Rapid Improvement in the Signs and Symptoms of Rheumatoid Arthritis Following Certolizumab Pegol Treatment Predicts Better Longterm Outcomes: Post-hoc Analysis of a Randomized Controlled Trial

被引:40
作者
Keystone, Edward C. [1 ]
Curtis, Jeffrey R. [2 ]
Fleischmann, Roy M. [3 ]
Furst, Daniel E. [4 ]
Khanna, Dinesh [4 ]
Smolen, Josef S. [5 ,6 ,8 ]
Mease, Philip J. [7 ]
Schiff, Michael H. [9 ]
Coteur, Geoffroy [10 ]
Davies, Owen [10 ]
Combe, Bernard [11 ]
机构
[1] Univ Toronto, Mt Sinai Hosp, Rebecca MacDonald Ctr Arthrit & Autoimmune Dis, Toronto, ON M5G 1X5, Canada
[2] Univ Alabama Birmingham, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[3] Univ Texas SW Med Ctr Dallas, Metroplex Clin Res Ctr, Dallas, TX 75390 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Rheumatol, Los Angeles, CA 90095 USA
[5] Med Univ Vienna, Div Rheumatol, Dept Med 3, Vienna, Austria
[6] Med Univ Vienna, Hietzing Hosp, Dept Med 2, Vienna, Austria
[7] Univ Washington, Sch Med, Seattle, WA USA
[8] Seattle Rheumatol Associates, Swedish Med Ctr, Seattle, WA USA
[9] Univ Colorado, Sch Med, Div Rheumatol, Denver, CO USA
[10] UCB Bioprod SA, Brussels, Belgium
[11] Univ Montpellier I, Hop Lapeyronie, Dept Rhumatol, Montpellier, France
关键词
CERTOLIZUMAB PEGOL; RHEUMATOID ARTHRITIS; DISEASE ACTIVITY PAIN; AMERICAN COLLEGE OF RHEUMATOLOGY RESPONSE; PHYSICAL FUNCTION; COLLEGE-OF-RHEUMATOLOGY; ANTITUMOR NECROSIS FACTOR; CONCOMITANT METHOTREXATE; MONOCLONAL-ANTIBODY; ADALIMUMAB; MANAGEMENT; THERAPY; RECOMMENDATIONS; ETANERCEPT; VALIDATION;
D O I
10.3899/jrheum.100935
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To assess the kinetics of response to certolizumab pegol (CZP), and association between rapid response and longterm outcomes, in patients with active rheumatoid arthritis (RA). Methods. This was a post-hoc analysis of the randomized, double-blind RAPID 1 study in patients who received methotrexate (MTX) and either CZP 200 mg subcutaneously or placebo every 2 weeks for 52 weeks. Clinical and radiographic outcomes at Week 52 were evaluated based on the Disease Activity Score 28 (DAS28) >= 1.2 and American College of Rheumatology 20% (ACR20) responses at Week 6 and Week 12. Results. Clinical responses [European League Against Rheumatism (EULAR), DAS28 >= 1.2, and ACR20 responses] were rapid in CZP-treated patients. Week 12 DAS28 >= 1.2 responders had better clinical and radiographic outcomes at Week 52 compared with nonresponders. Among Week 12 responders, incremental benefit of earlier response was observed: Week 6 DAS28 >= 1.2 responders and ACR20 responders had significantly higher ACR response rates and were more likely to achieve remission at Week 52 than Week 12 responders. Patients with a clinical response at Week 6 had faster, more meaningful sustained improvements in patient-derived outcomes than those responding by Week 12 only. Conclusion. Rapid attainment of clinical response in patients with RA is associated with improved longterm outcomes. Analysis of the kinetics of response to CZP during the first 12 weeks of therapy potentially permits informed prediction of clinical success or need to alter treatment. In patients not achieving a clinical response at Week 12 treatment adjustment should be considered. Trial registration NCT00152386. (First Release March 1 2011; J Rheumatol 2011;38:990-6; doi:10.3899/jrheum.100935)
引用
收藏
页码:990 / 996
页数:7
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