First-line options for systemic juvenile idiopathic arthritis treatment: an observational study of Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans

被引:9
|
作者
Beukelman, Timothy [1 ]
Tomlinson, George [2 ]
Nigrovic, Peter A. [3 ,4 ]
Dennos, Anne [5 ]
Del Gaizo, Vincent [6 ]
Jelinek, Marian [6 ]
Riordan, Mary Ellen [7 ]
Schanberg, Laura E. [5 ,8 ]
Mohan, Shalini
Pfeifer, Erin [9 ]
Kimura, Yukiko [7 ]
机构
[1] Univ Alabama Birmingham, 1601 4th Ave South,CPPN G10, Birmingham, AL 35233 USA
[2] Univ Toronto, Inst Hlth Policy Management & Evaluat, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[3] Boston Childrens Hosp, Div Immunol, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, Boston, MA 02115 USA
[5] Duke Univ, Duke Clin Res Inst, Durham, NC 27715 USA
[6] Childhood Arthrit & Rheumatol Res Alliance, Washington, DC USA
[7] Joseph M Sanzari Childrens Hosp, Hackensack Meridian Sch Med, Nutley, NJ 07110 USA
[8] Duke Univ, Sch Med, Dept Pediat, Durham, NC 27710 USA
[9] Genentech Inc, South San Francisco, CA 94080 USA
关键词
Systemic juvenile idiopathic arthritis; Juvenile idiopathic arthritis; Still's disease; Treatment; Biologics; PLACEBO-CONTROLLED TRIAL; DISEASE-ACTIVITY SCORE; DOUBLE-BLIND; CRITERIA; CLASSIFICATION; CANAKINUMAB;
D O I
10.1186/s12969-022-00768-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed consensus treatment plans (CTPs) to compare treatment initiation strategies for systemic juvenile idiopathic arthritis (sJIA). First-line options for sJIA treatment (FROST) was a prospective observational study to assess CTP outcomes using the CARRA Registry. Methods: Patients with new-onset sJIA were enrolled if they received initial treatment according to the biologic CTPs (IL-1 or IL-6 inhibitor) or non-biologic CTPs (glucocorticoid (GC) monotherapy or methotrexate). CTPs could be used with or without systemic GC. Primary outcome was achievement of clinical inactive disease (CID) at 9 months without current use of GC. Due to the small numbers of patients in the non-biologic CTPs, no statistical comparisons were made between the CTPs. Results: Seventy-three patients were enrolled: 63 (86%) in the biologic CTPs and 10 (14%) in the non-biologic CTPs. CTP choice appeared to be strongly influenced by physician preference. During the first month of follow-up, oral GC use was observed in 54% of biologic CTP patients and 90% of non-biologic CTPs patients. Five (50%) non-biologic CTP patients subsequently received biologics within 4 months of follow-up. Overall, 30/53 (57%) of patients achieved CID at 9 months without current GC use. Conclusion: Nearly all patients received treatment with biologics during the study period, and 46% of biologic CTP patients did not receive oral GC within the first month of treatment. The majority of patients had favorable short-term clinical outcomes. Increased use of biologics and decreased use of GC may lead to improved outcomes in sJIA.
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页数:10
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