Your browser doesn't support javascript.
JAK Inhibition with Ruxolitinib in Patients with COVID-19 and Severe Pneumonia: Multicenter Clinical Experience from a Compassionate Use Program in Italy.
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.
  • Vannucchi AM; Center Research Innovation of Myeloproliferative Neoplasms (CRIMM), SOD Hematology, University of Florence and AOU Careggi, 50134 Florence, Italy.
  • Mortara A; Department of Clinical Cardiology, Policlinico di Monza, 28100 Monza, Italy.
  • D'Alessio A; COVID Medical Department, Policlinico S. Marco, Gruppo San Donato University and Research Hospital, 24040 Zingonia, Italy.
  • Morelli M; Novartis Farma SpA, 21040 Origgio, Italy.
  • Tedeschi A; U.O.C. Medicina Generale, Ospedale Bolognini, ASST Bergamo Est, 24068 Seriate, Italy.
  • Festuccia MB; Azienda USL della Valle d'Aosta, Internal Medicine Division, 11100 Aosta, Italy.
  • Monforte AD; Institute of Infectious Diseases, Department of Health Sciences, University of Milan, 20153 Milan, Italy.
  • Capochiani E; UOC Ematologia, Azienda USL Toscana Nord Ovest, 57124 Livorno, Italy.
  • Selleri C; Hematology, Department of Medicine, Surgery and Dentistry, University of Salerno, 84081 Baronissi, Italy.
  • Simonetti F; UOC Ematologia, Azienda USL Toscana Nord Ovest, 55049 Versilia, Italy.
  • Saracino A; Clinica Malattie Infettive, Dip. Scienze Biomediche ed Oncologia Umana, Università degli Studi di Bari, 70124 Bari, Italy.
  • Rapezzi D; S.C. Ematologia Ospedale S. Croce e Carle, 12100 Cuneo, Italy.
  • Badagliacca MR; UOS UFA UOC Farmacia Ospedaliera Distretto Ospedaliero CL1-P.O.S. Elia, Azienda Sanitaria Provinciale di Caltanissetta, 93100 Caltanissetta, Italy.
  • Falasca K; Clinic of Infectious Diseases, Department of Medicine and Science of Aging, University G. d'Annunzio, Chieti-Pescara, 66100 Chieti, Italy.
  • Molteni A; UOC Ematologia e CTMO, ASST Cremona, 26100 Cremona, Italy.
  • Palazzolo R; Azienda Ospedaliera Valtellina Valchiavenna, 23100 Sondrio, Italy.
  • Schettino G; Malattie Infettive ASL Alessandria, 15121 Alessandria, Italy.
  • Bocchia M; Hematology Unit, University of Siena, Azienda Ospedaliero Universitaria Senese, 53100 Siena, Italy.
  • Turrini M; Division of Hematology, Department of Medicine, Valduce Hospital, 22100 Como, Italy.
  • Ascierto PA; Unit of Melanoma, Cancer Immunotherapy and Development Therapeutics, Istituto Nazionale per lo Studio e la Cura dei Tumori IRCCS Fondazione G. Pascale, 80131 Naples, Italy.
  • Zuurman M; Novartis Farma SpA, 21040 Origgio, Italy.
  • Paley C; Novartis Pharma BV, 1101 Amsterdam, The Netherlands.
  • Coco P; Novartis Oncology, East Hanover, NJ 07936, USA.
  • Saglio G; Novartis Farma SpA, 21040 Origgio, Italy.
J Clin Med ; 10(16)2021 Aug 23.
Article in English | MEDLINE | ID: covidwho-1367859
ABSTRACT
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.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Language: English Year: 2021 Document Type: Article Affiliation country: Jcm10163752

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Language: English Year: 2021 Document Type: Article Affiliation country: Jcm10163752