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  • Comparative effectiveness of less commonly used systemic monotherapies and common combination therapies for moderate to severe psoriasis in the clinical setting.

Comparative effectiveness of less commonly used systemic monotherapies and common combination therapies for moderate to severe psoriasis in the clinical setting.

Journal of the American Academy of Dermatology (2014-09-28)
Junko Takeshita, Shuwei Wang, Daniel B Shin, Kristina Callis Duffin, Gerald G Krueger, Robert E Kalb, Jamie D Weisman, Brian R Sperber, Michael B Stierstorfer, Bruce A Brod, Stephen M Schleicher, Andrew D Robertson, Kristin A Linn, Russell T Shinohara, Andrea B Troxel, Abby S Van Voorhees, Joel M Gelfand
ABSTRACT

The effectiveness of psoriasis therapies in real-world settings remains relatively unknown. We sought to compare the effectiveness of less commonly used systemic therapies and commonly used combination therapies for psoriasis. This was a multicenter cross-sectional study of 203 patients with plaque psoriasis receiving less common systemic monotherapy (acitretin, cyclosporine, or infliximab) or common combination therapies (adalimumab, etanercept, or infliximab and methotrexate) compared with 168 patients receiving methotrexate evaluated at 1 of 10 US outpatient dermatology sites participating in the Dermatology Clinical Effectiveness Research Network. In adjusted analyses, patients on acitretin (relative response rate 2.01; 95% confidence interval [CI] 1.18-3.41), infliximab (relative response rate 1.93; 95% CI 1.26-2.98), adalimumab and methotrexate (relative response rate 3.04; 95% CI 2.12-4.36), etanercept and methotrexate (relative response rate 2.22; 95% CI 1.25-3.94), and infliximab and methotrexate (relative response rate 1.72; 95% CI 1.10-2.70) were more likely to have clear or almost clear skin compared with patients on methotrexate. There were no differences among treatments when response rate was defined by health-related quality of life. Single time point assessment may result in overestimation of effectiveness. The efficacy of therapies in clinical trials may overestimate their effectiveness as used in clinical practice. Although physician-reported relative response rates were different among therapies, absolute differences were small and did not correspond to differences in patient-reported outcomes.

MATERIALS
Product Number
Brand
Product Description

Methotrexate for system suitability, European Pharmacopoeia (EP) Reference Standard
Supelco
Methotrexate solution, 1.0 mg/mL in methanol with 0.1N NaOH, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
Cyclosporin A solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
Sigma-Aldrich
Methotrexate hydrate, powder, BioReagent, suitable for cell culture, ≥98% (HPLC)
Sigma-Aldrich
Methotrexate hydrate, ≥98% (HPLC), powder
Sigma-Aldrich
Methotrexate, meets USP testing specifications
Sigma-Aldrich
Methotrexate hydrate, ≥99.0% (sum of enantiomers, HPLC)
USP
Acitretin Related Compound A, United States Pharmacopeia (USP) Reference Standard
Methotrexate for peak identification, European Pharmacopoeia (EP) Reference Standard
USP
Acitretin, United States Pharmacopeia (USP) Reference Standard
Supelco
Methotrexate, Pharmaceutical Secondary Standard; Certified Reference Material
Methotrexate, European Pharmacopoeia (EP) Reference Standard
Acitretin, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Acitretin, ≥98.0% (HPLC)
SAFC
Methotrexate