Comparative Effectiveness of Tocilizumab with either Methotrexate or Leflunomide in the Treatment of Rheumatoid Arthritis

被引:14
作者
Narvaez, Javier [1 ]
Diaz-Torne, Cesar [2 ]
Magallares, Berta [2 ]
Victoria Hernandez, Maria [3 ]
Reina, Delia [4 ]
Corominas, Hector [4 ]
Sanmart, Raimon [3 ]
Rodriguez de la Serna, Arturo [2 ]
Maria Llobet, Josep [2 ]
Nolla, Joan M. [1 ]
机构
[1] Hosp Univ Bellvitge IDIBELL, Dept Rheumatol, Barcelona, Spain
[2] Hosp Santa Creu & Sant Pau, Rheumatol Unit, Barcelona, Spain
[3] Hosp Clin Barcelona, IDIBAPS, Dept Rheumatol, Barcelona, Spain
[4] Hosp St Joan Despi, Dept Rheumatol, Consorci Sanitari Integral, Barcelona, Spain
来源
PLOS ONE | 2015年 / 10卷 / 04期
关键词
MODIFYING ANTIRHEUMATIC DRUGS; INADEQUATE RESPONSE; RECEPTOR INHIBITION; ADDING TOCILIZUMAB; DISEASE-ACTIVITY; MONOTHERAPY; COMBINATION; INTERLEUKIN-6; RITUXIMAB; UPDATE;
D O I
10.1371/journal.pone.0123392
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference treatment because of the superior long-term clinical and radiographic outcomes. Methotrexate (MTX) is the cornerstone of combination therapy but is in some cases contra-indicated or poorly tolerated. This observational study aimed to compare the effectiveness and safety of TCZ in combination with either MTX or leflunomide (LEF) in the treatment of patients with active rheumatoid arthritis (RA) and an inadequate response to one or more DMARDs and/or biological agents in a real-world setting. Methods We performed an ambispective review of 91 patients with active RA who were routinely treated with TCZ plus MTX or LEF. A comparative study between the two combinations of treatment was performed at 6 months of follow-up considering 3 outcomes: improvement of RA disease activity, evolution of functional disability, and tolerability and side effect profile. Results Of the 91 patients, 62 received TCZ with MTX and 29 received TCZ with LEF. Eighty-one patients were followed for 6 months, and the remaining 10 patients discontinued treatment due to serious adverse events. At baseline, there were no significant differences between the groups in terms of the main clinical and laboratory data or in the number of previous DMARDs and biological agents used. At 6 months, there were no significant differences between the combinations in terms of disease activity and functional disability. Serious adverse events occurred in 11% and 10% of the patients treated in combination with MTX and LEF, respectively. Conclusion Our preliminary data support the argument that LEF is an effective and safe (equivalent) alternative to MTX for combination treatment with TCZ.
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页数:9
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