Journal
JOURNAL OF RHEUMATOLOGY
Volume 43, Issue 9, Pages 1713-1717Publisher
J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.160275
Keywords
SECUKINUMAB; TUMOR NECROSIS FACTOR INHIBITOR; PSORIATIC ARTHRITIS; BIOLOGICS; INTERLEUKIN 17A
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Funding
- National Institute for Health Research [CL-2006-06-010] Funding Source: researchfish
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Objective. To determine the effect of prior tumor necrosis factor inhibitor (TNFi) therapy on secukinumab efficacy in psoriatic arthritis (PsA). Methods. Patients were randomized to secukinumab 300 mg, 150 mg, 75 mg, or placebo. Results. American College of Rheumatology 20 responses at Week 24 with secukinumab 300 mg, 150 mg, 75 mg, and placebo were 58.2%, 63.5%, 36.9%, and 15.9% in TNFi-naive (n = 258), and 45.5%, 29.7%, 14.7%, and 14.3% in TNFi-exposed patients (n = 139), respectively. Week 52 responses with secukinumab 300 mg, 150 mg, and 75 mg were 68.7%, 79.4%, and 58.5% in TNFi-naive, and 54.5%, 37.8%, and 35.3% in TNFi-exposed patients, respectively. Conclusion. Secukinumab was efficacious in TNFi-naive and TNFi-exposed patients with PsA, with greatest improvements in TNFi-naive patients.
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