New International League of Associations for Rheumatology (ILAR) recommendations are now available for the treatment of patients with psoriatic arthritis living in resource-poor regions, including Central and South America and Africa.
New International League of Associations for Rheumatology (ILAR) recommendations are now available for the treatment of patients with psoriatic arthritis (PsA) living in resource-poor regions, including Central and South America and Africa.
The new ILAR recommendations were adapted from existing PsA treatment recommendations developed by the European League Against Rheumatism (EULAR)1 and the Group for Research and Assessment of Psoriasis and PSA (GRAPPA),2 as well as expert opinion from these regions. EULAR and GRAPPA issued their respective recommendations for management of PsA in 2015, but there have been concerns that the guidelines were primarily based on studies conducted in resource-wealthy countries and thus might not be applicable to resource-poor countries. The study, by Musaab Elmamoun, MBBS, MRCPI, and a group of international expert colleagues, was presented at the annual European Congress of Rheumatology, held June 13-16, 2018, in Amsterdam, and hosted by EULAR.
The first part of the collaborative process was undertaken to assess and adapt EULAR and GRAPPA treatment recommendations for PsA to cover patients living in Central and South America and Africa:
The adaptation process resulted in the creation of 5 principles for the management of PsA that address goals of therapy, assessment of domains, assessment of relevant comorbidities, safety of pharmacotherapy and shared decision-making, and frequency of follow up.
Finally, the collaborative group developed the following 6 recommendations for the management of PsA:
References
Resolution of Injection Site Reactions After Switching to Adalimumab Biosimilar
February 22nd 2025A 15-year-old girl with ulcerative colitis who developed injection site reactions to the adalimumab reference product was successfully switched to the biosimilar LBAL without recurrence of symptoms, demonstrating the safety and effectiveness of switching for medical reasons, likely due to an allergic reaction to an excipient in the originator.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Breaking Barriers in Osteoporosis Care: New Denosumab Biosimilars Wyost, Jubbonti Approved
June 16th 2024In this episode, The Center for Biosimilars® delves into the FDA approval of the first denosumab biosimilars, Wyost and Jubbonti (denosumab-bbdz), and discuss their potential to revolutionize osteoporosis treatment with expert insights from 2 rheumatologists.
The Biosimilar Void: 90% of Biologics Coming Off Patent Will Lack Biosimilars
February 5th 2025Of the 118 biologics losing exclusivity over the next decade, only 10% have biosimilars in development, meaning a vast majority of biologics have no pipeline, which limits savings potential for the health care system.