Sustained efficacy of certolizumab pegol added to methotrexate in the treatment of rheumatoid arthritis: 2-year results from the RAPID 1 trial

被引:32
|
作者
Keystone, Edward C. [1 ]
Combe, Bernard [2 ]
Smolen, Josef [3 ]
Strand, Vibeke [4 ]
Goel, Niti [5 ]
van Vollenhoven, Ronald [6 ]
Mease, Philip [7 ,8 ]
Landewe, Robert [9 ,10 ]
Fleischmann, Roy [11 ]
Luijtens, Kristel
van der Heijde, Desiree [12 ]
机构
[1] Univ Toronto, Mt Sinai Hosp, Rebecca MacDonald Ctr Arthrit & Autoimmune Dis, Toronto, ON M5T 3L9, Canada
[2] Univ Montpellier, Hop Lapeyronie, Dept Rheumatol, F-34059 Montpellier, France
[3] Med Univ Vienna, Div Rheumatol, Vienna, Austria
[4] Stanford Univ, Div Rheumatol & Immunol, Palo Alto, CA 94304 USA
[5] Global Projects & Dev, UCB Pharma, Smyrna, GA USA
[6] Karolinska Inst, Dept Med, Stockholm, Sweden
[7] Swedish Med Ctr, Seattle, WA USA
[8] Univ Washington, Seattle, WA 98195 USA
[9] Univ Amsterdam, Acad Med Ctr, Dept Clin Immunol & Rheumatol, Heerlen, Netherlands
[10] Atrium Med Ctr, Heerlen, Netherlands
[11] Univ Texas SW Med Ctr Dallas, Metroplex Clin Res Ctr, Dallas, TX 75390 USA
[12] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
关键词
certolizumab pegol; rheumatoid arthritis; efficacy; RAPID; 1; ACR; ANTITUMOR NECROSIS FACTOR; ADALIMUMAB PLUS METHOTREXATE; COLLEGE-OF-RHEUMATOLOGY; DOUBLE-BLIND; PHYSICAL FUNCTION; CONCOMITANT METHOTREXATE; MONOCLONAL-ANTIBODY; CLINICAL-TRIAL; PHASE-III; MORTALITY;
D O I
10.1093/rheumatology/kes082
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To evaluate the safety and efficacy of 2-year administration of certolizumab pegol (CZP) + MTX in patients with active RA. Methods. Patients completing 52 weeks in the Rheumatoid Arthritis Prevention of Structural Damage (RAPID) 1 trial (52-week completers), or withdrawing at week 16 due to lack of ACR20 response were eligible for open-label treatment (CZP 400 mg every other week + MTX). After 2 years' treatment, HAQ-Disability Index response, ACR20/50/70 responses, DAS-28 and radiographic progression were assessed in 52-week completers. ACR20/50/70 and DAS-28 were also calculated for the intent-to-treat (ITT) population. Adverse events were assessed in patients who received one or more CZP doses during the study. Results. At week 100, 88.9% (n = 216) of 52-week completers who originally received CZP 200 mg + MTX and open-label treatment remained in the study. In this group, ACR20/50/70 at week 100 were 68.2, 55.2 and 35.6%, respectively. HAQ-DI and DAS-28 improvements were sustained throughout the open-label extension (mean change -0.79 and -3.5 at week 100, respectively). A total of 46.7% (n = 113) of CZP 200 mg + MTX 52-week completers achieved low disease activity by week 100. Inhibition of radiographic progression was maintained. Similar findings were observed in 52-week completers who originally received CZP 400 mg + MTX and in the ITT population. Rates of serious infection or malignancies did not increase over time and no new safety signals were observed. Conclusion. CZP + MTX provided sustained, 2-year inhibition of radiographic progression and sustained improvements in RA clinical signs and symptoms, with no new safety signals observed in patients who completed 2 years of treatment. Trial registration: clinicaltrials.gov, ext-link-type="uri" xlink:href="http://www.clinicaltrials.gov" xmlns:xlink="http://www.w3.org/1999/xlink">http://www.clinicaltrials.gov, NCT00175877.
引用
收藏
页码:1628 / 1638
页数:11
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