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肺癌中Ki-67表达与患者生存率:文献系统评价及荟萃分析

Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis.

作者信息

Martin B, Paesmans M, Mascaux C, Berghmans T, Lothaire P, Meert A-P, Lafitte J-J, Sculier J-P

机构信息

Critical Care Department and Thoracic Oncology, Institut Jules Bordet, Centre des Tumeurs de l'Université Libre de Bruxelles, Brussels, Belgium.

出版信息

Br J Cancer. 2004 Dec 13;91(12):2018-25. doi: 10.1038/sj.bjc.6602233.

Abstract

Among new biological markers that could become useful prognostic factors for lung carcinoma, Ki-67 is a nuclear protein involved in cell proliferation regulation. Some studies have suggested an association between Ki-67 and poor survival in lung cancer patients. In order to clarify this point, we have performed a systematic review of the literature, using the methodology already described by our Group, the European Lung Cancer Working Party. In total, 37 studies, including 3983 patients, were found to be eligible. In total, 49% of the patients were considered as having a tumour positive for the expression of Ki-67 according to the authors cutoff. In all, 29 of the studies dealt with non-small-cell lung carcinoma (NSCLC), one with small-cell carcinoma (SCLC), two with carcinoid tumours and five with any histology. In terms of survival results, Ki-67 was a bad prognosis factor for survival in 15 studies while it was not in 22. As there was no statistical difference in quality scores between the significant and nonsignificant studies evaluable for the meta-analysis, we were allowed to aggregate the survival results. The combined hazard ratio for NSCLC, calculated using a random-effects model was 1.56 (95% CI: 1.30-1.87), showing a worse survival when Ki-67 expression is increased. In conclusion, our meta-analysis shows that the expression of Ki-67 is a factor of poor prognosis for survival in NSCLC.

摘要

在可能成为肺癌有用预后因素的新型生物标志物中,Ki-67是一种参与细胞增殖调控的核蛋白。一些研究表明Ki-67与肺癌患者的不良生存之间存在关联。为了阐明这一点,我们采用本研究团队(欧洲肺癌工作组)已描述的方法对文献进行了系统综述。总共发现37项研究符合条件,涉及3983例患者。根据作者设定的临界值,总共49%的患者被认为肿瘤Ki-67表达呈阳性。其中,29项研究涉及非小细胞肺癌(NSCLC),1项涉及小细胞肺癌(SCLC),2项涉及类癌肿瘤,5项涉及任何组织学类型。在生存结果方面,15项研究中Ki-67是生存的不良预后因素,而在22项研究中则不是。由于可用于荟萃分析的有显著意义和无显著意义的研究在质量评分上没有统计学差异,我们得以汇总生存结果。使用随机效应模型计算的NSCLC合并风险比为1.56(95%CI:1.30 - 1.87),表明Ki-67表达增加时生存情况更差。总之,我们的荟萃分析表明Ki-67的表达是NSCLC生存不良预后的一个因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/121b/2409786/793c92131db8/91-6602233f1.jpg

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