Hoffman Gary S, Cid Maria C, Rendt-Zagar Karen E, Merkel Peter A, Weyand Cornelia M, Stone John H, Salvarani Carlo, Xu Weichun, Visvanathan Sudha, Rahman Mahboob U
Center for Vasculitis Care and Research, The Cleveland Clinic Foundation, Lerner College of Medicine, Cleveland, Ohio 44195, USA.
Ann Intern Med. 2007 May 1;146(9):621-30. doi: 10.7326/0003-4819-146-9-200705010-00004.
Tumor necrosis factor-alpha is present in arteries in giant cell arteritis.
To evaluate the efficacy of infliximab, an anti-tumor necrosis factor-alpha agent, in giant cell arteritis.
Randomized, controlled trial.
22 sites in the United States, the United Kingdom, Belgium, Italy, and Spain.
44 patients with newly diagnosed giant cell arteritis that was in glucocorticosteroid-induced remission.
Participants were randomly assigned in a 2:1 ratio to receive infliximab (5 mg/kg of body weight) or placebo. Sixteen patients were assigned to glucocorticosteroid plus placebo, and 28 patients to glucocorticosteroid plus infliximab.
End points were measured through week 22, when an interim analysis resulted in early stopping of the planned 54-week trial. Primary end points were the number of patients who remained free of relapse through week 22 and adverse events. Secondary end points were time to first relapse, biomarkers, cumulative glucocorticosteroid dose, and the number of patients who remained relapse-free while the glucocorticosteroid dosage was tapered to 10 mg/d.
Infliximab therapy did not increase the proportion of patients without relapse at week 22 compared with placebo (43% vs. 50%, respectively; difference, -7 percentage points [95% CI, -38 to 23 percentage points; P = 0.65), nor did it increase the proportion of patients whose glucocorticosteroid dosages were tapered to 10 mg/d without relapse (61% vs. 75%, respectively; difference, -14 percentage points [CI, -42 to 14 percentage points]; P = 0.31). The incidence of infection was 71% with infliximab and 56% with placebo (difference, 15 percentage points [CI, -14 to 45 percentage points]).
The sample was too small to rule out modest effects of infliximab and included only patients with a new diagnosis. Only one dose of infliximab was evaluated, and the study was terminated early.
This trial is too small to draw definitive conclusions, but it provides evidence that using infliximab as maintenance therapy in patients in glucocorticoid-induced remission of newly diagnosed giant cell arteritis is of no benefit and may be harmful. If infliximab has benefit, it is unlikely to be great. ClinicalTrials.gov registration number: NCT00076726.
肿瘤坏死因子-α存在于巨细胞动脉炎的动脉中。
评估抗肿瘤坏死因子-α药物英夫利昔单抗治疗巨细胞动脉炎的疗效。
随机对照试验。
美国、英国、比利时、意大利和西班牙的22个研究点。
44例新诊断的处于糖皮质激素诱导缓解期的巨细胞动脉炎患者。
参与者按2:1的比例随机分组,分别接受英夫利昔单抗(5 mg/kg体重)或安慰剂治疗。16例患者被分配接受糖皮质激素加安慰剂治疗,28例患者接受糖皮质激素加英夫利昔单抗治疗。
在第22周时测量终点指标,此时进行的中期分析导致原计划的54周试验提前终止。主要终点指标为至第22周仍未复发的患者数量和不良事件。次要终点指标为首次复发时间、生物标志物、糖皮质激素累积剂量,以及在糖皮质激素剂量减至10 mg/d时仍未复发的患者数量。
与安慰剂相比,英夫利昔单抗治疗在第22周时并未增加未复发患者的比例(分别为43%和50%;差异为-7个百分点[95%CI,-38至23个百分点;P = 0.65]),也未增加糖皮质激素剂量减至10 mg/d且未复发患者的比例(分别为61%和75%;差异为-14个百分点[CI,-42至14个百分点];P = 0.31)。英夫利昔单抗组感染发生率为71%,安慰剂组为56%(差异为15个百分点[CI,-14至45个百分点])。
样本量过小,无法排除英夫利昔单抗的适度疗效,且仅纳入了新诊断的患者。仅评估了一剂英夫利昔单抗,且研究提前终止。
该试验样本量过小,无法得出明确结论,但提供了证据表明,在新诊断的巨细胞动脉炎糖皮质激素诱导缓解期的患者中,使用英夫利昔单抗作为维持治疗无益处且可能有害。如果英夫利昔单抗有获益,也不太可能很大。ClinicalTrials.gov注册号:NCT00076726。