Dupilumab Drug Survival and Associated Predictors in Patients With Moderate to Severe Atopic Dermatitis: Long-term Results From the Daily Practice BioDay Registry.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 09 2022
Historique:
pubmed: 11 8 2022
medline: 24 9 2022
entrez: 10 8 2022
Statut: ppublish

Résumé

Long-term data on dupilumab drug survival in patients with atopic dermatitis (AD) are scarce. Furthermore, little is known about the factors associated with drug survival of dupilumab in AD. To describe the drug survival of dupilumab in patients with AD and to identify associated predictors. This cohort study was based on data from the multicenter prospective daily practice BioDay registry, in which 4 university and 10 nonuniversity hospitals in the Netherlands participated. Analysis included patients (age ≥18 years) participating in the BioDay registry with a follow-up of at least 4 weeks. The first patient treated with dupilumab was recorded in the BioDay registry in October 2017; data lock took place in December 2020, and data analysis was performed from October 2017 to December 2020. Drug survival was analyzed by Kaplan-Meier survival curves and associated characteristics by using univariate and multivariate Cox regression analysis. A total of 715 adult patients with AD (mean [SD] age, 41.8 [16.0] years; 418 [58.5%] were male) were included with a 1-year, 2-year, and 3-year overall dupilumab drug survival of 90.3%, 85.9%, and 78.6%, respectively. Characteristics associated with shorter drug survival owing to ineffectiveness were the use of immunosuppressant drugs at baseline (hazard ratio [HR], 2.64; 95% CI, 1.10-6.37) and being a nonresponder at 4 weeks (HR, 8.68; 95% CI, 2.97-25.35). Characteristics associated with shorter drug survival owing to adverse effects were the use of immunosuppressant drugs at baseline (HR, 2.69; 95% CI, 1.32-5.48), age 65 years or older (HR, 2.94; 95% CI, 1.10-7.87), and Investigator Global Assessment score of very severe AD (HR, 3.51; 95% CI, 1.20-10.28). This cohort study demonstrated a good overall 1-year, 2-year, and 3-year dupilumab drug survival. Patients using immunosuppressive therapy at baseline and those with an absence of treatment effect at week 4 tended to discontinue treatment owing to ineffectiveness more frequently. Using immunosuppressant drugs at baseline, older age, and Investigator Global Assessment score of very severe AD were characteristics associated with an increased risk for discontinuation owing to adverse effects. These data provide more insight and new perspectives regarding dupilumab treatment in AD and can contribute to the optimization of patient outcomes.

Identifiants

pubmed: 35947364
pii: 2794825
doi: 10.1001/jamadermatol.2022.3014
pmc: PMC9366658
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Immunosuppressive Agents 0
dupilumab 420K487FSG

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1048-1056

Auteurs

Lotte S Spekhorst (LS)

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

Marlies de Graaf (M)

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

Nicolaas P A Zuithoff (NPA)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.

Juul M P A van den Reek (JMPA)

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

Marijke Kamsteeg (M)

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

Celeste M Boesjes (CM)

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.

Laura Loman (L)

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

Inge Haeck (I)

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

Albert J Oosting (AJ)

Department of Dermatology, Spaarnegasthuis, Haarlem, the Netherlands.

Astrid de Boer-Brand (A)

Department of Dermatology, St Antonius Ziekenhuis, Nieuwegein, the Netherlands.

Wouter R H Touwslager (WRH)

Department of Dermatology, Catharina Ziekenhuis, Eindhoven, the Netherlands.

Annebeth Flinterman (A)

Department of Dermatology, Diakonessenhuis, Utrecht, the Netherlands.

Anneke M T van Lynden-van Nes (AMT)

Department of Dermatology, Meander Medisch Centrum, Amersfoort, the Netherlands.

Antoni H Gostynski (AH)

Department of Dermatology, University Medical Center Maastricht, Maastricht, 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.

Marie-Louise Schuttelaar (ML)

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

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