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dc.rights.licenseopenen_US
dc.contributor.authorROUYER, M.
dc.contributor.authorOUDARD, S.
dc.contributor.authorJOLY, F.
dc.contributor.authorFIZAZI, K.
dc.contributor.authorTUBACH, F.
dc.contributor.authorJOVE, J.
dc.contributor.authorLACUEILLE, C.
dc.contributor.authorLAMARQUE, S.
dc.contributor.authorGUIARD, E.
dc.contributor.authorBALESTRA, A.
dc.contributor.authorDROZ-PERROTEAU, C.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorFOURRIER-REGLAT, Annie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMOORE, Nicholas
dc.date.accessioned2020-07-10T14:54:11Z
dc.date.available2020-07-10T14:54:11Z
dc.date.issued2019-12
dc.identifier.issn1532-1827 (Electronic) 0007-0920 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/10416
dc.description.abstractEnBACKGROUND: Cabazitaxel is a treatment of metastatic castration-resistant prostate cancer (mCRPC) after docetaxel failure. The FUJI cohort aimed to confirm the real-life overall and progression-free survival (OS, PFS) and safety of cabazitaxel. METHODS: Multicentre, non-interventional cohort of French mCRPC patients initiating cabazitaxel between 2013 and 2015, followed 18 months. RESULTS: Four hundred one patients were recruited in 42 centres. At inclusion, median age was 70, main metastatic sites were bones (87%), lymph nodes (42%) and visceral (20%). 18% had cabazitaxel in 2nd-line treatment, 39% in 3rd-line and 43% in 4th-line or beyond. All had prior docetaxel, and 82% prior abiraterone, enzalutamide or both. Median duration of cabazitaxel treatment was 3.4 months. Median OS from cabazitaxel initiation was 11.9 months [95% CI: 10.1-12.9]. In multivariate analyses, grade >/= 3 adverse events, visceral metastases, polymedication, and >5 bone metastases were associated with a shorter OS. Main grade >/= 3 adverse events were haematological with 8% febrile neutropenia. CONCLUSION: Real-life survival with cabazitaxel in FUJI was shorter than in TROPIC (pivotal trial, median OS 15.1 months) or PROSELICA (clinical trial 20 vs 25 mg/m(2), median OS, respectively, 13.4 and 14.5 months). There was no effect of treatment-line on survival. No unexpected adverse concerns were identified. STUDY REGISTRATION: It was registered with the European Medicines Agency EUPASS registry, available at www.encepp.eu, as EUPAS10391. It has been approved as an ENCEPP SEAL study.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/us/
dc.subject.enPharmacoEpi-Drugs
dc.title.enOverall and progression-free survival with cabazitaxel in metastatic castration-resistant prostate cancer in routine clinical practice: the FUJI cohort
dc.title.alternativeBr J Canceren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41416-019-0611-6en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed31719685en_US
bordeaux.journalBritish Journal of Canceren_US
bordeaux.page1001-1008en_US
bordeaux.volume121en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue12en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-02896685
hal.version1
hal.date.transferred2020-07-10T14:54:16Z
hal.exporttrue
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