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首页> 外文期刊>The Australasian journal of dermatology >A Systematic review and Meta-Analysis of the survival and clinicopathological features of p63 expression in Merkel cell carcinoma
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A Systematic review and Meta-Analysis of the survival and clinicopathological features of p63 expression in Merkel cell carcinoma

机译:Merkel细胞癌P63表达的存活和临床病理特征的系统综述与荟萃分析

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摘要

Merkel cell carcinoma (MCC) is a rare skin tumour of neuroendocrine origin with aggressive behaviour. The aims of this study were to investigate the association of p63 + MCC with clinicopathological features and to estimate survival through a systematic review and meta-analysis. A comprehensive search of PubMed, Embase, Scopus and Virtual Health Library following the PRISMA guidelines was conducted on September 2017. DerSimonian and Lard random-effects models were used to calculate survival-weighted means and their corresponding 95% confidence intervals (CI) among studies. Five studies met our inclusion criteria after screening 77 citations and 36 full-text articles. The included studies enrolled 413 patients with MCC. We observed that p63 + MCC was significantly associated with mortality with OR 2.92 (95% CI [1.66-5.13]). The summary hazard ratio of multivariate analysis was 1.99 (95% CI [1.32-3.01]). The only clinicopathological feature associated with p63 + MCC with statistical significance was the Merkel cell polyomavirus (MCPyV) status. The presence of MCPyV was associated as a protective factor for the expression of p63 (OR 0.25, 95% CI [0.08-0.73]). These results support that p63 + MCC evaluated by immunohistochemistry has a poor outcome. Therefore, we suggest p63 to be performed when staging MCC.
机译:梅尔克尔细胞癌(MCC)是一种罕见的神经内分泌源性皮肤肿瘤,具有激进的行为。本研究的目的是探讨P63 + MCC与临床病理特征的关联,并通过系统审查和荟萃分析来估计生存。在2017年9月进行了Prisma准则之后的PubMed,Embase,Scopus和虚拟健康图书馆的全面搜索。狄奥尼昂和猪油随机效应模型用于计算生存加权手段及其相应的95%的置信区间(CI)研究。在筛选77个引文和36条全文文章后,五项研究达到了我们的纳入标准。本发明的研究注册了413例MCC患者。我们观察到P63 + MCC与222(95%CI [1.66-5.13]的死亡率显着相关。多变量分析的摘要危险比为1.99(95%CI [1.32-3.01])。与P63 + MCC相关的临床病理特征,具有统计学意义是Merkel细胞多瘤(MCPyV)状态。 McPyV的存在与P63表达的保护因子相关联(或0.25,95%CI [0.08-0.73])。这些结果支持通过免疫组织化学评估的P63 + MCC具有较差的结果。因此,我们建议在暂存MCC时进行P63。

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