The clinical relevance of dupilumab serum concentration in patients with atopic dermatitis: a two-center prospective cohort study.


Journal

The Journal of dermatological treatment
ISSN: 1471-1753
Titre abrégé: J Dermatolog Treat
Pays: England
ID NLM: 8918133

Informations de publication

Date de publication:
Dec 2023
Historique:
medline: 3 5 2023
pubmed: 26 4 2023
entrez: 26 4 2023
Statut: ppublish

Résumé

Dupilumab is prescribed in one dosage across adult atopic dermatitis patients. Differences in drug exposure may explain variation in treatment response. Investigating the clinical relevance of dupilumab serum concentration in atopic dermatitis in real-world practice. In two centers (Netherlands, UK), adults treated with dupilumab for atopic dermatitis were evaluated for effectiveness and safety pretreatment and at 2, 12, 24, and 48 weeks; trough serum samples were analyzed for dupilumab concentration at corresponding time points. In 149 patients, median dupilumab levels during follow-up ranged from 57.4 to 72.4 μg/mL. Levels showed high inter-patient and low intra-patient variability. No correlation was found between levels and ΔEASI. At 2 weeks, levels of ≥64.1 μg/mL predict EASI ≤7 at 24 weeks (specificity:100%, sensitivity:60%; At the on-label dosage, the measured range of dupilumab levels does not seem to yield differences in treatment effectiveness. However, disease activity does seem to influence dupilumab levels - higher baseline disease activity results in lower levels at follow-up.

Sections du résumé

BACKGROUND UNASSIGNED
Dupilumab is prescribed in one dosage across adult atopic dermatitis patients. Differences in drug exposure may explain variation in treatment response.
OBJECTIVE UNASSIGNED
Investigating the clinical relevance of dupilumab serum concentration in atopic dermatitis in real-world practice.
METHODS UNASSIGNED
In two centers (Netherlands, UK), adults treated with dupilumab for atopic dermatitis were evaluated for effectiveness and safety pretreatment and at 2, 12, 24, and 48 weeks; trough serum samples were analyzed for dupilumab concentration at corresponding time points.
RESULTS UNASSIGNED
In 149 patients, median dupilumab levels during follow-up ranged from 57.4 to 72.4 μg/mL. Levels showed high inter-patient and low intra-patient variability. No correlation was found between levels and ΔEASI. At 2 weeks, levels of ≥64.1 μg/mL predict EASI ≤7 at 24 weeks (specificity:100%, sensitivity:60%;
CONCLUSION UNASSIGNED
At the on-label dosage, the measured range of dupilumab levels does not seem to yield differences in treatment effectiveness. However, disease activity does seem to influence dupilumab levels - higher baseline disease activity results in lower levels at follow-up.

Identifiants

pubmed: 37098906
doi: 10.1080/09546634.2023.2193663
doi:

Substances chimiques

dupilumab 420K487FSG

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2193663

Auteurs

Angela L Bosma (AL)

Department of Dermatology, Amsterdam UMC, Location Academic Medical Center, University of Amsterdam, Amsterdam Public Health Research Institute, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.

Louise A A Gerbens (LAA)

Department of Dermatology, Amsterdam UMC, Location Academic Medical Center, University of Amsterdam, Amsterdam Public Health Research Institute, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.

Hajar El Khattabi (H)

Department of Dermatology, Amsterdam UMC, Location Academic Medical Center, University of Amsterdam, Amsterdam Public Health Research Institute, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.

Floris C Loeff (FC)

Sanquin Diagnostic Services, Amsterdam, The Netherlands.

Michael Duckworth (M)

St John's Institute of Dermatology, School of Basic and Medical Biosciences, King's College London, London, UK.

Richard T Woolf (RT)

St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Theo Rispens (T)

Department of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Catherine H Smith (CH)

St John's Institute of Dermatology, School of Basic and Medical Biosciences, King's College London, London, UK.
St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Phyllis I Spuls (PI)

Department of Dermatology, Amsterdam UMC, Location Academic Medical Center, University of Amsterdam, Amsterdam Public Health Research Institute, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH