Abstract | BACKGROUND: OBJECTIVE: METHODS: 190 patients with plaque psoriasis (at least 3% skin involvement) and active PsA were randomized to double-blind treatment with leflunomide (100 mg/day loading dose for 3 days followed by 20 mg/day orally) or placebo for 24 weeks. RESULTS: As previously reported, leflunomide resulted in a significantly higher Psoriatic Arthritis Response Criteria response rate than placebo (58.9 vs. 29.7%; p < 0.0001). Significant differences in favor of leflunomide were also observed in the Psoriasis Area and Severity Index (PASI 50 in 30.4% of patients vs. 18.9% for placebo; p = 0.05), target lesion response (46.4 vs. 25.3%; p = 0.0048), combined skin and joint response (27.2 vs. 8.9%; p < 0.0001), Dermatology Life Quality Index (improvement of 1.9 points vs. 0.2; p = 0.0173) and certain SF-36 subdomains. Dermatological responses were observed at the earliest examination (4 weeks) and increased throughout the 24-week study. CONCLUSION:
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Authors | Peter Nash, Diamant Thaçi, Frank Behrens, Franziska Falk, J Peter Kaltwasser |
Journal | Dermatology (Basel, Switzerland)
(Dermatology)
Vol. 212
Issue 3
Pg. 238-49
( 2006)
ISSN: 1018-8665 [Print] Switzerland |
PMID | 16549920
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial)
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Copyright | 2006 S. Karger AG, Basel |
Chemical References |
- Adjuvants, Immunologic
- Anti-Inflammatory Agents, Non-Steroidal
- Immunosuppressive Agents
- Isoxazoles
- Leflunomide
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Topics |
- Adjuvants, Immunologic
(administration & dosage, therapeutic use)
- Administration, Oral
- Adult
- Aged
- Anti-Inflammatory Agents, Non-Steroidal
(administration & dosage, therapeutic use)
- Arthritis, Psoriatic
(drug therapy)
- Double-Blind Method
- Female
- Humans
- Immunosuppressive Agents
(administration & dosage, therapeutic use)
- Isoxazoles
(administration & dosage, therapeutic use)
- Leflunomide
- Male
- Middle Aged
- Psoriasis
(drug therapy, pathology)
- Quality of Life
- Skin
(pathology)
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