Division of Paediatric Gastroenterology, Erasmus University Medical Center-Sophia Children's Hospital, Rotterdam Zuid-Holland, The Netherlands.
Intensive Care and Department of Paediatric Surgery, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, Zuid-Holland, The Netherlands.
J Pediatr Gastroenterol Nutr. 2020 Jun;70(6):763-776. doi: 10.1097/MPG.0000000000002631.
Infliximab (IFX), a monoclonal antibody directed against tumor necrosis factor alpha is a potent treatment option for inflammatory bowel disease (IBD). Dosing regimens in children are extrapolated from adult data using a fixed, weight-based dose, which is often not adequate. While clinical trials have focused on safety and efficacy, there is limited data on pharmacokinetic characteristics and immunogenicity of IFX in children. The objective was to provide a systematic overview of current literature on pharmacokinetic and immunogenicity of IFX in children with IBD, to assess the validity of current adult to pediatric dosing extrapolation.
A literature search identified publications up to October 2018. Eligibility criteria were study population consisting of children and/or adolescents with IBD, report of IFX trough levels and/or antibodies-to IFX, full text article or abstract, article in English, and original data.
Initial electronic search yielded 2360 potentially relevant articles, with 1831 remaining after removal of duplicates. An additional search yielded another 202 potentially relevant articles. Of the 2033 retrieved articles, 2000 articles were excluded based on title, abstract, or eligibility criteria. Clearance of IFX was increased in young children and children with extensive disease, leading to lower trough levels after extrapolated dosing of 5 mg/kg, antibodies-to IFX emergence, and subsequent reduced efficacy.
Adult to pediatric weight-based dosing extrapolation is often inadequate. We provide several considerations for optimal dosing of IFX in children and adolescents with IBD.
英夫利昔单抗(IFX)是一种针对肿瘤坏死因子-α的单克隆抗体,是炎症性肠病(IBD)的有效治疗选择。儿童剂量方案是从成人数据外推得出的,采用固定的基于体重的剂量,但往往不够。虽然临床试验主要关注安全性和疗效,但关于儿童 IFX 的药代动力学特征和免疫原性的数据有限。目的是系统综述目前关于 IBD 儿童 IFX 的药代动力学和免疫原性的文献,评估目前成人到儿科剂量外推的有效性。
文献检索截至 2018 年 10 月的出版物。纳入标准为研究人群为患有 IBD 的儿童和/或青少年,报告 IFX 谷浓度和/或抗 IFX,全文文章或摘要,英文文章,以及原始数据。
最初的电子搜索产生了 2360 篇潜在相关文章,去除重复后剩余 1831 篇。额外的搜索又产生了另外 202 篇潜在相关文章。在检索到的 2033 篇文章中,根据标题、摘要或纳入标准排除了 2000 篇文章。IFX 的清除率在幼儿和广泛疾病的儿童中增加,导致经外推 5mg/kg 剂量后谷浓度降低、抗 IFX 出现,随后疗效降低。
成人到儿科的基于体重的剂量外推往往不够。我们为 IBD 儿童和青少年 IFX 的最佳剂量提供了一些考虑因素。