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首页> 外文期刊>Interdisciplinary Neurosurgery >Role of chromosomal 1p/19q co-deletion on the prognosis of oligodendrogliomas: A systematic review and meta-analysis
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Role of chromosomal 1p/19q co-deletion on the prognosis of oligodendrogliomas: A systematic review and meta-analysis

机译:染色体1p / 19q共缺失在少突胶质细胞瘤预后中的作用:系统评价和荟萃分析

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Background The impact of chromosomal 1p/19q co-deletion on the prognosis of oligodendrogliomas has been measured in many studies previously. However most studies used 1p/19q co-deletion as a covariate to be adjusted for in a multivariable model that aimed to assess treatment effects, thus not directly measuring the effect of the 1p/19q co-deletion on prognosis. We conducted a systematic review and meta-analysis to synthesize the results and provide insight on how 1p/19q co-deletion affects prognoses of WHO grade II/III oligodendrogliomas. Methods Weighted mean difference (WMD), standardized mean difference (SMD), and hazard ratios (HRs) were used to report pooled effect of 1p/19q co-deletion on prognosis of oligodendrogliomas. The Meta-ANOVA model was used to obtain the pooled HRs. Results The difference in median overall survival (OS) time is 0.24 (95% CI: 0.15 to 0.33) and the WMD for 5-year OS rate is 6.87% (95% CI: 6.66% to 7.07%), favoring patients with co-deletion. The pooled hazard ratio (HR) for mortality is 0.28 (95% CI: 0.13 to 0.62), favoring 1p/19q co-deletion. For progression free survival (PFS), the SMD of median PFS time is 0.13 (95% CI: 0.04 to 0.21), in favor of 1p/19q co-deletion. When comparing therapies among patients with 1p/19q co-deletion, we found that those receiving radiation therapy (RT) and chemotherapy (CT) had a significantly better prognosis than those who received RT only, with pooled HR of 0.64 (95% CI: 0.51 to 0.80). Conclusions Our pooled results show that chromosomal 1p/19q co-deletion has a significant protective effect on prognosis of grade II/III oligodendrogliomas.
机译:背景技术先前已在许多研究中测量了染色体1p / 19q共缺失对少突胶质细胞瘤预后的影响。然而,大多数研究在旨在评估治疗效果的多变量模型中使用1p / 19q共删除作为要调整的协变量,因此并未直接测量1p / 19q共删除对预后的影响。我们进行了系统的综述和荟萃分析,以合成结果,并提供有关1p / 19q共缺失如何影响WHO II / III级少突胶质细胞瘤预后的见解。方法采用加权平均差(WMD),标准化平均差(SMD)和危险比(HRs)报告1p / 19q共缺失对少突胶质细胞瘤预后的综合作用。使用Meta-ANOVA模型获得合并的HR。结果中位总生存时间(OS)的差异为0.24(95%CI:0.15至0.33),而5年OS发生率的WMD为6.87%(95%CI:6.66%至7.07%),偏爱合并症患者-删除。死亡率的总危险比(HR)为0.28(95%CI:0.13至0.62),有利于1p / 19q共删除。对于无进展生存期(PFS),中位PFS时间的SMD为0.13(95%CI:0.04至0.21),有利于1p / 19q共删除。在比较1p / 19q共缺失患者中的治疗方法时,我们发现接受放射治疗(RT)和化学疗法(CT)的患者的预后明显优于仅接受RT治疗的患者,合并HR为0.64(95%CI 0.51至0.80)。结论我们的汇总结果表明,染色体1p / 19q共缺失对II / III级少突胶质细胞瘤的预后具有明显的保护作用。

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