TY - JOUR
T1 - A Randomized Trial of Etanercept as Monotherapy for Psoriasis
AU - Gottlieb, Alice B.
AU - Matheson, Robert T.
AU - Lowe, Nicholas
AU - Krueger, Gerald G.
AU - Kang, Sewon
AU - Goffe, Bernard S.
AU - Gaspari, Anthony A.
AU - Ling, Mark
AU - Weinstein, Gerald D.
AU - Nayak, Anjuli
AU - Gordon, Kenneth B.
AU - Zitnik, Ralph
AU - Naldi, Luigi
PY - 2003/12
Y1 - 2003/12
N2 - Objective: To determine safety and efficacy of monotherapy with etanercept. Design: Randomized, double-blind, placebo-controlled, multicenter study. Setting: Outpatient, ambulatory; private practice and university dermatology research centers. Patients: Patients aged at least 18 years, with plaque psoriasis involving 10% or more of body surface area; 148 were screened and 112 were randomly assigned to treatment groups and received study drug. Interventions: Patients received placebo or etanercept, 25 mg, subcutaneously twice a week for 24 weeks. Other psoriasis therapies were limited during the study. Main Outcome Measures: Safety measurements included tracking of adverse events and laboratory values. Efficacy was evaluated using the Psoriasis Area and Severity Index (PASI); the primary end point was a 75% improvement in PASI. Other efficacy measurements included patient and physician global assessments and quality-of-life measures. Results: After 12 weeks of treatment, 17 (30%) of the 57 etanercept-treated patients and 1 (2%) of the 55 placebo-treated patients had achieved PASI 75%, and after 24 weeks, 32 (56%) of etanercept-treated patients and 3 (5%) of placebo-treated patients had reached this level (P<.001 for both time points). By 24 weeks, psoriasis was clear or minimal by physician's global assessment in more than 50% of patients who received etanercept. Treatment failure (PASI response <50) occurred in 23% of patients at week 24. All other measures confirmed the efficacy of etanercept. Adverse events were similar among etanercept and placebo groups. Conclusion: Etanercept monotherapy provided significant benefit to patients with psoriasis and had a favorable safety profile.
AB - Objective: To determine safety and efficacy of monotherapy with etanercept. Design: Randomized, double-blind, placebo-controlled, multicenter study. Setting: Outpatient, ambulatory; private practice and university dermatology research centers. Patients: Patients aged at least 18 years, with plaque psoriasis involving 10% or more of body surface area; 148 were screened and 112 were randomly assigned to treatment groups and received study drug. Interventions: Patients received placebo or etanercept, 25 mg, subcutaneously twice a week for 24 weeks. Other psoriasis therapies were limited during the study. Main Outcome Measures: Safety measurements included tracking of adverse events and laboratory values. Efficacy was evaluated using the Psoriasis Area and Severity Index (PASI); the primary end point was a 75% improvement in PASI. Other efficacy measurements included patient and physician global assessments and quality-of-life measures. Results: After 12 weeks of treatment, 17 (30%) of the 57 etanercept-treated patients and 1 (2%) of the 55 placebo-treated patients had achieved PASI 75%, and after 24 weeks, 32 (56%) of etanercept-treated patients and 3 (5%) of placebo-treated patients had reached this level (P<.001 for both time points). By 24 weeks, psoriasis was clear or minimal by physician's global assessment in more than 50% of patients who received etanercept. Treatment failure (PASI response <50) occurred in 23% of patients at week 24. All other measures confirmed the efficacy of etanercept. Adverse events were similar among etanercept and placebo groups. Conclusion: Etanercept monotherapy provided significant benefit to patients with psoriasis and had a favorable safety profile.
UR - http://www.scopus.com/inward/record.url?scp=10744221697&partnerID=8YFLogxK
U2 - 10.1001/archderm.139.12.1627
DO - 10.1001/archderm.139.12.1627
M3 - Article
C2 - 14676082
AN - SCOPUS:10744221697
SN - 0003-987X
VL - 139
SP - 1627
EP - 1632
JO - Archives of Dermatology
JF - Archives of Dermatology
IS - 12
ER -