JAK Inhibition with Ruxolitinib in Patients with COVID-19 and Severe Pneumonia: Multicenter Clinical Experience from a Compassionate Use Program in Italy
Jak inhibitors are potent anti-inflammatory drugs that have the potential to dampen the hyperactive inflammatory response associated with severe COVID-19. We reviewed the clinical outcomes of 218 patients with COVID-19 hospitalized for severe pneumonia and treated with ruxolitinib through a compassi...
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Veröffentlicht in: | Journal of clinical medicine 2021-08, Vol.10 (16), p.3752 |
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creator | Vannucchi, Alessandro Maria Mortara, Andrea D’Alessio, Andrea Morelli, Mara Tedeschi, Alberto Festuccia, Moreno Benedetto Monforte, Antonella D’Arminio Capochiani, Enrico Selleri, Carmine Simonetti, Federico Saracino, Annalisa Rapezzi, Davide Badagliacca, Maria Rita Falasca, Katia Molteni, Alfredo Palazzolo, Roberto Schettino, Giuliano Bocchia, Monica Turrini, Mauro Ascierto, Paolo A. Zuurman, Mike Paley, Carole Coco, Paola Saglio, Giuseppe |
description | Jak inhibitors are potent anti-inflammatory drugs that have the potential to dampen the hyperactive inflammatory response associated with severe COVID-19. We reviewed the clinical outcomes of 218 patients with COVID-19 hospitalized for severe pneumonia and treated with ruxolitinib through a compassionate use program. Data on the duration of treatment; outcomes at 4, 7, 14, and 28 days; oxygen support requirements; clinical status; and laboratory parameters were retrospectively collected. Overall, according to the physician evaluation, 66.5% of patients showed improvement at follow-up; of these, 83.5% showed improvement by day 7. Oxygen support status also showed improvement, and by day 7, 21.6% of patients were on ambient air, compared with 1.4% at baseline, which increased to 48.2% by day 28. Significant decreases in C-reactive protein and increases in the lymphocyte total count were already observed by day 4, which seemed to correlate with a positive outcome. At the end of the observation period, 87.2% of patients were alive. No unexpected safety findings were observed, and grade 3/4 adverse events were reported in 6.9% of patients. |
doi_str_mv | 10.3390/jcm10163752 |
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We reviewed the clinical outcomes of 218 patients with COVID-19 hospitalized for severe pneumonia and treated with ruxolitinib through a compassionate use program. Data on the duration of treatment; outcomes at 4, 7, 14, and 28 days; oxygen support requirements; clinical status; and laboratory parameters were retrospectively collected. Overall, according to the physician evaluation, 66.5% of patients showed improvement at follow-up; of these, 83.5% showed improvement by day 7. Oxygen support status also showed improvement, and by day 7, 21.6% of patients were on ambient air, compared with 1.4% at baseline, which increased to 48.2% by day 28. Significant decreases in C-reactive protein and increases in the lymphocyte total count were already observed by day 4, which seemed to correlate with a positive outcome. At the end of the observation period, 87.2% of patients were alive. No unexpected safety findings were observed, and grade 3/4 adverse events were reported in 6.9% of patients.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm10163752</identifier><identifier>PMID: 34442045</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Clinical medicine ; Coronaviruses ; COVID-19 ; Cytokines ; Data collection ; Graft versus host disease ; Infections ; Inflammation ; Laboratories ; Lymphocytes ; Mortality ; Patients ; Pneumonia ; Severe acute respiratory syndrome coronavirus 2 ; Steroids</subject><ispartof>Journal of clinical medicine, 2021-08, Vol.10 (16), p.3752</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-3d5d2b0028d8ecf416713a9e7e2515be9946d1c35e89fbf7ae5e4910dbbca1da3</citedby><cites>FETCH-LOGICAL-c386t-3d5d2b0028d8ecf416713a9e7e2515be9946d1c35e89fbf7ae5e4910dbbca1da3</cites><orcidid>0000-0003-3538-3913 ; 0000-0003-0073-1789 ; 0000-0002-5861-8984 ; 0000-0002-6797-0410 ; 0000-0001-5299-8456 ; 0000-0002-3643-5861</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397012/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397012/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Vannucchi, Alessandro Maria</creatorcontrib><creatorcontrib>Mortara, Andrea</creatorcontrib><creatorcontrib>D’Alessio, Andrea</creatorcontrib><creatorcontrib>Morelli, Mara</creatorcontrib><creatorcontrib>Tedeschi, Alberto</creatorcontrib><creatorcontrib>Festuccia, Moreno Benedetto</creatorcontrib><creatorcontrib>Monforte, Antonella D’Arminio</creatorcontrib><creatorcontrib>Capochiani, Enrico</creatorcontrib><creatorcontrib>Selleri, Carmine</creatorcontrib><creatorcontrib>Simonetti, Federico</creatorcontrib><creatorcontrib>Saracino, Annalisa</creatorcontrib><creatorcontrib>Rapezzi, Davide</creatorcontrib><creatorcontrib>Badagliacca, Maria Rita</creatorcontrib><creatorcontrib>Falasca, Katia</creatorcontrib><creatorcontrib>Molteni, Alfredo</creatorcontrib><creatorcontrib>Palazzolo, Roberto</creatorcontrib><creatorcontrib>Schettino, Giuliano</creatorcontrib><creatorcontrib>Bocchia, Monica</creatorcontrib><creatorcontrib>Turrini, Mauro</creatorcontrib><creatorcontrib>Ascierto, Paolo A.</creatorcontrib><creatorcontrib>Zuurman, Mike</creatorcontrib><creatorcontrib>Paley, Carole</creatorcontrib><creatorcontrib>Coco, Paola</creatorcontrib><creatorcontrib>Saglio, Giuseppe</creatorcontrib><title>JAK Inhibition with Ruxolitinib in Patients with COVID-19 and Severe Pneumonia: Multicenter Clinical Experience from a Compassionate Use Program in Italy</title><title>Journal of clinical medicine</title><description>Jak inhibitors are potent anti-inflammatory drugs that have the potential to dampen the hyperactive inflammatory response associated with severe COVID-19. We reviewed the clinical outcomes of 218 patients with COVID-19 hospitalized for severe pneumonia and treated with ruxolitinib through a compassionate use program. Data on the duration of treatment; outcomes at 4, 7, 14, and 28 days; oxygen support requirements; clinical status; and laboratory parameters were retrospectively collected. Overall, according to the physician evaluation, 66.5% of patients showed improvement at follow-up; of these, 83.5% showed improvement by day 7. Oxygen support status also showed improvement, and by day 7, 21.6% of patients were on ambient air, compared with 1.4% at baseline, which increased to 48.2% by day 28. Significant decreases in C-reactive protein and increases in the lymphocyte total count were already observed by day 4, which seemed to correlate with a positive outcome. At the end of the observation period, 87.2% of patients were alive. No unexpected safety findings were observed, and grade 3/4 adverse events were reported in 6.9% of patients.</description><subject>Clinical medicine</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Cytokines</subject><subject>Data collection</subject><subject>Graft versus host disease</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Laboratories</subject><subject>Lymphocytes</subject><subject>Mortality</subject><subject>Patients</subject><subject>Pneumonia</subject><subject>Severe acute respiratory syndrome coronavirus 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subjects | Clinical medicine Coronaviruses COVID-19 Cytokines Data collection Graft versus host disease Infections Inflammation Laboratories Lymphocytes Mortality Patients Pneumonia Severe acute respiratory syndrome coronavirus 2 Steroids |
title | JAK Inhibition with Ruxolitinib in Patients with COVID-19 and Severe Pneumonia: Multicenter Clinical Experience from a Compassionate Use Program in Italy |
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