Pyo Jung-Soo, Kang Guhyun, Cho Hyunjin
Department of Pathology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Pathology, Inje University Sanggye Paik Hospital, Seoul, Korea.
J Gastric Cancer. 2016 Sep;16(3):141-151. doi: 10.5230/jgc.2016.16.3.141. Epub 2016 Sep 30.
The aim of the present study was to elucidate the clinicopathological significance and diagnostic accuracy of immunohistochemistry (IHC) for determining the mesenchymal epidermal transition (c-MET) expression in patients with gastric cancer (GC).
The present meta-analysis investigated the correlation between c-MET expression as determined by IHC and the clinicopathological parameters in 8,395 GC patients from 37 studies that satisfied the eligibility criteria. In addition, a concordance analysis was performed between c-MET expression as determined by IHC and amplification, and the diagnostic test accuracy was reviewed.
The estimated rate of c-MET overexpression was 0.403 (95% confidence interval [CI], 0.3270.484) and it was significantly correlated with male patients, poor differentiation, lymph node metastasis, higher TNM stage, and human epidermal growth factor receptor 2 (HER2) positivity in IHC analysis. There was a significant correlation between c-MET expression and worse overall survival rate (hazard ratio, 1.588; 95% CI, 1.2661.992). The concordance rates between c-MET expression and amplification were 0.967 (95% CI, 0.9160.987) and 0.270 (95% CI, 0.1730.395) for cases with non-overexpressed and overexpressed , respectively. In the diagnostic test accuracy review, the pooled sensitivity and specificity were 0.56 (95% CI, 0.500.63) and 0.79 (95% CI, 0.770.81), respectively.
The c-MET overexpression as determined by IHC was significantly correlated with aggressive tumor behavior and positive IHC status for HER2 in patients with GC. In addition, the c-MET expression status could be useful in the screening of amplification in patients with GC.
本研究旨在阐明免疫组织化学(IHC)检测胃癌(GC)患者间充质表皮转化(c-MET)表达的临床病理意义及诊断准确性。
本荟萃分析调查了37项符合纳入标准的研究中8395例GC患者经IHC检测的c-MET表达与临床病理参数之间的相关性。此外,对IHC检测的c-MET表达与基因扩增进行了一致性分析,并评估了诊断试验的准确性。
c-MET过表达的估计率为0.403(95%置信区间[CI],0.3270.484),在IHC分析中,其与男性患者、低分化、淋巴结转移、较高的TNM分期以及人表皮生长因子受体2(HER2)阳性显著相关。c-MET表达与较差的总生存率显著相关(风险比,1.588;95%CI,1.2661.992)。c-MET表达与基因扩增的一致性率在c-MET未过表达和过表达的病例中分别为0.967(95%CI,0.9160.987)和0.270(95%CI,0.1730.395)。在诊断试验准确性评估中,汇总的敏感性和特异性分别为0.56(95%CI,0.500.63)和0.79(95%CI,0.770.81)。
IHC检测的c-MET过表达与GC患者的侵袭性肿瘤行为及HER2的IHC阳性状态显著相关。此外,c-MET表达状态可能有助于GC患者基因扩增的筛查。