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首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Prognostic role of microvessel density in patients with renal cell carcinoma: a meta-analysis
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Prognostic role of microvessel density in patients with renal cell carcinoma: a meta-analysis

机译:微血管密度在肾细胞癌患者中的预后作用:一项荟萃分析

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摘要

Microvessel density (MVD), an indicator of angiogenesis, has been proposed to predict prognosis of patients with renal cell carcinoma (RCC), but its ability to predict survival of patients with RCC remains controversial. The present study sought to address this question rigorously by systematically reviewing the literature on MVD and RCC prognosis. We identified relevant studies in PubMed, EMBASE and the Cochrane Library, and two reviewers independently assessed study quality and extracted relevant data to compare survival based on MVD stratification in patients with RCC. We identified 15 studies that satisfied the inclusion criteria; eight studies assessed MVD in surgical samples by immunohistochemistry to label factor VIII; four studies, by immunohistochemistry to label CD34; two studies, CD31; and one study, CD105. Survival meta-analysis was performed using data pooled from 10 studies: five based on factor VIII, two based on CD34, two based on CD31 and one based on CD105. The overall survival hazard ratio describing the relationship between MVD and survival in all 10 pooled studies was 0.964 (95% CI: 0.873-1.065), while the individual hazard ratios for pooled studies based on factor VIII were 1.673 (95% CI: 0.860-3.252); CD34, 0.903 (95% CI: 0.853-0.956); and CD31, 0.926 (95% CI: 0.868-0.989). The corresponding result for the sole trial based on CD105 was 0.1759 (95% CI: 0.036-0.856). These findings suggest that MVD is not reliably associated with survival time of patients with RCC, which may reflect the need to take into account whether the microvasculature is differentiated or not. MVD as currently calculated may not be an ideal prognostic factor for patients with RCC.
机译:已经提出微血管密度(MVD)作为血管生成的指标来预测肾细胞癌(RCC)患者的预后,但是其预测RCC患者生存的能力仍存在争议。本研究试图通过系统地回顾有关MVD和RCC预后的文献来严格解决这个问题。我们在PubMed,EMBASE和Cochrane库中确定了相关研究,两名评价者独立评估了研究质量并提取了相关数据,以基于MVD分层比较RCC患者的生存率。我们确定了15项符合纳入标准的研究。八项研究通过免疫组织化学标记因子VIII评估了手术样品中的MVD;四项研究,通过免疫组织化学标记CD34;两项研究,CD31;一项研究是CD105。使用从10项研究中收集的数据进行生存率荟萃分析:五项基于VIII因子,两项基于CD34,两项基于CD31,一项基于CD105。描述所有10项合并研究的MVD与存活之间关系的总生存危险比为0.964(95%CI:0.873-1.065),而基于VIII因子的合并研究的个体危险比为1.673(95%CI:0.860- 3.252); CD34,0.903(95%CI:0.853-0.956); CD31为0.926(95%CI:0.868-0.989)。基于CD105的唯一试验的相应结果为0.1759(95%CI:0.036-0.856)。这些发现表明,MVD与RCC患者的生存时间并不可靠相关,这可能反映了需要考虑微脉管系统是否分化的需要。目前计算出的MVD对于RCC患者可能不是理想的预后因素。

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