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COVID-19 in persons with chronic myeloid leukaemia
We studied by questionnaire 530 subjects with chronic myeloid leukaemia (CML) in Hubei Province during the recent SARS-CoV-2 epidemic. Five developed confirmed (N = 4) or probable COVID-19 (N = 1). Prevalence of COVID-19 in our subjects, 0.9% (95% Confidence Interval, 0.1, 1.8%) was ninefold higher...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233329/ https://www.ncbi.nlm.nih.gov/pubmed/32424293 http://dx.doi.org/10.1038/s41375-020-0853-6 |
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author | Li, Weiming Wang, Danyu Guo, Jingming Yuan, Guolin Yang, Zhuangzhi Gale, Robert Peter You, Yong Chen, Zhichao Chen, Shiming Wan, Chucheng Zhu, Xiaojian Chang, Wei Sheng, Lingshuang Cheng, Hui Zhang, Youshan Li, Qing Qin, Jun Meng, Li Jiang, Qian |
author_facet | Li, Weiming Wang, Danyu Guo, Jingming Yuan, Guolin Yang, Zhuangzhi Gale, Robert Peter You, Yong Chen, Zhichao Chen, Shiming Wan, Chucheng Zhu, Xiaojian Chang, Wei Sheng, Lingshuang Cheng, Hui Zhang, Youshan Li, Qing Qin, Jun Meng, Li Jiang, Qian |
author_sort | Li, Weiming |
collection | PubMed |
description | We studied by questionnaire 530 subjects with chronic myeloid leukaemia (CML) in Hubei Province during the recent SARS-CoV-2 epidemic. Five developed confirmed (N = 4) or probable COVID-19 (N = 1). Prevalence of COVID-19 in our subjects, 0.9% (95% Confidence Interval, 0.1, 1.8%) was ninefold higher than 0.1% (0, 0.12%) reported in normals but lower than 10% (6, 17%) reported in hospitalised persons with other haematological cancers or normal health-care providers, 7% (4, 12%). Co-variates associated with an increased risk of developing COVID-19 amongst persons with CML were exposure to someone infected with SARS-CoV-2 (P = 0.037), no complete haematologic response (P = 0.003) and co-morbidity(ies) (P = 0.024). There was also an increased risk of developing COVID-19 in subjects in advanced phase CML (P = 0.004) even when they achieved a complete cytogenetic response or major molecular response at the time of exposure to SARS-CoV-2. 1 of 21 subjects receiving 3rd generation tyrosine kinase-inhibitor (TKI) developed COVID-19 versus 3 of 346 subjects receiving imatinib versus 0 of 162 subjects receiving 2nd generation TKIs (P = 0.096). Other co-variates such as age and TKI-therapy duration were not significantly associated with an increased risk of developing COVID-19. Persons with these risk factors may benefit from increased surveillance of SARS-CoV-2 infection and possible protective isolation. |
format | Online Article Text |
id | pubmed-7233329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72333292020-05-18 COVID-19 in persons with chronic myeloid leukaemia Li, Weiming Wang, Danyu Guo, Jingming Yuan, Guolin Yang, Zhuangzhi Gale, Robert Peter You, Yong Chen, Zhichao Chen, Shiming Wan, Chucheng Zhu, Xiaojian Chang, Wei Sheng, Lingshuang Cheng, Hui Zhang, Youshan Li, Qing Qin, Jun Meng, Li Jiang, Qian Leukemia Article We studied by questionnaire 530 subjects with chronic myeloid leukaemia (CML) in Hubei Province during the recent SARS-CoV-2 epidemic. Five developed confirmed (N = 4) or probable COVID-19 (N = 1). Prevalence of COVID-19 in our subjects, 0.9% (95% Confidence Interval, 0.1, 1.8%) was ninefold higher than 0.1% (0, 0.12%) reported in normals but lower than 10% (6, 17%) reported in hospitalised persons with other haematological cancers or normal health-care providers, 7% (4, 12%). Co-variates associated with an increased risk of developing COVID-19 amongst persons with CML were exposure to someone infected with SARS-CoV-2 (P = 0.037), no complete haematologic response (P = 0.003) and co-morbidity(ies) (P = 0.024). There was also an increased risk of developing COVID-19 in subjects in advanced phase CML (P = 0.004) even when they achieved a complete cytogenetic response or major molecular response at the time of exposure to SARS-CoV-2. 1 of 21 subjects receiving 3rd generation tyrosine kinase-inhibitor (TKI) developed COVID-19 versus 3 of 346 subjects receiving imatinib versus 0 of 162 subjects receiving 2nd generation TKIs (P = 0.096). Other co-variates such as age and TKI-therapy duration were not significantly associated with an increased risk of developing COVID-19. Persons with these risk factors may benefit from increased surveillance of SARS-CoV-2 infection and possible protective isolation. Nature Publishing Group UK 2020-05-18 2020 /pmc/articles/PMC7233329/ /pubmed/32424293 http://dx.doi.org/10.1038/s41375-020-0853-6 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2020 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 | Article Li, Weiming Wang, Danyu Guo, Jingming Yuan, Guolin Yang, Zhuangzhi Gale, Robert Peter You, Yong Chen, Zhichao Chen, Shiming Wan, Chucheng Zhu, Xiaojian Chang, Wei Sheng, Lingshuang Cheng, Hui Zhang, Youshan Li, Qing Qin, Jun Meng, Li Jiang, Qian COVID-19 in persons with chronic myeloid leukaemia |
title | COVID-19 in persons with chronic myeloid leukaemia |
title_full | COVID-19 in persons with chronic myeloid leukaemia |
title_fullStr | COVID-19 in persons with chronic myeloid leukaemia |
title_full_unstemmed | COVID-19 in persons with chronic myeloid leukaemia |
title_short | COVID-19 in persons with chronic myeloid leukaemia |
title_sort | covid-19 in persons with chronic myeloid leukaemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233329/ https://www.ncbi.nlm.nih.gov/pubmed/32424293 http://dx.doi.org/10.1038/s41375-020-0853-6 |
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