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Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial

BACKGROUND: The Clinical Trial of Sarilumab in Adults With COVID-19 (SARICOR) showed that patients with coronavirus disease 2019 (COVID-19) pneumonia and increased levels of interleukin (IL)-6 might benefit from blockade of the IL-6 pathway. However, the benefit from this intervention might not be u...

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Autores principales: Trigo-Rodríguez, Marta, Cárcel, Sheila, Navas, Ana, Espíndola-Gómez, Reinaldo, Garrido-Gracia, José Carlos, Esteban Moreno, María Ángeles, León-López, Rafael, Pérez-Crespo, Pedro María Martínez, Alonso, Eduardo Aguilar, Vinuesa, David, Romero-Palacios, Alberto, Pérez-Camacho, Inés, Gutiérrez-Gutiérrez, Belén, Martínez-Marcos, Francisco Javier, Fernández-Roldán, Concepción, León, Eva, Caño, Alexandra Aceituno, Corzo-Delgado, Juan E, Perez-Nadales, Elena, Riazzo, Cristina, de la Fuente, Carmen, Jurado, Aurora, Torre-Cisneros, Julián, Merchante, Nicolás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077828/
https://www.ncbi.nlm.nih.gov/pubmed/37035487
http://dx.doi.org/10.1093/ofid/ofad133
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author Trigo-Rodríguez, Marta
Cárcel, Sheila
Navas, Ana
Espíndola-Gómez, Reinaldo
Garrido-Gracia, José Carlos
Esteban Moreno, María Ángeles
León-López, Rafael
Pérez-Crespo, Pedro María Martínez
Alonso, Eduardo Aguilar
Vinuesa, David
Romero-Palacios, Alberto
Pérez-Camacho, Inés
Gutiérrez-Gutiérrez, Belén
Martínez-Marcos, Francisco Javier
Fernández-Roldán, Concepción
León, Eva
Caño, Alexandra Aceituno
Corzo-Delgado, Juan E
Perez-Nadales, Elena
Riazzo, Cristina
de la Fuente, Carmen
Jurado, Aurora
Torre-Cisneros, Julián
Merchante, Nicolás
author_facet Trigo-Rodríguez, Marta
Cárcel, Sheila
Navas, Ana
Espíndola-Gómez, Reinaldo
Garrido-Gracia, José Carlos
Esteban Moreno, María Ángeles
León-López, Rafael
Pérez-Crespo, Pedro María Martínez
Alonso, Eduardo Aguilar
Vinuesa, David
Romero-Palacios, Alberto
Pérez-Camacho, Inés
Gutiérrez-Gutiérrez, Belén
Martínez-Marcos, Francisco Javier
Fernández-Roldán, Concepción
León, Eva
Caño, Alexandra Aceituno
Corzo-Delgado, Juan E
Perez-Nadales, Elena
Riazzo, Cristina
de la Fuente, Carmen
Jurado, Aurora
Torre-Cisneros, Julián
Merchante, Nicolás
author_sort Trigo-Rodríguez, Marta
collection PubMed
description BACKGROUND: The Clinical Trial of Sarilumab in Adults With COVID-19 (SARICOR) showed that patients with coronavirus disease 2019 (COVID-19) pneumonia and increased levels of interleukin (IL)-6 might benefit from blockade of the IL-6 pathway. However, the benefit from this intervention might not be uniform. In this subanalysis, we sought to determine if other immunoactivation markers, besides IL-6, could identify which subgroup of patients benefit most from this intervention. METHODS: The SARICOR trial was a phase II, open-label, multicenter, controlled trial (July 2020–March 2021) in which patients were randomized to receive usual care (UC; control group), UC plus a single dose of sarilumab 200 mg (sarilumab-200 group), or UC plus a single dose of sarilumab 400 mg (sarilumab-400 group). Patients who had baseline serum samples for cytokine determination (IL-8, IL-10, monocyte chemoattractant protein–1, interferon-inducible protein [IP]-10) were included in this secondary analysis. Progression to acute respiratory distress syndrome (ARDS) according to cytokine levels and treatment received was evaluated. RESULTS: One hundred one (88%) of 115 patients enrolled in the SARICOR trial had serum samples (control group: n = 33; sarilumab-200: n = 33; sarilumab-400: n = 35). Among all evaluated biomarkers, IP-10 showed the strongest association with treatment outcome. Patients with IP-10 ≥2500 pg/mL treated with sarilumab-400 had a lower probability of progression (13%) compared with the control group (58%; hazard ratio, 0.19; 95% CI, 0.04–0.90; P = .04). Conversely, patients with IP-10 <2500 pg/mL did not show these differences. CONCLUSIONS: IP-10 may predict progression to ARDS in patients with COVID-19 pneumonia and IL-6 levels >40 pg/mL. Importantly, IP-10 value <2500 pg/mL might discriminate those individuals who might not benefit from sarilumab therapy among those with high IL-6 levels.
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spelling pubmed-100778282023-04-07 Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial Trigo-Rodríguez, Marta Cárcel, Sheila Navas, Ana Espíndola-Gómez, Reinaldo Garrido-Gracia, José Carlos Esteban Moreno, María Ángeles León-López, Rafael Pérez-Crespo, Pedro María Martínez Alonso, Eduardo Aguilar Vinuesa, David Romero-Palacios, Alberto Pérez-Camacho, Inés Gutiérrez-Gutiérrez, Belén Martínez-Marcos, Francisco Javier Fernández-Roldán, Concepción León, Eva Caño, Alexandra Aceituno Corzo-Delgado, Juan E Perez-Nadales, Elena Riazzo, Cristina de la Fuente, Carmen Jurado, Aurora Torre-Cisneros, Julián Merchante, Nicolás Open Forum Infect Dis Major Article BACKGROUND: The Clinical Trial of Sarilumab in Adults With COVID-19 (SARICOR) showed that patients with coronavirus disease 2019 (COVID-19) pneumonia and increased levels of interleukin (IL)-6 might benefit from blockade of the IL-6 pathway. However, the benefit from this intervention might not be uniform. In this subanalysis, we sought to determine if other immunoactivation markers, besides IL-6, could identify which subgroup of patients benefit most from this intervention. METHODS: The SARICOR trial was a phase II, open-label, multicenter, controlled trial (July 2020–March 2021) in which patients were randomized to receive usual care (UC; control group), UC plus a single dose of sarilumab 200 mg (sarilumab-200 group), or UC plus a single dose of sarilumab 400 mg (sarilumab-400 group). Patients who had baseline serum samples for cytokine determination (IL-8, IL-10, monocyte chemoattractant protein–1, interferon-inducible protein [IP]-10) were included in this secondary analysis. Progression to acute respiratory distress syndrome (ARDS) according to cytokine levels and treatment received was evaluated. RESULTS: One hundred one (88%) of 115 patients enrolled in the SARICOR trial had serum samples (control group: n = 33; sarilumab-200: n = 33; sarilumab-400: n = 35). Among all evaluated biomarkers, IP-10 showed the strongest association with treatment outcome. Patients with IP-10 ≥2500 pg/mL treated with sarilumab-400 had a lower probability of progression (13%) compared with the control group (58%; hazard ratio, 0.19; 95% CI, 0.04–0.90; P = .04). Conversely, patients with IP-10 <2500 pg/mL did not show these differences. CONCLUSIONS: IP-10 may predict progression to ARDS in patients with COVID-19 pneumonia and IL-6 levels >40 pg/mL. Importantly, IP-10 value <2500 pg/mL might discriminate those individuals who might not benefit from sarilumab therapy among those with high IL-6 levels. Oxford University Press 2023-03-11 /pmc/articles/PMC10077828/ /pubmed/37035487 http://dx.doi.org/10.1093/ofid/ofad133 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Trigo-Rodríguez, Marta
Cárcel, Sheila
Navas, Ana
Espíndola-Gómez, Reinaldo
Garrido-Gracia, José Carlos
Esteban Moreno, María Ángeles
León-López, Rafael
Pérez-Crespo, Pedro María Martínez
Alonso, Eduardo Aguilar
Vinuesa, David
Romero-Palacios, Alberto
Pérez-Camacho, Inés
Gutiérrez-Gutiérrez, Belén
Martínez-Marcos, Francisco Javier
Fernández-Roldán, Concepción
León, Eva
Caño, Alexandra Aceituno
Corzo-Delgado, Juan E
Perez-Nadales, Elena
Riazzo, Cristina
de la Fuente, Carmen
Jurado, Aurora
Torre-Cisneros, Julián
Merchante, Nicolás
Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title_full Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title_fullStr Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title_full_unstemmed Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title_short Role of IP-10 to Predict Clinical Progression and Response to IL-6 Blockade With Sarilumab in Early COVID-19 Pneumonia. A Subanalysis of the SARICOR Clinical Trial
title_sort role of ip-10 to predict clinical progression and response to il-6 blockade with sarilumab in early covid-19 pneumonia. a subanalysis of the saricor clinical trial
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077828/
https://www.ncbi.nlm.nih.gov/pubmed/37035487
http://dx.doi.org/10.1093/ofid/ofad133
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