Beneficial effects of apremilast on genital ulcers, skin lesions, and arthritis in patients with Behçet’s disease: A systematic review and meta-analysis

Author:

Iizuka Yuki1,Takase-Minegishi Kaoru1ORCID,Hirahara Lisa1,Kirino Yohei1ORCID,Soejima Yutaro1,Namkoong H o2ORCID,Horita Nobuyuki3,Yoshimi Ryusuke1,Takeuchi Masaki4,Takeno Mitsuhiro5ORCID,Mizuki Nobuhisa4,Nakajima Hideaki1

Affiliation:

1. Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan

2. Department of Infectious Diseases, Keio University School of Medicine, Tokyo, Japan

3. Chemotherapy Center, Yokohama City University Hospital, Yokohama, Japan

4. Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Yokohama, Japan

5. Department of Allergy and Rheumatology, Nippon Medical School Musashi Kosugi Hospital, Kawasaki, Japan

Abstract

ABSTRACT Objectives This study aimed to determine the clinical efficacy of apremilast for oral ulcers (OUs), extra-oral manifestations, and overall disease activity in patients with Behçet’s disease (BD). Methods A systematic literature search was performed in PubMed, Embase, Cochrane Library, and Web of Science Core Collection. Studies assessing the treatment effects of apremilast in BD were included. The odds ratios (ORs) of being symptom-free for individual manifestations and mean difference (MD) of Behçet’s Disease Current Activity Form (BDCAF) scores were calculated with 95% confidence intervals (CIs) at 12 and 24 weeks using a random-model meta-analysis. Results Of 259 screened articles, eight were included. After 12 weeks of apremilast treatment the OR of symptom-free was as followings: OUs, 45.76 (95% CI, 13.23–158.31); genital ulcers, 4.56 (95% CI, 2.47–8.44); erythema nodosum, 3.59 (95% CI, 1.11–11.61); pseudofolliculitis, 2.81 (95% CI, 1.29–6.15); and arthritis, 3.55 (95% CI, 1.71–7.40). Furthermore, BDCAF scores at 12 weeks were significantly reduced (MD=−1.38; −1.78 to −0.99). However, the proportion of oral-ulcer-free patients increased at 24 weeks (OR = 14.88; 4.81 to 46.07). Conclusions The currently accumulated data indicate an improvement in mucocutaneous and articular symptoms by short-term apremilast treatment in patients with BD.

Funder

Japanese Society for the Promotion of Science

Japan College of Rheumatology Next Generation

Health and Labour Sciences Research

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

Reference35 articles.

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2. The International Criteria for Behçet’s Disease (ICBD): a collaborative study of 27 countries on the sensitivity and specificity of the new criteria;International Team for the Revision of the International Criteria for Behçet’s Disease (ITR-ICBD);J Eur Acad Dermatol Venereol,2014

3. Behçet disease: evolution of clinical manifestations;Ideguchi;Medicine (Baltimore),2011

4. Clinical and genetic aspects of Behçet’s disease in Japan;Kirino;Intern Med,2019

5. Diagnostic criteria for Behcet’s disease in 1987, and guideline for treating Behcet’s disease;Mizushima;Saishin Igaku,1988

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