Reactivation After Teprotumumab Treatment for Active Thyroid Eye Disease

被引:9
|
作者
Hwang, Catherine J. [1 ]
Rebollo, Nicole P. [1 ]
Mechels, Keegan B. [1 ]
Perry, Julian D. [1 ,2 ]
机构
[1] Cole Eye Inst, Dept Oculofacial Plast Surg, Cleveland Clin, Cleveland, OH USA
[2] Cleveland Clin, Cole Eye Inst, Cleveland, OH 44195 USA
关键词
D O I
10.1016/j.ajo.2023.12.001
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
center dot PURPOSE: To determine the recurrence and reactivation rates after teprotumumab therapy for active thyroid eye disease. center dot DESIGN: Retrospective consecutive case series. center dot METHODS: This was a study of all patients followed for active thyroid eye disease at the Cole Eye Institute, Cleveland Clinic, treated with teprotumumab between May 2020 and May 2021. Patients with less than 6 months follow-up after completion of infusions were excluded. The primary outcome measure was reactivation, defined as a regression in proptosis (increase of > 2 mm in either eye and to within < 2 mm of pre-treatment level and Clinical Activity Score [CAS] worsening of 2 points or greater). Secondary outcome was diplopia response. center dot RESULTS: A total of 21 patients were included in the study. The average long-term improvement in proptosis in the eye with more proptosis after teprotumumab was 1.57mm (range, -3 to 4 mm). Of the 17 initial responders, there were 8 reactivations (47%) and 2 isolated proptosis regressions (12%); Overall, 7 of 21 patients (33%) responded throughout the study period. Average time to regression was 12.25 months (range, 2-22.5 months). There was no statistically significant change in diplopia at final visit in any subgroup ( P = 0.68 to > .99). center dot CONCLUSIONS: At most, 33% of patients demonstrate continued response 2 years after teprotumumab treatment. The proptosis and CAS regression occurs in the setting of disease reactivation in 80% of regressions. Teprotumumab treatment appears to offer minimal long-term improvement in diplopia. (Am J Ophthalmol 2024;263: 152-159. (c) 2023 Published by Elsevier Inc.)
引用
收藏
页码:152 / 159
页数:8
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