Barkham Nick, Keen Helen I, Coates Laura C, O'Connor Philip, Hensor Elizabeth, Fraser Alexander D, Cawkwell Lorna S, Bennett Alexander, McGonagle Dennis, Emery Paul
University of Leeds, Leeds, UK.
Arthritis Rheum. 2009 Apr;60(4):946-54. doi: 10.1002/art.24408.
To evaluate the efficacy of infliximab in HLA-B27-positive patients with magnetic resonance imaging (MRI)-determined early sacroiliitis, using both clinical and MRI assessments.
Forty patients with recent-onset inflammatory back pain, as assessed by the Calin criteria, HLA-B27 positivity, clinical disease activity as measured by the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), pain and morning stiffness, and magnetic resonance imaging (MRI)-determined sacroiliac joint bone edema were randomized in a double-blind manner to receive infliximab 5 mg/kg or placebo at 0, 2, 6, and 12 weeks. MRI scans were performed at baseline and 16 weeks and scored by 2 observers (blinded to both the order of the scans and to treatment group), using the Leeds scoring system. Clinical assessments included the BASDAI, the Bath Ankylosing Spondylitis Functional Index (BASFI), the Ankylosing Spondylitis Quality of Life (ASQoL) instrument, the ASsessment in Ankylosing Spondylitis International Working Group criteria (ASAS) for improvement, and markers of inflammation.
The mean reduction in the total MRI score from week 0 to week 16 was significantly greater in infliximab-treated patients compared with placebo-treated patients (P = 0.033). On average, significantly more lesions resolved in the infliximab group (P < 0.001), while significantly more new lesions developed in the placebo group (P = 0.004). Significantly greater improvement in the infliximab group versus the placebo group was also observed for changes from week 0 to week 16 in the BASDAI (P = 0.002), BASFI (P = 0.004), and ASQoL (P = 0.007) scores. Responses according to the ASAS criteria for 40% improvement, the ASAS criteria for 20% improvement in 5 of 6 domains, and ASAS partial remission were achieved by 61%, 44%, and 56% of infliximab-treated patients, respectively. Infliximab was well tolerated, and no serious adverse events were observed.
Infliximab was an effective therapy for early sacroiliitis, providing a reduction in disease activity by week 16. This study is the first to show that infliximab is effective for reducing clinical and imaging evidence of disease activity in patients with MRI-determined early axial spondylarthritis.
采用临床和磁共振成像(MRI)评估方法,评价英夫利昔单抗对MRI确诊的早期骶髂关节炎HLA - B27阳性患者的疗效。
40例近期出现炎性背痛(根据卡林标准评估)、HLA - B27阳性、采用巴斯强直性脊柱炎疾病活动指数(BASDAI)测量临床疾病活动度、有疼痛和晨僵症状且MRI显示骶髂关节骨水肿的患者,以双盲方式随机分组,在0、2、6和12周时接受5mg/kg英夫利昔单抗或安慰剂治疗。在基线和16周时进行MRI扫描,由2名观察者(对扫描顺序和治疗组均不知情)使用利兹评分系统进行评分。临床评估包括BASDAI、巴斯强直性脊柱炎功能指数(BASFI)、强直性脊柱炎生活质量(ASQoL)量表、强直性脊柱炎国际工作组改善标准(ASAS)以及炎症标志物。
与安慰剂治疗组相比,英夫利昔单抗治疗组患者从第0周至第16周MRI总评分的平均降低幅度显著更大(P = 0.033)。平均而言,英夫利昔单抗组有更多病变得以缓解(P < 0.001),而安慰剂组出现了更多新病变(P = 0.004)。从第0周至第16周,英夫利昔单抗组在BASDAI(P = 0.002)、BASFI(P = 0.004)和ASQoL(P = 0.007)评分方面的改善也显著大于安慰剂组。分别有61%、44%和56%接受英夫利昔单抗治疗的患者达到了ASAS标准中40%改善、6个领域中5个领域20%改善以及ASAS部分缓解的标准。英夫利昔单抗耐受性良好,未观察到严重不良事件。
英夫利昔单抗是早期骶髂关节炎的有效治疗方法,可在第16周时降低疾病活动度。本研究首次表明英夫利昔单抗对降低MRI确诊的早期中轴型脊柱关节炎患者疾病活动的临床和影像学证据有效。