Dupilumab shows long-term effectiveness in a large cohort of treatment-refractory atopic dermatitis patients in daily practice: 52-Week results from the Dutch BioDay registry.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 04 04 2020
revised: 27 08 2020
accepted: 30 08 2020
pubmed: 19 9 2020
medline: 26 8 2021
entrez: 18 9 2020
Statut: ppublish

Résumé

Real-life data on long-term effectiveness and safety of dupilumab in atopic dermatitis patients are limited. To study 52-week effectiveness and safety of dupilumab in a prospective multicenter cohort of adult patients with treatment-refractory atopic dermatitis. Patients treated with dupilumab and participating in the Dutch BioDay registry were included. Clinical effectiveness and safety were evaluated. Two hundred ten atopic dermatitis patients were included. Mean percentage change in Eczema Area and Severity Index score after 16 weeks was -70.0% (standard deviation 33.2%) and further decreased to -76.6% (standard deviation 30.6%) by week 52. A greater than or equal to 75% improvement in the score was achieved by 59.9% of individuals by week 16 and by 70.3% by week 52. The most reported adverse effect was conjunctivitis (34%). Limited patients (17; 8.1%) discontinued dupilumab treatment. Because of the lack of a control group and observational design, factors of bias may have been induced. Treatment with dupilumab resulted in a rapid improvement in clinical outcome measures, and effectiveness further improved during the 52-week follow-up period.

Sections du résumé

BACKGROUND BACKGROUND
Real-life data on long-term effectiveness and safety of dupilumab in atopic dermatitis patients are limited.
OBJECTIVE OBJECTIVE
To study 52-week effectiveness and safety of dupilumab in a prospective multicenter cohort of adult patients with treatment-refractory atopic dermatitis.
METHODS METHODS
Patients treated with dupilumab and participating in the Dutch BioDay registry were included. Clinical effectiveness and safety were evaluated.
RESULTS RESULTS
Two hundred ten atopic dermatitis patients were included. Mean percentage change in Eczema Area and Severity Index score after 16 weeks was -70.0% (standard deviation 33.2%) and further decreased to -76.6% (standard deviation 30.6%) by week 52. A greater than or equal to 75% improvement in the score was achieved by 59.9% of individuals by week 16 and by 70.3% by week 52. The most reported adverse effect was conjunctivitis (34%). Limited patients (17; 8.1%) discontinued dupilumab treatment.
LIMITATIONS CONCLUSIONS
Because of the lack of a control group and observational design, factors of bias may have been induced.
CONCLUSION CONCLUSIONS
Treatment with dupilumab resulted in a rapid improvement in clinical outcome measures, and effectiveness further improved during the 52-week follow-up period.

Identifiants

pubmed: 32946967
pii: S0190-9622(20)32618-9
doi: 10.1016/j.jaad.2020.08.127
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Antibodies, Monoclonal, Humanized 0
Immunosuppressive Agents 0
Receptors, Interleukin-4 0
dupilumab 420K487FSG

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1000-1009

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Lieneke F M Ariëns (LFM)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands. Electronic address: l.f.m.ariens@umcutrecht.nl.

Jorien van der Schaft (J)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Lotte S Spekhorst (LS)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Daphne S Bakker (DS)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Geertruida L E Romeijn (GLE)

Department of Dermatology, University Medical Center Groningen, Groningen, the Netherlands.

Tessa A Kouwenhoven (TA)

Department of Dermatology, Radboud University Medical Center Nijmegen, Nijmegen, the Netherlands.

Marijke Kamsteeg (M)

Department of Dermatology, Radboud University Medical Center Nijmegen, Nijmegen, the Netherlands.

Angelique N Voorberg (AN)

Department of Dermatology, University Medical Center Groningen, Groningen, the Netherlands.

Albert J Oosting (AJ)

Department of Dermatology, Spaarne Ziekenhuis, the Netherlands.

Ilona de Ridder (I)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Annemieke Sloeserwij (A)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Inge Haeck (I)

Department of Dermatology, Reinier de Graaf Gasthuis, Delft, the Netherlands.

Judith L Thijs (JL)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

Marie L A Schuttelaar (MLA)

Department of Dermatology, University Medical Center Groningen, Groningen, the Netherlands.

Marjolein S de Bruin-Weller (MS)

National Expertise Center for Atopic Dermatitis, Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.

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Classifications MeSH