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Effectiveness and Safety of Upadacitinib in the Treatment of Moderate-Severe Atopic Dermatitis: A Multicentric, Prospective, Real-World, Cohort Study

  • Andrea Chiricozzi*
  • , Niccolò Gori
  • , Alessandra Narcisi
  • , Anna Balato
  • , Alessio Gambardella
  • , Michela Ortoncelli
  • , Angelo Valerio Marzano
  • , Riccardo Balestri
  • , Giovanni Palazzo
  • , Michele Pellegrino
  • , Marco Romanelli
  • , Giovanni Tripepi
  • , Ketty Peris
  • , Antonio Costanzo
  • *Autore corrispondente per questo lavoro
  • IRCCS Istituto Clinico Humanitas - Rozzano (Milano)
  • Humanitas University
  • University of Campania Luigi Vanvitelli
  • University of Turin
  • IRCCS Fondazione Ca'Granda – Ospedale Maggiore Policlinico - Milano
  • University of Milan
  • Ospedale S. Chiara
  • Ospedale distrettuale “A. Lo Dico”
  • Ospedale della Misericordia, Grosseto
  • University of Pisa
  • CNR Institute of Clinical Physiology

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Background The efficacy and safety of upadacitinib in atopic dermatitis (AD) have been defined in clinical trials, but no real-world data are currently available. We aimed to assess the safety and effectiveness of upadacitinib in a real-world AD patient cohort that mostly included patients who failed the available systemic therapies, including dupilumab. Methods Prospective cohort study collecting data on upadacitinib-treated AD adult patients completing at least 16 weeks of therapy. Results Forty-three patients showed rapid and marked response to upadacitinib with significant reduction of all disease severity scores since the first follow-up visit. At week 16, Eczema Area and Severity Index (EASI) 75, EASI 90, and EASI 100 response was observed in 97.5%, 82.1%, and 69.2% of patients, respectively. EASI 90 response reflected the achievement of a clear or almost clear condition (POEM 0-2), self-evaluated by 79.5% of patients. Patients' quality of life improved as suggested by the achievement of DLQI 0/1 by 38.5% of patients at week 4, and by 76.9% at week 16. Conclusion Elevated effectiveness and favorable safety of upadacitinib were confirmed in patients unresponsive to dupilumab, who were not included in upadacitinib trials.
Lingua originaleInglese
pagine (da-a)1-8
Numero di pagine8
RivistaDRUGS IN R&D
Numero di pubblicazioneN/A
DOI
Stato di pubblicazionePubblicato - 2022

All Science Journal Classification (ASJC) codes

  • Farmacologia

Keywords

  • atopic dermatitis

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