Efficacy of tocilizumab therapy in Korean patients with adult-onset Still's disease: a multicentre retrospective study of 22 cases

被引:0
作者
Song, S. T. [1 ]
Kim, J. J. [1 ]
Lee, S. [1 ]
Kim, H. A. [2 ]
Lee, E. Y. [3 ]
Shin, K. C. [3 ]
Lee, J. H. [4 ]
Lee, K. H. [5 ]
Choi, S. T. [6 ]
Cha, H. S. [7 ]
Yoo, D. H. [1 ]
机构
[1] Hanyang Univ Hosp Rheumat Dis, Seoul, South Korea
[2] Ajou Univ, Sch Med, Suwon, South Korea
[3] Seoul Natl Univ, Coll Med, Seoul, South Korea
[4] Inje Univ, Ilsan Paik Hosp, Goyang, South Korea
[5] Dongguk Univ, Ilsan Hosp, Goyang, South Korea
[6] Chung Ang Univ, Coll Med, Seoul, South Korea
[7] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Seoul, South Korea
关键词
adult-onset Still's disease; refractory; biological agents; tocilizumab; interleukin; JUVENILE IDIOPATHIC ARTHRITIS; TUMOR-NECROSIS-FACTOR; COLLEGE-OF-RHEUMATOLOGY; RECEPTOR ANTAGONIST; CYTOKINE PROFILES; IL-6; RECEPTOR; DOUBLE-BLIND; INTERLEUKIN-6; ANAKINRA; TRIAL;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To evaluate the efficacy of tocilizumab (TCZ), a monoclonal antibody against the interleukin (IL)-6 receptor, for refractory adult-onset Still's disease (AOSD) in the Korean population. Methods. This retrospective study included 22 Korean patients with refractory AOSD who were given TCZ at one of seven university hospital-based clinics for rheumatic disease. Patients were subdivided into groups according to disease course: monocyclic, systemic polycyclic, and chronic articular. Modified Pouchot scores, including laboratory and clinical findings, were analysed at 6 months and 12 months. Results. TCZ was given at 4-8 mg/kg every 4-5 weeks (8 mglkg every 4-5 weeks in 18 patients, 6 mglkg every 4 weeks in 2, and 4 mglkg every 4 weeks in 2) for 7.5 months (median, IQR: 4.0-12 3). A good response (measured as a decrease of >2 in the modified Pouchot score) was achieved in 50.0% of patients (11 of 22) at 6 months and in 64.3% (9 of 14) at 12 months. The dose of corticosteroid dose was reduced from 11.5 mglday (median, IQR: 10.0-21.3) immediately before TCZ therapy to 7.5 mglday (median, IQR: 5.0-10.0, p=0.002) at 6 months and finally to 6.3 mg/day (median, IQR: 5.0-7.5, p=0.002) at 12 months. Only one patient discontinued TCZ treatment due to facial swelling accompanied by high blood pressure. In all others, adverse events subsided with delayed TCZ therapy, and TCZ therapy was continued successfully without problems. Conclusion. TCZ was effective for treating Korean AOSD patients who were refractory to conventional therapy or other anti-cytokine biologics, showing a corticosteroid-sparing effect and an acceptable tolerance profile.
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页码:S64 / S71
页数:8
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