TY - JOUR
T1 - COVID-19 Sequelae and the Host Proinflammatory Response
T2 - An Analysis From the OnCovid Registry
AU - on behalf of the OnCovid study group
AU - Cortellini, Alessio
AU - Gennari, Alessandra
AU - Pommeret, Fanny
AU - Patel, Grisma
AU - Newsom-Davis, Thomas
AU - Bertuzzi, Alexia
AU - Viladot, Margarita
AU - Aguilar-Company, Juan
AU - Mirallas, Oriol
AU - Felip, Eudald
AU - Lee, Alvin J.X.
AU - Pria, Alessia Dalla
AU - Sharkey, Rachel
AU - Brunet, Joan
AU - Carmona-Garcıa, Mcarmen
AU - Chester, John
AU - Mukherjee, Uma
AU - Scotti, Lorenza
AU - Dolly, Saoirse
AU - Sita-Lumsden, Ailsa
AU - Ferrante, Daniela
AU - Van Hemelrijck, Mieke
AU - Moss, Charlotte
AU - Russell, Beth
AU - Seguı, Elia
AU - Biello, Federica
AU - Krengli, Marco
AU - Marco-Hernandez, Javier
AU - Gaidano, Gianluca
AU - Patriarca, Andrea
AU - Bruna, Riccardo
AU - Roldan, Elisa
AU - Fox, Laura
AU - Pous, Anna
AU - Griscelli, Franck
AU - Salazar, Ramon
AU - Martinez-Vila, Clara
AU - Sureda, Anna
AU - Loizidou, Angela
AU - Maluquer, Clara
AU - Stoclin, Annabelle
AU - Iglesias, Maria
AU - Pedrazzoli, Paolo
AU - Rizzo, Gianpiero
AU - Santoro, Armando
AU - Rimassa, Lorenza
AU - Rossi, Sabrina
AU - Harbeck, Nadia
AU - de Torre, Ana Sanchez
AU - Pinato, David J.
N1 - Publisher Copyright:
© The Author(s) 2022. Published by Oxford University Press. All rights reserved.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - 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 ¼ .03), and the neutrophil to lymphocyte ratio (NLR; 6.0 vs 4.3, P ¼ .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 ¼ 0.66, 95% confidence interval [CI]: 0.63 to 0.69), followed by the NLR (AUC ¼ 0.58, 95% CI: 0.55 to 0.61) and lactate dehydrogenase (AUC ¼ 0.57, 95% CI: 0.52 to 0.61). Using a fixed categorical multivariable analysis, high CRP (odds ratio [OR] ¼ 2.56, 95% CI: 1.67 to 3.91) and NLR (OR ¼ 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 ¼ 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.
AB - 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 ¼ .03), and the neutrophil to lymphocyte ratio (NLR; 6.0 vs 4.3, P ¼ .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 ¼ 0.66, 95% confidence interval [CI]: 0.63 to 0.69), followed by the NLR (AUC ¼ 0.58, 95% CI: 0.55 to 0.61) and lactate dehydrogenase (AUC ¼ 0.57, 95% CI: 0.52 to 0.61). Using a fixed categorical multivariable analysis, high CRP (odds ratio [OR] ¼ 2.56, 95% CI: 1.67 to 3.91) and NLR (OR ¼ 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 ¼ 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.
UR - https://www.scopus.com/pages/publications/85134427068
U2 - 10.1093/jnci/djac057
DO - 10.1093/jnci/djac057
M3 - Article
SN - 0027-8874
VL - 114
SP - 979
EP - 987
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 7
ER -