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Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer

BACKGROUND: Consolidated evidence suggests spontaneous immunity from SARS-CoV-2 is not durable, leading to the risk of reinfection, especially in the context of newly emerging viral strains. In patients with cancer who survive COVID-19 prevalence and severity of SARS-CoV-2 reinfections are unknown....

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Autores principales: Cortellini, Alessio, Aguilar-Company, Juan, Salazar, Ramon, Bower, Mark, Sita-Lumsden, Ailsa, Plaja, Andrea, Lee, Alvin J. X., Bertuzzi, Alexia, Tondini, Carlo, Diamantis, Nikolaos, Martinez-Vila, Clara, Prat, Aleix, Apthorp, Eleanor, Gennari, Alessandra, Pinato, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395853/
https://www.ncbi.nlm.nih.gov/pubmed/35995934
http://dx.doi.org/10.1038/s41416-022-01952-x
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author Cortellini, Alessio
Aguilar-Company, Juan
Salazar, Ramon
Bower, Mark
Sita-Lumsden, Ailsa
Plaja, Andrea
Lee, Alvin J. X.
Bertuzzi, Alexia
Tondini, Carlo
Diamantis, Nikolaos
Martinez-Vila, Clara
Prat, Aleix
Apthorp, Eleanor
Gennari, Alessandra
Pinato, David J.
author_facet Cortellini, Alessio
Aguilar-Company, Juan
Salazar, Ramon
Bower, Mark
Sita-Lumsden, Ailsa
Plaja, Andrea
Lee, Alvin J. X.
Bertuzzi, Alexia
Tondini, Carlo
Diamantis, Nikolaos
Martinez-Vila, Clara
Prat, Aleix
Apthorp, Eleanor
Gennari, Alessandra
Pinato, David J.
author_sort Cortellini, Alessio
collection PubMed
description BACKGROUND: Consolidated evidence suggests spontaneous immunity from SARS-CoV-2 is not durable, leading to the risk of reinfection, especially in the context of newly emerging viral strains. In patients with cancer who survive COVID-19 prevalence and severity of SARS-CoV-2 reinfections are unknown. METHODS: We aimed to document natural history and outcome from SARS-CoV-2 reinfection in patients recruited to OnCovid (NCT04393974), an active European registry enrolling consecutive patients with a history of solid or haematologic malignancy diagnosed with COVID-19. RESULTS: As of December 2021, out of 3108 eligible participants, 1806 COVID-19 survivors were subsequently followed at participating institutions. Among them, 34 reinfections (1.9%) were reported after a median time of 152 days (range: 40–620) from the first COVID-19 diagnosis, and with a median observation period from the second infection of 115 days (95% CI: 27–196). Most of the first infections were diagnosed in 2020 (27, 79.4%), while most of reinfections in 2021 (25, 73.5%). Haematological malignancies were the most frequent primary tumour (12, 35%). Compared to first infections, second infections had lower prevalence of COVID-19 symptoms (52.9% vs 91.2%, P = 0.0008) and required less COVID-19-specific therapy (11.8% vs 50%, P = 0.0013). Overall, 11 patients (32.4%) and 3 (8.8%) were fully and partially vaccinated against SARS-CoV-2 before the second infection, respectively. The 14-day case fatality rate was 11.8%, with four death events, none of which among fully vaccinated patients. CONCLUSION: This study shows that reinfections in COVID-19 survivors with cancer are possible and more common in patients with haematological malignancies. Reinfections carry a 11% risk of mortality, which rises to 15% among unvaccinated patients, highlighting the importance of universal vaccination of patients with cancer.
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spelling pubmed-93958532022-08-23 Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer Cortellini, Alessio Aguilar-Company, Juan Salazar, Ramon Bower, Mark Sita-Lumsden, Ailsa Plaja, Andrea Lee, Alvin J. X. Bertuzzi, Alexia Tondini, Carlo Diamantis, Nikolaos Martinez-Vila, Clara Prat, Aleix Apthorp, Eleanor Gennari, Alessandra Pinato, David J. Br J Cancer Article BACKGROUND: Consolidated evidence suggests spontaneous immunity from SARS-CoV-2 is not durable, leading to the risk of reinfection, especially in the context of newly emerging viral strains. In patients with cancer who survive COVID-19 prevalence and severity of SARS-CoV-2 reinfections are unknown. METHODS: We aimed to document natural history and outcome from SARS-CoV-2 reinfection in patients recruited to OnCovid (NCT04393974), an active European registry enrolling consecutive patients with a history of solid or haematologic malignancy diagnosed with COVID-19. RESULTS: As of December 2021, out of 3108 eligible participants, 1806 COVID-19 survivors were subsequently followed at participating institutions. Among them, 34 reinfections (1.9%) were reported after a median time of 152 days (range: 40–620) from the first COVID-19 diagnosis, and with a median observation period from the second infection of 115 days (95% CI: 27–196). Most of the first infections were diagnosed in 2020 (27, 79.4%), while most of reinfections in 2021 (25, 73.5%). Haematological malignancies were the most frequent primary tumour (12, 35%). Compared to first infections, second infections had lower prevalence of COVID-19 symptoms (52.9% vs 91.2%, P = 0.0008) and required less COVID-19-specific therapy (11.8% vs 50%, P = 0.0013). Overall, 11 patients (32.4%) and 3 (8.8%) were fully and partially vaccinated against SARS-CoV-2 before the second infection, respectively. The 14-day case fatality rate was 11.8%, with four death events, none of which among fully vaccinated patients. CONCLUSION: This study shows that reinfections in COVID-19 survivors with cancer are possible and more common in patients with haematological malignancies. Reinfections carry a 11% risk of mortality, which rises to 15% among unvaccinated patients, highlighting the importance of universal vaccination of patients with cancer. Nature Publishing Group UK 2022-08-22 2022-11-09 /pmc/articles/PMC9395853/ /pubmed/35995934 http://dx.doi.org/10.1038/s41416-022-01952-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cortellini, Alessio
Aguilar-Company, Juan
Salazar, Ramon
Bower, Mark
Sita-Lumsden, Ailsa
Plaja, Andrea
Lee, Alvin J. X.
Bertuzzi, Alexia
Tondini, Carlo
Diamantis, Nikolaos
Martinez-Vila, Clara
Prat, Aleix
Apthorp, Eleanor
Gennari, Alessandra
Pinato, David J.
Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title_full Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title_fullStr Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title_full_unstemmed Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title_short Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
title_sort natural immunity to sars-cov-2 and breakthrough infections in vaccinated and unvaccinated patients with cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395853/
https://www.ncbi.nlm.nih.gov/pubmed/35995934
http://dx.doi.org/10.1038/s41416-022-01952-x
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