The American College of Rheumatology (ACR) and the Arthritis Foundation (AF) released guidelines for treating 2 subtypes of juvenile idiopathic arthritis (JIA), which affects nearly 300,000 children in the United States. One guideline discusses therapeutic approaches for non-systemic polyarthritis, sacroiliitis, and enthesitis; the other focuses on the screening, monitoring, and treatment of JIA with associated uveitis. The second guideline focuses on uveitis, which can be a chronic or acute disease.
The American College of Rheumatology (ACR) and the Arthritis Foundation (AF) this week released guidelines for treating 2 subtypes of juvenile idiopathic arthritis (JIA), which affects nearly 300,000 children in the United States.
One guideline discusses therapeutic approaches for non-systemic polyarthritis, sacroiliitis, and enthesitis; the other focuses on the screening, monitoring, and treatment of JIA with associated uveitis.
Juvenile arthritis is an umbrella term used to describe the autoimmune and inflammatory conditions or pediatric rheumatic diseases, like JIA, that can develop in children younger than 16, according to the AF.
To address polyarthritis, guideline development teams created Patient/Population, Intervention, Comparison, and Outcomes (PICO) questions, and conducted a systematic review to compile evidence for the benefits and harms associated with treatments for these conditions.
As opposed to previously published guidelines, which use a different model to address the quality of the evidence, this report uses GRADE (Grading of Recommendations Assessment, Development and Evaluation) methodology, which the authors say provides greater transparency.
From that, 39 recommendations were developed (8 strong and 31 conditional). While the quality of supporting evidence was very low or low for 90% of the recommendations, the report said recommendations should not be used to limit or deny access to therapies.
In addition, the report noted that “quality” as used in the review does not refer to methodologic quality of studies mentioned, but instead to rate the article(s) in relation to the PICO question, such as if the population or intervention being studied does not completely match what is being asked by the question.
The report noted that there was a debate among the voting panel regarding the appropriateness of the use of biologics as initial therapy in children with polyarthritis, particularly for those with risk factors.
Ultimately, non—biologic disease-modifying antirheumatic drug (DMARD) therapy was recommended, but the report said there may be some patients for whom initial biologic therapy is indicated. Current studies may better clarify which patients are most likely to benefit from first-line biologic therapy.
Some of the recommendations from the polyarthritis guideline include:
The second guideline focuses on uveitis, which can be a chronic or acute disease. Chronic anterior uveitis (CAU) develops in 10% to 20% of children with JIA; it is usually asymptomatic, and there is rarely external evidence of inflammation.
Acute anterior uveitis (AAU) is a distinctly different form of uveitis and typically occurs in children with spondyloarthritis.
Due to a lack of literature with good quality of evidence, recommendations were formulated on the basis of available evidence and a consensus expert opinion.
Similar to the other guideline, the report said the quality of evidence was very low, and most recommendations were therefore conditional; however, the guideline fills an important clinical gap in the care of children with JIA-associated uveitis until better evidence becomes available.
Methotrexate is the usual first-line systemic immunosuppressive agent, followed by tumor necrosis factor (TNF) inhibitors like infliximab and adalimumab.
Despite the frequency with which these drugs are used for uveitis, only 1 large randomized controlled trial studying children with JIA-associated uveitis has been published.
JIA-associated uveitis guideline recommendations include:
Perceptions of Biosimilar Switching Among Veterans With IBD
December 2nd 2024Veterans with inflammatory bowel disease (IBD) prioritize shared decision-making, transparency, and individualized care in biosimilar switching, favoring delayed switching for severe cases and greater patient control.
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.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
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.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.