Abstract |
Traditional disease-modifying antirheumatic drugs ( DMARD) remain the first-line treatment of psoriatic arthritis (PsA), despite lack of randomized controlled trials, and with evidence based on observational studies. Anti- tumor necrosis factor agents remain a top choice for biologic treatment, complemented with new biologics with different targets ( IL12-23 and IL17). Unmet needs have been identified for patients who do not respond to treatment. Among targeted small molecules Apremilast is approved for the treatment of PsA and Tofactitinib is under investigation. The drugs discussed herein have the potential to address unmet needs; however, additional research is required to identify more effective therapies for PsA.
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Authors | Enrique R Soriano |
Journal | Rheumatic diseases clinics of North America
(Rheum Dis Clin North Am)
Vol. 41
Issue 4
Pg. 711-22
(Nov 2015)
ISSN: 1558-3163 [Electronic] United States |
PMID | 26476228
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Antirheumatic Agents
- Tumor Necrosis Factor-alpha
- Thalidomide
- apremilast
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Topics |
- Anti-Inflammatory Agents, Non-Steroidal
(therapeutic use)
- Antirheumatic Agents
(therapeutic use)
- Arthritis, Psoriatic
(drug therapy, metabolism)
- Disease Management
- Humans
- Molecular Targeted Therapy
(methods)
- Thalidomide
(analogs & derivatives, therapeutic use)
- Treatment Outcome
- Tumor Necrosis Factor-alpha
(antagonists & inhibitors)
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