Efficacy of Tocilizumab in Refractory Graves Orbitopathy From Real-World Clinical Practice: An Observational Study.

IF 3 Q2 ENDOCRINOLOGY & METABOLISM
Journal of the Endocrine Society Pub Date : 2024-11-02 eCollection Date: 2024-10-29 DOI:10.1210/jendso/bvae193
Mingyang Wang, Bixuan Qin, Cuihong Liu, Honglei Liu, Dongmei Li
{"title":"Efficacy of Tocilizumab in Refractory Graves Orbitopathy From Real-World Clinical Practice: An Observational Study.","authors":"Mingyang Wang, Bixuan Qin, Cuihong Liu, Honglei Liu, Dongmei Li","doi":"10.1210/jendso/bvae193","DOIUrl":null,"url":null,"abstract":"<p><strong>Context: </strong>The efficacy of tocilizumab (TCZ) in treating Graves orbitopathy (GO) remains uncertain due to the small sample sizes of earlier studies, and there is a lack of research on the drug for juvenile GO.</p><p><strong>Objective: </strong>To evaluate the effectiveness of TCZ in treating GO that is resistant to conventional therapy.</p><p><strong>Design: </strong>This observational study at a tertiary care center included 79 Chinese GO patients, 15 of whom were pediatric patients, with 52 of these patients having moderate to severe active GO (all adult patients having steroid-resistant GO). Intravenous infusion of TCZ 8 mg/kg was given every 28 days for 4 months. Changes from baseline in visual acuity (VA), intraocular pressure (IOP), proptosis, clinical activity score (CAS), and thyrotropin receptor antibody (TRAb) levels throughout TCZ therapy were assessed at baseline (T0), the fifth month (T4), and follow-up (T5). Additionally, improvements in CAS by at least 2 points and CAS < 4 points at T4 and T5 were evaluated.</p><p><strong>Results: </strong>Significant improvements were found in VA, IOP, proptosis, CAS, and TRAb levels in the adult group, and proptosis in the pediatric group at T5 (<i>P</i> < .05). Additionally, significant improvements were identified in TRAb levels and CAS (active GO at T0) in the pediatric group at T4 (<i>P</i> < .05). In the adult and pediatric group with active GO at T5, 71.4% and 60% experienced a decrease in CAS by ≥ 2 points, respectively; 89.3% and 60% achieved the response criterion of low activity disease (CAS < 4 points), respectively.</p><p><strong>Conclusion: </strong>TCZ emerged as a valuable therapeutic option for Chinese patients with active, corticosteroid-resistant, moderate to severe GO.</p>","PeriodicalId":17334,"journal":{"name":"Journal of the Endocrine Society","volume":"8 12","pages":"bvae193"},"PeriodicalIF":3.0000,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11574614/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Endocrine Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1210/jendso/bvae193","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/29 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Context: The efficacy of tocilizumab (TCZ) in treating Graves orbitopathy (GO) remains uncertain due to the small sample sizes of earlier studies, and there is a lack of research on the drug for juvenile GO.

Objective: To evaluate the effectiveness of TCZ in treating GO that is resistant to conventional therapy.

Design: This observational study at a tertiary care center included 79 Chinese GO patients, 15 of whom were pediatric patients, with 52 of these patients having moderate to severe active GO (all adult patients having steroid-resistant GO). Intravenous infusion of TCZ 8 mg/kg was given every 28 days for 4 months. Changes from baseline in visual acuity (VA), intraocular pressure (IOP), proptosis, clinical activity score (CAS), and thyrotropin receptor antibody (TRAb) levels throughout TCZ therapy were assessed at baseline (T0), the fifth month (T4), and follow-up (T5). Additionally, improvements in CAS by at least 2 points and CAS < 4 points at T4 and T5 were evaluated.

Results: Significant improvements were found in VA, IOP, proptosis, CAS, and TRAb levels in the adult group, and proptosis in the pediatric group at T5 (P < .05). Additionally, significant improvements were identified in TRAb levels and CAS (active GO at T0) in the pediatric group at T4 (P < .05). In the adult and pediatric group with active GO at T5, 71.4% and 60% experienced a decrease in CAS by ≥ 2 points, respectively; 89.3% and 60% achieved the response criterion of low activity disease (CAS < 4 points), respectively.

Conclusion: TCZ emerged as a valuable therapeutic option for Chinese patients with active, corticosteroid-resistant, moderate to severe GO.

从真实世界的临床实践看托珠单抗对难治性巴塞杜氏眼病的疗效:一项观察性研究。
背景:由于早期研究的样本量较小,托西珠单抗(TCZ)治疗巴塞杜氏眶病(Graves orbitopathy,GO)的疗效仍不确定,而且缺乏对该药物治疗青少年GO的研究:评估TCZ治疗对常规疗法耐药的GO的疗效:这项在一家三级医疗中心进行的观察性研究纳入了79名中国GO患者,其中15名为儿童患者,52名患者为中度至重度活动性GO(所有成人患者均为类固醇耐药GO)。每28天静脉输注一次8毫克/千克的TCZ,持续4个月。在基线(T0)、第5个月(T4)和随访(T5)期间,对TCZ治疗期间视力(VA)、眼压(IOP)、突眼、临床活动评分(CAS)和促甲状腺激素受体抗体(TRAb)水平与基线相比的变化进行评估。此外,CAS 至少提高 2 个点,CAS 结果显示,TCZ 的治疗效果显著:成人组的 VA、眼压、眼球突出、CAS 和 TRAb 水平均有显著改善,儿童组的眼球突出在 T5 时也有显著改善(P < .05)。此外,儿童组的 TRAb 水平和 CAS(T0 时活跃的 GO)在 T4 时也有明显改善(P < .05)。在T5活动性GO的成人组和儿童组中,分别有71.4%和60%的患者CAS下降≥2点;分别有89.3%和60%的患者达到了低活动性疾病(CAS<4点)的应答标准:结论:TCZ对皮质类固醇耐药的中重度活动性GO患者来说是一种有价值的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of the Endocrine Society
Journal of the Endocrine Society Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.50
自引率
0.00%
发文量
2039
审稿时长
9 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信