Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/72976
Campo DC Valoridioma
dc.contributor.authorGadgeel, Shirish M.en_US
dc.contributor.authorGarassino, Marina Chiaraen_US
dc.contributor.authorEsteban, Emilioen_US
dc.contributor.authorSperanza, Giovannaen_US
dc.contributor.authorFelip, Enriquetaen_US
dc.contributor.authorHochmair, Maximilian J.en_US
dc.contributor.authorPowell, Steven Francisen_US
dc.contributor.authorCheng, Susanna Y.en_US
dc.contributor.authorBischoff, Helgeen_US
dc.contributor.authorPeled, Niren_US
dc.contributor.authorHui, Rinaen_US
dc.contributor.authorReck, Martinen_US
dc.contributor.authorKurata, Takayasuen_US
dc.contributor.authorGaron, Edward B.en_US
dc.contributor.authorBoyer, Michael J.en_US
dc.contributor.authorYang, Jingen_US
dc.contributor.authorPietanza, Maria Catherineen_US
dc.contributor.authorRodriguez-Abreu, Delvysen_US
dc.date.accessioned2020-06-04T10:47:17Z-
dc.date.available2020-06-04T10:47:17Z-
dc.date.issued2019en_US
dc.identifier.issn0732-183Xen_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/72976-
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 NSCLCen_US
dc.languageengen_US
dc.relation.ispartofJournal of Clinical Oncologyen_US
dc.sourceJournal Of Clinical Oncology [ISSN 0732-183X], v. 37 (15) sup. S, Abstract 9013, (Mayo 2019)en_US
dc.subject32 Ciencias médicasen_US
dc.titleKEYNOTE-189: Updated OS and progression after the next line of therapy (PFS2) with pembrolizumab (pembro) plus chemo with pemetrexed and platinum vs placebo plus chemo for metastatic nonsquamous NSCLC.en_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.typeConferenceObjecten_US
dc.relation.conferenceAnnual Meeting of the American-Society-of-Clinical-Oncology (ASCO)en_US
dc.identifier.isi000487345806458-
dc.identifier.eissn1527-7755-
dc.identifier.issue15-
dc.relation.volume37en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Actas de congresosen_US
dc.contributor.daisngid56826-
dc.contributor.daisngid135391-
dc.contributor.daisngid97657-
dc.contributor.daisngid31498955-
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.daisngid31417340-
dc.contributor.daisngid305985-
dc.contributor.daisngid1064006-
dc.description.numberofpages2en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Gadgeel, SM-
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, SF-
dc.contributor.wosstandardWOS:Cheng, SY-
dc.contributor.wosstandardWOS:Bischoff, H-
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, MJ-
dc.contributor.wosstandardWOS:Yang, J-
dc.contributor.wosstandardWOS:Pietanza, MC-
dc.contributor.wosstandardWOS:Rodriguez-Abreu, D-
dc.date.coverdateMayo 2019en_US
dc.identifier.supplementS-
dc.identifier.abstractid9013-
dc.identifier.conferenceidevents121171-
dc.identifier.ulpgces
dc.description.sjr10,054
dc.description.jcr32,956
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.event.eventsstartdate31-05-2019-
crisitem.event.eventsenddate04-06-2019-
Colección:Actas de congresos
Vista resumida

Google ScholarTM

Verifica


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.