Tocilizumab combined with short-term high-dose glucocorticoids for rapid disease activity control and glucocorticoid reduction in adult-onset Still’s disease: a single-center retrospective study

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Authors: Shi-Lei Zhong, Yan-Ping Lei, Li-Xuan Zhou, Ai-xia Niu, Bo Liu, Yonglong He, Qi-Bin Yang
Cited by: 0
References: 35

Abstract

Objectives This study aimed to evaluate the effectiveness of tocilizumab (TCZ) combined with short-term high-dose glucocorticoids in rapidly controlling disease activity and reducing glucocorticoid use in patients with adult-onset Still’s disease (AOSD). Methods In this single-center retrospective study, all patients meeting the inclusion criteria were enrolled. Patients receiving short-term high-dose glucocorticoids (5 mg/kg/day for 3 days) with TCZ (400 mg every 4 weeks) were assigned to the TCZ group, while those receiving standard-dose glucocorticoids (1 mg/kg/day) without TCZ formed the non-TCZ group. Efficacy was evaluated based on laboratory data, clinical and Pouchot scores. Glucocorticoids -retention rate was estimated by the Kaplan-Meier method. Results Fifty patients (11 men, 39 women) were included (19 in the TCZ group and 31 in the non-TCZ group). The TCZ group had a higher incidence of skin rash (100% vs 58.1%, P = 0.003) and sore throat (84.2% vs 29.0%, P < 0.001). Over the follow-up period, inflammatory markers (CRP, ESR, SF), liver enzymes (AST, ALT), and WBC counts significantly declined in the TCZ group ( P < 0.05). Remission rates were higher in the TCZ group at months 1 (63.2% vs 9.7%), 3 (88.9% vs 20.0%), and 6 (83.3% vs 25.9%) ( P < 0.001). Despite a higher initial glucocorticoid dose, no significant differences in subsequent doses were observed between groups. By 36 months, the TCZ group showed a significantly higher glucocorticoid discontinuation rate (77.0% vs 30.9%, P = 0.0046). TCZ treatment was also associated with improved liver function indicators and reduced liver injury (10.5% vs 32.3%). Conclusion Tocilizumab combined with short-term high-dose glucocorticoids may provide rapid disease control and facilitate glucocorticoid tapering in AOSD. More prospective studies are needed to confirm these findings.

Fields of Study & Subjects

Autoimmune and Inflammatory Disorders Research Kawasaki Disease and Coronary Complications Rheumatoid Arthritis Research and Therapies

Publication details

Journal / source
Frontiers in Immunology
Volume
17
Pages
1732826–1732826
Publication date
5 February 2026
Language
EN