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dc.rights.licenseopenen_US
dc.contributor.authorROSELLINI, Pietro
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorAMINTAS, Samuel
dc.contributor.authorCAUMONT, Charline
dc.contributor.authorVEILLON, Remi
dc.contributor.authorGALLAND-GIRODET, Sigolene
dc.contributor.authorCUGUILLIERE, Alain
dc.contributor.authorNGUYEN, Laurent
hal.structure.identifierImmunology from Concept and Experiments to Translation [ImmunoConcept]
dc.contributor.authorDOMBLIDES, Charlotte
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorGOUVERNEUR, Amandine
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMERLIO, Jean-Philippe
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBEZIN, Julien
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorGIRODET, Pierre-Olivier
dc.date.accessioned2023-02-20T13:45:34Z
dc.date.available2023-02-20T13:45:34Z
dc.date.issued2022-09
dc.identifier.issn1879-0852 (Electronic) 0959-8049 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172002
dc.description.abstractEnBACKGROUND: Mutations in STK11/LKB1 gene present a negative impact on tumour immune microenvironment, especially with concomitant activating KRAS mutation. These recent data may explain a decreased response to immunotherapy treatment in STK11 mutant non-small cell lung cancer (NSCLC). OBJECTIVE: The primary objective is to evaluate, in a real-life setting, overall survival (OS) in patients with NSCLC according to the presence of STK11 mutation. The secondary objective is to assess time to treatment failure (TTF) for the first-line chemotherapy or immunotherapy. METHODS: This observational multicentric study was conducted in Nouvelle-Aquitaine (France), for 24 months. Clinical, histopathological and imagery data were collected in each centre while the next-generation sequencing analysis was performed in Bordeaux Hospital University. Patient's data were longitudinally followed from NSCLC diagnosis date to the occurrence of censoring events (therapeutic failure or death, as applicable) or until the study end date. RESULTS: median OS from the first drug administration was significantly longer for STK11(wt) patients than STK11(mut) patients (16.2 months [11 - nr] versus 4.7 months [2.5-9.4]; Log-rank test P < 0.001). The Presence of STK11 mutation was significantly associated with shortened OS (RR = 2.26 [1.35-3.79], P = 0.002). First-line TTF was significantly shorter in STK11(mut) population and the presence of the mutation was significantly associated with an increase in treatment failures (RR = 1.87 [1.21-2.89], P = 0.005). The type of treatment (chemotherapy, immunotherapy) does not influence the amplitude of reduced TTF in patients with STK11(mut). CONCLUSION: The presence of STK11 mutation is associated with poor prognosis in NSCLC.
dc.language.isoENen_US
dc.subject.enNSCLC
dc.subject.enSTK11
dc.subject.enOverall survival
dc.subject.enTTF
dc.subject.enImmunotherapy
dc.subject.enKRAS
dc.title.enClinical impact of STK11 mutation in advanced-stage non-small cell lung cancer
dc.title.alternativeEur J Canceren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.ejca.2022.05.026en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed35759814en_US
bordeaux.journalEuropean Journal of Canceren_US
bordeaux.page85-95en_US
bordeaux.volume172en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCNRS
bordeaux.teamAHEAD_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03997235
hal.version1
hal.date.transferred2023-02-20T13:45:47Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=European%20Journal%20of%20Cancer&amp;rft.date=2022-09&amp;rft.volume=172&amp;rft.spage=85-95&amp;rft.epage=85-95&amp;rft.eissn=1879-0852%20(Electronic)%200959-8049%20(Linking)&amp;rft.issn=1879-0852%20(Electronic)%200959-8049%20(Linking)&amp;rft.au=ROSELLINI,%20Pietro&amp;AMINTAS,%20Samuel&amp;CAUMONT,%20Charline&amp;VEILLON,%20Remi&amp;GALLAND-GIRODET,%20Sigolene&amp;rft.genre=article


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