Bertin Luisa, Savarino Edoardo Vincenzo
Gastroenterology Unit, Azienda Ospedale Università Padova, Padova, Italy.
Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
United European Gastroenterol J. 2025 May;13(4):505-507. doi: 10.1002/ueg2.12716. Epub 2024 Nov 29.
JAK inhibitors are pivotal in treating immune-mediated inflammatory diseases (IMIDs) like rheumatoid arthritis (RA) and inflammatory bowel disease. However, emerging safety concerns warrant careful evaluation. A recent analysis of the FDA Adverse Event Reporting System (FAERS) revealed that RA patients using JAK inhibitors face nearly double the risk of gastrointestinal perforations (GIPs) compared to those on biologics, particularly with concurrent steroid or NSAID use. Additionally, the FDA's ORAL Surveillance study linked tofacitinib with higher rates of cancer and cardiovascular events, prompting regulatory restrictions. These findings highlight the importance of balancing JAK inhibitors' therapeutic benefits with potential risks, emphasizing the need for patient-centred risk assessment and vigilant monitoring to optimize outcomes.
JAK抑制剂在治疗类风湿性关节炎(RA)和炎症性肠病等免疫介导的炎症性疾病(IMID)中起着关键作用。然而,新出现的安全问题值得仔细评估。最近对美国食品药品监督管理局不良事件报告系统(FAERS)的分析显示,与使用生物制剂的类风湿性关节炎患者相比,使用JAK抑制剂的患者发生胃肠道穿孔(GIP)的风险几乎高出一倍,尤其是在同时使用类固醇或非甾体抗炎药的情况下。此外,美国食品药品监督管理局的口服监测研究将托法替布与更高的癌症和心血管事件发生率联系起来,促使监管机构出台限制措施。这些发现凸显了在JAK抑制剂的治疗益处与潜在风险之间取得平衡的重要性,强调了以患者为中心进行风险评估和 vigilant monitoring以优化治疗结果的必要性。 (注:原文中“vigilant monitoring”此处直接保留英文未翻译,因为不清楚是否是特定医学术语,若有准确中文对应可替换。)