Université François Rabelais de Tours, CNRS, UMR 6239, Tours, France.
Ther Drug Monit. 2010 Apr;32(2):232-6. doi: 10.1097/FTD.0b013e3181cc6fef.
Infliximab is a chimeric monoclonal antibody that binds to human tumor necrosis factor alpha and is approved for refractory rheumatoid arthritis. We studied the association between infliximab concentration and long-term control of disease activity in patients with rheumatoid arthritis treated on a routine basis both in cross-sectional analysis and over the long term. Trough serum infliximab concentrations were measured in patients with rheumatoid arthritis receiving infliximab infusions during the period August to October 2006. Disease activity was assessed by the Disease Activity Score for 28 Joints (DAS28) and usual biologic markers. During a 42-week follow-up period, patients were classified into two groups: those continuing with the same or lower doses of infliximab (Group A = treatment success) and those who switched to another biopharmaceutical or required an increase in infliximab dose (Group B = treatment failure). Treatment maintenance for Group A was analyzed by categories of infliximab concentration at baseline and compared by the log rank test. In 28 patients, C-reactive protein and infliximab concentrations were inversely related. Infliximab concentration in patients with low disease activity (DAS28 3.2 or less) was higher than in those with persistent active disease (DAS28 greater than 3.2); median values were 3.26 and 0.16 mg/L, respectively (P < 0.01). Analysis after 42 weeks showed that patients in Group A had higher infliximab concentrations at baseline than those with treatment failure (P < 0.01). In rheumatoid arthritis, infliximab concentration is predictive of sustained efficacy with the same infliximab regimen and should be considered on a routine basis.
英夫利昔单抗是一种嵌合型单克隆抗体,可与人肿瘤坏死因子-α结合,被批准用于治疗难治性类风湿关节炎。我们研究了在常规基础上接受英夫利昔单抗治疗的类风湿关节炎患者的英夫利昔单抗浓度与疾病活动长期控制之间的关系,分析方法包括横断面分析和长期随访。2006 年 8 月至 10 月期间,我们对接受英夫利昔单抗输注的类风湿关节炎患者进行了血清英夫利昔单抗浓度检测。采用 28 关节疾病活动评分(DAS28)和常用的生物学标志物评估疾病活动度。在 42 周的随访期间,我们将患者分为两组:继续使用相同或较低剂量英夫利昔单抗的患者(A 组=治疗成功)和改用其他生物制剂或需要增加英夫利昔单抗剂量的患者(B 组=治疗失败)。对 A 组的治疗维持情况进行了分类分析,并通过对数秩检验进行了比较。在 28 例患者中,C 反应蛋白和英夫利昔单抗浓度呈负相关。低疾病活动度(DAS28 3.2 或以下)患者的英夫利昔单抗浓度高于持续活动疾病患者(DAS28 大于 3.2);中位数分别为 3.26 和 0.16 mg/L(P < 0.01)。42 周后分析显示,A 组患者的基线英夫利昔单抗浓度高于治疗失败组(P < 0.01)。在类风湿关节炎中,英夫利昔单抗浓度可预测相同英夫利昔单抗方案的持续疗效,应常规进行评估。