The Jules Stein Eye Institute University of California, Los Angeles, Los Angeles, CA, USA.
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
Eye (Lond). 2021 Sep;35(9):2607-2612. doi: 10.1038/s41433-020-01297-w. Epub 2020 Nov 21.
Teprotumumab, a blocking antibody to the insulin like growth factor 1 receptor (IGF-1R) has been shown to significantly reduce proptosis in recent phase 2 and 3 trials in patients with inflammatory thyroid eye disease (TED). Herein, we investigate the impact of teprotumumab on patients with non-inflammatory TED. We also investigate the expression of the IGF-1R on orbital tissues from patients with inflammatory and non-inflammatory TED compared to controls.
Consecutive patients with non-inflammatory TED (clinical activity score, CAS ≤ 1, for at least 4 months, were treated with teprotumumab. They received a complete course (total eight infusions) of teprotumumab (10 mg/kg for the first infusion and 20 mg/kg for subsequent infusions every 3 weeks). The primary outcome was a proptosis response at week 24. Further, IGF-1R α and β expression was evaluated on orbital tissue from patients with inflammatory and non-inflammatory TED, as well as healthy controls. Non-biased histological analysis of IGF-1R expression was performed using ImageJ.
Four patients met eligibility criteria for the clinical study, with a mean (SD) CAS of 0 (0). Following teprotumumab treatment, there was a mean (SD) reduction in proptosis of 2.6 mm (1.2). Five patients were included for each group of the histological study; inflammatory TED, non-inflammatory TED and controls. IGF-1Rα and IGF-1Rβ expression was significantly greater in the orbital tissues of patients with inflammatory TED and non-inflammatory TED, when compared to controls.
Our findings demonstrate for the first time, that teprotumumab, a blocking antibody to the IGF-1R reduces proptosis in a series of patients with non-inflammatory TED. Overexpression of the IGF-1R in orbital tissue from patients with non-inflammatory disease compared to controls may be an important consideration for effect.
胰岛素样生长因子 1 受体(IGF-1R)阻断抗体特罗鲁单抗已在最近的 2 期和 3 期临床试验中显示出可显著降低炎症性甲状腺眼病(TED)患者的眼球突出。在此,我们研究了特罗鲁单抗对非炎症性 TED 患者的影响。我们还比较了炎症性和非炎症性 TED 患者与对照组眼眶组织中 IGF-1R 的表达。
连续患有非炎症性 TED(临床活动评分,CAS≤1,至少 4 个月)的患者接受特罗鲁单抗治疗。他们接受了特罗鲁单抗的完整疗程(首剂 10mg/kg,随后每 3 周 20mg/kg)。主要结局是 24 周时的眼球突出反应。此外,还评估了炎症性和非炎症性 TED 患者以及健康对照组眼眶组织中 IGF-1Rα和β的表达。使用 ImageJ 对 IGF-1R 表达进行了无偏倚的组织学分析。
4 名患者符合临床研究的入选标准,平均(标准差)CAS 为 0(0)。特罗鲁单抗治疗后,眼球突出平均(标准差)减少 2.6mm(1.2)。组织学研究每组纳入 5 名患者;炎症性 TED、非炎症性 TED 和对照组。与对照组相比,炎症性 TED 和非炎症性 TED 患者眼眶组织中的 IGF-1Rα和 IGF-1Rβ表达明显更高。
我们的研究结果首次表明,IGF-1R 阻断抗体特罗鲁单抗可降低一系列非炎症性 TED 患者的眼球突出。与对照组相比,非炎症性疾病患者眼眶组织中 IGF-1R 的过度表达可能是影响疗效的重要考虑因素。