Zaans Medical Center, Zaandam and Emma Children's Hospital, Amsterdam UMC, Pediatric Immunology, Rheumatology and Infectious Diseases, University of Amsterdam, Amsterdam, The Netherlands.
Emma Children's Hospital, Amsterdam UMC, Pediatric Immunology, Rheumatology and Infectious Diseases, University of Amsterdam, Amsterdam, The Netherlands.
Pediatr Rheumatol Online J. 2021 Apr 29;19(1):59. doi: 10.1186/s12969-021-00545-x.
Anti-tumor necrosis factor (TNF) drugs have improved the prognosis for juvenile idiopathic arthritis (JIA) significantly. However, evidence for individual treatment decisions based on serum anti-TNF drug levels and the presence of anti-drug antibodies (ADAbs) in children is scarce. We aimed to assess if anti-TNF drug levels and/or ADAbs influenced physician's treatment decisions in children with JIA.
Patients' records in our center were retrospectively screened for measurements of anti-TNF drug levels and ADAbs in children with JIA using etanercept, adalimumab or infliximab. Clinical characteristics and disease activity were retrieved from patient charts.
We analyzed 142 measurements of anti-TNF drug levels in 65 children with JIA. Of these, ninety-seven (68.3%) were trough concentrations. N = 14/97 (14.4%) of these showed trough concentrations within the therapeutic drug range known for adults with RA and IBD. ADAbs against adalimumab were detected in seven patients and against infliximab in one patient. Seven (87,5%) of these ADAb-positive patients had non-detectable drug levels. A flowchart was made on decisions including rational dose escalation, stopping treatment in the presence of ADAbs and undetectable drug levels, showing that 45% of measurements influenced treatment decisions, which concerned 65% of patients (n = 42/65).
In the majority of patients, measurement of anti-TNF drug levels led to changes in treatment. A wide variation of anti-TNF drug levels was found possibly due to differences in drug clearance in different age groups. There is need for determination of therapeutic drug ranges and pharmacokinetic curves for anti-TNF and other biologics in children with JIA.
抗肿瘤坏死因子(TNF)药物显著改善了幼年特发性关节炎(JIA)的预后。然而,基于儿童血清抗 TNF 药物水平和抗药物抗体(ADAb)的个体治疗决策的证据仍然缺乏。我们旨在评估抗 TNF 药物水平和/或 ADAb 是否影响 JIA 儿童的医生治疗决策。
我们回顾性筛选了使用依那西普、阿达木单抗或英夫利昔单抗治疗的 JIA 儿童的抗 TNF 药物水平和 ADAb 的中心患者记录。从患者病历中检索临床特征和疾病活动度。
我们分析了 65 名 JIA 儿童的 142 项抗 TNF 药物水平测量值。其中 97 项(68.3%)为谷浓度。在这些谷浓度中,n = 14/97(14.4%)处于已知成人 RA 和 IBD 的治疗药物范围内。检测到 7 名患者存在针对阿达木单抗的 ADAb,1 名患者存在针对英夫利昔单抗的 ADAb。这 7 名 ADAb 阳性患者中有 7 名(87.5%)的药物水平无法检测到。制作了一个流程图,用于决策,包括合理的剂量递增、存在 ADAb 和无法检测到药物水平时停止治疗,结果显示 45%的测量结果影响了治疗决策,这涉及 65%的患者(n = 42/65)。
在大多数患者中,抗 TNF 药物水平的测量导致了治疗的改变。发现抗 TNF 药物水平存在广泛差异,可能是由于不同年龄组药物清除率的差异所致。需要确定 JIA 儿童的抗 TNF 和其他生物制剂的治疗药物范围和药代动力学曲线。