COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry

  • A. Cortellini
  • , Alessandra Gennari
  • , F. Pommeret
  • , G. Patel
  • , T. Newsom-Davis
  • , A. Bertuzzi
  • , M. Viladot
  • , J. Aguilar-Company
  • , O. Mirallas
  • , E. Felip
  • , A. J. X. Lee
  • , A. D. Pria
  • , R. Sharkey
  • , J. Brunet
  • , M. Carmona-Garcia
  • , J. Chester
  • , U. Mukherjee
  • , Lorenza Scotti
  • , S. Dolly
  • , A. Sita-Lumsden
  • Daniela FERRANTE, Hemelrijck M. Van, C. Moss, B. Russell, E. Segui, F. Biello, M. Krengli, J. Marco-Hernandez, Gianluca GAIDANO, A. Patriarca, R. Bruna, E. Roldan, L. Fox, A. Pous, F. Griscelli, R. Salazar, C. Martinez-Vila, A. Sureda, A. Loizidou, C. Maluquer, A. Stoclin, M. Iglesias, P. Pedrazzoli, G. Rizzo, A. Santoro, L. Rimassa, S. Rossi, N. Harbeck, A. S. de Torre, B. Vincenzi, M. Libertini, S. Provenzano, D. Generali, S. Grisanti, R. Berardi, M. Tucci, F. Mazzoni, M. Lambertini, M. Tagliamento, A. Parisi, F. Zoratto, P. Queirolo, R. Giusti, A. Guida, A. Zambelli, C. Tondini, A. Maconi, M. Betti, E. Colomba, N. Diamantis, A. Sinclair, M. Bower, I. Ruiz-Camps, David James PINATO

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Background: 15% of patients with cancer experience symptomatic sequelae, which impair post COVID-19 outcomes. In this study we investigated whether a pro-inflammatory status is associated with the development of COVID-19 sequelae. Methods: OnCovid recruited 2795 consecutive patients, diagnosed with SARS-CoV-2 infection between 27/02/2020-14/02/2021. This analysis focused on COVID-19 survivors who underwent a clinical re-assessment after the exclusion of patients with haematological malignancies. We evaluated the association of inflammatory markers collected at COVID-19 diagnosis with sequelae, considering the impact of prior systemic anticancer therapy (SACT). Results: Out of 1339 patients eligible, 203 experienced at least one sequela (15.2%). Median baseline C-reactive protein (CRP, 77.5 mg/L vs 22.2 mg/L, p<.001), lactate dehydrogenase (LDH, 310 UI/L vs 274 UI/L, p=.028) and neutrophil-to-lymphocyte ratio (NLR, 6.0 vs 4.3, p=.001) were statistically significantly higher among patients who experienced sequelae, while no association were reported for platelet-to-lymphocyte ratio (PLR) and the OnCovid Inflammatory Score (OIS), which includes albumin and lymphocytes. The widest Area under the ROC curve was reported for baseline CRP (AUC 0.66,95%CI:0.63-0.69), followed by the NLR (AUC0.58,95%CI:0.55-0.61) and LDH (AUC=0.57,95%CI:0.52-0.61). Using a fixed categorical multivariable analysis high CRP (OR 2.56,95%CI:1.67-3.91) and NLR (OR 1.45,95%CI:1.01-2.10) were confirmed to be statistically significantly associated with an increased risk of sequelae. Exposure to chemotherapy was associated with a decreased risk of sequelae (OR 0.57,95%CI:0.36-0.91), while no associations with immune checkpoint inhibitors, endocrine therapy, and other types of SACT were found. Conclusions: Although the association between inflammatory status, recent chemotherapy and sequelae warrants further investigations, our findings suggest that a deranged pro-inflammatory reaction at COVID-19 diagnosis may predict for sequelae development.
Lingua originaleInglese
pagine (da-a)979-987
Numero di pagine9
RivistaJournal of the National Cancer Institute
Volume114
Numero di pubblicazione7
DOI
Stato di pubblicazionePubblicato - 2022

Keywords

  • COVID-19
  • SARS-CoV-2
  • autoimmunity
  • inflammation
  • sequelae

Fingerprint

Entra nei temi di ricerca di 'COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry'. Insieme formano una fingerprint unica.

Cita questo