From Department of Oculofacial Plastic Surgery, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, USA.
From Department of Oculofacial Plastic Surgery, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Am J Ophthalmol. 2024 Jul;263:152-159. doi: 10.1016/j.ajo.2023.12.001. Epub 2023 Dec 23.
To determine the recurrence and reactivation rates after teprotumumab therapy for active thyroid eye disease.
Retrospective consecutive case series.
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.
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).
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.
确定替普妥单抗治疗活动性甲状腺眼病后的复发和再激活率。
回顾性连续病例系列。
这是一项在克利夫兰诊所科尔眼研究所对 2020 年 5 月至 2021 年 5 月期间接受替普妥单抗治疗的活动性甲状腺眼病患者进行的研究。排除了输注完成后随访时间少于 6 个月的患者。主要结局指标是再激活,定义为眼球突出度(任何一只眼的退缩增加≥2mm,且恢复至治疗前水平并临床活动评分[CAS]恶化 2 分或以上)。次要结局是复视反应。
共有 21 例患者纳入研究。替普妥单抗治疗后眼球突出度较大的那只眼的长期平均突出度改善为 1.57mm(范围为-3 至 4mm)。在 17 名初始反应者中,有 8 名出现再激活(47%)和 2 名孤立性眼球突出度回退(12%);总的来说,21 名患者中有 7 名(33%)在整个研究期间均有反应。平均再激活时间为 12.25 个月(范围为 2-22.5 个月)。在任何亚组中,最终随访时复视均无统计学显著变化(P = 0.68 至>.99)。
最多只有 33%的患者在替普妥单抗治疗 2 年后仍持续有反应。80%的回退发生在疾病再激活的情况下,出现眼球突出度和 CAS 回退。替普妥单抗治疗似乎在长期改善复视方面效果有限。