Department of Pathophysiology, National and Kapodistrian University of Athens, Athens, Greece.
Front Endocrinol (Lausanne). 2023 Jun 22;14:1186105. doi: 10.3389/fendo.2023.1186105. eCollection 2023.
Graves' orbitopathy (GO) is an autoimmune disorder affecting the orbital fat and muscles. A significant role of IL-6 in the pathogenesis of GO has been described and tocilizumab (TCZ), an IL-6 inhibitor targeting IL-6R has been given in some patients. The aim of our case study was to evaluate the therapeutic outcome of TCZ in non-responders to first line treatments with corticosteroids.
We conducted an observational study of patients with moderate to severe GO. Twelve patients received TCZ in intravenous infusions at a dose of 8mg/kg every 28 days for 4 months and followed up for additionally 6 weeks. The primary outcome was improvement in CAS by at least 2 points, 6 weeks after the last dose of TCZ. Secondary outcomes included CAS <3 (inactive disease) 6 weeks after TCZ last dose, reduced TSI levels, proptosis reduction by > 2mm and diplopia response.
The primary outcome, was achieved in all patients 6 weeks after treatment course. Furthermore all patients had inactive disease 6 weeks after treatment cessation. Treatment with TCZ reduced significantly median CAS by 3 units (p=0.002), TSI levels by 11.02 IU/L (p=0.006), Hertel score on the right eye by 2.3 mm (p=0.003), Hertel score on the left eye by 1.6 mm (p=0.002), while diplopia persisted in fewer patients (25%) after treatment with TCZ (not statistically significant, p=0.250). After treatment with TCZ, there was a radiological improvement in 75% of patients, while 16.7% showed no response, and in 8.3% of patients deterioration was established.
Tocilizumab appears to be a safe and cost effective therapeutic option for patients with active, corticosteroid-resistant, moderate to severe Graves' orbitopathy.
格雷夫斯眼病(GO)是一种影响眼眶脂肪和肌肉的自身免疫性疾病。IL-6 在 GO 的发病机制中具有重要作用,已有研究表明靶向 IL-6R 的 IL-6 抑制剂托珠单抗(TCZ)已在一些患者中使用。本病例研究的目的是评估 TCZ 在对皮质类固醇治疗无反应的患者中的治疗效果。
我们对中重度 GO 患者进行了一项观察性研究。12 例患者接受 TCZ 静脉输注,剂量为 8mg/kg,每 28 天一次,共 4 个月,并在最后一次 TCZ 剂量后额外随访 6 周。主要结局是在最后一次 TCZ 剂量后 6 周,CAS 至少改善 2 分。次要结局包括 TCZ 最后一次剂量后 6 周时 CAS <3(无活动疾病)、TSI 水平降低、突眼度增加>2mm 和复视反应。
所有患者在治疗后 6 周达到主要结局。此外,所有患者在治疗停止后 6 周时均无疾病活动。TCZ 治疗可显著降低 CAS 中位数 3 分(p=0.002)、TSI 水平 11.02 IU/L(p=0.006)、右眼 Hertel 评分 2.3mm(p=0.003)、左眼 Hertel 评分 1.6mm(p=0.002),而在 TCZ 治疗后,复视患者减少(25%,但无统计学意义,p=0.250)。TCZ 治疗后,75%的患者影像学改善,16.7%无反应,8.3%的患者病情恶化。
TCZ 似乎是治疗活动期、皮质类固醇耐药、中重度格雷夫斯眼病患者的安全且经济有效的治疗选择。