Baricitinib 2 mg for the treatment of atopic dermatitis in North America: Long-term efficacy and patient-reported outcomes.


Journal

Dermatologic therapy
ISSN: 1529-8019
Titre abrégé: Dermatol Ther
Pays: United States
ID NLM: 9700070

Informations de publication

Date de publication:
12 2022
Historique:
received: 12 05 2022
accepted: 06 10 2022
pubmed: 22 10 2022
medline: 21 12 2022
entrez: 21 10 2022
Statut: ppublish

Résumé

To address the need for long-term efficacy and patient-reported outcomes (PROs) data for patients with atopic dermatitis (AD) treated with baricitinib 2 mg, a study was conducted to evaluate the efficacy of baricitinib 2 mg in adult patients with moderate-to-severe AD. Data presented here provided efficacy and outcomes data for patients treated for 52 weeks. Patients who participated in the originating study, BREEZE-AD5 (NCT03435081), and met additional eligibility criteria could enroll in the multicenter, open-label, Phase 3, long-term extension study BREEZE-AD6 (NCT03559270). Patients received baricitinib 2 mg for the duration of BREEZE-AD6. In BREEZE-AD6, the proportion of patients who achieved a 75% improvement in the Eczema Area and Severity Index (EASI75) and validated Investigator Global Assessment for AD (vIGA-AD™) of 0 (clear) or 1 (almost clear) were assessed through 52 weeks, in addition to several PROs. At week 52, the proportion of patients treated with baricitinib 2 mg daily achieving EASI75 was 48.6% (70/144), and 31.3% (45/144) of patients achieved a vIGA-AD score of 0 or 1 (clear or almost clear). Improvements in PROs such as SCORing Atopic Dermatitis (SCORAD, itch and sleep) scores, Dermatology Life Quality Index (DLQI) total score, and DLQI ≤5 response were observed, and these responses were sustained through 52 weeks. Long-term efficacy of baricitinib in patients with AD was demonstrated by both clinician and patient-reported outcome measures.

Identifiants

pubmed: 36270978
doi: 10.1111/dth.15954
doi:

Substances chimiques

baricitinib ISP4442I3Y

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15954

Subventions

Organisme : Eli Lilly and Company

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Eric Simpson (E)

Department of Dermatology, Oregon Health and Science University, Portland, Oregon, USA.

April Armstrong (A)

Department of Dermatology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Mark Boguniewicz (M)

Division of Allergy-Immunology, Department of Pediatrics, National Jewish Health and University of Colorado School of Medicine, Denver, Colorado, USA.

Zelma C Chiesa Fuxench (ZC)

Department of Dermatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Meghan Feely (M)

Eli Lilly and Company, Indianapolis, Indiana, USA.
Department of Dermatology, Mount Sinai Health System, New York, New York, USA.

Evangeline Pierce (E)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Luna Sun (L)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Yun-Fei Chen (YF)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Robinette Angle (R)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Jonathan I Silverberg (JI)

Department of Dermatology, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.

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