Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/112559
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dc.contributor.authorGadgeel, Sen_US
dc.contributor.authorRodríguez Abreu, Delvysen_US
dc.contributor.authorSperanza, Gen_US
dc.contributor.authorEsteban, Een_US
dc.contributor.authorFelip, Een_US
dc.contributor.authorDomine, Men_US
dc.contributor.authorHui, RNen_US
dc.contributor.authorHochmair, MJen_US
dc.contributor.authorClingan, Pen_US
dc.contributor.authorPowell, SFen_US
dc.contributor.authorCheng, SYSen_US
dc.contributor.authorBischoff, HGen_US
dc.contributor.authorPeled, Nen_US
dc.contributor.authorGrossi, Fen_US
dc.contributor.authorJennens, RRen_US
dc.contributor.authorReck, Men_US
dc.contributor.authorGaron, EBen_US
dc.contributor.authorNovello, Sen_US
dc.contributor.authorRubio-Viqueira, Ben_US
dc.contributor.authorBoyer, Men_US
dc.contributor.authorKurata, Ten_US
dc.contributor.authorGray, JEen_US
dc.contributor.authorYang, Jen_US
dc.contributor.authorBas, Ten_US
dc.contributor.authorPietanza, MCen_US
dc.contributor.authorGarassino, MCen_US
dc.date.accessioned2021-11-04T15:15:36Z-
dc.date.available2021-11-04T15:15:36Z-
dc.date.issued2020en_US
dc.identifier.issn0732-183Xen_US
dc.identifier.urihttp://hdl.handle.net/10553/112559-
dc.description.abstractPURPOSE In KEYNOTE-189, first-line pembrolizumab plus pemetrexed-platinum significantly improved overall survival (OS) and progression-free survival (PFS) compared with placebo plus pemetrexed-platinum in patients with metastatic nonsquamous non‒small-cell lung cancer (NSCLC), irrespective of tumor programmed death-ligand 1 (PD-L1) expression. We report an updated analysis from KEYNOTE-189 (ClinicalTrials.gov: NCT02578680). METHODS Patients were randomly assigned (2:1) to receive pemetrexed and platinum plus pembrolizumab (n = 410) or placebo (n = 206) every 3 weeks for 4 cycles, then pemetrexed maintenance plus pembrolizumab or placebo for up to a total of 35 cycles. Eligible patients with disease progression in the placebo-combination group could cross over to pembrolizumab monotherapy. Response was assessed per RECIST (version 1.1) by central review. No alpha was assigned to this updated analysis. RESULTS As of September 21, 2018 (median follow-up, 23.1 months), the updated median (95% CI) OS was 22.0 (19.5 to 25.2) months in the pembrolizumab-combination group versus 10.7 (8.7 to 13.6) months in the placebo-combination group (hazard ratio [HR], 0.56; 95% CI, 0.45 to 0.70]). Median (95% CI) PFS was 9.0 (8.1 to 9.9) months and 4.9 (4.7 to 5.5) months, respectively (HR, 0.48; 95% CI, 0.40 to 0.58). Median (95% CI) time from randomization to objective tumor progression on next-line treatment or death from any cause, whichever occurred first (progression-free-survival-2; PFS-2) was 17.0 (15.1 to 19.4) months and 9.0 (7.6 to 10.4) months, respectively (HR, 0.49; 95% CI, 0.40 to 0.59). OS and PFS benefits with pembrolizumab were observed regardless of PD-L1 expression or presence of liver/brain metastases. Incidence of grade 3-5 adverse events was similar in the pembrolizumab-combination (71.9%) and placebo-combination (66.8%) groups. CONCLUSION First-line pembrolizumab plus pemetrexed-platinum continued to demonstrate substantially improved OS and PFS in metastatic nonsquamous NSCLC, regardless of PD-L1 expression or liver/brain metastases, with manageable safety and tolerability.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Clinical Oncologyen_US
dc.sourceJournal of Clinical Oncology [ISSN 0732-183X], v. 38(14), p. 1505-1517en_US
dc.subject32 Ciencias médicasen_US
dc.subject320101 Oncologíaen_US
dc.subject.otherKEYNOTE-189en_US
dc.subject.otherPembrolizumaben_US
dc.subject.otherPlaceboen_US
dc.subject.otherPemetrexeden_US
dc.subject.otherNon–small-cell lung canceren_US
dc.titleUpdated Analysis From KEYNOTE-189: Pembrolizumab or Placebo Plus Pemetrexed and Platinum for Previously Untreated Metastatic Nonsquamous Non-Small-Cell Lung Canceren_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typearticleen_US
dc.identifier.doi10.1200/JCO.19.03136en_US
dc.identifier.pmid32150489-
dc.identifier.scopus2-s2.0-85083573113-
dc.identifier.isiWOS:000537768800002-
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dc.description.lastpage1517en_US
dc.identifier.issue14-
dc.description.firstpage1505en_US
dc.relation.volume38en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages13en_US
dc.utils.revisionen_US
dc.date.coverdateMayo 2020en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr10,482
dc.description.jcr44,544
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextopen-
item.fulltextCon 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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