Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/69923
Campo DC | Valor | idioma |
---|---|---|
dc.contributor.author | Salas-Salas, B. G. | en_US |
dc.contributor.author | Domínguez-Nuez, D. J. | en_US |
dc.contributor.author | Cabrera, R. | en_US |
dc.contributor.author | Ferrera-Alayón, L. | en_US |
dc.contributor.author | Lloret Sáez-Bravo, Marta | en_US |
dc.contributor.author | Lara Jiménez, Pedro Carlos | en_US |
dc.date.accessioned | 2020-02-05T12:51:19Z | - |
dc.date.available | 2020-02-05T12:51:19Z | - |
dc.date.issued | 2019 | en_US |
dc.identifier.issn | 1699-048X | en_US |
dc.identifier.other | Scopus | - |
dc.identifier.uri | http://hdl.handle.net/10553/69923 | - |
dc.description.abstract | Background: 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.language | eng | en_US |
dc.relation.ispartof | Clinical and Translational Oncology | en_US |
dc.source | Clinical and Translational Oncology [ISSN 1699-048X], v. 22, p. 151–157 | en_US |
dc.subject | 320101 Oncología | en_US |
dc.subject | 320111 Radiología | en_US |
dc.subject.other | Conservative Treatment | en_US |
dc.subject.other | Larynx Cancer | en_US |
dc.subject.other | Local Control | en_US |
dc.subject.other | Overall Survival | en_US |
dc.subject.other | Radiotherapy Scheme | en_US |
dc.subject.other | T1 | en_US |
dc.title | Hypofractionation vs. conventional radiotherapy fractionation in the conservative treatment of T1 glottic cancer: a prospective cohort study | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1007/s12094-019-02118-7 | en_US |
dc.identifier.scopus | 85066618902 | - |
dc.identifier.isi | 000511608200016 | - |
dc.contributor.authorscopusid | 57209142019 | - |
dc.contributor.authorscopusid | 57209141394 | - |
dc.contributor.authorscopusid | 57189214490 | - |
dc.contributor.authorscopusid | 57209144026 | - |
dc.contributor.authorscopusid | 7003855087 | - |
dc.contributor.authorscopusid | 7004374085 | - |
dc.identifier.eissn | 1699-3055 | - |
dc.description.lastpage | 157 | en_US |
dc.identifier.issue | 1 | - |
dc.description.firstpage | 151 | en_US |
dc.relation.volume | 22 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.contributor.daisngid | 34822381 | - |
dc.contributor.daisngid | 34833731 | - |
dc.contributor.daisngid | 3702110 | - |
dc.contributor.daisngid | 34822854 | - |
dc.contributor.daisngid | 802813 | - |
dc.contributor.daisngid | 591076 | - |
dc.description.numberofpages | 7 | en_US |
dc.utils.revision | Sí | en_US |
dc.contributor.wosstandard | WOS:Salas-Salas, BG | - |
dc.contributor.wosstandard | WOS:Dominguez-Nuez, DJ | - |
dc.contributor.wosstandard | WOS:Cabrera, R | - |
dc.contributor.wosstandard | WOS:Ferrera-Alayon, L | - |
dc.contributor.wosstandard | WOS:Lloret, M | - |
dc.contributor.wosstandard | WOS:Lara, PC | - |
dc.date.coverdate | Enero 2020 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 0,833 | |
dc.description.jcr | 2,737 | |
dc.description.sjrq | Q2 | |
dc.description.jcrq | Q3 | |
dc.description.scie | SCIE | |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | Departamento de Ciencias Clínicas | - |
crisitem.author.fullName | Lloret Sáez-Bravo, Marta | - |
crisitem.author.fullName | Lara Jiménez, Pedro Carlos | - |
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