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树突状细胞瘤苗治疗胶质母细胞瘤患者的有效性和安全性的 Meta 分析:随机对照试验研究。

Efficacy and safety of dendritic cell vaccines for patients with glioblastoma: A meta-analysis of randomized controlled trials.

机构信息

Department of Neurosurgery, First Affiliated Hospital, University of South China, Hengyang 421001, Hunan Providence, China.

Department of Neurosurgery, First Affiliated Hospital, University of South China, Hengyang 421001, Hunan Providence, China.

出版信息

Int Immunopharmacol. 2020 Jun;83:106336. doi: 10.1016/j.intimp.2020.106336. Epub 2020 Mar 23.

Abstract

BACKGROUND

Dendritic cell (DC)-based vaccination has been suggested to be promising for glioblastoma. However, the evidence in randomized controlled trials (RCTs) is inconsistent. We aimed to systematically evaluate the efficacy and safety of DC vaccine for glioblastoma via a meta-analysis of RCTs.

METHODS

Related randomized controlled trials (RCTs) were identified via a search of PubMed, Embase, and Cochrane's Library. We used a random-effect model to pool the results.

RESULTS

Six phase II RCTs with 347 patients with newly diagnosed or recurrent glioblastoma that underwent conventional treatments were included. Compared to the control group with placebo or blank treatment, DC vaccine was associated with significantly improved overall survival in patients with glioblastoma (hazard ratio [HR]: 0.69, 95% confidence interval [CI]: 0.49 to 0.97, p = 0.03) with moderate heterogeneity (p for Cochrane's Q test = 0.07, I = 51%). A trend of improved progression-free survival was also detected in patients allocated to the DC vaccine group compared to those in the control group (HR: 0.76, 95% CI: 0.56 to 1.02, p = 0.07), with no significant heterogeneity (I = 0%). Moreover, the incidence of adverse events was not significant between patients treated with DC vaccine or control (odds ratio = 1.52, 95% CI: 0.88 to 2.62, p = 0.14; I = 0%).

CONCLUSIONS

Evidence based on phase II RCTs suggests that DC vaccine may improve the survival of patients with glioblastoma. Large-scale RCTs are needed to validate the findings and determine the optimal regimens for DC vaccine.

摘要

背景

树突状细胞(DC)为基础的疫苗接种被认为对胶质母细胞瘤有希望。然而,随机对照试验(RCT)的证据并不一致。我们旨在通过对 RCT 的荟萃分析系统地评估 DC 疫苗治疗胶质母细胞瘤的疗效和安全性。

方法

通过检索 PubMed、Embase 和 Cochrane 图书馆,确定了相关的随机对照试验(RCT)。我们使用随机效应模型来汇总结果。

结果

纳入了 6 项 II 期 RCT,共 347 例接受常规治疗的新诊断或复发性胶质母细胞瘤患者。与接受安慰剂或空白治疗的对照组相比,DC 疫苗与胶质母细胞瘤患者的总生存期显著改善相关(风险比 [HR]:0.69,95%置信区间 [CI]:0.49 至 0.97,p = 0.03),异质性中等(Cochrane's Q 检验 p 值 = 0.07,I = 51%)。与对照组相比,接受 DC 疫苗治疗的患者的无进展生存期也有改善的趋势(HR:0.76,95%CI:0.56 至 1.02,p = 0.07),异质性不显著(I = 0%)。此外,接受 DC 疫苗或对照治疗的患者不良反应发生率无显著差异(优势比 = 1.52,95%CI:0.88 至 2.62,p = 0.14;I = 0%)。

结论

基于 II 期 RCT 的证据表明,DC 疫苗可能改善胶质母细胞瘤患者的生存。需要大规模 RCT 来验证这些发现,并确定 DC 疫苗的最佳方案。

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