Journal
JOURNAL OF RHEUMATOLOGY
Volume 36, Issue 4, Pages 801-808Publisher
J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.081048
Keywords
ADALIMUMAB; ANKYLOSING SPONDYLITIS; EXTRAAXIAL ARTHRITIS; PREDICTOR; TUMOR NECROSIS FACTOR ANTAGONIST
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Funding
- Abbott Laboratories, Abbott Park, Illinois, USA
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Objective. We evaluated the effectiveness and safety of adalimumab in a large cohort of patients with active ankylosing spondylitis (AS) and identified clinical predictors of good clinical response. Methods. Patients with active AS [Bath AS Disease Activity Index (BASDAI) >= 4] received adalimumab 40 mg every other week in addition to their standard antirheumatic therapies in a multinational 12-week, open-label study. We used 3 definitions of good clinical response: 50% improvement in the BASDAI (BASDAI = 50), 40% improvement in the ASsessments of SpondyloArthritis International Society criteria (ASAS40), or ASAS partial remission. Response predictors were determined by logistic regression with backward elimination (selection level 5%). Results. Of 1250 patients, 1159 (92.7%) completed 12 weeks of adalimumab treatment. At Week 12, 57.2% of patients achieved BASDAI 50, 53.7% achieved ASAS40, and 27.7% achieved ASAS partial remission. Important predictors of good clinical response (BASDAI 50, ASAS40, and partial remission) were Younger age (p < 0.001), and greater C-reactive protein (CRP) concentration (p <= 0.001), HLA-B27 positivity (p <= 0.01), and tumor necrosis factor (TNF) antagonist naivety (p < 0.00 1). Conclusion. Adalimumab was effective in this large cohort of patients with AS, with more than half of patients achieving a BASDAI 50 or ASAS40 response and more than a quarter of patients reaching partial remission at Week 12. Younger age, greater CRP concentrations, HLA-B27 positivity. and TNF antagonist naivety were strongly associated with BASDAI 50, ASAS40, and partial remission responses. ClinicalTrials.gov identifier: NCT00478660. (First Release March 1 2009; J Rheumatol 2009;36:801-8; doi: 10.3899/jrheum.081048)
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