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-LumsdenDaniela 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, Torre A. S. de, 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

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