Article (Scientific journals)
Real-Life Experience of Tralokinumab for the Treatment of Adult Patients with Severe Atopic Dermatitis: A Multicentric Prospective Study.
De Greef, Axel; Ghislain, Pierre-Dominique; Bulinckx, Audrey et al.
2023In Clinical Drug Investigation, 43 (4), p. 299 - 306
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Keywords :
tralokinumab; Antibodies, Monoclonal; Humans; Adult; Prospective Studies; Treatment Outcome; Injections, Subcutaneous; Double-Blind Method; Antibodies, Monoclonal/adverse effects; Severity of Illness Index; Dermatitis, Atopic/diagnosis; Dermatitis, Atopic/drug therapy; Conjunctivitis/chemically induced; Conjunctivitis/drug therapy; Eczema/chemically induced; Eczema/drug therapy; Conjunctivitis; Dermatitis, Atopic; Eczema; Pharmacology (medical)
Abstract :
[en] [en] BACKGROUND: Tralokinumab, the first fully human monoclonal antibody that binds specifically to interleukin-13, was safe and effective for treating atopic dermatitis (AD) in clinical trials, but real-life experience is still limited. OBJECTIVES: The objective of this study was to evaluate the effectiveness and safety of tralokinumab in severe AD in a real-life multicenter prospective cohort. METHODS: Adult patients with severe AD were enrolled between January 2022 and July 2022 and received tralokinumab subcutaneously for 16 weeks. Objective and subjective scores were collected at baseline, weeks 6 and 16. Adverse events were reported throughout the study. RESULTS: Twenty-one patients were included. An improvement of at least 75% on the Eczema Area and Severity Index (EASI 75) was achieved in 66.7% of patients at week 16. The median objective and subjective scores at week 16 were significantly (p < 0.001) lower than those at baseline. Combination with cyclosporine was sometimes necessary at the beginning of treatment, and addition of upadacitinib was required for some patients with very severe disease during the treatment. The most frequent adverse events were flares of eczema (23.8%) and reactions at injection site (19.0%). No cases of conjunctivitis were reported. Four patients (19.0%) discontinued treatment. CONCLUSIONS: Tralokinumab is an effective first-line biotherapy for severe AD. However, therapeutic response may be progressive. Safety data were reassuring. Atopic dermatitis flares or reactions at the injection site may lead to discontinuation of treatment. A history of conjunctivitis on dupilumab is not a contraindication to the initiation of tralokinumab.
Disciplines :
Dermatology
Author, co-author :
De Greef, Axel ;  Department of Dermatology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Avenue Hippocrate 10, 1200, Brussels, Belgium. axel.degreef@saintluc.uclouvain.be
Ghislain, Pierre-Dominique;  Department of Dermatology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Avenue Hippocrate 10, 1200, Brussels, Belgium
Bulinckx, Audrey;  Department of Dermatology, Grand Hôpital de Charleroi, Charleroi, Belgium
Coster, Alison;  Department of Dermatology, CHU UCL Namur Sainte-Elisabeth, Namur, Belgium
de Halleux, Céline;  Department of Dermatology, Clinique Saint-Jean, Brussels, Belgium
Damsin, Thomas ;  Centre Hospitalier Universitaire de Liège - CHU > > Service de dermatologie
Jacobs, Marie-Claude;  Private Dermatology Practice, Woluwe-Saint-Pierre, Brussels, Belgium
Suys, Erwin;  Private Dermatology Practice, Kortrijk, Belgium
Zoghaib, Samer;  Department of Dermatology, CHU Ambroise Paré, Mons, Belgium
Baeck, Marie;  Department of Dermatology, Cliniques universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Avenue Hippocrate 10, 1200, Brussels, Belgium
Language :
English
Title :
Real-Life Experience of Tralokinumab for the Treatment of Adult Patients with Severe Atopic Dermatitis: A Multicentric Prospective Study.
Publication date :
April 2023
Journal title :
Clinical Drug Investigation
ISSN :
1173-2563
eISSN :
1179-1918
Publisher :
Adis, New Zealand
Volume :
43
Issue :
4
Pages :
299 - 306
Peer reviewed :
Peer Reviewed verified by ORBi
Funding text :
No funding was used to conduct this study. Open Access fee was funded by the authors.
Available on ORBi :
since 29 November 2024

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