Glucocorticoids in the treatment of IgG4-related disease-Prospects for new international treatment guidelines

被引:17
作者
Yoshifuji, Hajime [1 ]
Umehara, Hisanori [2 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Rheumatol & Clin Immunol, Kyoto, Japan
[2] Nagahama City Hosp, Ctr RA & Autoimmune Dis, Nagahama, Shiga, Japan
关键词
IgG4-related disease; glucocorticoids; mycophenolate mofetil; leflunomide; rituximab; AUTOIMMUNE PANCREATITIS; RELAPSE; THERAPY; DACRYOADENITIS; INTERVENTION; SIALADENITIS; PREDICTORS; INDUCTION; RITUXIMAB; EFFICACY;
D O I
10.1093/mr/roac097
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immunoglobulin G4-related disease (IgG4-RD) is a chronic fibro-inflammatory disease that may cause dysfunction in various organs. Worldwide multidisciplinary experts attending the Fourth International Symposium on IgG4-Related Disease in Japan in 2021 discussed treatments for IgG4-RD, especially glucocorticoid (GC) therapy. This review describes the efficacy, safety, and cost of treatments for IgG4-RD based on findings presented at the international symposium. A medium dose of GC was considered appropriate for the initial treatment of IgG4-RD. A randomized controlled trial and an open-label prospective study have shown that long-term maintenance GC therapy (prednisolone >= 5 mg/day) could prevent disease relapse. In addition, two open-label randomized controlled trials reported the effects of combinational use of GC and synthetic immunosuppressive agents, mycophenolate mofetil and leflunomide, on relapse prevention. Moreover, an open-label single-arm study showed an excellent rate of clinical response to rituximab. Many observational studies have shown the efficacy of an appropriate GC regimen in patients with IgG4-RD. Synthetic immunosuppressive agents and a molecular-targeted agent can be potent alternatives to GCs, but additional studies are required comparing their efficacy, risk of infection, and costs.
引用
收藏
页码:252 / 257
页数:6
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