Effectiveness of Adalimumab in Non-radiographic Axial Spondyloarthritis Evaluation of Clinical and Magnetic Resonance Imaging Outcomes in a Monocentric Cohort

被引:14
作者
Cantarini, Luca [1 ]
Fabbroni, Marta [1 ]
Talarico, Rosaria [2 ]
Costa, Luisa [3 ]
Caso, Francesco [4 ]
Cuneo, Gian Luca [5 ]
Frediani, Bruno [1 ]
Faralli, Gabriele [6 ]
Vitale, Antonio [1 ]
Brizi, Maria Giuseppina [1 ]
Sabadini, Luciano [7 ]
Galeazzi, Mauro [1 ]
机构
[1] Univ Siena, Rheumatol Unit, Dept Med Sci Surg & Neurosci, I-53100 Siena, Italy
[2] Univ Pisa, Rheumatol Unit, Dept Clin & Expt Med, Pisa, Italy
[3] Univ Naples Federico II, Dept Clin & Expt Med, Rheumatol Res Unit, Naples, Italy
[4] Univ Padua, Rheumatol Unit, Dept Med DIMED, Padua, Italy
[5] S Donato Hosp, Cardiovasc & Neurol Dept, Neuroradiol Unit, Arezzo, Italy
[6] S Donato Hosp, Dept Diagnost & Clin Pathol, Radiol Unit, Arezzo, Italy
[7] Dept Internal Med, Rheumatol Unit, Arezzo, Italy
关键词
SOCIETY CLASSIFICATION CRITERIA; ANTI-TNF AGENTS; ANKYLOSING-SPONDYLITIS; SACROILIAC JOINT; SCORING SYSTEM; SPONDYLARTHROPATHY; ABNORMALITIES; VALIDATION; BLOCKERS; EFFICACY;
D O I
10.1097/MD.0000000000001170
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The primary aim of the study was to evaluate the long-term effectiveness of adalimumab (ADA) in a cohort of non-radiographic axial spondyloarthritis (nr-axSpA), and the secondary aims were to identify predictive factors of response and evaluate radiological progression.We evaluated 37 patients (male/female: 12/25; mean age 4914; mean disease duration: 6.35.8) with active nr-axSpA (Assessment of SpondyloArthritis International Society criteria), despite the treatment with 1 nonsteroidal anti-inflammatory drug for at least 3 months, initiating the treatment with ADA 40mg every other week. Patients were treated for 24 months, and evaluated at baseline, 6, 12, and 24 months. Outcome measures included Ankylosing Spondylitis Disease Activity Score, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), and Bath Ankylosing Spondylitis Functional Index. Radiograph of the spine and sacroiliac joints and magnetic resonance of the sacroiliac joints were performed at baseline and according to the standard of assessment for the disease.The proportion of patients that achieved a BASDAI50 response at 6, 12 and 24 months was 51.3%, 70.3%, and 76.8%, respectively. Treatment was well tolerated with no unexpected adverse events and/or serious adverse events. All patients remained on treatment for 2 years, with a good compliance. We did not identify any predictive factor of response to therapy. Moreover, modified Stoke Ankylosing Spondylitis Spine Score and Spondyloarthritis Research Consortium of Canada scores showed a trend of improvement during the study period.ADA was effective on clinical and radiological outcomes at 2-year follow-up; thus, early treatment with ADA may prevent radiographic damage and be associated with low disease activity or remission. Moreover, data from this cohort study have confirmed safety and tolerability profile of ADA in nr-axSpA in the long term.
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页数:4
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