Evaluation of standard treatments for managing adult Japanese patients with inadequately controlled moderate-to-severe atopic dermatitis: Two-year data from the ADDRESS-J disease registry.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Sep 2022
Historique:
revised: 04 05 2022
received: 11 11 2021
accepted: 22 05 2022
pubmed: 19 6 2022
medline: 8 9 2022
entrez: 18 6 2022
Statut: ppublish

Résumé

Atopic dermatitis (AD), a chronic relapsing inflammatory skin disease with a high disease burden, is one of the most common dermatological conditions in Japan. Herein, we report the disease profiles and current AD treatment during 2-year management of Japanese adults with moderate-to-severe AD. ADDRESS-J was a prospective, longitudinal, observational study that evaluated real-world effectiveness and safety of current AD treatments of adult patients with moderate-to-severe AD (Investigator's Global Assessment score 3 or 4) in Japan. The maximum follow-up period was 2 years. Among 300 patients enrolled, 288 had ≥1 post-baseline evaluation and were analyzed (mean age, 35.5 years; 60.1% male). Almost all patients (99.7%) received topical therapy; the most commonly used therapy was topical corticosteroids of the second-highest potency (86.5%) (e.g., 0.1% mometasone furoate) followed by medium-potency topical corticosteroids (50.3%) (e.g., 0.05% clobetasol butyrate). At month 12 of the study, 10.4% of patients had Investigator's Global Assessment 0/1, similarly at month 24 (10.8%). A total of 132 patients (45.8%) had ≥1 AD flare-up during the observation period, with the majority of first flares occurring within the first year of the study. Various physician- and patient-reported outcomes improved considerably during the first 3 months of the study, with only minor changes after this time. In this cohort, 16.7% of patients had skin infections requiring treatment; 7.3% had adverse events (AE) potentially related to treatment; 1.7% had serious AE; and 1.0% had treatment discontinuations due to AE. Limitations include missing data at later timepoints and the inclusion criteria limiting generalizability. In summary, this analysis of the ADDRESS-J study showed that some patients with moderate or severe AD respond to conventional therapies, while others do not. For those with inadequately controlled moderate-to-severe AD, the newly emerged systemic agents, such as biologics, may provide a potential strategy for long-term disease management.

Identifiants

pubmed: 35715964
doi: 10.1111/1346-8138.16485
pmc: PMC9543354
doi:

Substances chimiques

Glucocorticoids 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

903-911

Subventions

Organisme : Sanofi and Regeneron Pharmaceuticals, Inc.

Informations de copyright

© 2022 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association.

Références

Br J Dermatol. 2003 Jan;148(1):128-33
pubmed: 12534606
Curr Opin Allergy Clin Immunol. 2015 Oct;15(5):453-60
pubmed: 26226355
Asia Pac Allergy. 2011 Jul;1(2):64-72
pubmed: 22053299
J Dermatol. 2021 Feb;48(2):140-151
pubmed: 33377547
Allergy. 2012 Jan;67(1):99-106
pubmed: 21951293
Br J Dermatol. 2018 Apr;178(4):925-930
pubmed: 29048751
Dermatology. 2015;230(1):27-33
pubmed: 25613671
Ann Allergy Asthma Immunol. 2021 Jan;126(1):21-31
pubmed: 32818591
J Dermatol. 2019 Apr;46(4):290-300
pubmed: 30756423
Br J Dermatol. 2017 Nov;177(5):1316-1321
pubmed: 28485036
Arch Dermatol. 2004 Dec;140(12):1513-9
pubmed: 15611432
Allergol Int. 2017 Jan;66(1):3-7
pubmed: 27634668
Allergy. 2012 Sep;67(9):1111-7
pubmed: 22844983
Clin Exp Dermatol. 1994 May;19(3):210-6
pubmed: 8033378
Exp Dermatol. 2001 Feb;10(1):11-8
pubmed: 11168575
J Dermatol Sci. 2015 Sep;79(3):279-87
pubmed: 26255207
J Dermatol. 2011 Apr;38(4):310-20
pubmed: 21426384
J Dermatol. 2008 Aug;35(8):477-83
pubmed: 18789066
JAMA. 1983 Apr 1;249(13):1743-5
pubmed: 6827763
J Dermatol. 2019 Dec;46(12):1053-1101
pubmed: 31599013
J Dermatol. 2006 Nov;33(11):817-9
pubmed: 17074002
J Dermatol. 2022 Sep;49(9):903-911
pubmed: 35715964
Br J Dermatol. 2020 Nov;183(5):891-898
pubmed: 32107772

Auteurs

Norito Katoh (N)

Department of Dermatology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, Kyoto, Japan.

Hidehisa Saeki (H)

Department of Dermatology, Nippon Medical School, Tokyo, Japan.

Yoko Kataoka (Y)

Department of Dermatology, Osaka Habikino Medical Center, Osaka, Japan.

Takafumi Etoh (T)

Atago Dermatology Clinic, Tokyo, Japan.
Department of Dermatology, Tokyo Teishin Hospital, Tokyo, Japan.

Satoshi Teramukai (S)

Department of Biostatistics, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Hiroki Takagi (H)

Sanofi K.K., Tokyo, Japan.

Hiroyuki Fujita (H)

Sanofi K.K., Tokyo, Japan.

Marius Ardeleanu (M)

Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.

Elena Rizova (E)

Sanofi, Cambridge, Massachusetts, USA.

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Classifications MeSH