Department of Internal Medicine, Hematology, and Oncology, University Hospital Brno, Brno, Czech Republic; School of Medicine, Masaryk University, Brno, Czech Republic.
Department of Mathematics and Statistics, Faculty of Science, Masaryk University, Brno, Czech Republic.
Oral Oncol. 2017 Nov;74:68-76. doi: 10.1016/j.oraloncology.2017.09.009. Epub 2017 Sep 27.
The hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (c-MET) ligand/receptor axis has been implicated in pathogenesis of malignant diseases including squamous cell carcinoma of the head and neck (SCCHN). Overexpression of c-MET has been reported as a common molecular abnormality in SCCHN, although its prognostic and predictive value remains to be validated.
We systematically searched literature for studies evaluating c-MET expression on immunohistochemistry in newly diagnosed, non-metastatic SCCHN. The c-MET expressing cases were classified into three categories according to predefined cut-off values for positivity. Our aim was to assess the prevalence of c-MET expression and its relationship with selected clinicopathological variables.
Twenty-eight studies with 2019 cases were included. Relative frequencies of c-MET expression above cut-off levels I, II, and III were 81.8%, 63.8%, and 46.2%, respectively. Differences between these three values were statistically significant (p<1.0×10). Above cut-off level II, c-MET positivity was associated with worse overall survival (p=4.0×10), positive nodal status (p=1.0×10), higher disease stage (p=7.0×10), older age (p=2.1×10), disease recurrence (p=2.0×10), and primary tumour localization in the oral cavity (p=2.3×10). Above cut-off level III, c-MET positivity was associated with worse disease-free or progression-free survival (p=9.0×10), p16 negativity (p=2.4×10), worse overall survival (p=4.0×10), positive epidermal growth factor receptor (EGFR) status (p=7.2×10), and larger primary tumours (p=4.6×10).
In SCCHN, immunohistochemical overexpression of c-MET above cut-off levels III and particularly II was associated with inferior survival outcomes and advanced disease. Moreover, it represents a promising predictive biomarker for c-MET targeting, yet the optimal scoring method remains to be defined.
肝细胞生长因子(HGF)/间质上皮转化因子(c-MET)配体/受体轴已被认为与包括头颈部鳞状细胞癌(SCCHN)在内的恶性疾病的发病机制有关。c-MET 的过表达已被报道为 SCCHN 中的常见分子异常,尽管其预后和预测价值仍有待验证。
我们系统地检索了评估新诊断的非转移性 SCCHN 中免疫组织化学 c-MET 表达的文献。根据阳性预设截断值,将 c-MET 表达病例分为三类。我们的目的是评估 c-MET 表达的流行率及其与选定临床病理变量的关系。
共纳入 28 项研究,共 2019 例。截定点水平 I、II 和 III 以上的 c-MET 表达的相对频率分别为 81.8%、63.8%和 46.2%。这三个值之间的差异具有统计学意义(p<1.0×10)。截定点 II 以上,c-MET 阳性与总生存时间较差(p=4.0×10)、淋巴结阳性(p=1.0×10)、疾病分期较高(p=7.0×10)、年龄较大(p=2.1×10)、疾病复发(p=2.0×10)和口腔原发肿瘤定位(p=2.3×10)有关。截定点 III 以上,c-MET 阳性与疾病无进展或无进展生存时间较差(p=9.0×10)、p16 阴性(p=2.4×10)、总生存时间较差(p=4.0×10)、表皮生长因子受体(EGFR)状态阳性(p=7.2×10)和原发肿瘤较大(p=4.6×10)有关。
在 SCCHN 中,免疫组织化学 c-MET 过表达截定点 III 以上,尤其是 II 以上与生存结局较差和疾病进展有关。此外,它代表了一种有前途的 c-MET 靶向预测生物标志物,但最佳评分方法仍有待确定。