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dc.rights.licenseopenen_US
hal.structure.identifierUniversité de Bordeaux [UB]
dc.contributor.authorHAIK, Laura
dc.contributor.authorGONTHIER, Aurore
dc.contributor.authorQUIVY, Amandine
dc.contributor.authorGROSS-GOUPIL, Marine
dc.contributor.authorVEILLON, Remi
hal.structure.identifierUniversité de Bordeaux [UB]
dc.contributor.authorFRISON, Eric
dc.contributor.authorRAVAUD, Alain
hal.structure.identifierImmunology from Concept and Experiments to Translation [ImmunoConcept]
dc.contributor.authorDOMBLIDES, Charlotte
hal.structure.identifierUniversité de Bordeaux [UB]
dc.contributor.authorDASTE, Amaury
dc.date.accessioned2022-11-14T15:35:28Z
dc.date.available2022-11-14T15:35:28Z
dc.date.created2021-09-22
dc.date.issued2021-09-22
dc.identifier.issn0284-186X (print) 1651-226X (online)en_US
dc.identifier.otherhttps://www.tandfonline.com/doi/suppl/10.1080/0284186X.2021.1978540en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170256
dc.description.abstractEnBackground : Evidence suggests that sarcopenia is a significant predictive factor of worst outcomes and treatment-associated toxicities in patients with metastatic solid tumours. The aim of this study was to explore the relationship between low muscle mass and clinical outcomes and immune-related severe toxicities (IrST) in patients treated with immune checkpoint inhibitors (ICIs). Methods : A retrospective cohort of 261 consecutive metastatic solid tumour patients treated with ICIs were included in our study. Low muscle mass was defined as skeletal muscle index <41 cm2/m2 for females and <43 cm2/m2 for males if body mass index (BMI) <25 kg/m2 or <53 cm2/m2 if BMI ≥ 25 kg/m2. Severe toxicities (ST), including grade III-IV toxicities and side effects leading to treatment interruption, were recorded. Results : The majority of patients (n = 179; 69%) included in this study had metastatic lung cancer. The prevalence of low muscle mass was 47%. The median progression-free survival (PFS) was 32.2 weeks for low muscle mass patients and 24.3 weeks for non-low muscle mass patients (adjusted HR, 0.80; 95% CI, 0.60–1.055; p = 0.11). For low muscle mass and non-low muscle mass lung cancer patients, median PFS was 24.0 weeks and 18.8 weeks (adjusted HR, 0.70; 95% CI, 0.50–0.98; p = 0.04) and median overall survival was 50.7 weeks and 41.1 weeks (adjusted HR, 0.77; 95% CI, 0.54–1.10, p = 0.15) respectively. Immune-related severe toxicities occurred in 3.3% and 9.4% of low muscle mass and non-low muscle mass patients respectively (adjusted OR, 0.69; 95% CI: 0.31–1.49; p = 0.35). Conclusion : No difference in outcomes and safety was observed for low muscle mass and non-low muscle mass patients treated with ICIs.
dc.language.isoENen_US
dc.subject.enImmune checkpoint inhibitors
dc.subject.enImmune-related severe toxicity
dc.subject.enImmunotherapy
dc.subject.enLow muscle mass
dc.title.enThe impact of sarcopenia on the efficacy and safety of immune checkpoint inhibitors in patients with solid tumours
dc.typeArticle de revueen_US
dc.identifier.doi10.1080/0284186X.2021.1978540en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed34549686en_US
bordeaux.journalActa Oncologicaen_US
bordeaux.page1597-1603en_US
bordeaux.volume60en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue12en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
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=Acta%20Oncologica&amp;rft.date=2021-09-22&amp;rft.volume=60&amp;rft.issue=12&amp;rft.spage=1597-1603&amp;rft.epage=1597-1603&amp;rft.eissn=0284-186X%20(print)%201651-226X%20(online)&amp;rft.issn=0284-186X%20(print)%201651-226X%20(online)&amp;rft.au=HAIK,%20Laura&amp;GONTHIER,%20Aurore&amp;QUIVY,%20Amandine&amp;GROSS-GOUPIL,%20Marine&amp;VEILLON,%20Remi&amp;rft.genre=article


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