Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43062
Campo DC Valoridioma
dc.contributor.authorLara, Pedro C.
dc.contributor.authorBordón, Elisa
dc.contributor.authorRey, Agustín
dc.contributor.authorMoreno, Mercedes
dc.contributor.authorLloret, Marta
dc.contributor.authorHenríquez-Hernández, Luis Alberto
dc.date.accessioned2018-11-21T12:18:50Z-
dc.date.available2018-11-21T12:18:50Z-
dc.date.issued2011
dc.identifier.issn1368-8375
dc.identifier.urihttp://hdl.handle.net/10553/43062-
dc.description.abstractTo 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.
dc.publisher1368-8375
dc.relation.ispartofOral Oncology
dc.sourceOral Oncology[ISSN 1368-8375],v. 47, p. 615-619
dc.subject.otherFactor-I Receptor
dc.subject.otherGrowth-Factor Receptor
dc.subject.otherDisease-Free Survival
dc.subject.otherBreast-Cancer
dc.subject.otherInsulin-Like-Growth-Factor-1 Receptor
dc.subject.otherRadiation-Therapy
dc.subject.otherDown-Regulation
dc.subject.otherSurgery
dc.subject.otherBinding
dc.subject.otherRecurrence
dc.titleIGF-1R expression predicts clinical outcome in patients with locally advanced oral squamous cell carcinoma
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.oraloncology.2011.05.005
dc.identifier.scopus79959708903-
dc.identifier.isi000292024500012
dc.contributor.authorscopusid7004374085
dc.contributor.authorscopusid24402677200
dc.contributor.authorscopusid7202860969
dc.contributor.authorscopusid56328294100
dc.contributor.authorscopusid7003855087
dc.contributor.authorscopusid15829708200
dc.description.lastpage619
dc.description.firstpage615
dc.relation.volume47
dc.type2Artículoes
dc.contributor.daisngid591076
dc.contributor.daisngid2045042
dc.contributor.daisngid4381521
dc.contributor.daisngid3955607
dc.contributor.daisngid802813
dc.contributor.daisngid465624
dc.contributor.wosstandardWOS:Lara, PC
dc.contributor.wosstandardWOS:Bordon, E
dc.contributor.wosstandardWOS:Rey, A
dc.contributor.wosstandardWOS:Moreno, M
dc.contributor.wosstandardWOS:Lloret, M
dc.contributor.wosstandardWOS:Henriquez-Hernandez, LA
dc.date.coverdateJulio 2011
dc.identifier.ulpgces
dc.description.sjr1,243
dc.description.jcr2,857
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Medio Ambiente y Salud-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0003-3237-0316-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameBordón Rodríguez, Elisa de los Reyes-
crisitem.author.fullNameHenríquez Hernández, Luis Alberto-
Colección:Artículos
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