Bob A, Nielen F, Krediet J, Schmitter J, Freundt D, Terhorst D, Röwert-Huber J, Kanitakis J, Stockfleth E, Ulrich Ch, Weichenthal M, Egberts F, Lange-Asschenfeldt B
Department of Dermatology, Venerology and Allergology, Charité University Medicine Berlin, Berlin, Germany.
Department of Dermatology, Schleswig-Holstein University Hospital, Campus Kiel, Kiel, Germany.
J Cancer Res Clin Oncol. 2017 Oct;143(10):1999-2010. doi: 10.1007/s00432-017-2455-x. Epub 2017 Jun 21.
Merkel cell carcinoma (MCC) is a rare but aggressive neuroendocrine tumor of the skin with an increasing incidence. The clinical course is variable and reliable prognostic factors are scarce. Tumor angiogenesis has been shown to have prognostic impact in different types of cancer. The aim of our study was to determine potential prognostic factors, including tumor vascularization, for clinical outcome of MCC.
The medical records of 46 patients with MCC diagnosed between 1997 and 2010 were analyzed retrospectively. Tissue samples were immune-stained for the lymphatic endothelial vessel marker podoplanin/D2-40 and the panvascular marker CD31. These immunostained sections were analyzed using computer-assisted morphometric image analyses. Aside from the parameters of tumor vascularization, clinicopathologic features were investigated, and progression-free survival (PFS) and tumor-specific survival (TSS) were assessed. Univariate and multivariate analyses were performed to determine prognostic factors.
Male sex of the MCC patients and a high cross-sectional whole vessel area (WVA) in relation to the entire tumor area as determined on CD31-stained tumor sections were found to be negative prognostic factors for PFS in a univariate and multivariate regression analysis. Ulceration of the primary tumor was significantly associated with both impaired PFS and TSS.
Our results indicate a high prognostic impact of tumor vascularization on the clinical outcome of MCC patients. Male sex and ulceration of the primary MCC were identified as independent unfavorable prognostic markers for the clinical outcome. As an outlook, MCC patients with increased angiogenesis might be identified and subjected to a targeted anti-angiogenic treatment.
默克尔细胞癌(MCC)是一种罕见但侵袭性强的皮肤神经内分泌肿瘤,其发病率呈上升趋势。临床病程多变,可靠的预后因素稀缺。肿瘤血管生成已被证明在不同类型的癌症中具有预后影响。我们研究的目的是确定包括肿瘤血管化在内的潜在预后因素对MCC临床结局的影响。
回顾性分析1997年至2010年间确诊的46例MCC患者的病历。组织样本用淋巴管内皮细胞标志物血小板内皮细胞黏附分子/D2-40和全血管标志物CD31进行免疫染色。使用计算机辅助形态计量图像分析对这些免疫染色切片进行分析。除了肿瘤血管化参数外,还研究了临床病理特征,并评估了无进展生存期(PFS)和肿瘤特异性生存期(TSS)。进行单因素和多因素分析以确定预后因素。
在单因素和多因素回归分析中,发现MCC患者的男性性别以及在CD-31染色的肿瘤切片上确定的与整个肿瘤面积相关的高横断面全血管面积(WVA)是PFS的负面预后因素。原发肿瘤溃疡与PFS和TSS受损均显著相关。
我们的结果表明肿瘤血管化对MCC患者的临床结局具有高度预后影响。男性性别和原发性MCC溃疡被确定为临床结局的独立不良预后标志物。展望未来,血管生成增加的MCC患者可能会被识别出来并接受靶向抗血管生成治疗。