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dc.rights.licenseopenen_US
dc.contributor.authorITALIANO, A.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBELLERA, Carine
dc.contributor.authorD'ANGELO, S.
dc.date.accessioned2021-01-27T08:31:59Z
dc.date.available2021-01-27T08:31:59Z
dc.date.issued2020
dc.identifier.issn1756-8722en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26043
dc.description.abstractEnImmune checkpoint inhibitors, especially the programmed cell death receptor-1/ligand 1 (PD-1/L1) inhibitors, displayed promising efficacy in several solid tumor types and hematological malignancies. Data related to their activity in soft-tissue sarcomas (STS) are scarce.We performed a pooled analysis of clinical trials investigating a PD1 or PD-L1 antagonist in patients with advanced STS. Three hundred eighty-four patients were included in the pooled analysis; of those, 153 (39.8%) received a PD1/PD-L1 antagonist as a single agent. In patients treated with anti-PD1/PDL1 as a single agent, the overall response rate (ORR) and non-progression rate (NPR) were 15.1% and 58.5% respectively. In patients treated with a combination regimen, the ORR and NPR were 13.4% and 55.8% respectively. Analysis by histological subtype revealed that patients with alveolar soft part sarcoma and undifferentiated pleomorphic sarcoma exhibited the highest response rates and leiomyosarcoma the lowest. PD-L1 expression rate was low and inconsistently associated with objective response.PD-1/PD-L1 antagonists have limited activity in unselected STS. Future studies should implement histology and immune-based stratification of STS in their design as well as sequential blood and tissue sampling to better understand the mechanisms of resistance and response given sarcomas inherent heterogeneity.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectEPICENE
dc.title.enPD1/PD-L1 targeting in advanced soft-tissue sarcomas: a pooled analysis of phase II trials
dc.title.alternativeJ Hematol Oncolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s13045-020-00891-5en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed32430039en_US
bordeaux.journalJournal of Hematology and Oncologyen_US
bordeaux.page55en_US
bordeaux.volume13en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamEPICENE_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03122472
hal.version1
hal.date.transferred2021-01-27T08:32:02Z
hal.exporttrue
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