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Systemic pro-inflammatory response identifies patients with cancer with adverse outcomes from SARS-CoV-2 infection: the OnCovid Inflammatory Score.
Dettorre, Gino M; Dolly, Saoirse; Loizidou, Angela; Chester, John; Jackson, Amanda; Mukherjee, Uma; Zambelli, Alberto; Aguilar-Company, Juan; Bower, Mark; Sng, Christopher C T; Salazar, Ramon; Bertuzzi, Alexia; Brunet, Joan; Mesia, Ricard; Sita-Lumsden, Ailsa; Seguí, Elia; Biello, Federica; Generali, Daniele; Grisanti, Salvatore; Seeva, Pavetha; Rizzo, Gianpiero; Libertini, Michela; Maconi, Antonio; Moss, Charlotte; Russell, Beth; Harbeck, Nadia; Vincenzi, Bruno; Bertulli, Rossella; Ottaviani, Diego; Liñan, Raquel; Marrari, Andrea; Carmona-García, M Carmen; Chopra, Neha; Tondini, Carlo Alberto; Mirallas, Oriol; Tovazzi, Valeria; Fotia, Vittoria; Cruz, Claudia Andrea; Saoudi-Gonzalez, Nadia; Felip, Eudald; Roqué, Ariadna; Lee, Alvin J X; Newsom-Davis, Tom; García-Illescas, David; Reyes, Roxana; Wong, Yien Ning Sophia; Ferrante, Daniela; Scotti, Lorenza; Marco-Hernández, Javier; Ruiz-Camps, Isabel.
  • Dettorre GM; Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.
  • Dolly S; Medical Oncology, Guy's and St Thomas' NHS Foundation Trust (GSTT), London, UK.
  • Loizidou A; Department of Infectious Diseases, Internal Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
  • Chester J; Medical Oncology, School of Medicine, Cardiff University, Cardiff, UK.
  • Jackson A; Medical Oncology, Velindre Cancer Centre, Cardiff, UK.
  • Mukherjee U; Clinical Trials, Velindre Cancer Centre, Cardiff, UK.
  • Zambelli A; Medical Oncology, Barts Health NHS Trust, London, UK.
  • Aguilar-Company J; Oncology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Bower M; Medical Oncology, Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain.
  • Sng CCT; Infectious Diseases, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Salazar R; Department of Oncology and National Centre for HIV Malignancy, Chelsea and Westminster Hospital, London, UK.
  • Bertuzzi A; Cancer Division, University College London Hospitals, London, UK.
  • Brunet J; Department of Medical Oncology, ICO L'Hospitalet, Oncobell Program (IDIBELL), CIBERONC, Hospitalet de Llobregat, Spain.
  • Mesia R; Medical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.
  • Sita-Lumsden A; Department of Medical Oncology, Catalan Institute of Oncology, University Hospital Josep Trueta, Girona, Spain.
  • Seguí E; Department of Medical Oncology, Catalan Institute of Oncology, Badalona, Spain.
  • Biello F; Medical Oncology, Guy's and St Thomas' NHS Foundation Trust (GSTT), London, UK.
  • Generali D; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Grisanti S; Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale and Maggiore della Carità Hospital, Novara, Italy.
  • Seeva P; Multidisciplinary Breast Pathology and Translational Research Unit, ASST Cremona, Cremona, Italy.
  • Rizzo G; Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
  • Libertini M; Medical Oncology Unit, Spedali Civili, Brescia, Italy.
  • Maconi A; Medical Oncology, Guy's and St Thomas' NHS Foundation Trust (GSTT), London, UK.
  • Moss C; Medical Oncology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Russell B; Medical Oncology Unit, Fondazione Poliambulanza Istituto Ospedaliero, Brescia, Italy.
  • Harbeck N; Infrastruttura Ricerca Formazione Innovazione, Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
  • Vincenzi B; Translational Oncology and Urology Research (TOUR), School of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
  • Bertulli R; Translational Oncology and Urology Research (TOUR), School of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
  • Ottaviani D; Department of Gynecology and Obstetrics, Breast Center and Gynecological Cancer Center and CCC Munich, University Hospital Munich, Munich, Germany.
  • Liñan R; Medical Oncology, Policlinico Universitario Campus Bio-Medico, Rome, Italy.
  • Marrari A; Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
  • Carmona-García MC; Cancer Division, University College London Hospitals, London, UK.
  • Chopra N; Department of Medical Oncology, Catalan Institute of Oncology, University Hospital Josep Trueta, Girona, Spain.
  • Tondini CA; Medical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.
  • Mirallas O; Department of Medical Oncology, Catalan Institute of Oncology, University Hospital Josep Trueta, Girona, Spain.
  • Tovazzi V; Cancer Division, University College London Hospitals, London, UK.
  • Fotia V; Oncology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Cruz CA; Medical Oncology, Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain.
  • Saoudi-Gonzalez N; Medical Oncology Unit, Spedali Civili, Brescia, Italy.
  • Felip E; Oncology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Roqué A; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Lee AJX; Medical Oncology, Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain.
  • Newsom-Davis T; Department of Medical Oncology, Catalan Institute of Oncology, Badalona, Spain.
  • García-Illescas D; Department of Medical Oncology, Catalan Institute of Oncology, University Hospital Josep Trueta, Girona, Spain.
  • Reyes R; Cancer Division, University College London Hospitals, London, UK.
  • Wong YNS; Department of Oncology and National Centre for HIV Malignancy, Chelsea and Westminster Hospital, London, UK.
  • Ferrante D; Medical Oncology, Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain.
  • Scotti L; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Marco-Hernández J; Cancer Division, University College London Hospitals, London, UK.
  • Ruiz-Camps I; Department of Translational Medicine, Unit of Cancer Epidemiology, CPO-Piemonte, University of Eastern Piedmont, Novara, Italy.
J Immunother Cancer ; 9(3)2021 03.
Article in English | MEDLINE | ID: covidwho-1147333
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 neutrophillymphocyte ratio (NLR); plateletlymphocyte 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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 Drug Treatment / Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Language: English Year: 2021 Document Type: Article Affiliation country: Jitc-2020-002277

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 Drug Treatment / Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Language: English Year: 2021 Document Type: Article Affiliation country: Jitc-2020-002277