Liau MeiQi May, Oon Hazel H
Division of Dermatology, University Medicine Cluster, National University Hospital, Singapore.
National Skin Centre, Singapore;
Biologics. 2019 Jul 5;13:127-132. doi: 10.2147/BTT.S188286. eCollection 2019.
Biologics are an important component of the armamentarium of drugs in the treatment of moderate to severe psoriasis. There is increasing evidence that therapeutic drug monitoring (TDM) encompassing the measurement of trough concentrations and anti-drug antibodies (ADA), together with clinical response is emerging as a valuable tool for clinical decision making. It aids in targeted dose adjustments in patients with low drug concentrations, monitoring of adherence and assessment of patients who lose response to biologics or do not respond at all. The high prevalence of psoriasis, its impact on patients' lives and costs spent on therapy motivate an evidence-based and cost-effective utility of biologics. We performed a literature review on the TDM of TNF alpha antagonists (adalimumab, infliximab, etanercept), IL12/23 antagonists (ustekinumab, guselkumab, tildrakizumab), IL17A inhibitors (secukinumab, ixekizumab) and biosimilars used in the treatment of psoriasis. Although establishing target therapeutic ranges for biologics is ideal, this has only been explored in adalimumab. We also propose a treatment algorithm for the practical application of TDM depending on drug trough concentrations, presence/absence of anti-drug antibodies and clinical response of patients. The practice of TDM is recommended in routine clinical practice where possible.
生物制剂是治疗中重度银屑病药物库的重要组成部分。越来越多的证据表明,包括谷浓度和抗药物抗体(ADA)测量以及临床反应的治疗药物监测(TDM)正在成为临床决策的宝贵工具。它有助于对药物浓度低的患者进行靶向剂量调整,监测依从性,并评估对生物制剂失去反应或根本无反应的患者。银屑病的高患病率、其对患者生活的影响以及治疗费用促使人们对生物制剂进行循证且具有成本效益的应用。我们对用于治疗银屑病的肿瘤坏死因子α拮抗剂(阿达木单抗、英夫利昔单抗、依那西普)、白细胞介素12/23拮抗剂(乌司奴单抗、古塞库单抗、替拉珠单抗)、白细胞介素17A抑制剂(司库奇尤单抗、依奇珠单抗)和生物类似药的TDM进行了文献综述。虽然为生物制剂确定目标治疗范围是理想的,但这仅在阿达木单抗中进行了探索。我们还根据药物谷浓度、抗药物抗体的有无以及患者的临床反应,提出了一种TDM实际应用的治疗算法。建议在可能的情况下,在常规临床实践中采用TDM做法。