The position of monoclonal antibodies and small molecules in the treatment of thyroid orbitopathy.

Mariusz Nowak, Wojciech Nowak, Bogdan Marek, Beata Kos-Kudła, Lucyna Siemińska, Magdalena Londzin-Olesik, Dariusz Kajdaniuk
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Abstract

Since the European Thyroid Association guidelines for the management of thyroid orbitopathy (TO) were published in 2016, a number of randomised clinical trials (RCTs) investigating the use of biologic drugs for the treatment of moderate to severe and active TO have been published. Therefore, new recommendations for its treatment were developed and published in 2021. Treatment of active TO includes 2 types of immunosuppressive agents: non-specific and specific. Specific immunosuppressive agents used to treat TO include adalimumab (ADA), infliximab (IFX), etanercept (ETA), rituximab (RTX), tocilizumab (TCZ), teprotumumab (TEP), and batoclimab (BAT). In the manuscript, we present a review of the literature on RCTs, retrospective studies, and case reports on their use in the treatment of TO. The authors emphasise the beneficial effects of TEP, indicating, however, the lack of data on its long-term efficacy and safety and the lack of head-to-head comparison with i.v. glucocorticosteroids and its huge limitation is also the high price of the drug. TCZ is a therapeutic option for glucocorticosteroid-resistant TO and should be considered for second-line treatment (due to the cost of treatment, among other reasons) or first-line treatment in patients with contraindications to i.v. glucocorticosteroids. Given its side-effect profile, especially some risk of optic nerve neuropathy (DON), RTX is considered by the authors as a second- or even third-line treatment option. The current 2021 European Group on Graves' Orbitopathy (EUGOGO) recommendations include RTX, TCZ, and TEP among the second-line drugs for the treatment of moderate to severe and active TO. BAT is under clinical trials. Given the numerous advantages of biologic drugs over glucocorticosteroids, further RCTs are indicated to confirm their possible place also as first-line treatment in TO.

单克隆抗体和小分子在甲状腺眼病治疗中的地位。
自2016年欧洲甲状腺协会甲状腺眼病(TO)管理指南发布以来,已经发表了许多随机临床试验(rct),研究生物药物治疗中重度和活动性TO的使用。因此,制定了新的治疗建议,并于2021年公布。活动性TO的治疗包括两种类型的免疫抑制剂:非特异性和特异性。用于治疗to的特异性免疫抑制剂包括阿达木单抗(ADA)、英夫利昔单抗(IFX)、依那西普(ETA)、利妥昔单抗(RTX)、托珠单抗(TCZ)、teprotumumab (TEP)和巴托利单抗(BAT)。在原稿中,我们对随机对照试验、回顾性研究和病例报告的文献进行了综述。作者强调了TEP的有益作用,然而,缺乏关于其长期疗效和安全性的数据,缺乏与静脉注射糖皮质激素的正面比较,其巨大的局限性也是该药的高价格。TCZ是糖皮质激素抵抗性TO的一种治疗选择,应考虑用于二线治疗(由于治疗费用等原因)或静脉注射糖皮质激素禁忌症患者的一线治疗。考虑到RTX的副作用,尤其是视神经病变(DON)的风险,作者认为RTX是二线甚至三线治疗选择。目前2021年欧洲格雷夫斯眼病小组(EUGOGO)推荐的二线药物包括RTX、TCZ和TEP,用于治疗中度至重度和活动性to。BAT正在进行临床试验。鉴于生物药物相对于糖皮质激素的众多优势,进一步的随机对照试验表明,它们也可能作为to的一线治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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