Systemic pro-inflammatory response identifies patients with cancer with adverse outcomes from SARS-CoV-2 infection: the OnCovid Inflammatory Score

dc.contributor.authorDettorre, Gino M.
dc.contributor.authorDolly, Saoirse
dc.contributor.authorLoizidou, Angela
dc.contributor.authorChester, John
dc.contributor.authorJackson, Amanda
dc.contributor.authorMukherjee, Uma
dc.contributor.authorZambelli, Alberto
dc.contributor.authorAguilar Company, Juan
dc.contributor.authorBower, Mark
dc.contributor.authorSng, Christopher C. T.
dc.contributor.authorSalazar Soler, Ramón
dc.contributor.authorBertuzzi, Alexia
dc.contributor.authorBrunet, Joan
dc.contributor.authorMesía Nin, Ricard
dc.contributor.authorSita-Lumsden, Ailsa
dc.contributor.authorSeguí, Elia
dc.contributor.authorBiello, Federica
dc.contributor.authorGenerali, Daniele
dc.contributor.authorGrisanti, Salvatore
dc.contributor.authorSeeva, Pavetha
dc.contributor.authorRizzo, Gianpiero
dc.contributor.authorLibertini, Michela
dc.contributor.authorMaconi, Antonio
dc.contributor.authorMoss, Charlotte
dc.contributor.authorRussell, Beth
dc.contributor.authorHarbeck, Nadia
dc.contributor.authorVincenzi, Bruno
dc.contributor.authorBertulli, Rossella
dc.contributor.authorOttaviani, Diego
dc.contributor.authorLiñan, Raquel
dc.contributor.authorMarrari, Andrea
dc.contributor.authorCarmona García, M. Carmen
dc.contributor.authorChopra, Neha
dc.contributor.authorTondini, Carlo Alberto
dc.contributor.authorMirallas, Oriol
dc.contributor.authorTovazzi, Valeria
dc.contributor.authorFotia, Vittoria
dc.contributor.authorCruz, Claudia Andrea
dc.contributor.authorSaoudi González, Nadia
dc.contributor.authorFelip, Eudald
dc.contributor.authorRoqué, Ariadna
dc.contributor.authorLee, Alvin J. X.
dc.contributor.authorNewsom-Davis, Tom
dc.contributor.authorGarcía Illescas, David
dc.contributor.authorReyes, Roxana
dc.contributor.authorWong, Yien Ning Sophia
dc.contributor.authorFerrante, Daniela
dc.contributor.authorScotti, Lorenza
dc.contributor.authorMarco Hernández, Javier
dc.contributor.authorRuiz, Isabel (Ruiz Camps)
dc.contributor.authorPatriarca, Andrea
dc.contributor.authorRimassa, Lorenza
dc.contributor.authorChiudinelli, Lorenzo
dc.contributor.authorFranchi, Michela
dc.contributor.authorSantoro, Armando
dc.contributor.authorPrat Aparicio, Aleix
dc.contributor.authorGennari, Alessandra
dc.contributor.authorVan Hemelrijck, Mieke
dc.contributor.authorTabernero Caturla, Josep
dc.contributor.authorDiamantis, Nikolaos
dc.contributor.authorPinato, David J.
dc.contributor.authorOnCovid study group
dc.date.accessioned2021-04-08T08:49:32Z
dc.date.available2021-04-08T08:49:32Z
dc.date.issued2021-03-01
dc.date.updated2021-04-08T08:02:43Z
dc.description.abstractBackground: Patients with cancer are particularly susceptible to SARS-CoV-2 infection. The systemic inflammatory response is a pathogenic mechanism shared by cancer progression and COVID-19. We investigated systemic inflammation as a driver of severity and mortality from COVID-19, evaluating the prognostic role of commonly used inflammatory indices in SARS-CoV-2-infected patients with cancer accrued to the OnCovid study. Methods: In a multicenter cohort of SARS-CoV-2-infected patients with cancer in Europe, we evaluated dynamic changes in neutrophil:lymphocyte ratio (NLR); platelet:lymphocyte ratio (PLR); Prognostic Nutritional Index (PNI), renamed the OnCovid Inflammatory Score (OIS); modified Glasgow Prognostic Score (mGPS); and Prognostic Index (PI) in relation to oncological and COVID-19 infection features, testing their prognostic potential in independent training (n=529) and validation (n=542) sets. Results: We evaluated 1071 eligible patients, of which 625 (58.3%) were men, and 420 were patients with malignancy in advanced stage (39.2%), most commonly genitourinary (n=216, 20.2%). 844 (78.8%) had ≥1 comorbidity and 754 (70.4%) had ≥1 COVID-19 complication. NLR, OIS, and mGPS worsened at COVID-19 diagnosis compared with pre-COVID-19 measurement (p<0.01), recovering in survivors to pre-COVID-19 levels. Patients in poorer risk categories for each index except the PLR exhibited higher mortality rates (p<0.001) and shorter median overall survival in the training and validation sets (p<0.01). Multivariable analyses revealed the OIS to be most independently predictive of survival (validation set HR 2.48, 95% CI 1.47 to 4.20, p=0.001; adjusted concordance index score 0.611). Conclusions: Systemic inflammation is a validated prognostic domain in SARS-CoV-2-infected patients with cancer and can be used as a bedside predictor of adverse outcome. Lymphocytopenia and hypoalbuminemia as computed by the OIS are independently predictive of severe COVID-19, supporting their use for risk stratification. Reversal of the COVID-19-induced proinflammatory state is a putative therapeutic strategy in patients with cancer.
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec717453
dc.identifier.pmid33753569
dc.identifier.urihttps://hdl.handle.net/2445/176045
dc.language.isoeng
dc.publisherBMJ
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1136/jitc-2020-002277
dc.relation.ispartofJournal for ImmunoTherapy of Cancer, 2021, vol. 9, num. 3
dc.relation.urihttps://doi.org/10.1136/jitc-2020-002277
dc.rightscc by (c) Dettorre et al., 2021
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationCàncer
dc.subject.classificationSARS-CoV-2
dc.subject.classificationCOVID-19
dc.subject.otherCancer
dc.subject.otherSARS-CoV-2
dc.subject.otherCOVID-19
dc.titleSystemic pro-inflammatory response identifies patients with cancer with adverse outcomes from SARS-CoV-2 infection: the OnCovid Inflammatory Score
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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