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SARS-CoV-2 infection in patients with primary central nervous system lymphoma
BACKGROUND: Cancer patients may be at higher risk for severe coronavirus infectious disease-19 (COVID-19); however, the outcome of Primary Central Nervous System Lymphoma (PCNSL) patients with SARS-CoV-2 infection has not been described yet. METHODS: We conducted a retrospective study within the Lym...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776286/ https://www.ncbi.nlm.nih.gov/pubmed/33387015 http://dx.doi.org/10.1007/s00415-020-10311-w |
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author | Laurenge, Alice Ursu, Renata Houillier, Caroline Abdi, Basma Tebano, Gianpiero Quemeneur, Cyril Choquet, Sylvain Di Blasi, Roberta Lozano, Fernando Morales, Andrea Durán-Peña, Alberto Sirven-Villaros, Lila Mathon, Bertrand Mokhtari, Karima Bielle, Franck Martin-Duverneuil, Nadine Delattre, Jean-Yves Marcelin, Anne-Geneviève Pourcher, Valérie Alentorn, Agusti Idbaih, Ahmed Carpentier, Antoine F. Leblond, Véronique Hoang-Xuan, Khê Touat, Mehdi |
author_facet | Laurenge, Alice Ursu, Renata Houillier, Caroline Abdi, Basma Tebano, Gianpiero Quemeneur, Cyril Choquet, Sylvain Di Blasi, Roberta Lozano, Fernando Morales, Andrea Durán-Peña, Alberto Sirven-Villaros, Lila Mathon, Bertrand Mokhtari, Karima Bielle, Franck Martin-Duverneuil, Nadine Delattre, Jean-Yves Marcelin, Anne-Geneviève Pourcher, Valérie Alentorn, Agusti Idbaih, Ahmed Carpentier, Antoine F. Leblond, Véronique Hoang-Xuan, Khê Touat, Mehdi |
author_sort | Laurenge, Alice |
collection | PubMed |
description | BACKGROUND: Cancer patients may be at higher risk for severe coronavirus infectious disease-19 (COVID-19); however, the outcome of Primary Central Nervous System Lymphoma (PCNSL) patients with SARS-CoV-2 infection has not been described yet. METHODS: We conducted a retrospective study within the Lymphomes Oculo-Cérébraux national network (LOC) to assess the clinical characteristics and outcome of SARS-CoV-2 infection in PCNSL patients (positive real-time polymerase chain reaction of nasopharyngeal swab or evocative lung computed tomography scan). We compared clinical characteristics between patients with severe (death and/or intensive care unit admission) and mild disease. RESULTS: Between March and May 2020, 13 PCNSL patients were diagnosed with SARS-CoV-2 infection, 11 (85%) of whom were undergoing chemotherapy at the time of infection. The mortality rate was 23% (3/13), and two additional patients (15%) required mechanical ventilation. Two patients (15%) had no COVID-19 symptoms. History of diabetes mellitus was more common in severe patients (3/5 vs 0/8, p = 0.03). Two patients recovered from COVID-19 after mechanical ventilation during more than two weeks and resumed chemotherapy. In all, chemotherapy was resumed after COVID-19 recovery in nine patients (69%) after a median delay of 16 days (range 3–32), none of whom developed unusual chemotherapy complication nor SARS-Cov2 reactivation. CONCLUSION: This preliminary analysis suggests that, while being at higher risk be for severe illness, PCNSL patients with COVID-19 might be treated maximally especially if they achieved oncological response at the time of SARS-CoV-2 infection. Chemotherapy might be resumed without prolonged delay in PCNSL patients with COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-10311-w) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7776286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-77762862021-01-04 SARS-CoV-2 infection in patients with primary central nervous system lymphoma Laurenge, Alice Ursu, Renata Houillier, Caroline Abdi, Basma Tebano, Gianpiero Quemeneur, Cyril Choquet, Sylvain Di Blasi, Roberta Lozano, Fernando Morales, Andrea Durán-Peña, Alberto Sirven-Villaros, Lila Mathon, Bertrand Mokhtari, Karima Bielle, Franck Martin-Duverneuil, Nadine Delattre, Jean-Yves Marcelin, Anne-Geneviève Pourcher, Valérie Alentorn, Agusti Idbaih, Ahmed Carpentier, Antoine F. Leblond, Véronique Hoang-Xuan, Khê Touat, Mehdi J Neurol Original Communication BACKGROUND: Cancer patients may be at higher risk for severe coronavirus infectious disease-19 (COVID-19); however, the outcome of Primary Central Nervous System Lymphoma (PCNSL) patients with SARS-CoV-2 infection has not been described yet. METHODS: We conducted a retrospective study within the Lymphomes Oculo-Cérébraux national network (LOC) to assess the clinical characteristics and outcome of SARS-CoV-2 infection in PCNSL patients (positive real-time polymerase chain reaction of nasopharyngeal swab or evocative lung computed tomography scan). We compared clinical characteristics between patients with severe (death and/or intensive care unit admission) and mild disease. RESULTS: Between March and May 2020, 13 PCNSL patients were diagnosed with SARS-CoV-2 infection, 11 (85%) of whom were undergoing chemotherapy at the time of infection. The mortality rate was 23% (3/13), and two additional patients (15%) required mechanical ventilation. Two patients (15%) had no COVID-19 symptoms. History of diabetes mellitus was more common in severe patients (3/5 vs 0/8, p = 0.03). Two patients recovered from COVID-19 after mechanical ventilation during more than two weeks and resumed chemotherapy. In all, chemotherapy was resumed after COVID-19 recovery in nine patients (69%) after a median delay of 16 days (range 3–32), none of whom developed unusual chemotherapy complication nor SARS-Cov2 reactivation. CONCLUSION: This preliminary analysis suggests that, while being at higher risk be for severe illness, PCNSL patients with COVID-19 might be treated maximally especially if they achieved oncological response at the time of SARS-CoV-2 infection. Chemotherapy might be resumed without prolonged delay in PCNSL patients with COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-10311-w) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2021-01-02 2021 /pmc/articles/PMC7776286/ /pubmed/33387015 http://dx.doi.org/10.1007/s00415-020-10311-w Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 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 | Original Communication Laurenge, Alice Ursu, Renata Houillier, Caroline Abdi, Basma Tebano, Gianpiero Quemeneur, Cyril Choquet, Sylvain Di Blasi, Roberta Lozano, Fernando Morales, Andrea Durán-Peña, Alberto Sirven-Villaros, Lila Mathon, Bertrand Mokhtari, Karima Bielle, Franck Martin-Duverneuil, Nadine Delattre, Jean-Yves Marcelin, Anne-Geneviève Pourcher, Valérie Alentorn, Agusti Idbaih, Ahmed Carpentier, Antoine F. Leblond, Véronique Hoang-Xuan, Khê Touat, Mehdi SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title | SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title_full | SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title_fullStr | SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title_full_unstemmed | SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title_short | SARS-CoV-2 infection in patients with primary central nervous system lymphoma |
title_sort | sars-cov-2 infection in patients with primary central nervous system lymphoma |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776286/ https://www.ncbi.nlm.nih.gov/pubmed/33387015 http://dx.doi.org/10.1007/s00415-020-10311-w |
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