Effectiveness of tocilizumab with and without synthetic disease-modifying antirheumatic drugs in rheumatoid arthritis: results from a European collaborative study

被引:54
作者
Gabay, Cem [1 ]
Riek, Myriam [2 ]
Hetland, Merete Lund [3 ,4 ]
Hauge, Ellen-Margrethe [5 ]
Pavelka, Karel [6 ]
Tomsic, Matija [7 ]
Canhao, Helena [8 ]
Chatzidionysiou, Katerina [9 ]
Lukina, Galina [10 ]
Nordstrom, Dan C. [11 ,12 ]
Lie, Elisabeth [13 ]
Ancuta, Ioan [14 ]
Victoria Hernandez, M. [15 ]
van Riel, Piet L. M. C. [16 ]
van Vollenhoven, Ronald [9 ]
Kvien, Tore K. [13 ]
机构
[1] Univ Hosp Geneva, Div Rheumatol, Geneva, Switzerland
[2] SCQM Fdn, Zurich, Switzerland
[3] Rigshosp, Ctr Rheumatol & Spine Dis, DANBIO, Glostrup, Denmark
[4] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Glostrup, Denmark
[5] Aarhus Univ Hosp, Dept Rheumatol, DK-8000 Aarhus, Denmark
[6] Charles Univ Prague, Inst Rheumatol & Clin Rheumatol, Prague, Czech Republic
[7] Univ Med Ctr, Ljubljana, Slovenia
[8] Inst Mol Med, Rheumatol Res Unit, Lisbon, Portugal
[9] Karolinska Inst, Stockholm, Sweden
[10] Russian Acad Med Sci, Inst Rheumatol, Moscow 109801, Russia
[11] Univ Helsinki, Cent Hosp, Dept Med, Helsinki, Finland
[12] Univ Helsinki, Helsinki, Finland
[13] Diakonhjemmet Hosp, Dept Rheumatol, Oslo, Norway
[14] Cantacuzino Hosp, Bucharest, Romania
[15] Hosp Clin Barcelona, Dept Rheumatol, Barcelona, Spain
[16] Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
关键词
DOUBLE-BLIND; ADDING TOCILIZUMAB; INADEQUATE RESPONSES; MULTIPLE IMPUTATION; RECEPTOR INHIBITION; RA PATIENTS; METHOTREXATE; MONOTHERAPY; OUTCOMES; COMBINATION;
D O I
10.1136/annrheumdis-2015-207760
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To examine the effectiveness of tocilizumab (TCZ) with and without synthetic disease-modifying antirheumatic drugs (sDMARDs) in a large observational study. Methods Patients with rheumatoid arthritis treated with TCZ who had a baseline visit and information on concomitant sDMARDs were included. According to baseline data, patients were considered as taking TCZ as monotherapy or combination with sDMARDs. Main study outcomes were the change of Clinical Disease Activity Index (CDAI) and TCZ retention. The prescription of TCZ as monotherapy was analysed using logistic regression. CDAI change was analysed with a mixed-effects model for longitudinal data. TCZ retention was analysed with a stratified extended Cox model. Results Multiple-adjusted analysis suggests that prescription of TCZ as monotherapy varied according to age, corticosteroid use, country of the registry and year of treatment initiation. The change of disease activity assessed by CDAI as well as the likelihood to be in remission were not significantly different whether TCZ was used as monotherapy or in combination with sDMARDs in a covariate-adjusted analysis. Estimates for unadjusted median TCZ retention were 2.3 years (95% CI 1.8 to 2.7) for monotherapy and 3.7 years (lower 95% CI limit 3.1, upper limit not estimable) for combination therapies. In a covariate-adjusted analysis, TCZ retention was also reduced when used as monotherapy, with an increasing difference between mono and combination therapy over time after 1.5 years (p=0.002). Conclusions TCZ with or without concomitant sDMARDs resulted in comparable clinical response as assessed by CDAI change, but TCZ retention was shorter under monotherapy of TCZ.
引用
收藏
页码:1336 / 1342
页数:7
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