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Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic
PURPOSE OF REVIEW: Chronic lymphocytic leukemia (CLL) is the most frequent lymphoproliferative disease in the elderly of the western world. Immune defective responses and treatment can worsen the immune system’s competence of CLL patients. Consequently, they may present a higher incidence of recurre...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778499/ https://www.ncbi.nlm.nih.gov/pubmed/35061199 http://dx.doi.org/10.1007/s11912-022-01198-z |
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author | Arellano-Llamas, Abril Adriana Vela-Ojeda, Jorge Hernandez-Caballero, Alvaro |
author_facet | Arellano-Llamas, Abril Adriana Vela-Ojeda, Jorge Hernandez-Caballero, Alvaro |
author_sort | Arellano-Llamas, Abril Adriana |
collection | PubMed |
description | PURPOSE OF REVIEW: Chronic lymphocytic leukemia (CLL) is the most frequent lymphoproliferative disease in the elderly of the western world. Immune defective responses and treatment can worsen the immune system’s competence of CLL patients. Consequently, they may present a higher incidence of recurrent severe infections, second malignancies, and reduced efficacy of vaccines. The outbreak of COVID-19 is an ongoing pandemic, and patients with comorbidities experience more severe forms of the disease. Hematological malignancies are associated with higher case fatality rates (CFRs) than other cancers. Knowledge about COVID-19 incidence, clinical course, and immune response to the infection and vaccination in CLL may contribute to design strategies that improve the outcomes of patients in the future. RECENT FINDINGS: The prevalence of SARS-CoV-2 positivity in CLL is not significantly higher than seen in the general population. CFRs for CLL patients are 16.5-fold more elevated than the median reported worldwide and even higher in older patients, those who require hospitalization have significant comorbidities or need oxygen therapy. CLL status decreases the anti-SARS-CoV-2 positivity after infection or vaccination by around 40%, and the spike-specific antibody titers are 74-fold lower than healthy age-matched controls. The response rate to COVID-19 vaccines is even worse in patients with active CLL-directed therapies like BTKi, BCL-2 antagonists, or anti-CD20 monoclonal antibodies. SUMMARY: CLL patients are at a greater risk of death from COVID-19. Inherent immunosuppression of CLL and immune deficiencies caused by treatment significantly decrease the ability to produce natural or vaccine-induced anti-SARS-CoV-2 immune responses. |
format | Online Article Text |
id | pubmed-8778499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-87784992022-01-21 Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic Arellano-Llamas, Abril Adriana Vela-Ojeda, Jorge Hernandez-Caballero, Alvaro Curr Oncol Rep Leukemia (A Aguayo, Section Editor) PURPOSE OF REVIEW: Chronic lymphocytic leukemia (CLL) is the most frequent lymphoproliferative disease in the elderly of the western world. Immune defective responses and treatment can worsen the immune system’s competence of CLL patients. Consequently, they may present a higher incidence of recurrent severe infections, second malignancies, and reduced efficacy of vaccines. The outbreak of COVID-19 is an ongoing pandemic, and patients with comorbidities experience more severe forms of the disease. Hematological malignancies are associated with higher case fatality rates (CFRs) than other cancers. Knowledge about COVID-19 incidence, clinical course, and immune response to the infection and vaccination in CLL may contribute to design strategies that improve the outcomes of patients in the future. RECENT FINDINGS: The prevalence of SARS-CoV-2 positivity in CLL is not significantly higher than seen in the general population. CFRs for CLL patients are 16.5-fold more elevated than the median reported worldwide and even higher in older patients, those who require hospitalization have significant comorbidities or need oxygen therapy. CLL status decreases the anti-SARS-CoV-2 positivity after infection or vaccination by around 40%, and the spike-specific antibody titers are 74-fold lower than healthy age-matched controls. The response rate to COVID-19 vaccines is even worse in patients with active CLL-directed therapies like BTKi, BCL-2 antagonists, or anti-CD20 monoclonal antibodies. SUMMARY: CLL patients are at a greater risk of death from COVID-19. Inherent immunosuppression of CLL and immune deficiencies caused by treatment significantly decrease the ability to produce natural or vaccine-induced anti-SARS-CoV-2 immune responses. Springer US 2022-01-21 2022 /pmc/articles/PMC8778499/ /pubmed/35061199 http://dx.doi.org/10.1007/s11912-022-01198-z Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Leukemia (A Aguayo, Section Editor) Arellano-Llamas, Abril Adriana Vela-Ojeda, Jorge Hernandez-Caballero, Alvaro Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title | Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title_full | Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title_fullStr | Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title_full_unstemmed | Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title_short | Chronic Lymphocytic Leukemia in the SARS-CoV-2 Pandemic |
title_sort | chronic lymphocytic leukemia in the sars-cov-2 pandemic |
topic | Leukemia (A Aguayo, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778499/ https://www.ncbi.nlm.nih.gov/pubmed/35061199 http://dx.doi.org/10.1007/s11912-022-01198-z |
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