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dc.contributor.authorCastro, Javier dees_ES
dc.contributor.authorGonzález-Larriba, J. L.es_ES
dc.contributor.authorVázquez-Estévez, Sergioes_ES
dc.contributor.authorMassutí, Bartomeues_ES
dc.contributor.authorSánchez-Torres, J. M.es_ES
dc.contributor.authorDómine, Manueles_ES
dc.contributor.authorGarrido, Pilares_ES
dc.contributor.authorCalles, A.es_ES
dc.contributor.authorArtal, A.es_ES
dc.contributor.authorCollado, Rosaes_ES
dc.contributor.authorGarcía, R.es_ES
dc.contributor.authorSereno, M.es_ES
dc.contributor.authorMajem, M.es_ES
dc.contributor.authorMacías, J. A.es_ES
dc.contributor.authorJuan-Vidal, Óscares_ES
dc.contributor.authorGómez-Codina, J.es_ES
dc.contributor.authorHernández, B.es_ES
dc.contributor.authorLázaro, M.es_ES
dc.contributor.authorOrtega, A. L.es_ES
dc.contributor.authorCobo, M.es_ES
dc.contributor.authorTrigo, José Manueles_ES
dc.contributor.authorCarcereny Costa, Enrices_ES
dc.contributor.authorRolfo, C.es_ES
dc.contributor.authorMaciá, S.es_ES
dc.contributor.authorMuñoz, J.es_ES
dc.contributor.authorDiz, Paulaes_ES
dc.contributor.authorMéndez, M.es_ES
dc.contributor.authorRosillo, F.es_ES
dc.contributor.authorPaz-Ares, Luises_ES
dc.contributor.authorCardona, J. V.es_ES
dc.contributor.authorIsla, María Doloreses_ES
dc.date.accessioned2020-01-22T13:33:18Z-
dc.date.available2020-01-22T13:33:18Z-
dc.date.issued2017-02-
dc.identifierdoi: 10.1007/s12094-016-1527-8-
dc.identifierissn: 1699-048X-
dc.identifiere-issn: 1699-3055-
dc.identifier.citationClinical and Translational Oncology 19(2): 219-226 (2017)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/198669-
dc.description.abstract[Background/Aim] First-line bevacizumab-based therapies have been shown to improve clinical outcomes in patients with non-squamous non-small-cell lung cancer (NSCLC). We aimed to descriptively analyse patients with non-squamous NSCLC who received a long-term period of maintenance bevacizumab.-
dc.description.abstract[Patients and methods] This retrospective study included 104 patients who had already reached a progression-free survival (PFS) of at least 9 months.-
dc.description.abstract[Results] Median overall survival and PFS were 30.7 and 15.1 months, respectively. The overall response rate was 83 %. Weight loss ≤5 %, ECOG PS = 0, or low number of metastatic sites seem to be predictive factors of good evolution. The incidence of bevacizumab-related adverse events appeared to be similar as the previous studies.-
dc.description.abstract[Conclusion] Our findings show that there is a long-term survivor group whom the administration of bevacizumab resulted in a relevant prolongation of response without new safety signals. Due to the population heterogeneity, it was not possible to identify the standardised predictive factors.-
dc.description.sponsorshipThis work was supported by Roche Farma, S.A., Spain.-
dc.languageeng-
dc.publisherSpringer Naturees_ES
dc.rightsclosedAccess-
dc.subjectNon-squamous NSCLC-
dc.subjectFirst-line treatment-
dc.subjectBevacizumab-
dc.subjectBevacizumab maintenance therapy-
dc.subjectRoutine clinical practice setting-
dc.subjectObservational study-
dc.titleLong-term survival in advanced non-squamous NSCLC patients treated with first-line bevacizumab-based therapyes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1007/s12094-016-1527-8-
dc.relation.publisherversionhttp://dx.doi.org/10.1007/s12094-016-1527-8-
dc.date.updated2020-01-22T13:33:18Z-
dc.contributor.funderRoche-
dc.relation.csices_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100004337es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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