Miles Nicholas, Masters Andi, Desta Zeruesenay, Goldman Jennifer L, Suppes Sarah L, Tillman Emma M
Division of Clinical Pharmacology (NM, ZD, ET), Indiana University School of Medicine, Indianapolis, IN.
Indiana University Comprehensive Cancer Center (AM), Indiana University School of Medicine, Indianapolis, IN.
J Pediatr Pharmacol Ther. 2023;28(7):643-648. doi: 10.5863/1551-6776-28.7.643. Epub 2023 Nov 23.
Etoposide, a topoisomerase II inhibitor used clinically to treat cancer, has been associated with severe anaphylactic infusion related adverse drug reactions (ADRs). In a previous study we identified a hydrophilic polyethersulfone filter as a possible cause of increased rates of pediatric etoposide infusion reactions. In this multidisciplinary follow-up analytical study, we aimed to assess the chemical structure of etoposide after passing through the same hydrophilic polyethersulfone filter.
An etoposide 0.4 mg/mL infusion was prepared under aseptic conditions and then passed through a standard IV infusion set with an in-line filter in place. Samples were taken in triplicate using a needle-less access system to include sampling sites directly from the IV bag port and from the IV tubing both before and after the in-line filter. Samples were diluted into mobile phase, then an aliquot was injected into a high-performance liquid chromatography mass spectrometry HPLC-MS (Thermo TSQ Quantum Ultra) system coupled to a Diode Array Detector (DAD) (Thermo Dionex Ultimate 3000). Etoposide was monitored using a selected reaction monitoring scan (SRM) of 606.2/228.8 and wavelengths of 210, 220, 254, and 280 nm for 30 minutes.
No detectable differences were observed upon comparing the three samples. Based on these results, a chemical change in etoposide resulting from an in-line filter is unlikely to be the primary cause of increased rates of infusion reactions.
Pharmacists working in healthcare systems, observe many ADRs, but rarely have the resources necessary to investigate the potential etiology or causality. This report highlights importance of multi-disciplinary collaboration to investigate serious ADRs.
依托泊苷是一种临床上用于治疗癌症的拓扑异构酶II抑制剂,与严重的过敏性输注相关药物不良反应(ADR)有关。在之前的一项研究中,我们确定一种亲水性聚醚砜过滤器可能是小儿依托泊苷输注反应发生率增加的原因。在这项多学科随访分析研究中,我们旨在评估依托泊苷通过同一亲水性聚醚砜过滤器后的化学结构。
在无菌条件下制备0.4mg/mL的依托泊苷输注液,然后通过带有在线过滤器的标准静脉输液装置。使用无针接入系统一式三份取样,包括直接从静脉输液袋端口以及在线过滤器前后的静脉输液管处取样。将样品稀释到流动相中,然后取一份注入与二极管阵列检测器(DAD)(Thermo Dionex Ultimate 3000)联用的高效液相色谱-质谱(HPLC-MS)(Thermo TSQ Quantum Ultra)系统。使用606.2/228.8的选择反应监测扫描(SRM)以及210、220、254和280nm的波长监测依托泊苷30分钟。
比较三个样品时未观察到可检测到的差异。基于这些结果,在线过滤器导致依托泊苷发生化学变化不太可能是输注反应发生率增加的主要原因。
在医疗保健系统工作的药剂师会观察到许多药物不良反应,但很少有必要的资源来调查潜在的病因或因果关系。本报告强调了多学科合作调查严重药物不良反应的重要性。