From the Department of Paediatric Gastroenterology, Hepatology and Nutrition, Royal Hospital for Children and Young People, Edinburgh, UK.
Paediatric Specialist Pharmacist, Royal Hospital for Children and Young People, Edinburgh, UK.
J Pediatr Gastroenterol Nutr. 2023 Aug 1;77(2):235-239. doi: 10.1097/MPG.0000000000003838. Epub 2023 May 23.
No real-world data are available on subcutaneous infliximab (SC-IFX) in pediatric inflammatory bowel disease (PIBD). We report a single-center cohort experience of an elective switching program from biosimilar intravenous infliximab to SC-IFX, 120 mg fortnightly, as maintenance. Clinical and laboratory data were collected for 7 patients with infliximab trough levels collected prior and at 6 and 40 weeks after the switch. High treatment persistence was registered with a single patient discontinuing the treatment due to high IFX antibodies, already present before switching. All patients remained in clinical remission with no significant changes in laboratory markers and median infliximab trough levels (12.3 µg/mL at baseline; 13.9 and 14.0 µg/mL at 6 and 40 weeks respectively). No newly-developed IFX antibodies were detected and no adverse reactions or rescue therapies were recorded. Our real-world data support the feasibility of an elective switch to SC-IFX in PIBD as maintenance with potential advantages concerning medical resources and patient satisfaction.
尚无关于儿童炎症性肠病(PIBD)患者皮下注射英夫利昔单抗(SC-IFX)的真实世界数据。我们报告了一项单中心队列经验,即对接受生物类似静脉注射英夫利昔单抗治疗的患者进行择期转换方案,转换为每两周皮下注射 SC-IFX,120mg,作为维持治疗。收集了 7 名患者的临床和实验室数据,在转换前以及转换后 6 周和 40 周时采集了英夫利昔单抗谷浓度。高治疗持续性,仅有 1 名患者因高英夫利昔单抗抗体而停止治疗,该抗体在转换前已经存在。所有患者均保持临床缓解,实验室标志物和中位数英夫利昔单抗谷浓度均无显著变化(基线时为 12.3μg/mL;分别在第 6 周和第 40 周时为 13.9 和 14.0μg/mL)。未检测到新产生的英夫利昔单抗抗体,也未记录到不良反应或抢救治疗。我们的真实世界数据支持将 PIBD 患者作为维持治疗进行择期转换为 SC-IFX 的可行性,这可能在医疗资源和患者满意度方面具有优势。