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COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry
BACKGROUND: Fifteen percent of patients with cancer experience symptomatic sequelae, which impair post–COVID-19 outcomes. In this study, we investigated whether a proinflammatory status is associated with the development of COVID-19 sequelae. METHODS: OnCovid recruited 2795 consecutive patients who...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047221/ https://www.ncbi.nlm.nih.gov/pubmed/35417006 http://dx.doi.org/10.1093/jnci/djac057 |
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author | Cortellini, Alessio Gennari, Alessandra Pommeret, Fanny Patel, Grisma Newsom-Davis, Thomas Bertuzzi, Alexia Viladot, Margarita Aguilar-Company, Juan Mirallas, Oriol Felip, Eudald Lee, Alvin J X Dalla Pria, Alessia Sharkey, Rachel Brunet, Joan Carmona-García, MCarmen Chester, John Mukherjee, Uma Scotti, Lorenza Dolly, Saoirse Sita-Lumsden, Ailsa Ferrante, Daniela Van Hemelrijck, Mieke Moss, Charlotte Russell, Beth Seguí, Elia Biello, Federica Krengli, Marco Marco-Hernández, Javier Gaidano, Gianluca Patriarca, Andrea Bruna, Riccardo Roldán, Elisa Fox, Laura Pous, Anna Griscelli, Franck Salazar, Ramon Martinez-Vila, Clara Sureda, Anna Loizidou, Angela Maluquer, Clara Stoclin, Annabelle Iglesias, Maria Pedrazzoli, Paolo Rizzo, Gianpiero Santoro, Armando Rimassa, Lorenza Rossi, Sabrina Harbeck, Nadia Sanchez de Torre, Ana Vincenzi, Bruno Libertini, Michela Provenzano, Salvatore Generali, Daniele Grisanti, Salvatore Berardi, Rossana Tucci, Marco Mazzoni, Francesca Lambertini, Matteo Tagliamento, Marco Parisi, Alessandro Zoratto, Federica Queirolo, Paola Giusti, Raffaele Guida, Annalisa Zambelli, Alberto Tondini, Carlo Maconi, Antonio Betti, Marta Colomba, Emeline Diamantis, Nikolaos Sinclair, Alasdair Bower, Mark Ruiz-Camps, Isabel Pinato, David J |
author_facet | Cortellini, Alessio Gennari, Alessandra Pommeret, Fanny Patel, Grisma Newsom-Davis, Thomas Bertuzzi, Alexia Viladot, Margarita Aguilar-Company, Juan Mirallas, Oriol Felip, Eudald Lee, Alvin J X Dalla Pria, Alessia Sharkey, Rachel Brunet, Joan Carmona-García, MCarmen Chester, John Mukherjee, Uma Scotti, Lorenza Dolly, Saoirse Sita-Lumsden, Ailsa Ferrante, Daniela Van Hemelrijck, Mieke Moss, Charlotte Russell, Beth Seguí, Elia Biello, Federica Krengli, Marco Marco-Hernández, Javier Gaidano, Gianluca Patriarca, Andrea Bruna, Riccardo Roldán, Elisa Fox, Laura Pous, Anna Griscelli, Franck Salazar, Ramon Martinez-Vila, Clara Sureda, Anna Loizidou, Angela Maluquer, Clara Stoclin, Annabelle Iglesias, Maria Pedrazzoli, Paolo Rizzo, Gianpiero Santoro, Armando Rimassa, Lorenza Rossi, Sabrina Harbeck, Nadia Sanchez de Torre, Ana Vincenzi, Bruno Libertini, Michela Provenzano, Salvatore Generali, Daniele Grisanti, Salvatore Berardi, Rossana Tucci, Marco Mazzoni, Francesca Lambertini, Matteo Tagliamento, Marco Parisi, Alessandro Zoratto, Federica Queirolo, Paola Giusti, Raffaele Guida, Annalisa Zambelli, Alberto Tondini, Carlo Maconi, Antonio Betti, Marta Colomba, Emeline Diamantis, Nikolaos Sinclair, Alasdair Bower, Mark Ruiz-Camps, Isabel Pinato, David J |
author_sort | Cortellini, Alessio |
collection | PubMed |
description | BACKGROUND: Fifteen percent of patients with cancer experience symptomatic sequelae, which impair post–COVID-19 outcomes. In this study, we investigated whether a proinflammatory status is associated with the development of COVID-19 sequelae. METHODS: OnCovid recruited 2795 consecutive patients who were diagnosed with Severe Acute Respiratory Syndrome Coronavirus 2 infection between February 27, 2020, and February 14, 2021. This analysis focused on COVID-19 survivors who underwent a clinical reassessment after the exclusion of patients with hematological malignancies. We evaluated the association of inflammatory markers collected at COVID-19 diagnosis with sequelae, considering the impact of previous systemic anticancer therapy. All statistical tests were 2-sided. RESULTS: Of 1339 eligible patients, 203 experienced at least 1 sequela (15.2%). Median baseline C-reactive protein (CRP; 77.5 mg/L vs 22.2 mg/L, P < .001), lactate dehydrogenase (310 UI/L vs 274 UI/L, P = .03), and the neutrophil to lymphocyte ratio (NLR; 6.0 vs 4.3, P = .001) were statistically significantly higher among patients who experienced sequelae, whereas no association was reported for the platelet to lymphocyte ratio and the OnCovid Inflammatory Score, which includes albumin and lymphocytes. The widest area under the ROC curve (AUC) was reported for baseline CRP (AUC = 0.66, 95% confidence interval [CI]: 0.63 to 0.69), followed by the NLR (AUC = 0.58, 95% CI: 0.55 to 0.61) and lactate dehydrogenase (AUC = 0.57, 95% CI: 0.52 to 0.61). Using a fixed categorical multivariable analysis, high CRP (odds ratio [OR] = 2.56, 95% CI: 1.67 to 3.91) and NLR (OR = 1.45, 95% CI: 1.01 to 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 to 0.91), whereas no associations with immune checkpoint inhibitors, endocrine therapy, and other types of systemic anticancer therapy were found. CONCLUSIONS: Although the association between inflammatory status, recent chemotherapy and sequelae warrants further investigation, our findings suggest that a deranged proinflammatory reaction at COVID-19 diagnosis may predict for sequelae development. |
format | Online Article Text |
id | pubmed-9047221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90472212022-04-28 COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry Cortellini, Alessio Gennari, Alessandra Pommeret, Fanny Patel, Grisma Newsom-Davis, Thomas Bertuzzi, Alexia Viladot, Margarita Aguilar-Company, Juan Mirallas, Oriol Felip, Eudald Lee, Alvin J X Dalla Pria, Alessia Sharkey, Rachel Brunet, Joan Carmona-García, MCarmen Chester, John Mukherjee, Uma Scotti, Lorenza Dolly, Saoirse Sita-Lumsden, Ailsa Ferrante, Daniela Van Hemelrijck, Mieke Moss, Charlotte Russell, Beth Seguí, Elia Biello, Federica Krengli, Marco Marco-Hernández, Javier Gaidano, Gianluca Patriarca, Andrea Bruna, Riccardo Roldán, Elisa Fox, Laura Pous, Anna Griscelli, Franck Salazar, Ramon Martinez-Vila, Clara Sureda, Anna Loizidou, Angela Maluquer, Clara Stoclin, Annabelle Iglesias, Maria Pedrazzoli, Paolo Rizzo, Gianpiero Santoro, Armando Rimassa, Lorenza Rossi, Sabrina Harbeck, Nadia Sanchez de Torre, Ana Vincenzi, Bruno Libertini, Michela Provenzano, Salvatore Generali, Daniele Grisanti, Salvatore Berardi, Rossana Tucci, Marco Mazzoni, Francesca Lambertini, Matteo Tagliamento, Marco Parisi, Alessandro Zoratto, Federica Queirolo, Paola Giusti, Raffaele Guida, Annalisa Zambelli, Alberto Tondini, Carlo Maconi, Antonio Betti, Marta Colomba, Emeline Diamantis, Nikolaos Sinclair, Alasdair Bower, Mark Ruiz-Camps, Isabel Pinato, David J J Natl Cancer Inst Articles BACKGROUND: Fifteen percent of patients with cancer experience symptomatic sequelae, which impair post–COVID-19 outcomes. In this study, we investigated whether a proinflammatory status is associated with the development of COVID-19 sequelae. METHODS: OnCovid recruited 2795 consecutive patients who were diagnosed with Severe Acute Respiratory Syndrome Coronavirus 2 infection between February 27, 2020, and February 14, 2021. This analysis focused on COVID-19 survivors who underwent a clinical reassessment after the exclusion of patients with hematological malignancies. We evaluated the association of inflammatory markers collected at COVID-19 diagnosis with sequelae, considering the impact of previous systemic anticancer therapy. All statistical tests were 2-sided. RESULTS: Of 1339 eligible patients, 203 experienced at least 1 sequela (15.2%). Median baseline C-reactive protein (CRP; 77.5 mg/L vs 22.2 mg/L, P < .001), lactate dehydrogenase (310 UI/L vs 274 UI/L, P = .03), and the neutrophil to lymphocyte ratio (NLR; 6.0 vs 4.3, P = .001) were statistically significantly higher among patients who experienced sequelae, whereas no association was reported for the platelet to lymphocyte ratio and the OnCovid Inflammatory Score, which includes albumin and lymphocytes. The widest area under the ROC curve (AUC) was reported for baseline CRP (AUC = 0.66, 95% confidence interval [CI]: 0.63 to 0.69), followed by the NLR (AUC = 0.58, 95% CI: 0.55 to 0.61) and lactate dehydrogenase (AUC = 0.57, 95% CI: 0.52 to 0.61). Using a fixed categorical multivariable analysis, high CRP (odds ratio [OR] = 2.56, 95% CI: 1.67 to 3.91) and NLR (OR = 1.45, 95% CI: 1.01 to 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 to 0.91), whereas no associations with immune checkpoint inhibitors, endocrine therapy, and other types of systemic anticancer therapy were found. CONCLUSIONS: Although the association between inflammatory status, recent chemotherapy and sequelae warrants further investigation, our findings suggest that a deranged proinflammatory reaction at COVID-19 diagnosis may predict for sequelae development. Oxford University Press 2022-04-13 /pmc/articles/PMC9047221/ /pubmed/35417006 http://dx.doi.org/10.1093/jnci/djac057 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Cortellini, Alessio Gennari, Alessandra Pommeret, Fanny Patel, Grisma Newsom-Davis, Thomas Bertuzzi, Alexia Viladot, Margarita Aguilar-Company, Juan Mirallas, Oriol Felip, Eudald Lee, Alvin J X Dalla Pria, Alessia Sharkey, Rachel Brunet, Joan Carmona-García, MCarmen Chester, John Mukherjee, Uma Scotti, Lorenza Dolly, Saoirse Sita-Lumsden, Ailsa Ferrante, Daniela Van Hemelrijck, Mieke Moss, Charlotte Russell, Beth Seguí, Elia Biello, Federica Krengli, Marco Marco-Hernández, Javier Gaidano, Gianluca Patriarca, Andrea Bruna, Riccardo Roldán, Elisa Fox, Laura Pous, Anna Griscelli, Franck Salazar, Ramon Martinez-Vila, Clara Sureda, Anna Loizidou, Angela Maluquer, Clara Stoclin, Annabelle Iglesias, Maria Pedrazzoli, Paolo Rizzo, Gianpiero Santoro, Armando Rimassa, Lorenza Rossi, Sabrina Harbeck, Nadia Sanchez de Torre, Ana Vincenzi, Bruno Libertini, Michela Provenzano, Salvatore Generali, Daniele Grisanti, Salvatore Berardi, Rossana Tucci, Marco Mazzoni, Francesca Lambertini, Matteo Tagliamento, Marco Parisi, Alessandro Zoratto, Federica Queirolo, Paola Giusti, Raffaele Guida, Annalisa Zambelli, Alberto Tondini, Carlo Maconi, Antonio Betti, Marta Colomba, Emeline Diamantis, Nikolaos Sinclair, Alasdair Bower, Mark Ruiz-Camps, Isabel Pinato, David J COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title | COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title_full | COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title_fullStr | COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title_full_unstemmed | COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title_short | COVID-19 Sequelae and the Host Proinflammatory Response: An Analysis From the OnCovid Registry |
title_sort | covid-19 sequelae and the host proinflammatory response: an analysis from the oncovid registry |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047221/ https://www.ncbi.nlm.nih.gov/pubmed/35417006 http://dx.doi.org/10.1093/jnci/djac057 |
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