2nd Medical School and University Hospital Motol, Department of Pathology and Molecular Medicine, Charles University, Prague, Czech Republic.
Pathol Oncol Res. 2009 Dec;15(4):605-14. doi: 10.1007/s12253-009-9160-2. Epub 2009 Mar 20.
Distinction between grade II ependymomas and anaplastic ependymomas based on histopathological examination solely is problematic and, therefore, the management of intracranial ependymomas remains controversial. The aim of this study was to conduct a systematic review (SR) and meta-analysis (MA) of data published on immunohistochemical prognostic markers (IPM) in intracranial ependymomas (IE), and to establish an evidence-based perspective on their clinical value. Following the extensive search based on a strictly defined group of key words, 30 studies reporting results on IPM in IE were identified. Due to a pronounced inter-study heterogeneity, only 14 publications fulfilled the criteria for inclusion into SR. From the total of 67 immunohistochemical markers, 18 were found to correlate with prognosis. However, owing to inadequate data publishing, MA could be performed only with data on proliferation marker MIB-1 (Ki-67) from 5 publications, including 337 patients: The pooled hazard ratio for overall survival was 3.16 (95% confidence interval = 1.96-5.09; p < 0.001) implicating that patients suffering from tumors with higher immunohistochemical expression of MIB-1 had a significantly worse outcome. Marked inter-study heterogeneity and incomplete data publishing in primary studies significantly limited extent of the SR, and the possibility of performing MA. Although the prognostic impact of MIB-1 immunoexpression in IE could be confirmed, there remains lack of further reliable IPM that could be used in routine diagnosis. We encourage to search for new, useful markers, as well as to standardize lab-techniques and data interpretation algorithms across laboratories in order to increase data compatibility.
仅基于组织病理学检查来区分 II 级室管膜瘤和间变室管膜瘤存在问题,因此,颅内室管膜瘤的治疗仍然存在争议。本研究旨在对颅内室管膜瘤(IE)中免疫组织化学预后标志物(IPM)的已发表数据进行系统评价(SR)和荟萃分析(MA),并从循证医学的角度评估其临床价值。在基于严格定义的一组关键词进行广泛搜索后,确定了 30 项报告 IE 中 IPM 结果的研究。由于研究间存在明显的异质性,只有 14 项符合 SR 纳入标准的出版物。在总共 67 种免疫组织化学标志物中,有 18 种与预后相关。然而,由于数据发布不充分,仅对 5 项出版物中关于增殖标志物 MIB-1(Ki-67)的数据进行了 MA,其中包括 337 例患者:总生存的合并危险比为 3.16(95%置信区间=1.96-5.09;p<0.001),这表明 MIB-1 免疫组织化学表达较高的患者预后明显较差。研究间的显著异质性和原始研究中数据发布不完整,极大地限制了 SR 的范围,以及进行 MA 的可能性。尽管可以确认 IE 中 MIB-1 免疫表达的预后影响,但仍然缺乏可在常规诊断中使用的其他可靠的 IPM。我们鼓励寻找新的、有用的标志物,并在实验室之间标准化实验室技术和数据解释算法,以提高数据的兼容性。