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Intravenous tocilizumab improves clinical activity in moderate-to-severe thyroid eye disease patients.

Intravenous tocilizumab improves clinical activity in moderate-to-severe thyroid eye disease patient…
Photo by César Badilla Miranda / Unsplash
Key Takeaway
Consider intravenous tocilizumab for moderate-to-severe thyroid eye disease based on preliminary single-center evidence.

A retrospective cohort study was conducted at Beijing Tongren Hospital involving 234 patients with moderate-to-severe thyroid eye disease. The intervention consisted of intravenous tocilizumab administered at 8 mg/kg every 4 weeks. No comparator group was reported, and follow-up duration was not reported.

Treatment response was defined as a reduction in Clinical Activity Score (CAS) of ≥2 points from baseline. The CAS decreased from 3.42 ± 0.61 to 1.70 ± 0.67 (P < 0.001). Additionally, TRAb levels declined from 10.35 ± 11.99 IU/L to 4.46 ± 6.73 IU/L (P < 0.001). Among responders, fibrinogen, HDL-cholesterol, and disease duration showed specific changes, with a responder rate of 155 of 234 patients (66.2%).

Multivariate analysis identified shorter disease duration (OR = 0.962 per month; 95% CI 0.928–0.998, P = 0.038), higher TRAb (OR = 1.036 per IU/L; 95% CI 1.004–1.068, P = 0.025), higher fibrinogen (OR = 1.869 per g/L; 95% CI 1.097–3.184, P = 0.021), and higher HDL-C (OR = 2.665 per mmol/L; 95% CI 1.175–6.041, P = 0.019) as predictive factors. The composite model AUC was 0.695 (95% CI 0.625–0.765, P < 0.001). Safety data, including adverse events and tolerability, were not reported.

Limitations include the single-center setting and retrospective nature of the data. The study offers a preliminary framework to inform patient selection but does not establish causality or long-term safety.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundTocilizumab (TCZ), an interleukin-6 receptor antagonist, is recommended as a second-line therapy for thyroid eye disease (TED), yet the clinical determinants of treatment response remain poorly defined. Identifying reliable predictors of response is essential for patient selection and precision use.MethodsWe conducted a single-center retrospective cohort study of 234 patients with moderate-to-severe TED treated with intravenous TCZ (8 mg/kg every 4 weeks) at Beijing Tongren Hospital from January 2023 to December 2025. Treatment response was defined as a reduction in Clinical Activity Score (CAS) of ≥2 points from baseline. Candidate predictors were entered into a multivariate binary logistic regression. ROC analysis identified optimal cut-off values.ResultsFollowing TCZ treatment, CAS decreased significantly from 3.42 ± 0.61 to 1.70 ± 0.67 (P < 0.001), and TRAb declined from 10.35 ± 11.99 IU/L to 4.46 ± 6.73 IU/L (P < 0.001). Of 234 patients with complete paired data, 155 (66.2%) were Responders. Responders had higher TRAb (12.17 vs. 7.07 IU/L), fibrinogen (FIB; 2.83 vs. 2.58 g/L), and HDL-cholesterol (HDL-C; 1.37 vs. 1.24 mmol/L), and shorter disease duration (7.91 vs. 10.08 months; all P < 0.05). Multivariate analysis identified four independent predictors: shorter disease duration (OR = 0.962 per month, 95% CI 0.928–0.998, P = 0.038), higher TRAb (OR = 1.036 per IU/L, 95% CI 1.004–1.068, P = 0.025), higher FIB (OR = 1.869 per g/L, 95% CI 1.097–3.184, P = 0.021), and higher HDL-C (OR = 2.665 per mmol/L, 95% CI 1.175–6.041, P = 0.019). The composite model achieved AUC = 0.695 (95% CI 0.625–0.765, P < 0.001).ConclusionsTCZ produces clinically meaningful and multi-dimensionally validated response with moderate-to-severe TED. Shorter disease duration, higher baseline TRAb, FIB, and HDL-C independently predict response, offering a preliminary framework to inform patient selection. These findings provide the largest real-world evidence to date for guiding precision use of TCZ in TED.
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