Literature DB >> 33753569

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

Gino M Dettorre1, Saoirse Dolly2, Angela Loizidou3, John Chester4,5, Amanda Jackson6, Uma Mukherjee7, Alberto Zambelli8, Juan Aguilar-Company9,10, Mark Bower11, Christopher C T Sng12, Ramon Salazar13, Alexia Bertuzzi14, Joan Brunet15, Ricard Mesia16, Ailsa Sita-Lumsden2, Elia Seguí17, Federica Biello18, Daniele Generali19,20, Salvatore Grisanti21, Pavetha Seeva2, Gianpiero Rizzo22, Michela Libertini23, Antonio Maconi24, Charlotte Moss25, Beth Russell25, Nadia Harbeck26, Bruno Vincenzi27, Rossella Bertulli28, Diego Ottaviani12, Raquel Liñan15, Andrea Marrari14, M Carmen Carmona-García15, Neha Chopra12, Carlo Alberto Tondini8, Oriol Mirallas9, Valeria Tovazzi21, Vittoria Fotia8, Claudia Andrea Cruz17, Nadia Saoudi-Gonzalez9, Eudald Felip16, Ariadna Roqué15, Alvin J X Lee12, Tom Newsom-Davis11, David García-Illescas9, Roxana Reyes17, Yien Ning Sophia Wong12, Daniela Ferrante29, Lorenza Scotti29, Javier Marco-Hernández30, Isabel Ruiz-Camps10, Andrea Patriarca31, Lorenza Rimassa32, Lorenzo Chiudinelli8, Michela Franchi8, Armando Santoro32, Aleix Prat33, Alessandra Gennari18, Mieke Van Hemelrijck2,25, Josep Tabernero34, Nikolaos Diamantis7, David J Pinato35,18.   

Abstract

BACKGROUND: 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. © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.

Entities:  

Keywords:  COVID-19; inflammation; inflammation mediators

Mesh:

Year:  2021        PMID: 33753569      PMCID: PMC7985977          DOI: 10.1136/jitc-2020-002277

Source DB:  PubMed          Journal:  J Immunother Cancer        ISSN: 2051-1426            Impact factor:   13.751


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