Comparison of tocilizumab and tumour necrosis factor inhibitors in rheumatoid arthritis: a retrospective analysis of 1603 patients managed in routine clinical practice

被引:0
作者
Marina Backhaus
Jörg Kaufmann
Constanze Richter
Siegfried Wassenberg
Anne-Eve Roske
Peter Hellmann
Markus Gaubitz
机构
[1] Charité-Universitätsmedizin Berlin,Medizinische Klinik mit Schwerpunkt Rheumatologie und klinische Immunologie
[2] Praxis Dr. med Jörg Kaufmann,undefined
[3] Internistisch-rheumatologische Schwerpunktpraxis,undefined
[4] Fachkrankenhaus Ratingen - Rheumatologische Klinik,undefined
[5] Rheumazentrum Ratingen,undefined
[6] Roche Pharma AG,undefined
[7] Chugai Pharma,undefined
[8] Akademie für Manuelle Therapie an der WWU Münster,undefined
[9] Interdisziplinäre Diagnostik und Therapie,undefined
来源
Clinical Rheumatology | 2015年 / 34卷
关键词
DMARDs; Patient-reported outcomes; Remission; Rheumatoid arthritis; Routine practice; Tocilizumab; Tumour necrosis factor inhibitors;
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学科分类号
摘要
Tocilizumab (TCZ) and tumour necrosis factor inhibitors (TNFi) are recommended for the treatment of rheumatoid arthritis (RA) in patients with inadequate response (IR) to prior disease-modifying antirheumatic drugs (DMARDs). This retrospective analysis assessed the efficacy of TCZ and TNFi, alone or in combination with DMARDs, in 1603 patients with IR to previous treatment with either DMARDs (DMARD-IR) and/or TNFi (TNFi-IR), initiating treatment with TCZ or a TNFi, managed in routine clinical practice. Patients were grouped according to treatment history and treatment initiated: DMARD-IR patients initiating treatment with TCZ + DMARD (DMARD-IR TCZ) or TNFi + DMARD (DMARD-IR TNFi), DMARD-IR and/or TNFi-IR patients initiating treatment with TCZ monotherapy (TCZ mono) or TNFi monotherapy (TNFi mono), and TNFi-IR patients initiating treatment with TCZ + DMARD (TNFi-IR TCZ) or TNFi + DMARD (TNFi-IR TNFi). Patients initiating treatment with TCZ generally had more severe disease and longer disease duration compared with the corresponding TNFi group. Significantly more patients achieved remission (DAS28 ESR <2.6) in the TCZ groups compared with corresponding TNFi groups (DMARD-IR, TCZ 44.0 % vs. TNFi 29.6 %; monotherapy, TCZ 37.2 % vs. TNFi 30.2 %; TNF-IR, TCZ 41.3 % vs. TNFi 19.2 %; p < 0.001 for all comparisons). More patients achieved moderate–good responses (EULAR criteria) in the TCZ treatment groups (79–85 %) compared with TNFi treatment groups (65–81 %). Patient-reported outcomes showed greater improvements in TCZ compared with TNFi groups. In patients with inadequate response to DMARDs and/or TNFi treated in routine clinical practice, TCZ in combination with DMARDs or as monotherapy resulted in significantly more patients achieving remission and more marked improvements in patient-reported outcomes compared with TNF inhibitors.
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页码:673 / 681
页数:8
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