Aims: This review aims to provide an overview of the current understanding of TED and its pathophysiology. To describe the evidence base for current consensus treatment recommendations and newer biological therapies available as well as to present future therapeutic research.
Methods: We reviewed and assessed the peer-reviewed literature placing particular emphasis on recent studies evaluating the pathophysiology of TED, landmark trials forming the basis of current management and recent clinical trials informing future therapeutics. Searched were made in MEDLINE Ovid, Embase Ovid, US National Institutes of Health Ongoing Trials Register and EU Clinical Trials Register. Keywords included: "Thyroid Eye Disease", "Graves Orbitopathy", "Thyroid Orbitopathy" and "Graves' Ophthalmopathy".
Results and conclusions: The pathophysiology of TED involves a complex array of cellular and humoral based autoimmune dysfunction. Previous therapies have been broad-based acting as a blunt instrument on this mechanism with varying efficacy but often accompanied with a significant side effect profile. The recent development of targeted therapy, spearheaded by Teprotumumab has led to an array of treatments focusing on specific components of the molecular pathway optimising their impact whilst possibly minimising their side effect profile. Future challenges involve identifying the most effective target for each patient rather than any single agent being a panacea. Long-term safety profiles will require clarification as unintended immunological consequence downstream may become manifest as seen in other diseases. Finally, future novel therapeutics will entail significant expenditure and may lead to a divergence of available treatment modalities between healthcare systems due to funding disparities.
摘要: 本文旨在对目前对甲状腺眼病 (TED) 及其病理生理学进行概述。阐述当前共识治疗建议和可用的新生物疗法的证据基础, 并介绍未来的治疗研究。我们回顾并评估了同行评审的文献, 特别强调了评估TED病理生理学的最新研究、构成当前管理基础的里程碑式试验以及为未来治疗提供信息的最新临床试验。在MEDLINE Ovid、Embase Ovid, 美国国立卫生研究院正在进行的试验注册和欧盟临床试验注册中进行了检索。关键词包括: “甲状腺眼病”、“Graves眼眶病”、“甲状腺眼眶病”和“Graves眼病”。TED的病理生理学涉及一系列复杂的细胞免疫和体液免疫障碍。既往治疗方法在该机制上起到了广泛的作用, 取得了不同程度的成功, 但往往伴随着严重的副作用。Teprotumumab介导的靶向治疗的发展带来了一系列针对分子通路特定治疗方法, 在优化疗效的同时可能将副作用降至最低。未来的挑战包括为每位患者确定最有效的靶点, 而不是将任何单一药物视为万能药物。对于靶向药物的下游有可能出现免疫反应, 因此需要明确长期安全性, 这一点在其他疾病中也有所表现。最后, 未来的新型疗法将耗费大量支出, 并可能由于资金差异而导致医疗系统间可用治疗模式的差异。.
© 2024. The Author(s).