Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/47714
DC FieldValueLanguage
dc.contributor.authorClavo, B.en_US
dc.contributor.authorRobaina, F.en_US
dc.contributor.authorFiuza, D.en_US
dc.contributor.authorRuiz, A.en_US
dc.contributor.authorLloret, M.en_US
dc.contributor.authorRey-Baltar, D.en_US
dc.contributor.authorLlontop, P.en_US
dc.contributor.authorRiveros, A.en_US
dc.contributor.authorRivero, J.en_US
dc.contributor.authorCastañeda, F.en_US
dc.contributor.authorQuintero, S.en_US
dc.contributor.authorSantana-Rodríguez, N.en_US
dc.date.accessioned2018-11-23T15:48:38Z-
dc.date.available2018-11-23T15:48:38Z-
dc.date.issued2017en_US
dc.identifier.issn1699-048Xen_US
dc.identifier.urihttp://hdl.handle.net/10553/47714-
dc.description.abstractPurpose Hypoxia has predictive value in head and neck cancer (HNC). It has been well described, albeit in a small number of clinical Centres. The aim of this study was to describe our experience using the polarographic probe technique to assess the predictive value of tumour oxygenation in patients with advanced HNC treated with hyperfractionated radio-chemotherapy. Hypoxia modification was induced using percutaneous spinal cord stimulation (SCS). Methods/patients Male patients (n = 12; stage IVb n = 8; IVa n = 4; mean age 58: range 46–70 years) with advanced HNC were evaluated. Planned therapy was hyperfractionated-radiotherapy, oral tegafur (precursor of 5-fluorouracil) and hypoxia modification using SCS. Pre-treatment analyses included: haemoglobin levels and tumour oxygenation (using the Eppendorf polarographic probe device). Oxygenation was expressed as median-pO2 (in mmHg) and hypoxia as the percentage of pO2 values ≤5 mmHg (HP5) and ≤2.5 mmHg (HP2.5). Results Lower haemoglobin levels were directly correlated with median pO2 (p = 0.017) and inversely correlated with HP5 (p = 0.020) and more advanced stages (IVb vs. IVa; p = 0.028). Patients who subsequently developed systemic metastasis had tumours that were more hypoxic, with lower median pO2 (p = 0.036) and higher HP5 (p = 0.036). The subgroup of patients with HP2.5 above the median (the most hypoxic tumours) had lower loco-regional control (p = 0.027), cause-specific survival (p = 0.008), and overall survival (p = 0.008). Conclusions Higher tumour hypoxia showed predictive value in HNC in our study, and was significantly associated with lower overall survival, cause-specific survival, and loco-regional control. Tumour hypoxia determination could be used to select patients who would most benefit by hypoxia modification during chemo-radiotherapy of HNC.en_US
dc.languageengen_US
dc.relation.ispartofClinical and Translational Oncologyen_US
dc.sourceClinical and Translational Oncology[ISSN 1699-048X],v. 19, p. 419-424en_US
dc.subject32 Ciencias médicasen_US
dc.subject320101 Oncologíaen_US
dc.subject.otherAnaemiaen_US
dc.subject.otherHead and neck canceren_US
dc.subject.otherPolarographic probesen_US
dc.subject.otherPredictive and prognostic valueen_US
dc.subject.otherSpinal cord stimulationen_US
dc.subject.otherTumour hypoxia modificationen_US
dc.titlePredictive value of hypoxia in advanced head and neck cancer after treatment with hyperfractionated radio-chemotherapy and hypoxia modificationen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s12094-016-1541-xen_US
dc.identifier.scopus2-s2.0-84982171393-
dc.contributor.authorscopusid57190093030-
dc.contributor.authorscopusid6603449723-
dc.contributor.authorscopusid6506332517-
dc.contributor.authorscopusid57195620232-
dc.contributor.authorscopusid7003855087-
dc.contributor.authorscopusid6505717937-
dc.contributor.authorscopusid37041705700-
dc.contributor.authorscopusid57190667426-
dc.contributor.authorscopusid7006478796-
dc.contributor.authorscopusid57190671639-
dc.contributor.authorscopusid57190666191-
dc.contributor.authorscopusid56072780900-
dc.description.lastpage424en_US
dc.description.firstpage419en_US
dc.relation.volume19en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages6en_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,392-
dc.description.jcrqQ3-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0003-2522-1064-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameClavo Varas,Bernardino-
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