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Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis

COVID‐19 carries a high risk of severe disease course, particularly in patients with comorbidities. Therapy of severe COVID‐19 infection has relied on supportive intensive care measures. More specific approaches including drugs that limit the detrimental “cytokine storm”, such as Janus‐activated kin...

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Autores principales: Koschmieder, Steffen, Jost, Edgar, Cornelissen, Christian, Müller, Tobias, Schulze‐Hagen, Maximilian, Bickenbach, Johannes, Marx, Gernot, Kleines, Michael, Marx, Nikolaus, Brümmendorf, Tim H., Dreher, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361537/
https://www.ncbi.nlm.nih.gov/pubmed/32593209
http://dx.doi.org/10.1111/ejh.13480
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author Koschmieder, Steffen
Jost, Edgar
Cornelissen, Christian
Müller, Tobias
Schulze‐Hagen, Maximilian
Bickenbach, Johannes
Marx, Gernot
Kleines, Michael
Marx, Nikolaus
Brümmendorf, Tim H.
Dreher, Michael
author_facet Koschmieder, Steffen
Jost, Edgar
Cornelissen, Christian
Müller, Tobias
Schulze‐Hagen, Maximilian
Bickenbach, Johannes
Marx, Gernot
Kleines, Michael
Marx, Nikolaus
Brümmendorf, Tim H.
Dreher, Michael
author_sort Koschmieder, Steffen
collection PubMed
description COVID‐19 carries a high risk of severe disease course, particularly in patients with comorbidities. Therapy of severe COVID‐19 infection has relied on supportive intensive care measures. More specific approaches including drugs that limit the detrimental “cytokine storm”, such as Janus‐activated kinase (JAK) inhibitors, are being discussed. Here, we report a compelling case of a 55‐yo patient with proven COVID‐19 pneumonia, who was taking the JAK1/2 inhibitor ruxolitinib in‐label for co‐existing primary myelofibrosis for 15 months prior to coronavirus infection. The patient had significant comorbidities, including chronic kidney disease, arterial hypertension, and obesity, and our previous cohort suggested that he was thus at high risk for acute respiratory distress syndrome (ARDS) and death from COVID‐19. Since abrupt discontinuation of ruxolitinib may cause fatal cytokine storm and ARDS, ruxolitinib treatment was continued and was well tolerated, and the patient´s condition remained stable, without the need for mechanical ventilation or vasopressors. The patient became negative for SARS‐CoV‐2 and was discharged home after 15 days. In conclusion, our report provides clinical evidence that ruxolitinib treatment is feasible and can be beneficial in patients with COVID‐19 pneumonia, preventing cytokine storm and ARDS.
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spelling pubmed-73615372020-07-15 Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis Koschmieder, Steffen Jost, Edgar Cornelissen, Christian Müller, Tobias Schulze‐Hagen, Maximilian Bickenbach, Johannes Marx, Gernot Kleines, Michael Marx, Nikolaus Brümmendorf, Tim H. Dreher, Michael Eur J Haematol Case Reports COVID‐19 carries a high risk of severe disease course, particularly in patients with comorbidities. Therapy of severe COVID‐19 infection has relied on supportive intensive care measures. More specific approaches including drugs that limit the detrimental “cytokine storm”, such as Janus‐activated kinase (JAK) inhibitors, are being discussed. Here, we report a compelling case of a 55‐yo patient with proven COVID‐19 pneumonia, who was taking the JAK1/2 inhibitor ruxolitinib in‐label for co‐existing primary myelofibrosis for 15 months prior to coronavirus infection. The patient had significant comorbidities, including chronic kidney disease, arterial hypertension, and obesity, and our previous cohort suggested that he was thus at high risk for acute respiratory distress syndrome (ARDS) and death from COVID‐19. Since abrupt discontinuation of ruxolitinib may cause fatal cytokine storm and ARDS, ruxolitinib treatment was continued and was well tolerated, and the patient´s condition remained stable, without the need for mechanical ventilation or vasopressors. The patient became negative for SARS‐CoV‐2 and was discharged home after 15 days. In conclusion, our report provides clinical evidence that ruxolitinib treatment is feasible and can be beneficial in patients with COVID‐19 pneumonia, preventing cytokine storm and ARDS. John Wiley and Sons Inc. 2020-07-16 2020-11 /pmc/articles/PMC7361537/ /pubmed/32593209 http://dx.doi.org/10.1111/ejh.13480 Text en © 2020 The Authors. European Journal of Haematology published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Koschmieder, Steffen
Jost, Edgar
Cornelissen, Christian
Müller, Tobias
Schulze‐Hagen, Maximilian
Bickenbach, Johannes
Marx, Gernot
Kleines, Michael
Marx, Nikolaus
Brümmendorf, Tim H.
Dreher, Michael
Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title_full Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title_fullStr Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title_full_unstemmed Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title_short Favorable COVID‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
title_sort favorable covid‐19 course despite significant comorbidities in a ruxolitinib‐treated patient with primary myelofibrosis
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361537/
https://www.ncbi.nlm.nih.gov/pubmed/32593209
http://dx.doi.org/10.1111/ejh.13480
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