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首页> 外文期刊>Journal of neuro-oncology. >Prognostic utility of gene therapy with herpes simplex virus thymidine kinase for patients with high-grade malignant gliomas: A systematic review and meta analysis
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Prognostic utility of gene therapy with herpes simplex virus thymidine kinase for patients with high-grade malignant gliomas: A systematic review and meta analysis

机译:单纯疱疹病毒胸苷激酶基因治疗对高度恶性神经胶质瘤患者的预后作用:系统评价和荟萃分析

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摘要

The aim of this study was to assess the effectiveness of adding viral vector-mediated gene therapy with herpes simplex virus thymidine kinase (HSV-tk) to standard treatment, in comparison with standard treatment alone to treat patients with high-grade gliomas (HGGs). A literature search of the databases PubMed, Embase, the Cochrane Library, Web of Science, and Chinese biomedicine was performed to identify eligible studies. Three randomized controlled trials (involving a total of 532 patients) were included in this systematic review. A meta-analysis of included studies demonstrated a significant increase in median survival time (MST) in patients who were treated with HSV-tk gene therapy (mean deviation 0.59, 95 % CI: 0.41-0.76, p < 0.0001). The results of pooled analysis for different patient groups show that overall survival (OS) for all HGG patients was improved by adding gene therapy [hazard ratio (HR) = 0.91, 95 % CI: 0.74-1.13, p = 0.42], while a different result was seen for glioblastoma multiforme (GBM) patients (HR = 1.06, 95 % CI: 0.80-1.41, p = 0.70). Furthermore, the combined results for tumor progression implied that standard therapy was superior to gene therapy [odds ratio (OR) = 1.31, p = 0.09]; yet differences in HR and OR between experimental groups and control groups had no statistical significance (p > 0.05). Based on the best available evidence, it appears that adding gene therapy with HSV-tk has some effect in treating HGG patients, especially with respect to MST. However, neither the pooled analysis of OS, nor the combined analysis of tumor progress indicates any significant advantage to adding gene therapy compared with standard treatment alone. More prospective studies are needed to draw solid conclusions about whether gene therapy has significant prognostic advantage.
机译:这项研究的目的是评估将单纯疱疹病毒胸苷激酶(HSV-tk)病毒载体介导的基因疗法与标准疗法相结合的有效性,与仅标准疗法治疗高级别神经胶质瘤(HGGs)的疗效相比。对数据库PubMed,Embase,Cochrane图书馆,Web of Science和中国生物医学进行了文献检索,以鉴定合格的研究。该系统评价包括三项随机对照试验(总共532例患者)。对纳入研究的荟萃分析显示,接受HSV-tk基因治疗的患者的中位生存时间(MST)显着增加(平均偏差0.59,95%CI:0.41-0.76,p <0.0001)。对不同患者组进行汇总分析的结果显示,通过添加基因治疗可以提高所有HGG患者的总体生存率[风险比(HR)= 0.91,95%CI:0.74-1.13,p = 0.42],而多形性胶质母细胞瘤(GBM)患者的观察结果不同(HR = 1.06,95%CI:0.80-1.41,p = 0.70)。此外,肿瘤进展的综合结果表明标准疗法优于基因疗法[比值比(OR)= 1.31,p = 0.09];然而,实验组和对照组之间的HR和OR差异无统计学意义(p> 0.05)。根据现有的最佳证据,似乎在HSG-tk中加入基因治疗对HGG患者有一定疗效,尤其是在MST方面。但是,与单独的标准治疗相比,对OS的汇总分析或对肿瘤进展的综合分析均未显示出添加基因治疗的任何明显优势。需要更多的前瞻性研究来得出关于基因治疗是否具有明显的预后优势的可靠结论。

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