Epidermal growth factor receptor expression is associated with poor outcome in cutaneous squamous cell carcinoma

表皮生长因子受体 免疫组织化学 病理 医学 转移 淋巴结 癌症研究 癌症 肿瘤科 生物 内科学
作者
Javier Cañueto,E. Cardeñoso,Juan Luis Garcı́a,Ángel Santos‐Briz,Andrés Castellanos,Emilia Fernández‐López,Adrián Blanco-Gómez,Jesús Pérez-Losada,Concepción Román‐Curto
出处
期刊:British Journal of Dermatology [Wiley]
卷期号:176 (5): 1279-1287 被引量:67
标识
DOI:10.1111/bjd.14936
摘要

Cutaneous squamous cell carcinoma (CSCC) is the second most frequent cancer in humans after basal cell carcinoma, and its incidence is dramatically rising. CSCC is rarely problematic, but given its high frequency, the absolute number of complicated cases is also high. It is necessary to identify molecular markers in order to recognize those CSCCs with poor prognosis. There is controversy concerning the role of epidermal growth factor receptor (EGFR) as a marker of prognosis in CSCC. In addition, EGFR-targeted therapies have emerged in recent years and a better understanding of the role of EGFR in CSCC may be of help for some patients in predicting prognosis and guiding curative management.To evaluate the role of EGFR as a prognostic factor in CSCC.We evaluated clinical and histopathological features, including events of poor clinical evolution, in a series of 94 cases of CSCC. We also analysed EGFR expression by immunohistochemistry, fluorescent in situ hybridization and quantitative polymerase chain reaction.We detected EGFR in 85 cases (90%), with overexpression in 33 cases (35%), and aberrant EGFR expression in the cytoplasm in 50 cases (53%). EGFR overexpression in the primary tumours was associated with lymph node progression, tumour-nodes-metastasis stage progression and proliferation (Ki-67 staining) in CSCC. EGFR overexpression and poor grade of differentiation were the strongest independent variables defining lymph node metastasis and progression in CSCC in a logistic regression model.We demonstrate that EGFR overexpression has prognostic implications associated with lymph node metastasis and progression in CSCC.
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