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Review
. 2014 Dec;15(6):467-78.
doi: 10.1007/s40257-014-0097-1.

Use of biologic agents in combination with other therapies for the treatment of psoriasis

Affiliations
Review

Use of biologic agents in combination with other therapies for the treatment of psoriasis

Jennifer C Cather et al. Am J Clin Dermatol. 2014 Dec.

Abstract

Psoriasis is a chronic inflammatory skin disorder, which is associated with a significant negative impact on a patient's quality of life. Traditional therapies for psoriasis are often not able to meet desired treatment goals, and high-dose and/or long-term use is associated with toxicities that can result in end-organ damage. An improved understanding of the involvement of cytokines in the etiology of psoriasis has led to the development of biologic agents targeting tumor necrosis factor (TNF)-α and interleukins (ILs)-12/23. While biologic agents have improved treatment outcomes, they are not effective in all individuals with psoriasis. The combination of biologic agents with traditional therapies may provide improved therapeutic options for patients who inadequately respond to a single drug or when efficacy may be increased with supplementation of another treatment. In addition, combination therapy may reduce safety concerns and cumulative toxicity, as lower doses of individual agents may be efficacious when used together. This article reviews the current evidence available on the efficacy and safety of combining biologic agents with systemic therapies (methotrexate, cyclosporine, or retinoids) or with phototherapy, and the combination of biologic agents themselves. Guidance is provided to help physicians identify situations and the characteristics of patients who would benefit from combination therapy with a biologic agent. Finally, the potential clinical impact of biologic therapies in development (e.g., those targeting IL-17A, IL-17RA, or IL-23 alone) is analyzed.

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Conflict of interest statement

Dr. Cather has served as a speaker or consultant for AbbVie, Janssen, Leo, and Novartis. She has served as an investigator in clinical trials for Amgen, Celgene, Galderma, Lilly, Merck, Novartis, Pfizer, and Tolmar. She owns no stock and has no ownership interest in any pharmaceutical company.

Dr. Crowley has served as a speaker or consultant for, and has received research grants from, AbbVie and Amgen. He has served as a consultant for, and has received research support from, Celgene, Janssen, Lilly, and Pfizer. He has received research grants from Maruho, Merck, and Regeneron. He owns no stock and has no ownership interest in any pharmaceutical company.

Figures

Fig. 1
Fig. 1
Proportions of patients with moderate-to-severe plaque psoriasis showing improvements in the Psoriasis Area Severity Index of ≥50 % (PASI 50), ≥75 % (PASI 75), and ≥90 % (PASI 90) at 12 and 24 weeks during treatment with etanercept, alone or combined with methotrexate. Reproduced with permission from Gottlieb et al. [57]. © 2012 The Authors. BJD © 2012 British Association of Dermatologists
Fig. 2
Fig. 2
Psoriasis Area Severity Index of ≥50 % (PASI 50) and ≥75 % (PASI 75) response rates at 24 weeks in patients with active plaque psoriasis treated with acitretin, etanercept twice weekly, or the two agents in combination with reduced use of etanercept (etanercept once weekly plus daily acitretin) [53]

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