Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/69923
DC FieldValueLanguage
dc.contributor.authorSalas-Salas, B. G.en_US
dc.contributor.authorDomínguez-Nuez, D. J.en_US
dc.contributor.authorCabrera, R.en_US
dc.contributor.authorFerrera-Alayón, L.en_US
dc.contributor.authorLloret Sáez-Bravo, Martaen_US
dc.contributor.authorLara Jiménez, Pedro Carlosen_US
dc.date.accessioned2020-02-05T12:51:19Z-
dc.date.available2020-02-05T12:51:19Z-
dc.date.issued2019en_US
dc.identifier.issn1699-048Xen_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/69923-
dc.description.abstractBackground: Definitive radiotherapy is an effective single-modality in T1 glottic cancer. Hypofractionated schemes could offer excellent results in a shorter treatment period. We aimed to evaluate the clinical outcomes and toxicity comparing conventional vs. hypofractionated radiotherapy treatment in T1N0M0-glottic cancer. Patients and Methods: Between Jan-1st, 2005 and August-1st, 2017, in a prospective cohort study, with 10-year follow-up, 138 patients were treated with conventional schedule 2 Gy/day, total dose 70 Gy/7 weeks (N = 71) or hypofractionated schedule 2, 2–2, 25 Gy/day, total dose 63, 8–63 Gy/5, 5 weeks (N = 67). Endpoints were clinical-response rate, local relapse-free survival (LRFS), laryngectomy-free survival (LFS), toxicity rates, relapse-free survival (RFS), metastasis-free survival (MFS), second tumour-free survival (2TFS), and overall survival (OS). Results: All patients showed a complete clinical response. No differences were found for LRFS (p = 0.869), LFS (p = 0.975), RFS (p = 0.767), MFS (p = 0.601), 2TFS (p = 0.293), or OS (p = 0.685). Acute toxicity for skin and mucosae was similar (p = 0.550 and p = 0.698). Acute laryngeal toxicity was higher in the hypofractionation group (p = 0.004), due to an increase in slight moderate grade. No differences in late laryngeal edema were found (p = 0.989). Conclusion: Radiotherapy offers high rate survival, local control, and larynx preservation after 5–10-year follow-up. A hypofractionation could be preferable, since it offers the same results as conventional with fewer treatment sessions.en_US
dc.languageengen_US
dc.relation.ispartofClinical and Translational Oncologyen_US
dc.sourceClinical and Translational Oncology [ISSN 1699-048X], v. 22, p. 151–157en_US
dc.subject320101 Oncologíaen_US
dc.subject320111 Radiologíaen_US
dc.subject.otherConservative Treatmenten_US
dc.subject.otherLarynx Canceren_US
dc.subject.otherLocal Controlen_US
dc.subject.otherOverall Survivalen_US
dc.subject.otherRadiotherapy Schemeen_US
dc.subject.otherT1en_US
dc.titleHypofractionation vs. conventional radiotherapy fractionation in the conservative treatment of T1 glottic cancer: a prospective cohort studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s12094-019-02118-7en_US
dc.identifier.scopus85066618902-
dc.identifier.isi000511608200016-
dc.contributor.authorscopusid57209142019-
dc.contributor.authorscopusid57209141394-
dc.contributor.authorscopusid57189214490-
dc.contributor.authorscopusid57209144026-
dc.contributor.authorscopusid7003855087-
dc.contributor.authorscopusid7004374085-
dc.identifier.eissn1699-3055-
dc.description.lastpage157en_US
dc.identifier.issue1-
dc.description.firstpage151en_US
dc.relation.volume22en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid34822381-
dc.contributor.daisngid34833731-
dc.contributor.daisngid3702110-
dc.contributor.daisngid34822854-
dc.contributor.daisngid802813-
dc.contributor.daisngid591076-
dc.description.numberofpages7en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Salas-Salas, BG-
dc.contributor.wosstandardWOS:Dominguez-Nuez, DJ-
dc.contributor.wosstandardWOS:Cabrera, R-
dc.contributor.wosstandardWOS:Ferrera-Alayon, L-
dc.contributor.wosstandardWOS:Lloret, M-
dc.contributor.wosstandardWOS:Lara, PC-
dc.date.coverdateEnero 2020en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,833
dc.description.jcr2,737
dc.description.sjrqQ2
dc.description.jcrqQ3
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.fullNameLloret Sáez-Bravo, Marta-
crisitem.author.fullNameLara Jiménez, Pedro Carlos-
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