Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/41319
Campo DC | Valor | idioma |
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dc.contributor.author | Gandhi, Leena | en_US |
dc.contributor.author | Rodríguez Abreu, Delvys | en_US |
dc.contributor.author | Gadgeel, Shirish M. | en_US |
dc.contributor.author | Esteban, Emilio | en_US |
dc.contributor.author | Felip, Enriqueta | en_US |
dc.contributor.author | De Angelis, Flavia | en_US |
dc.contributor.author | Dómine, Manuel | en_US |
dc.contributor.author | Clingan, Phillip R. | en_US |
dc.contributor.author | Hochmair, Maximilian J. | en_US |
dc.contributor.author | Powell, Steven F. | en_US |
dc.contributor.author | Cheng, Susanna Yee Shan | en_US |
dc.contributor.author | Bischoff, Helge G. | en_US |
dc.contributor.author | Peled, Nir | en_US |
dc.contributor.author | Grossi, Francesco | en_US |
dc.contributor.author | Jennens, Ross R. | en_US |
dc.contributor.author | Reck, Martin | en_US |
dc.contributor.author | Hui, Rina | en_US |
dc.contributor.author | Garon, Edward B. | en_US |
dc.contributor.author | Boyer, Michael | en_US |
dc.contributor.author | Rubio-Viqueira, Belén | en_US |
dc.contributor.author | Novello, Silvia | en_US |
dc.contributor.author | Kurata, Takayasu | en_US |
dc.contributor.author | Gray, Jhanelle E. | en_US |
dc.contributor.author | Vida, John | en_US |
dc.contributor.author | Wei, Ziwen | en_US |
dc.contributor.author | Yang, Jing | en_US |
dc.contributor.author | Raftopoulos, Harry | en_US |
dc.contributor.author | Pietanza, Maria Catherine | en_US |
dc.contributor.author | Garassino, Marina Chiara | en_US |
dc.contributor.author | KEYNOTE | en_US |
dc.date.accessioned | 2018-06-19T09:50:53Z | - |
dc.date.available | 2018-06-19T09:50:53Z | - |
dc.date.issued | 2018 | en_US |
dc.identifier.issn | 0028-4793 | en_US |
dc.identifier.other | WoS | - |
dc.identifier.uri | http://hdl.handle.net/10553/41319 | - |
dc.description.abstract | Background. 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.language | eng | en_US |
dc.relation.ispartof | New England Journal of Medicine | en_US |
dc.source | New England Journal Of Medicine [ISSN 0028-4793], v. 378 (22), p. 2078-2092, (Mayo 2018) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 320101 Oncología | en_US |
dc.subject.other | Cáncer de pulmón | en_US |
dc.subject.other | Metástasis | en_US |
dc.title | Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1056/NEJMoa1801005 | en_US |
dc.identifier.scopus | 85047328215 | - |
dc.identifier.isi | 000435693800004 | - |
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dc.identifier.eissn | 1533-4406 | - |
dc.description.lastpage | 2092 | en_US |
dc.identifier.issue | 22 | - |
dc.description.firstpage | 2078 | en_US |
dc.relation.volume | 378 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
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dc.description.numberofpages | 15 | en_US |
dc.utils.revision | Sí | en_US |
dc.contributor.wosstandard | WOS:Gandhi, L | - |
dc.contributor.wosstandard | WOS:Rodriguez-Abreu, D | - |
dc.contributor.wosstandard | WOS:Gadgeel, S | - |
dc.contributor.wosstandard | WOS:Esteban, E | - |
dc.contributor.wosstandard | WOS:Felip, E | - |
dc.contributor.wosstandard | WOS:De Angelis, F | - |
dc.contributor.wosstandard | WOS:Domine, M | - |
dc.contributor.wosstandard | WOS:Clingan, P | - |
dc.contributor.wosstandard | WOS:Hochmair, MJ | - |
dc.contributor.wosstandard | WOS:Powell, SF | - |
dc.contributor.wosstandard | WOS:Cheng, SYS | - |
dc.contributor.wosstandard | WOS:Bischoff, HG | - |
dc.contributor.wosstandard | WOS:Peled, N | - |
dc.contributor.wosstandard | WOS:Grossi, F | - |
dc.contributor.wosstandard | WOS:Jennens, RR | - |
dc.contributor.wosstandard | WOS:Reck, M | - |
dc.contributor.wosstandard | WOS:Hui, R | - |
dc.contributor.wosstandard | WOS:Garon, EB | - |
dc.contributor.wosstandard | WOS:Boyer, M | - |
dc.contributor.wosstandard | WOS:Rubio-Viqueira, B | - |
dc.contributor.wosstandard | WOS:Novello, S | - |
dc.contributor.wosstandard | WOS:Kurata, T | - |
dc.contributor.wosstandard | WOS:Gray, JE | - |
dc.contributor.wosstandard | WOS:Vida, J | - |
dc.contributor.wosstandard | WOS:Wei, Z | - |
dc.contributor.wosstandard | WOS:Yang, J | - |
dc.contributor.wosstandard | WOS:Raftopoulos, H | - |
dc.contributor.wosstandard | WOS:Pietanza, MC | - |
dc.contributor.wosstandard | WOS:Garassino, MC | - |
dc.date.coverdate | Mayo 2018 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 19,524 | |
dc.description.jcr | 70,67 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q1 | |
dc.description.scie | SCIE | |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | GIR Nanomaterials and Corrosion | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0003-0506-1366 | - |
crisitem.author.parentorg | Departamento de Ingeniería Mecánica | - |
crisitem.author.fullName | Rodríguez Abreu, Delvys | - |
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