Pérez-Guijo Veronica C, Cravo Ana Rita, Castro Maria del Carmen, Font Pilar, Muñoz-Gomariz Elisa, Collantes-Estevez Eduardo
Department of Rheumatology, Reina Sofia University Hospital of Córdoba, Menendez Pidal, s/n, 14004 Cordoba, Spain.
Joint Bone Spine. 2007 May;74(3):254-8. doi: 10.1016/j.jbspin.2006.08.005. Epub 2007 Mar 1.
The aims of this study were to assess the efficacy of infliximab (IFX) combined with methotrexate (MTX) versus IFX alone in the treatment of ankylosing spondylitis (AS).
The study was a 30weeks open label and prospective study of parallel groups in 19 patients with active AS. These patients had shown incomplete therapeutic response to standard therapy (full dose of non-steroidal anti-inflammatory drugs: NSAIDs) and disease modifying antirheumatic drugs: DMARDs (MTX or sulfasalazine: SLZ) for a period of at least 12 weeks and were treated with IFX (5mg/kg). Patients were divided into two treatment groups according to the previous treatment: in Group A, 9 patients previously treated with 7.5mg/week of MTX were treated with IFX in addition to MTX (IFX+MTX); in Group B, 10 patients previously treated only with NSAIDs were treated with IFX (5mg/kg) as monotherapy (IFX). The primary outcome was improvement in disease activity shown by the BASDAI50 at week 30; the secondary outcome included comparison of the proportions of subjects in each group achieving response criteria proposed by the ASAS group. BASDAI, BASFI, ESR, CRP, pain, inflammation and Patient Global Assessment were also recorded.
Both groups were similar in sex ratio, clinical forms and B27. Differences between groups occurred only in the disease duration and age of the patient. At 14 and 30 weeks only 50% and 10% respectively of the patients from the IFX group achieved BASDAI50 response compared to 89% of patients from the IFX+MTX group. The difference between groups at 30 weeks was statistically significant (p=0.001; percentage of difference: 79%; 95% confidence interval (CI): 26-93%:). ASAS50 was reached in 67% and 55.6% of patients from the IFX+MTX group at 14 and 30 weeks respectively, compared with 30% and 0% of patients from the IFX group The difference between groups at 30 weeks was statistically significant (p=0.011; percentage of difference: 57%; 95% CI: 8-84.7%).
Infliximab in combination with MTX seems to increase the efficacy of the therapeutic response in active AS patients, but more wide-ranging studies are necessary, mainly long-term studies.
本研究旨在评估英夫利昔单抗(IFX)联合甲氨蝶呤(MTX)与单用IFX治疗强直性脊柱炎(AS)的疗效。
本研究为一项针对19例活动期AS患者的30周开放标签平行组前瞻性研究。这些患者对标准治疗(全剂量非甾体抗炎药:NSAIDs)和改善病情抗风湿药(DMARDs,MTX或柳氮磺胺吡啶:SLZ)治疗至少12周显示治疗反应不完全,并接受IFX(5mg/kg)治疗。根据既往治疗情况将患者分为两个治疗组:A组,9例既往接受7.5mg/周MTX治疗的患者,除MTX外还接受IFX治疗(IFX+MTX);B组,10例既往仅接受NSAIDs治疗的患者,接受IFX(5mg/kg)单药治疗(IFX)。主要结局为第30周时BASDAI50显示的疾病活动改善;次要结局包括比较两组中达到ASAS组提出的反应标准的受试者比例。还记录了BASDAI、BASFI、ESR、CRP、疼痛、炎症和患者整体评估情况。
两组在性别比例、临床类型和B27方面相似。组间差异仅存在于病程和患者年龄。在第14周和第30周时,IFX组分别仅有50%和10%的患者达到BASDAI50反应,而IFX+MTX组为89%。两组在第30周时的差异具有统计学意义(p=0.001;差异百分比:79%;95%置信区间(CI):26-93%)。IFX+MTX组在第14周和第30周时分别有67%和55.6%的患者达到ASAS50,而IFX组分别为30%和0%。两组在第30周时的差异具有统计学意义(p=0.011;差异百分比:57%;95%CI:8-84.7%)。
英夫利昔单抗联合MTX似乎可提高活动期AS患者的治疗反应疗效,但需要更广泛的研究,主要是长期研究。