Long-term outcomes in patients with polyarticular juvenile idiopathic arthritis receiving adalimumab with or without methotrexate

被引:18
|
作者
Lovell, Daniel J. [1 ]
Brunner, Hermine, I [1 ]
Reiff, Andreas O. [2 ,3 ]
Jung, Lawrence [4 ]
Jarosova, Katerina [5 ,6 ]
Nemcova, Dana [7 ,8 ]
Mouy, Richard [9 ,10 ]
Sandborg, Christy [11 ]
Bohnsack, John F. [12 ]
Elewaut, Dirk [13 ,14 ]
Gabriel, Christos [15 ]
Higgins, Gloria [16 ]
Kone-Paut, Isabelle [17 ,18 ]
Jones, Olcay Y. [19 ]
Vargova, Veronika [20 ]
Chalom, Elizabeth [21 ]
Wouters, Carine [22 ]
Lagunes, Ivan [23 ]
Song, Yanna [23 ]
Martini, Alberto [24 ]
Ruperto, Nicolino [25 ]
机构
[1] Univ Cincinnati, Dept Pediat, Cincinnati Childrens Hosp Med Ctr, PRCSG Coordinating Ctr,Div Rheumatol, Cincinnati, OH 45221 USA
[2] Univ Southern Calif, Dept Pediat, Keck Sch Med, Los Angeles, CA USA
[3] Childrens Hosp Los Angeles, Div Rheumatol, Los Angeles, CA USA
[4] Childrens Natl Med Ctr Canc & Immunol Res, Dept Rheumatol, Washington, DC USA
[5] Inst Rheumatol, Prague, Czech Republic
[6] Charles Univ Prague, Fac Med 1, Dept Rheumatol, Prague, Czech Republic
[7] Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic
[8] Gen Univ Hosp, Prague, Czech Republic
[9] Univ Paris 05, Pediat Rheumatol, Paris, France
[10] Hop Necker Enfants Malad, Paris, France
[11] Lucile Packard Childrens Hosp Stanford, Pediat Rheumatol, Palo Alto, CA USA
[12] Univ Utah, Dept Pediat, Div Allergy Immunol & Pediat Rheumatol, Salt Lake City, UT USA
[13] Univ Hosp Gent, Rheumatol, Ghent, Belgium
[14] Univ Ghent, VIB Ctr Inflammat Res, Ghent, Belgium
[15] Childrens Hosp Kings Daughters, Pediat Rheumatol, Norfolk, VA USA
[16] Ohio State Univ, Dept Pediat, Coll Med, Columbus, OH USA
[17] Hop Bicetre, Natl Reference Ctr Auto Inflammatory Dis, Dept Paediat Rheumatol, Paris, France
[18] Hop Bicetre, Natl Reference Ctr Auto Inflammatory Dis, CEREMAI, Paris, France
[19] Walter Reed Natl Mil Med Ctr, Pediat Rheumatol, Bethesda, MD USA
[20] Fac Hosp, Pediat Rheumatol Unit, Kosice, Slovakia
[21] St Barnabas Hosp, Pediat Rheumatol, Livingston, NJ USA
[22] Univ Hosp Gasthuisberg, Pediat Immunol, Leuven, Belgium
[23] AbbVie Inc, N Chicago, IL USA
[24] Univ Genoa, Dipartimento Neurosci Riabilitaz Oftalmol Genet &, Genoa, Italy
[25] IRCCS, Clin Pediat & Reumatol PRINTO, Ist Giannina Gaslini, Genoa, Italy
来源
RMD OPEN | 2020年 / 6卷 / 02期
关键词
Juvenile Idiopathic Arthritis; Anti-TNF; Adult Onset Still's Disease; Methotrexate; Arthritis; Dermatomyositis; Lupus Erythematosus; Systemic; Familial Mediterranean Fever; Autoimmune Diseases; INFLIXIMAB PLUS METHOTREXATE; RHEUMATOID-ARTHRITIS; PEDIATRIC-PATIENTS; CLINICAL-RESPONSE; DISEASE-ACTIVITY; DOUBLE-BLIND; SAFETY; CHILDREN; EFFICACY; THERAPY;
D O I
10.1136/rmdopen-2020-001208
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Long-term safety and efficacy of adalimumab among patients with juvenile idiopathic arthritis (JIA) was evaluated through 6 years of treatment. Methods Children aged 4-17 years with polyarticular JIA were enrolled in a phase III, randomised-withdrawal, double-blind, placebo-controlled trial consisting of a 16-week open-label lead-in period, 32-week randomised double-blind period and 360-week long-term extension. Patients were stratified by baseline methotrexate use. Adverse events (AEs) were monitored, and efficacy assessments included JIA American College of Rheumatology (JIA ACR) 30%, 50%, 70% or 90% responses and the proportions of patients achieving 27-joint Juvenile Arthritis Disease Activity Score (JADAS27) low disease activity (LDA, <3.8) and inactive disease (ID, <1). Results Of 171 patients enrolled, 62 (36%) completed the long-term extension. Twelve serious infections in 11 patients were reported through 592.8 patient-years of exposure. No cases of congestive heart failure-related AEs, demyelinating disease, lupus-like syndrome, malignancies, tuberculosis or deaths were reported. JIA ACR 30/50/70/90 responses and JADAS27 LDA were achieved in 66% to 96% of patients at week 104, and 63 (37%) patients achieved clinical remission (JADAS27 ID sustained for >= 6 continuous months) during the study. Attainment of JIA ACR 50 or higher and JADAS27 LDA or ID in the initial weeks were the best predictors of clinical remission. Mean JADAS27 decreased from baseline, 22.5 (n=170), to 2.5 (n=30) at week 312 (observed analysis). Conclusions Through 6 years of exposure, adalimumab was well tolerated with significant clinical response (up to clinical remission) and a relatively low retention rate.
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页数:11
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