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Dupilumab for the treatment of atopic dermatitis: real-world data from the Czech Republic BIOREP registry.
Kojanova, Martina; Tanczosova, Milena; Strosova, Daniela; Cetkovska, Petra; Fialova, Jorga; Dolezal, Tomas; Machovcova, Alena; Gkalpakiotis, Spyridon.
  • Kojanova M; Department of Dermatovenereology, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.
  • Tanczosova M; Department of Dermatovenereology, Third Faculty of Medicine, Charles University, Kralovske Vinohrady University Hospital, Prague, Czechia.
  • Strosova D; Value Outcomes, Prague, Czechia.
  • Cetkovska P; Department of Dermatovenereology, Faculty of Medicine in Pilsen, Charles University, Prague, Czechia.
  • Fialova J; Department of Dermatovenereology, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.
  • Dolezal T; Value Outcomes, Prague, Czechia.
  • Machovcova A; Motol University Hospital, Prague, Czechia.
  • Gkalpakiotis S; Department of Dermatovenereology, Third Faculty of Medicine, Charles University, Kralovske Vinohrady University Hospital, Prague, Czechia.
J Dermatolog Treat ; 33(5): 2578-2586, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-1692399
ABSTRACT

BACKGROUND:

Dupilumab has been approved to treat moderate-to-severe atopic dermatitis; however, the data in a real-world setting are still limited.

OBJECTIVE:

To analyze the effectiveness and safety of dupilumab.

METHODS:

This was a real-life Czech multicenter retrospective study from patients treated with dupilumab for severe AD.

RESULTS:

A total of 360 patients were included. At 16 weeks, 66.6, 34.1, and 5.5% of patients achieved EASI75/90 and EASI100, respectively. Improvement continued with the time, and the proportion of patients with EASI75/90 and EASI100 increased to 89.5, 55.6, and 12.9% after one year of treatment and reached 95.8, 60.4, and 27.1% in the second year of therapy, respectively. A significant reduction was observed in the DLQI scores. The most common adverse events were infections in 5.8% of patients, followed by ocular complications in 2.5% of patients. Persistence rates were 98.2% at four months to 93.1% at month 24, and lack of effectiveness was the most common reason for discontinuation.

CONCLUSION:

This real-life study confirmed the effectiveness and safety of dupilumab in a real-life setting during the COVID-19 pandemic. Our study revealed a higher frequency of infections and a lower conjunctivitis frequency than other real-life studies and clinical trials.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Dermatitis, Atopic / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Country/Region as subject: Europa Language: English Journal: J Dermatolog Treat Journal subject: Dermatology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Dermatitis, Atopic / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Country/Region as subject: Europa Language: English Journal: J Dermatolog Treat Journal subject: Dermatology Year: 2022 Document Type: Article