Gjefsen Elisabeth, Bråten Lars C, Ponzi Erica, Dagestad Magnhild H, Marchand Gunn H, Kadar Thomas, Bakland Gunnstein, Haugen Anne J, Granviken Fredrik, Flørenes Tonje W, Vetti Nils, Grøvle Lars, Nilsen Aksel T, Lunestad Astrid, Holmgard Thor E, Valberg Morten, Bolstad Nils, Espeland Ansgar, Brox Jens I, Goll Guro L, Storheim Kjersti, Zwart John-Anker
Oslo University Hospital and University of Oslo, Oslo, Norway.
Oslo University Hospital, Oslo, Norway.
Arthritis Rheumatol. 2025 May;77(5):615-623. doi: 10.1002/art.43073. Epub 2025 Jan 15.
The efficacy of tumor necrosis factor inhibitors for treating chronic low-back pain with Modic changes is uncertain. This study investigated the superiority of infliximab over placebo in patients with Modic type 1 changes.
In this multicenter, randomized, triple-blind, placebo-controlled trial, patients aged 18 to 65 years with moderate to severe chronic low-back pain and Modic type 1 changes were enrolled from five Norwegian public hospitals between January 2019 and October 2022. Participants were randomly assigned to four intravenous infusions of 5 mg/kg infliximab or placebo. The primary outcome was difference in change in the Oswestry Disability Index (ODI) score from baseline to five months. Secondary outcomes included changes in low-back pain intensity, disability, and health-related quality of life. A linear mixed model was used for efficacy analyses.
A total of 128 patients (mean age 43 years, 65.6% women) participated (64 in each group). All patients who received at least one dose of the allocated infusion were included in the primary analyses. The average ODI score (±SD) change was -7.0 (±9.7) in the group who received infliximab and -6.4 (±10.4) in the group who received placebo. The difference in the ODI score change between the two groups was 1.3 ODI points (95% confidence interval -2.1 to 4.6, P = 0.45). Analyses showed no effect of infliximab compared to placebo on secondary outcomes. Adverse event rates were similar between groups.
Infliximab did not demonstrate superiority over placebo in reducing pain-related disability in patients with moderate to severe chronic low-back pain with Modic type 1 changes at five months.
肿瘤坏死因子抑制剂治疗伴有Modic改变的慢性下腰痛的疗效尚不确定。本研究调查了英夫利昔单抗对比安慰剂治疗Modic 1型改变患者的优越性。
在这项多中心、随机、三盲、安慰剂对照试验中,2019年1月至2022年10月期间从挪威五家公立医院招募了年龄在18至65岁、患有中度至重度慢性下腰痛且有Modic 1型改变的患者。参与者被随机分配接受4次静脉输注5mg/kg英夫利昔单抗或安慰剂。主要结局是从基线到五个月时奥斯威斯功能障碍指数(ODI)评分的变化差异。次要结局包括下腰痛强度、功能障碍以及与健康相关的生活质量的变化。采用线性混合模型进行疗效分析。
共有128名患者(平均年龄43岁,65.6%为女性)参与(每组64名)。所有接受至少一剂分配输注的患者均纳入主要分析。接受英夫利昔单抗治疗的组ODI评分(±标准差)平均变化为-7.0(±9.7),接受安慰剂治疗的组为-6.4(±10.4)。两组之间ODI评分变化的差异为1.3个ODI点(95%置信区间为-2.1至4.6,P = 0.45)。分析表明,与安慰剂相比,英夫利昔单抗对次要结局无影响。两组的不良事件发生率相似。
对于患有Modic 1型改变的中度至重度慢性下腰痛患者,在五个月时,英夫利昔单抗在减轻疼痛相关功能障碍方面并未显示出优于安慰剂的效果。