Clinical, Functional, and Radiographic Benefits of Longterm Adalimumab Plus Methotrexate: Final 10-year Data in Longstanding Rheumatoid Arthritis

被引:40
作者
Keystone, Edward C. [1 ]
van der Heijde, Desiree [2 ]
Kavanaugh, Arthur [3 ]
Kupper, Hartmut [4 ]
Liu, Shufang [5 ]
Guerette, Benoit [5 ]
Mozaffarian, Neelufar [5 ]
机构
[1] Univ Toronto, Toronto, ON, Canada
[2] Leiden Univ, Med Ctr, Leiden, Netherlands
[3] Univ Calif San Diego, La Jolla, CA 92093 USA
[4] AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany
[5] AbbVie Inc, N Chicago, IL USA
关键词
ADALIMUMAB; METHOTREXATE; RHEUMATOID ARTHRITIS; RANDOMIZED CONTROLLED TRIAL; ANTITUMOR NECROSIS FACTOR; RECEIVING CONCOMITANT METHOTREXATE; LOW DISEASE-ACTIVITY; MONOCLONAL-ANTIBODY; EULAR RECOMMENDATIONS; PHYSICAL FUNCTION; PHASE-III; THERAPY; INFLIXIMAB; TRIALS;
D O I
10.3899/jrheum.120964
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To examine the longterm effectiveness and safety of adalimumab in patients with longstanding rheumatoid arthritis (RA) and an inadequate response to methotrexate (MTX), and to assess the effect of a 1-year delay in initiation of combination therapy. Methods. DE019 was a 1-year randomized controlled trial (RCT) in which patients received adalimumab 20 mg weekly, adalimumab 40 mg every other week (eow), or placebo; all received concomitant MTX. Patients completing the RCT could receive open-label adalimumab 40 mg eow + MTX for an additional 9 years. Clinical, functional, and radiographic outcomes were assessed using composite measures of disease activity (e.g., American College of Rheumatology responses, 28-joint Disease Activity Score with C-reactive protein, Simplified Disease Activity Index), Health Assessment Questionnaire-Disability Index, and the modified total Sharp score (mTSS), respectively. Results. Of the 619 patients randomized, 457 entered the open-label extension; 202 completed 10 years. At Year 10, patients demonstrated effective disease control and inhibition of radiographic progression. Differences in clinical and functional responses between adalimumab + MTX and placebo + MTX observed during the RCT became less apparent at Year 10. Still, patients who initially received adalimumab + MTX had significantly lower mean Delta mTSS at Year 10 compared with patients who initially received placebo + MTX. No new safety signals arose following up to 10 years of adalimumab + MTX exposure. Conclusion. During up to 10 years of treatment with adalimumab + MTX, patients with longstanding RA experienced effective disease control with no change to the expected safety profile. A 1-year delay in receipt of adalimumab + MTX was associated with reduced effectiveness, suggesting that a window of opportunity to prevent irreversible damage exists even in a population with established RA.
引用
收藏
页码:1487 / 1497
页数:11
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