Afficher la notice abrégée

dc.rights.licenseopenen_US
dc.contributor.authorCOUSIN, Sophie
dc.contributor.authorTOULMONDE, Maud
dc.contributor.authorKIND, Michele
dc.contributor.authorGUEGAN, Jean-Philippe
dc.contributor.authorBESSEDE, Alban
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorCANTAREL, Coralie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBELLERA, Carine
dc.contributor.authorITALIANO, Antoine
dc.date.accessioned2023-02-15T09:10:22Z
dc.date.available2023-02-15T09:10:22Z
dc.date.issued2022-12-06
dc.identifier.issn2162-3619en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/171952
dc.description.abstractEnBreast cancer is one the most common cause of cancer death in women worldwide. We report here the first phase II study investigating a virus genetically engineered for tumor-selective replication in patients with breast cancer. Ten patients were treated with a combination of low-dose oral cyclophosphamide and intra-venous JX-594, a thymidine kinase gene-inactivated oncolytic vaccinia virus engineered for the expression of transgenes encoding human granulocyte-macrophage colony-stimulating factor (GM-CSF) and β-galactosidase. Best response as per RECIST criteria was stable disease for 2 patients and progressive disease for 8 patients. Median progression-free and overall survival were 1.6 months (95% CI: [1.1-1.9]) and 14.4 months (95% CI: [2.0 - NA]) respectively. High throughput analysis of sequential plasma samples revealed an upregulation of protein biomarkers reflecting immune induction such as IFN gamma. Whether the combination of JX-594 with an immune checkpoint inhibitor is associated with meaningful clinical activity is therefore worth to investigate.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enBreast cancer
dc.subject.enOncolytic virus
dc.subject.enJX-594
dc.title.enPhase 2 trial of intravenous oncolytic virus JX-594 combined with low-dose cyclophosphamide in patients with advanced breast cancer
dc.title.alternativeExp Hematol Oncolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s40164-022-00338-2en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed36474303en_US
bordeaux.journalExperimental Hematology & Oncologyen_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamEPICENE_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDInstitut National Du Canceren_US
bordeaux.identifier.funderIDAssociation pour la Recherche sur le Canceren_US
hal.identifierhal-03989918
hal.version1
hal.date.transferred2023-02-15T09:10:24Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Experimental%20Hematology%20&%20Oncology&rft.date=2022-12-06&rft.volume=11&rft.issue=1&rft.eissn=2162-3619&rft.issn=2162-3619&rft.au=COUSIN,%20Sophie&TOULMONDE,%20Maud&KIND,%20Michele&GUEGAN,%20Jean-Philippe&BESSEDE,%20Alban&rft.genre=article


Fichier(s) constituant ce document

Thumbnail
Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée