Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/154586
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dc.contributor.authorGarassino, Marina C.en_US
dc.contributor.authorGadgeel, Shirishen_US
dc.contributor.authorSperanza, Giovannaen_US
dc.contributor.authorFelip, Enriquetaen_US
dc.contributor.authorEsteban, Emilioen_US
dc.contributor.authorDomine, Manuelen_US
dc.contributor.authorHochmair, Maximilian J.en_US
dc.contributor.authorPowell, Steven F.en_US
dc.contributor.authorBischoff, Helge G.en_US
dc.contributor.authorPeled, Niren_US
dc.contributor.authorGrossi, Francescoen_US
dc.contributor.authorJennens, Ross R.en_US
dc.contributor.authorReck, Martinen_US
dc.contributor.authorHui, Rinaen_US
dc.contributor.authorGaron, Edward B.en_US
dc.contributor.authorKurata, Takayasuen_US
dc.contributor.authorGray, Jhanelle E.en_US
dc.contributor.authorSchwarzenberger, Paulen_US
dc.contributor.authorJensen, Erinen_US
dc.contributor.authorPietanza, M. Catherineen_US
dc.contributor.authorRodríguez Abreu, Delvysen_US
dc.date.accessioned2026-01-09T19:33:41Z-
dc.date.available2026-01-09T19:33:41Z-
dc.date.issued2023en_US
dc.identifier.issn0732-183Xen_US
dc.identifier.otherWoS-
dc.identifier.urihttps://accedacris.ulpgc.es/jspui/handle/10553/154586-
dc.description.abstractClinical trials frequently include multiple end points that mature at different times. The initial report, typically on the based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.We present 5-year outcomes from the phase 3 KEYNOTE-189 study (ClinicalTrials.gov identifier: NCT02578680). Eligible patients with previously untreated metastatic nonsquamous non-small-cell lung cancer without EGFR/ALK alterations were randomly assigned 2:1 to pembrolizumab 200 mg or placebo once every 3 weeks for up to 35 cycles with pemetrexed and investigator's choice of carboplatin/cisplatin for four cycles, followed by maintenance pemetrexed until disease progression or unacceptable toxicity. Primary end points were overall survival (OS) and progression-free survival (PFS). Among 616 randomly assigned patients (n = 410, pembrolizumab plus pemetrexed-platinum; n = 206, placebo plus pemetrexed-platinum), median time from random assignment to data cutoff (March 8, 2022) was 64.6 (range, 60.1-72.4) months. Hazard ratio (95% CI) for OS was 0.60 (0.50 to 0.72) and PFS was 0.50 (0.42 to 0.60) for pembrolizumab plus platinum-pemetrexed versus placebo plus platinum-pemetrexed. 5-year OS rates were 19.4% versus 11.3%. Toxicity was manageable. Among 57 patients who completed 35 cycles of pembrolizumab, objective response rate was 86.0% and 3-year OS rate after completing 35 cycles (approximately 5 years after random assignment) was 71.9%. Pembrolizumab plus pemetrexed-platinum maintained OS and PFS benefits versus placebo plus pemetrexed-platinum, regardless of programmed cell death ligand-1 expression. These data continue to support pembrolizumab plus pemetrexed-platinum as a standard of care in previously untreated metastatic non-small-cell lung cancer without EGFR/ALK alterations.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Clinical Oncologyen_US
dc.sourceJournal Of Clinical Oncology[ISSN 0732-183X],v. 41 (11), (Abril 2023)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3209 Farmacologíaen_US
dc.subject320713 Oncologíaen_US
dc.subject.otherChemotherapyen_US
dc.titlePembrolizumab Plus Pemetrexed and Platinum in Nonsquamous Non-Small-Cell Lung Cancer: 5-Year Outcomes From the Phase 3 KEYNOTE-189 Studyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1200/JCO.22.01989en_US
dc.identifier.isi001648015500003-
dc.identifier.eissn1527-7755-
dc.identifier.issue11-
dc.relation.volume41en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
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dc.description.numberofpages14en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Garassino, MC-
dc.contributor.wosstandardWOS:Gadgeel, S-
dc.contributor.wosstandardWOS:Speranza, G-
dc.contributor.wosstandardWOS:Felip, E-
dc.contributor.wosstandardWOS:Esteban, E-
dc.contributor.wosstandardWOS:Domine, M-
dc.contributor.wosstandardWOS:Hochmair, MJ-
dc.contributor.wosstandardWOS:Powell, SF-
dc.contributor.wosstandardWOS:Bischoff, HG-
dc.contributor.wosstandardWOS:Peled, N-
dc.contributor.wosstandardWOS:Grossi, F-
dc.contributor.wosstandardWOS:Jennens, RR-
dc.contributor.wosstandardWOS:Reck, M-
dc.contributor.wosstandardWOS:Hui, RN-
dc.contributor.wosstandardWOS:Garon, EB-
dc.contributor.wosstandardWOS:Kurata, T-
dc.contributor.wosstandardWOS:Gray, JE-
dc.contributor.wosstandardWOS:Schwarzenberger, P-
dc.contributor.wosstandardWOS:Jensen, E-
dc.contributor.wosstandardWOS:Pietanza, MC-
dc.contributor.wosstandardWOS:Rodríguez-Abreu, D-
dc.date.coverdateAbril 2023en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr10,639
dc.description.jcr42,1
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds11,0
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR Nanomaterials and Corrosion-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0003-0506-1366-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.fullNameRodríguez Abreu, Delvys-
Colección:Artículos
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