Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Feb;133(2):429-38.
doi: 10.1016/j.jaci.2013.07.049. Epub 2013 Oct 24.

Efficacy and safety of systemic treatments for moderate-to-severe atopic dermatitis: a systematic review

Affiliations

Efficacy and safety of systemic treatments for moderate-to-severe atopic dermatitis: a systematic review

Evelien Roekevisch et al. J Allergy Clin Immunol. 2014 Feb.

Abstract

Background: Many patients with moderate-to-severe atopic dermatitis (AD) require systemic immunomodulating treatment to achieve adequate disease control.

Objective: We sought to systematically evaluate the efficacy and safety of systemic treatments for moderate-to-severe AD.

Methods: A systematic literature search was performed in MEDLINE, EMBASE, and CENTRAL (until June 2012). Randomized controlled trials (RCTs) evaluating systemic immunomodulating treatments for moderate-to-severe AD were included. Selection, data extraction, quality assessment, and generation of treatment recommendations using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach were performed independently by 2 reviewers. Efficacy outcomes were clinical signs, symptoms, quality of life, and the course of AD. Safety data were compared by calculating the weekly incidence rates (as percentages) for adverse events.

Results: Thirty-four RCTs with 12 different systemic treatments and totaling 1653 patients were included. Fourteen trials consistently indicate that cyclosporin A efficaciously improves clinical signs of AD. Cyclosporin A is recommended as first-line treatment for short-term use. A second-line treatment option is azathioprine, but efficacy is lower, and evidence is weaker. Methotrexate can be considered a third-line treatment option. Recommendations are impossible for mycophenolate, montelukast, intravenous immunoglobulins, and systemic glucocorticosteroids because of limited evidence. A meta-analysis was not performed because of a lack of standardization in outcome measures.

Conclusion: Although 12 different interventions for moderate-to-severe AD have been studied in 34 RCTs, strong recommendations are only possible for the short-term use of cyclosporin A. Methodological limitations in the majority of trials prevent evidence-based conclusions. Large head-to-head trials evaluating long-term treatments are required.

Keywords: AD; AE; AZA; Adverse event; Atopic dermatitis; Azathioprine; CsA; Cyclosporin A; EASI; EC-MPS; Eczema Area and Severity Index; Enteric-coated mycophenolate sodium; GRADE; Grading of Recommendations Assessment, Development and Evaluation; IVIG; Intravenous immunoglobulin; MTX; Methotrexate; RCT; Randomized controlled trial; SAE; Serious adverse event; TCHM; TP-5; Thymopentin; Traditional Chinese herbal medicine; evidence-based medicine/systematic review; immunomodulator; immunosuppressive therapy; recommendations; systemic treatment.

PubMed Disclaimer

Publication types

MeSH terms