Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/326481
Type: Artigo
Title: Epidermal Growth Factor Receptor As An Adverse Survival Predictor In Squamous Cell Carcinoma Of The Penis
Author: Thomaz da Silva Amancio
Alice Muglia; da Cunha
Isabela Werneck; Neves
Jose Ivanildo; Quetz
Josiane da Silva; Carraro
Dirce Maria; Rocha
Rafael Malagoli; Zequi
Stenio Cassio; Cubilla
Antonio Leopoldo; da Fonseca
Francisco Paulo; Lopes
Ademar; Socorro Saldanha da Cunha
Maria do Perpetuo; Alves Lima
Marcos Venicio; Vassallo
Jose; Guimaraes
Gustavo Cardoso; Soares
Fernando Augusto
Abstract: Penile carcinoma (PC) is more frequent in underdeveloped countries, generally is diagnosed at an advanced stage when therapeutic options are restricted, and thus is associated with high morbidity/mortality rates. Recent studies have demonstrated clinical benefits with epidermal growth factor receptor (EGFR) targeted therapy in patients with PC, although there is no test that provides accurate patient selection. The aim of the present study was to evaluate the prognostic value of EGFR gene and protein status in tumor samples from patients with primary penile squamous cell carcinoma. We assessed the expression of wild type and 2 mutant EGFR isoforms (delA746-E750 and mL858R) by immunohistochemistry in 139 samples, of which 49 were also evaluated for EGFR copy number by fluorescence in situ hybridization (FISH). Positive immunohistochemical staining of wild-typeand mutant EGFR was evidenced by complete and strong membranous staining. For FISH analysis, cases were considered unaltered, polysomic, or amplified, as determined by signals of the EGFR gene and chromosome 7. An independent cohort of 107 PC samples was evaluated for mutations in EGFR, KRAS, and BRAF. Protein overexpression was noted in nearly half of the cases and was associated with cancer recurrence (P =.004) and perineural invasion (P =.005). Expression of the 2 mutated EGFR isoforms was not observed. The FISH status was not associated with protein expression. Altered FISH (polysomy and gene amplification) was an independent risk factor for dying of cancer. Only 1 patient of 107 presented KRAS mutations, and no mutations of EGFR or BRAF were observed. (C) 2017 Elsevier Inc. All rights reserved.
Subject: Egfr
Penile Cancer
Immunohistoehemistry
Fish
Prognosis
Editor: W B Saunders Co-Elsevier Inc
Philadelphia
Rights: fechado
Identifier DOI: 10.1016/j.humpath.2016.07.041
Address: http://www-sciencedirect-com.ez88.periodicos.capes.gov.br/science/article/pii/S0046817716303100
Date Issue: 2017
Appears in Collections:Unicamp - Artigos e Outros Documentos

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