Efficacy and safety of infliximab monotherapy for plaque-type psoriasis: arandomised trial

Background Currently available treatments for moderate to severe psoriasis are either incompletely effective in some patients, or are associated with toxic effects. Since tumour necrosis factor alpha (TNF-alpha) is thought to have a role in the pathogenesis of psoriasis, we did a double-blind, rando mised trial to assess the clinical benefit and safety of infliximab-a monoc lonal antibody against TNF-alpha. Methods 33 patients with moderate to severe plaque psoriasis were randomly assigned intravenous placebo (n=11), infliximab 5 mg/kg (n=11), or inflixim ab 10 mg/kg (n=11) at weeks 0, 2, and 6. Patients were assessed at week 10 for the primary endpoint (score on the physician's global assessment [PGA]) . Analysis was by intention to treat. Findings Of the 33 patients enrolled, three dropped out. Nine of 11 (82%) p atients in the Infliximab 5 mg/kg group were responders (good, excellent, o r clear rating on PGA), compared with two of 11 (18%) In the placebo group (difference 64% [95% CI 20-89], p=0.0089), and ten of 11 (91%) patients in the infliximab 10 mg/kg group were responders (difference from placebo 73% [30-94], p=0.0019). The median time to response was 4 weeks for patients in both infliximab groups. There were no serious adverse events, and inflixim ab was well tolerated. Interpretation In this controlled trial, patients receiving the anti-TNF-al pha agent infliximab as monotherapy experienced a high degree of clinical b enefit and rapid time to response In the treatment of moderate to severe pl aque psoriasis compared with patients who received placebo. These findings suggest that TNF-alpha has a pivotal role in the pathogenesis of psoriasis.