理,并讨论了最近采用基因治疗恶性脑肿瘤的临床试验结果。

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