BACKGROUND: Biologics are a safe and efficacious therapy for psoriasis. The drug survival of biologics may be disappointing, primarily due to loss of efficacy. Therefore, safe combination treatments are sought to improve their clinical response. OBJECTIVE: To assess the efficacy, safety and tolerability of the combination therapy of etanercept with fumarates versus etanercept monotherapy. METHODS:Thirty-three patients with psoriasis were randomized 1:1 to receive etanercept combined with fumarates or etanercept monotherapy. The primary outcome measure was the difference in PASI-75 response after 24 weeks; additionally, a longitudinal analysis was performed. An important secondary outcome measure was the proportion of patients with a Physician Global Assessment (PGA) of clear or almost clear. Adverse events were collected throughout the study. RESULTS: In the combination therapy group, 78% (14 out of 18 patients) reached PASI-75 at week 24 versus 57% (8 out of 14 patients) in the monotherapy group (p = 0.27). The longitudinal analysis showed a PASI reduction of 5.97% per week for the combination therapy group and of 4.76% for the monotherapy group (p = 0.11). In the combination therapy group, 94% (17 out of 18 patients) of patients had a PGA of clear/almost clear versus 64% (9 out of 14 patients) in the monotherapy group (p = 0.064). The incidence of mild gastrointestinal complaints was higher in the combination group than in the monotherapy group. CONCLUSION: Using the PGA, combination therapy showed a trend towards faster improvement in the first 24 weeks. The difference in the PASI score between the two groups was not statistically significant. Addition of fumarates to etanercept for 48 weeks appeared safe with an acceptable tolerability.
RCT Entities:
BACKGROUND: Biologics are a safe and efficacious therapy for psoriasis. The drug survival of biologics may be disappointing, primarily due to loss of efficacy. Therefore, safe combination treatments are sought to improve their clinical response. OBJECTIVE: To assess the efficacy, safety and tolerability of the combination therapy of etanercept with fumarates versus etanercept monotherapy. METHODS: Thirty-three patients with psoriasis were randomized 1:1 to receive etanercept combined with fumarates or etanercept monotherapy. The primary outcome measure was the difference in PASI-75 response after 24 weeks; additionally, a longitudinal analysis was performed. An important secondary outcome measure was the proportion of patients with a Physician Global Assessment (PGA) of clear or almost clear. Adverse events were collected throughout the study. RESULTS: In the combination therapy group, 78% (14 out of 18 patients) reached PASI-75 at week 24 versus 57% (8 out of 14 patients) in the monotherapy group (p = 0.27). The longitudinal analysis showed a PASI reduction of 5.97% per week for the combination therapy group and of 4.76% for the monotherapy group (p = 0.11). In the combination therapy group, 94% (17 out of 18 patients) of patients had a PGA of clear/almost clear versus 64% (9 out of 14 patients) in the monotherapy group (p = 0.064). The incidence of mild gastrointestinal complaints was higher in the combination group than in the monotherapy group. CONCLUSION: Using the PGA, combination therapy showed a trend towards faster improvement in the first 24 weeks. The difference in the PASI score between the two groups was not statistically significant. Addition of fumarates to etanercept for 48 weeks appeared safe with an acceptable tolerability.
Authors: Stephen Tyring; Alice Gottlieb; Kim Papp; Ken Gordon; Craig Leonardi; Andrea Wang; Deepa Lalla; Michael Woolley; Angelika Jahreis; Ralph Zitnik; David Cella; Ranga Krishnan Journal: Lancet Date: 2006-01-07 Impact factor: 79.321
Authors: Charlotte L Krieckaert; Anna Jamnitski; Michael T Nurmohamed; Piet J Kostense; Maarten Boers; Gertjan Wolbink Journal: Arthritis Rheum Date: 2012-12
Authors: K A Papp; S Tyring; M Lahfa; J Prinz; C E M Griffiths; A M Nakanishi; R Zitnik; P C M van de Kerkhof; Linda Melvin Journal: Br J Dermatol Date: 2005-06 Impact factor: 9.302
Authors: April W Armstrong; Jerry Bagel; Abby S Van Voorhees; Andrew D Robertson; Paul S Yamauchi Journal: JAMA Dermatol Date: 2015-04 Impact factor: 10.282
Authors: Maarten L Zandvliet; Jine S van Bezooijen; Mariska A Bos; Errol P Prens; Martijn van Doorn; Ilona Bijen; Marco W J Schreurs; Vincent H J van der Velden; Birgit C P Koch; Teun van Gelder Journal: Ther Drug Monit Date: 2013-10 Impact factor: 3.681