Effect of disease duration and prior disease-modifying antirheumatic drug use on treatment outcomes in patients with rheumatoid arthritis

被引:46
作者
Aletaha, Daniel [1 ]
Maa, Jen-Fue [2 ]
Chen, Su [2 ]
Park, Sung-Hwan [3 ]
Nicholls, Dave [4 ]
Florentinus, Stefan [5 ]
Furtner, Daniel [6 ]
Smolen, Josef S. [1 ]
机构
[1] Med Univ Vienna, Dept Rheumatol, Vienna, Austria
[2] AbbVie Inc, Data & Stat Sci, N Chicago, IL USA
[3] Catholic Univ Korea, Seoul St Marys Hosp, Div Rheumatol, Dept Internal Med, Seoul, South Korea
[4] Univ Sunshine Coast, Clin Trials Ctr, Maroochydore, Qld, Australia
[5] AbbVie, Global Med Affairs, Hoofddorp, Netherlands
[6] AbbVie, Global Med Affairs, Mascot, NSW, Australia
关键词
ADALIMUMAB PLUS METHOTREXATE; ANTITUMOR NECROSIS FACTOR; CONCOMITANT METHOTREXATE; MONOCLONAL-ANTIBODY; CERTOLIZUMAB PEGOL; CLINICAL-TRIAL; THERAPY; MULTICENTER; REMISSION; IMPROVEMENT;
D O I
10.1136/annrheumdis-2018-214918
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To determine if disease duration and number of prior disease-modifying antirheumatic drugs (DMARDs) affect response to therapy in patients with established rheumatoid arthritis (RA). Methods Associations between disease duration or number of prior DMARDs and response to therapy were assessed using data from two randomised controlled trials in patients with established RA (mean duration, 11 years) receiving adalimumab+methotrexate. Response to therapy was assessed at week 24 using disease activity outcomes, including 28-joint Disease Activity Score based on C-reactive protein (DAS28(CRP)), Simplified Disease Activity Index (SDAI) and Health Assessment Questionnaire Disability Index (HAQ-DI), and proportions of patients with 20%/50%/70% improvement in American College of Rheumatology (ACR) responses. Results In the larger study (N=207), a greater number of prior DMARDs (>2 vs 0-1) was associated with smaller improvements in DAS28(CRP) (-1.8 vs -2.2), SDAI (-22.1 vs -26.9) and HAQ-DI (-0.43 vs -0.64) from baseline to week 24. RA duration of >10 years versus <1 year was associated with higher HAQ-DI scores (1.1 vs 0.7) at week 24, but results on DAS28(CRP) and SDAI were mixed. A greater number of prior DMARDs and longer RA duration were associated with lower ACR response rates at week 24. Data from the second trial (N=67) generally confirmed these findings. Conclusions Number of prior DMARDs and disease duration affect responses to therapy in patients with established RA. Furthermore, number of prior DMARDs, regardless of disease duration, has a limiting effect on the potential response to adalimumab therapy.
引用
收藏
页码:1609 / 1615
页数:7
相关论文
共 30 条
[1]   Treatment-related improvement in physical function varies with duration of rheumatoid arthritis: a pooled analysis of clinical trial results [J].
Aletaha, D. ;
Strand, V. ;
Smolen, J. S. ;
Ward, M. M. .
ANNALS OF THE RHEUMATIC DISEASES, 2008, 67 (02) :238-243
[2]   Duration of rheumatoid arthritis influences the degree of functional improvement in clinical trials [J].
Aletaha, D ;
Ward, MM .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (02) :227-233
[3]  
Anderson JJ, 2000, ARTHRITIS RHEUM, V43, P22, DOI 10.1002/1529-0131(200001)43:1<22::AID-ANR4>3.0.CO
[4]  
2-9
[5]  
Andersson Maria L E, 2013, Open Rheumatol J, V7, P105, DOI 10.2174/1874312901307010105
[6]   The PREMIER study - A multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment [J].
Breedveld, FC ;
Weisman, MH ;
Kavanaugh, AF ;
Cohen, SB ;
Pavelka, K ;
van Vollenhoven, R ;
Sharp, J ;
Perez, JL ;
Spencer-Green, GT .
ARTHRITIS AND RHEUMATISM, 2006, 54 (01) :26-37
[7]   Induction therapy with adalimumab plus methotrexate for 24 weeks followed by methotrexate monotherapy up to week 48 versus methotrexate therapy alone for DMARD-naive patients with early rheumatoid arthritis: HIT HARD, an investigator-initiated study [J].
Detert, Jacqueline ;
Bastian, Hans ;
Listing, Joachim ;
Weiss, Anja ;
Wassenberg, Siegfried ;
Liebhaber, Anke ;
Rockwitz, Karin ;
Alten, Rieke ;
Krueger, Klaus ;
Rau, Rolf ;
Simon, Christina ;
Gremmelsbacher, Eva ;
Braun, Tanja ;
Marsmann, Bettina ;
Hoehne-Zimmer, Vera ;
Egerer, Karl ;
Buttgereit, Frank ;
Burmester, Gerd-R .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (06) :844-850
[8]   Combination etanercept and methotrexate provides better disease control in very early (≤4 months) versus early rheumatoid arthritis (&gt;4 months and &lt;2 years): post hoc analyses from the COMET study [J].
Emery, Paul ;
Kvien, Tore K. ;
Combe, Bernard ;
Freundlich, Bruce ;
Robertson, Deborah ;
Ferdousi, Tahmina ;
Bananis, Eustratios ;
Pedersen, Ronald ;
Koenig, Andrew S. .
ANNALS OF THE RHEUMATIC DISEASES, 2012, 71 (06) :989-992
[9]   Greater Likelihood of Remission in Rheumatoid Arthritis Patients Treated Earlier in the Disease Course: Results From the Consortium of Rheumatology Researchers of North America Registry [J].
Furst, Daniel E. ;
Pangan, Aileen L. ;
Harrold, Leslie R. ;
Chang, Hong ;
Reed, George ;
Kremer, Joel M. ;
Greenberg, Jeffrey D. .
ARTHRITIS CARE & RESEARCH, 2011, 63 (06) :856-864
[10]  
Goekoop-Ruiterman YPM, 2005, ARTHRITIS RHEUM-US, V52, P3381, DOI [10.1002/art.21405, 10.1002/art.23364]