Clinical and Experimental Rheumatology | |
The role of low-dose glucocorticoids for rheumatoid arthritis in the biologic era | |
Monica Todoerti1  Carlomaurizio Montecucco1  Carlo Alberto Scirè1  Roberto Caporali1  | |
关键词: Rheumatoid arthritis; glucocorticoid; biologics; remission; discontinuation; Discontinuation of therapy; rheumatoid arthritis; glucocorticoids; | |
DOI : | |
学科分类:医学(综合) | |
来源: Pacini Editore SpA | |
【 摘 要 】
In rheumatoid arthritis (RA), low-dose glucocorticoid (GC) therapy has a well-established effect on disease activity. Particularly in early RA, robust evidence demonstrates that GC treatment in association with standard disease-modifying anti-rheumatic drugs (DMARDs) is effective in inducing high remission rates, earlier and more persistently. Despite international recommendations that discourage long-term concomitant GC use, the majority of the clinical trials and observational registries on biologic agents include a high proportion (up to 80%) of patients in treatment with GC. From an analysis of the literature, a substantial lack of reliable information about the efficacy of GC in association with biologic agents emerges; in particular, the role of GC co-therapy in sustaining remission after biological therapy discontinuation remains to be clarified. Given the increasing prevalence of patients in sustained remission, a rational discontinuation strategy should include low-dose GCs in the experimental design to elucidate their role in inducing and maintaining biologic-free remission, for efficacy, safety and pharmacoeconomic considerations.
【 授权许可】
Unknown
【 预 览 】
Files | Size | Format | View |
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RO201912020417485ZK.pdf | 312KB | download |