Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43062
Título: IGF-1R expression predicts clinical outcome in patients with locally advanced oral squamous cell carcinoma
Autores/as: Lara, Pedro C.
Bordón, Elisa 
Rey, Agustín
Moreno, Mercedes
Lloret, Marta
Henríquez-Hernández, Luis Alberto 
Palabras clave: Factor-I Receptor
Growth-Factor Receptor
Disease-Free Survival
Breast-Cancer
Insulin-Like-Growth-Factor-1 Receptor, et al.
Fecha de publicación: 2011
Editor/a: 1368-8375
Publicación seriada: Oral Oncology 
Resumen: To assess the expression of IGF-1R in oral cavity squamous cell carcinoma patients, to explore its relation with clinical and pathologic prognostic factors and its role in predicting clinical outcome. One hundred and thirty-one consecutive patients suffering from oral cavity squamous cell carcinoma were included in this study from July 1989 to April 2005. Follow-up was closed in May 2010. The mean follow-up for survivors was 110.26 +/- 47.42 months. Patients were staged following the TNM classification. Patients in tumour stages I and II were referred to surgery. Patients in stages III-IV were referred to postoperative radiotherapy. Radiation therapy was administered up to a mean dose of 62.13 +/- 7.74 Gy in 1.8-2 Gy fractions. IGF-1R expression was studied by immunohistochemistry in paraffin-embedded tumour tissue. IGF-1R was expressed in 101 patients (77.1%). IGF-1R expression was related to tumour grade (P = 0.012). Tumour stage was the most important prognostic factor for survival. Low (negative and fairly) IGF-1R tumour expression was correlated to better long-term Local Disease Free Survival (P = 0.016), Disease-Free Survival (P = 0.029), and Survival (P = 0.009) in patients achieving tumour stages III-IV. Low IGF-1R expression was related to better long-term control in patients suffering locally advanced oral carcinoma. (C) 2011 Elsevier Ltd. All rights reserved.
URI: http://hdl.handle.net/10553/43062
ISSN: 1368-8375
DOI: 10.1016/j.oraloncology.2011.05.005
Fuente: Oral Oncology[ISSN 1368-8375],v. 47, p. 615-619
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