Asioli Sofia, Righi Alberto, Volante Marco, Eusebi Vincenzo, Bussolati Gianni
Department of Biomedical Sciences and Human Oncology, University of Turin, Italy.
Cancer. 2007 Aug 1;110(3):640-7. doi: 10.1002/cncr.22828.
Merkel cell carcinoma (MCC) is an aggressive neuroendocrine skin tumor, mostly affecting elderly individuals. The histogenesis of this rare tumor as well as its prognostic criteria are a matter of dispute.
An immunohistochemical analysis of markers of proliferation (Ki-67/MIB-1), neuroendocrine differentiation (chromogranin A and synaptophysin), and basal cell differentiation (p63) was performed in a series of 47 cases of MCC. The significance of pathologic data and of immunoreactivity with different markers was evaluated using the chi-square test. Survival curves were calculated using the Kaplan-Meyer method. The survival difference was estimated using the Wilcoxon or Mantel-Cox test.
Immunohistochemical evidence of neuroendocrine differentiation and immunopositivity for cytokeratin 20 were observed in all cases, whereas positivity for p63 was detected in approximately half of the cases (25 of 47 cases; 53.2%). Cases that were positive for p63 demonstrated a more aggressive clinical course than those that were negative (Z value of 2.93; P = .0003; hazards ratio of 22.22).
Data from the current study indicate that p63 expression is associated with a worse prognosis in patients with MCC and represents a new independent marker of clinical evolution.
默克尔细胞癌(MCC)是一种侵袭性神经内分泌皮肤肿瘤,主要影响老年人。这种罕见肿瘤的组织发生及其预后标准存在争议。
对47例MCC病例进行了增殖标志物(Ki-67/MIB-1)、神经内分泌分化标志物(嗜铬粒蛋白A和突触素)以及基底细胞分化标志物(p63)的免疫组化分析。使用卡方检验评估病理数据和不同标志物免疫反应性的意义。采用Kaplan-Meier法计算生存曲线。使用Wilcoxon或Mantel-Cox检验估计生存差异。
所有病例均观察到神经内分泌分化的免疫组化证据和细胞角蛋白20免疫阳性,而约一半病例(47例中的25例;53.2%)检测到p63阳性。p63阳性病例的临床病程比阴性病例更具侵袭性(Z值为2.93;P = .0003;风险比为22.22)。
本研究数据表明,p63表达与MCC患者预后较差相关,是临床进展的一个新的独立标志物。