Review and Feature Article
Expert Perspectives on Management of Moderate-to-Severe Atopic Dermatitis: A Multidisciplinary Consensus Addressing Current and Emerging Therapies

https://doi.org/10.1016/j.jaip.2017.08.005Get rights and content
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Atopic dermatitis (AD) is a common, chronic, relapsing, inflammatory skin disease that affects children and adults. Until recently, the only Food and Drug Administration–approved systemic treatment option for patients with moderate-to-severe AD was systemic steroids, which are not recommended by current guidelines and are commonly associated with disease rebound. Instead, clinicians choose from several off-label immunosuppressants, which can have serious adverse effects. A significant number of these patients go untreated. Research on the immunopathogenesis of AD has paved the way for new, targeted, systemic therapies for moderate-to-severe AD. In early 2017, the Food and Drug Administration approved dupilumab for adults with moderate-to-severe AD whose disease is not adequately controlled with topical therapies. Although the national guidelines can be very helpful to clinicians, the process for updating them does not allow for timely incorporation of novel therapies. A steering committee of AD experts, including dermatologists, allergists, and a patient advocacy group representative, developed recommendations on the basis of a literature review and expert opinion to help clinicians understand how new therapies fit into the current treatment paradigm and to provide practical recommendations for assessing AD severity, treatment response, and treatment failure.

Key words

Atopic dermatitis
Eczema
Recommendations
Diagnosis
Treatment
Allergy

Abbreviations used

AAD
American Academy of Dermatology
AD
Atopic dermatitis
BSA
Body surface area
EASI
Eczema Area and Severity Index
FDA
Food and Drug Administration
QOL
Quality of life
SC
Steering committee
TCS
Topical corticosteroid
UV
Ultraviolet

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This work was supported by the Sanofi-Genzyme and Regeneron Alliance. The Sanofi-Genzyme and Regeneron Alliance provided funding for the 3AD program but had no influence on the development of the recommendations. Sanofi-Genzyme and Regeneron had no influence on the development of the manuscript nor did they review the content of the manuscript. The authors (all of whom are members of the 3AD Steering Committee) determined and approved the final content of the manuscript. The Steering Committee has been assisted by Lighthouse Medical Communications US (formerly known as Lucid US), a specialist medical communications company, which was funded by Sanofi-Genzyme and Regeneron, for the organization of the program and editorial support of the manuscript. The authors maintained complete control over the direction and content of the paper. No payments were made to the authors for the writing of this manuscript.

Conflicts of interest: M. Boguniewicz has received consultancy fees and travel support from Anacor and Lucid; has received consultancy and lecture fees from Regeneron and Sanofi-Genzyme; has received research support from Regeneron; and has received payment for developing educational presentations from Regeneron. A. F. Alexis has received consultancy fees, provision of writing assistance from, and is on the advisory board for Regeneron; has been a consultant for Anacor, Galderma, and Sanofi-Genzyme; and has received research support from Galderma. L. A. Beck has received consultancy fees and travel support from Sanofi-Regeneron; has received consultancy fees from AbbVie, Celgene, Hoffman-LaRoche, Janssen, Lilly, Novan, Realm Therapeutics, Regeneron, and Genentech; has received research support from Regeneron, Pfizer, and AbbVie; was a participant in atopic dermatitis clinical trials for AbbVie and Regeneron; and has stock/stock options in Pfizer and Medtronics. J. Block has received consultancy fees and travel support from Sanofi-Genzyme and Regeneron and has received research support from corporate sponsors. (The National Eczema Association receives funding from various corporate sponsors, which are guided by our Corporate Relations Policy and disclosed to the public.) L. F. Eichenfield has received consultancy fees and travel support from Lucid in proxy for Regeneron/Sanofi and has received consultancy fees from Allergan, Anacor/Pfizer, DS Biopharma, Galderma, Genentech, Lilly, Otsuka/Medimetriks, Ralaxar, Regeneron/Sanofi, and Valeant. L. Fonacier has received consultancy fees and travel support from Sanofi-Genzyme and Regeneron; is on the boards for the American Board of Allergy and Immunology and the American College of Allergy, Asthma and Immunology; has received consultancy fees from Church and Dwight Co, Inc; has received research support from Genentech and Baxter on behalf of NYU Winthrop Hospital; and has received lecture fees from regional allergy societies. E. Guttman-Yassky has received research support from Celgene, Dermira, Janssen Biotech, LEO Pharmaceuticals, Merck, Novartis, Regeneron, and BMS and has received consultancy fees from AbbVie, Amgen, Anacor, Celgene, Celsus Therapeutics, Dermira, Drais, Galderma, Genentech, Glenmark, LEO Pharmaceuticals, Novartis, Pfizer, Regeneron, Sanofi-Genzyme, Stiefel/GlaxoSmithKline, Vitae, Mitsubishi Tanabe, Eli Lilly, Bristol-Myers Squibb, Allergan, Escalier, and Afecta. A. S. Paller has received consultancy fees and travel support from Sanofi-Genzyme and Regeneron; has received consultancy fees from Pfizer, Eli Lilly, Galderma, GlaxoSmithKline-Stiefel, Pierre Fabre, Puricore (Realm), Regeneron/Sanofi, Roivant, and Valeant; and has received lecture fees from Expanscience Laboratories (Mustela). D. Pariser has received consultancy fees from Bickel Biotechnology, Biofrontera AG, Celgene Corporation, Dermira, DUSA Pharmaceuticals, LEO Pharma, Novartis, Pfizer, Promius Pharmaceuticals, Regeneron, Sanofi-Genzyme, TheraVida, and Valeant Pharmaceuticals International; has received research support from LEO Pharma, Abbott Laboratories, Amgen, Bickel Biotechnology, Celgene Corporation, Eli Lilly, Novartis, Novo Nordisk A/S, Ortho Dermatologics, Peplin Ic, Photocure ASA, Promius Pharmaceuticals, Regeneron, Stiefel/GSK, and Valeant; and is on the Pfizer Advisory Board. J. I. Silverberg has received research support from GlaxoSmithKline; has received consultancy fees from AbbVie, Anacor, Eli Lilly, GSK, Galderma, Kiniksa, Menlo, Pfizer, Realm-1, Sanofi-Genzyme, and Regeneron; has received fees for participation in review activities from Eli Lilly, Anacor, and Regeneron-Sanofi; and has received lecture fees from Regeneron-Sanofi. M. Lebwohl has received research support from Taro, LEO Pharma, Regeneron, Sanofi-Genzyme, and Valeant.