Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/41319
DC FieldValueLanguage
dc.contributor.authorGandhi, Leenaen_US
dc.contributor.authorRodríguez Abreu, Delvysen_US
dc.contributor.authorGadgeel, Shirish M.en_US
dc.contributor.authorEsteban, Emilioen_US
dc.contributor.authorFelip, Enriquetaen_US
dc.contributor.authorDe Angelis, Flaviaen_US
dc.contributor.authorDómine, Manuelen_US
dc.contributor.authorClingan, Phillip R.en_US
dc.contributor.authorHochmair, Maximilian J.en_US
dc.contributor.authorPowell, Steven F.en_US
dc.contributor.authorCheng, Susanna Yee Shanen_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.authorBoyer, Michaelen_US
dc.contributor.authorRubio-Viqueira, Belénen_US
dc.contributor.authorNovello, Silviaen_US
dc.contributor.authorKurata, Takayasuen_US
dc.contributor.authorGray, Jhanelle E.en_US
dc.contributor.authorVida, Johnen_US
dc.contributor.authorWei, Ziwenen_US
dc.contributor.authorYang, Jingen_US
dc.contributor.authorRaftopoulos, Harryen_US
dc.contributor.authorPietanza, Maria Catherineen_US
dc.contributor.authorGarassino, Marina Chiaraen_US
dc.contributor.authorKEYNOTEen_US
dc.date.accessioned2018-06-19T09:50:53Z-
dc.date.available2018-06-19T09:50:53Z-
dc.date.issued2018en_US
dc.identifier.issn0028-4793en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/41319-
dc.description.abstractBackground. First-line therapy for advanced non–small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial. Methods. In this double-blind, phase 3 trial, we randomly assigned (in a 2:1 ratio) 616 patients with metastatic nonsquamous NSCLC without sensitizing EGFR or ALK mutations who had received no previous treatment for metastatic disease to receive pemetrexed and a platinum-based drug plus either 200 mg of pembrolizumab or placebo every 3 weeks for 4 cycles, followed by pembrolizumab or placebo for up to a total of 35 cycles plus pemetrexed maintenance therapy. Crossover to pembrolizumab monotherapy was permitted among the patients in the placebo-combination group who had verified disease progression. The primary end points were overall survival and progression-free survival, as assessed by blinded, independent central radiologic review. Results. After a median follow-up of 10.5 months, the estimated rate of overall survival at 12 months was 69.2% (95% confidence interval [CI], 64.1 to 73.8) in the pembrolizumab-combination group versus 49.4% (95% CI, 42.1 to 56.2) in the placebo-combination group (hazard ratio for death, 0.49; 95% CI, 0.38 to 0.64; P<0.001). Improvement in overall survival was seen across all PD-L1 categories that were evaluated. Median progression-free survival was 8.8 months (95% CI, 7.6 to 9.2) in the pembrolizumab-combination group and 4.9 months (95% CI, 4.7 to 5.5) in the placebo-combination group (hazard ratio for disease progression or death, 0.52; 95% CI, 0.43 to 0.64; P<0.001). Adverse events of grade 3 or higher occurred in 67.2% of the patients in the pembrolizumab-combination group and in 65.8% of those in the placebo-combination group. Conclusions. In patients with previously untreated metastatic nonsquamous NSCLC without EGFR or ALK mutations, the addition of pembrolizumab to standard chemotherapy of pemetrexed and a platinum-based drug resulted in significantly longer overall survival and progression-free survival than chemotherapy alone.en_US
dc.languageengen_US
dc.relation.ispartofNew England Journal of Medicineen_US
dc.sourceNew England Journal Of Medicine [ISSN 0028-4793], v. 378 (22), p. 2078-2092, (Mayo 2018)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320101 Oncologíaen_US
dc.subject.otherCáncer de pulmónen_US
dc.subject.otherMetástasisen_US
dc.titlePembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Canceren_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1056/NEJMoa1801005en_US
dc.identifier.scopus85047328215-
dc.identifier.isi000435693800004-
dc.contributor.authorscopusid36933707100-
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dc.contributor.authorscopusid7201708870-
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dc.contributor.authorscopusid6506071717-
dc.contributor.authorscopusid8739577000-
dc.contributor.authorscopusid16232960200-
dc.identifier.eissn1533-4406-
dc.description.lastpage2092en_US
dc.identifier.issue22-
dc.description.firstpage2078en_US
dc.relation.volume378en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
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dc.description.numberofpages15en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Gandhi, L-
dc.contributor.wosstandardWOS:Rodriguez-Abreu, D-
dc.contributor.wosstandardWOS:Gadgeel, S-
dc.contributor.wosstandardWOS:Esteban, E-
dc.contributor.wosstandardWOS:Felip, E-
dc.contributor.wosstandardWOS:De Angelis, F-
dc.contributor.wosstandardWOS:Domine, M-
dc.contributor.wosstandardWOS:Clingan, P-
dc.contributor.wosstandardWOS:Hochmair, MJ-
dc.contributor.wosstandardWOS:Powell, SF-
dc.contributor.wosstandardWOS:Cheng, SYS-
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, R-
dc.contributor.wosstandardWOS:Garon, EB-
dc.contributor.wosstandardWOS:Boyer, M-
dc.contributor.wosstandardWOS:Rubio-Viqueira, B-
dc.contributor.wosstandardWOS:Novello, S-
dc.contributor.wosstandardWOS:Kurata, T-
dc.contributor.wosstandardWOS:Gray, JE-
dc.contributor.wosstandardWOS:Vida, J-
dc.contributor.wosstandardWOS:Wei, Z-
dc.contributor.wosstandardWOS:Yang, J-
dc.contributor.wosstandardWOS:Raftopoulos, H-
dc.contributor.wosstandardWOS:Pietanza, MC-
dc.contributor.wosstandardWOS:Garassino, MC-
dc.date.coverdateMayo 2018en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr19,524
dc.description.jcr70,67
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
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-
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