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基因与病毒治疗脑胶质瘤:临床试验及未来方向的综述

Gene and viral therapy for glioblastoma: a review of clinical trials and future directions.

机构信息

Department of Neurological Surgery, Dardinger Laboratory for Neuro-Oncology and Neurosciences, The James Comprehensive Cancer Center and The Ohio State University Medical Center, Columbus, OH, USA.

出版信息

Cancer J. 2012 Jan-Feb;18(1):82-8. doi: 10.1097/PPO.0b013e3182458b13.

Abstract

Progress in improving the prognosis of patients with glioblastoma has been modest and has predominantly relied on informative imaging, optimization of medical and surgical treatment, and approval of new drugs with modest benefits on overall and/or progression-free survival. This has frustrated clinicians and demoralized patients but has underscored the importance of pursuing novel treatment strategies in hopes of mounting a decisive assault on this disease. Although initially not intuitive, the use of a pathogen to treat cancer has become a radical and sophisticated strategy to combat the aggressive phenotype of this disease. In fact, the engineering of viruses to fight cancer is a field that has now reached scientific maturity and has rapidly progressed from preclinical stages to clinical testing with considerable safety but disappointing efficacy. Here we review the milestones of this therapy focusing on landmark clinical trials, shed light on the limitations of this approach, and describe the recent and future strategies aimed at bringing promising efficacy to this mode of therapy.

摘要

提高胶质母细胞瘤患者预后的进展一直较为有限,主要依赖于有信息价值的影像学检查、优化的医疗和手术治疗,以及批准对总生存期和/或无进展生存期有适度获益的新药。这让临床医生感到沮丧,也让患者感到失望,但凸显了寻求新的治疗策略的重要性,以期对这种疾病发起决定性的攻击。尽管最初并非直观,但利用病原体治疗癌症已成为一种激进而复杂的策略,可对抗这种疾病侵袭性的表型。事实上,利用病毒治疗癌症的工程已经达到了科学成熟的阶段,并迅速从临床前阶段进展到临床试验,具有相当的安全性,但疗效却令人失望。在这里,我们重点回顾了该疗法的里程碑式临床试验,阐明了该方法的局限性,并描述了最近和未来旨在为这种治疗模式带来有前景疗效的策略。

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