Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/72689
Campo DC Valoridioma
dc.contributor.authorGadgeel, S.en_US
dc.contributor.authorGarassino, M. C.en_US
dc.contributor.authorEsteban, E.en_US
dc.contributor.authorSperanza, G.en_US
dc.contributor.authorFelip, E.en_US
dc.contributor.authorHochmair, M. J.en_US
dc.contributor.authorPowell, S.en_US
dc.contributor.authorCheng, S. Y. -S.en_US
dc.contributor.authorBischoff, H. G.en_US
dc.contributor.authorPeled, N.en_US
dc.contributor.authorHui, R.en_US
dc.contributor.authorReck, M.en_US
dc.contributor.authorKurata, T.en_US
dc.contributor.authorGaron, E. B.en_US
dc.contributor.authorBoyer, M.en_US
dc.contributor.authorYang, J.en_US
dc.contributor.authorPietanza, M. C.en_US
dc.contributor.authorRodriguez-Abreu, D.en_US
dc.date.accessioned2020-05-20T17:07:15Z-
dc.date.available2020-05-20T17:07:15Z-
dc.date.issued2019en_US
dc.identifier.issn1556-0864en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/72689-
dc.description.abstractBackground: Pembro + chemo significantly improved OS and PFS over chemo alone and had manageable safety as 1L therapy for metastatic nonsquamous NSCLC in the KEYNOTE-189 study (NCT02578680). The benefit was observed irrespective of PD-L1 TPS. We present updated OS based on longer follow-up and, for the first time, PFS2. Methods: Eligible pts were randomized 2:1 to pembro (n = 410) or placebo (n = 206) + pemetrexed and carboplatin or cisplatin for 4 cycles followed by pembro or placebo for up to 35 cycles + maintenance pemetrexed. Pts in the chemo arm could crossover to pembro alone upon PD. Poststudy anticancer therapy and outcomes were collected. PFS2 was defined as time from randomization to PD per investigator after start of 2L therapy or death, whichever occurred first. There was no multiplicity adjustment, and all P values are nominal. Data cutoff was 21 Sep 2018. Results: With 18.7-mo median follow-up, pembro + chemo continued to provide longer OS (HR 0.56 [95% CI 0.45-0.70], P < .00001; median 22.0 mo vs 10.7 mo) and PFS (HR 0.48 [95% CI 0.40-0.58], P < .00001). Benefit was seen in all PD-L1 TPS groups (Table). 2L+ therapy was received by 45% in the pembro + chemo arm and 59% (54% 2L+ immunotherapy) in the placebo + chemo arm. PFS2 was longer for 1L pembro + chemo (HR 0.49 [95% CI 0.40-0.59], P < .00001; median 17.0 mo vs 9.0 mo), with no difference by TPS (Table). Conclusions: 1L pembro + pemetrexed/platinum continued to show substantial OS benefit in metastatic nonsquamous NSCLC, regardless of PD-L1 TPS and despite 54% of pts in the placebo + chemo arm receiving subsequent immunotherapy. Median OS, PFS and PFS2 were approximately doubled with pembro + chemo. These data confirm that pembro should be given as part of 1L therapy to maximize outcomes in both PD-L1 expressing and PD-L1 non-expressing NSCLC.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Thoracic Oncologyen_US
dc.sourceJournal Of Thoracic Oncology [ISSN 1556-0864], v. 14 (11) sup. 2, p. S1153, (Noviembre 2019)en_US
dc.subject32 Ciencias médicasen_US
dc.subject.otherPd-L1en_US
dc.subject.otherPembrolizumaben_US
dc.subject.otherChemotherapyen_US
dc.subject.otherNsclcen_US
dc.titleKEYNOTE-189: OS Update and Progression After the Next Line of Therapy (PFS2) with Pembrolizumab plus Chemotherapy for Metastatic Nonsquamous NSCLCen_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.typeConferenceObjecten_US
dc.identifier.isi000494945000004-
dc.identifier.eissn1556-1380-
dc.description.lastpageS1153en_US
dc.identifier.issue11-
dc.description.firstpageS1153en_US
dc.relation.volume14en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Actas de congresosen_US
dc.contributor.daisngid56826-
dc.contributor.daisngid135391-
dc.contributor.daisngid31464946-
dc.contributor.daisngid6056846-
dc.contributor.daisngid21074-
dc.contributor.daisngid745745-
dc.contributor.daisngid7427581-
dc.contributor.daisngid3041915-
dc.contributor.daisngid254414-
dc.contributor.daisngid60442-
dc.contributor.daisngid30184843-
dc.contributor.daisngid15815-
dc.contributor.daisngid292593-
dc.contributor.daisngid99177-
dc.contributor.daisngid14675-
dc.contributor.daisngid17159771-
dc.contributor.daisngid305985-
dc.contributor.daisngid1064006-
dc.description.numberofpages1en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Gadgeel, S-
dc.contributor.wosstandardWOS:Garassino, MC-
dc.contributor.wosstandardWOS:Esteban, E-
dc.contributor.wosstandardWOS:Speranza, G-
dc.contributor.wosstandardWOS:Felip, E-
dc.contributor.wosstandardWOS:Hochmair, MJ-
dc.contributor.wosstandardWOS:Powell, S-
dc.contributor.wosstandardWOS:Cheng, SYS-
dc.contributor.wosstandardWOS:Bischoff, HG-
dc.contributor.wosstandardWOS:Peled, N-
dc.contributor.wosstandardWOS:Hui, R-
dc.contributor.wosstandardWOS:Reck, M-
dc.contributor.wosstandardWOS:Kurata, T-
dc.contributor.wosstandardWOS:Garon, EB-
dc.contributor.wosstandardWOS:Boyer, M-
dc.contributor.wosstandardWOS:Yang, J-
dc.contributor.wosstandardWOS:Pietanza, MC-
dc.contributor.wosstandardWOS:Rodriguez-Abreu, D-
dc.date.coverdateNoviembre 2019en_US
dc.identifier.supplement2-
dc.identifier.ulpgces
dc.description.sjr3,218
dc.description.jcr13,357
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
Colección:Actas de congresos
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