Risk of infection with biologic antirheumatic therapies in patients with rheumatoid arthritis

被引:71
作者
Lahiri, Manjari [1 ,2 ]
Dixon, William G. [3 ]
机构
[1] Natl Univ Hlth Syst, Univ Med Cluster, Div Rheumatol, Singapore, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore 117595, Singapore
[3] Univ Manchester, Arthrit Res UK Ctr Epidemiol, Manchester Acad Hlth Sci Ctr, Manchester M13 9PT, Lancs, England
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2015年 / 29卷 / 02期
关键词
Rheumatoid arthritis; Biological therapy; Infection; NECROSIS-FACTOR-ALPHA; LONG-TERM SAFETY; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; ANTI-TNF THERAPY; INTERLEUKIN-6 RECEPTOR INHIBITION; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RITUXIMAB PLUS METHOTREXATE; RANDOMIZED CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; EVERY; WEEKS;
D O I
10.1016/j.berh.2015.05.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There are currently 10 licensed biologic therapies for the treatment of rheumatoid arthritis in 2014. In this article, we review the risk of serious infection (SI) for biologic therapies. This risk has been closely studied over the last 15 years within randomised controlled trials, long-term extension studies and observational drug registers, especially for the first three antitumour necrosis factor (TNF) drugs, namely infliximab, etanercept and adalimumab. The risk of SI with the newer biologics rituximab, tocilizumab, abatacept and tofacitinib is also reviewed, although further data from long-term observational studies are awaited. Beyond all-site SI, we review the risk of tuberculosis, other opportunistic infections and herpes zoster, and the effect of screening on TB rates. Lastly, we review emerging opportunities for stratifying the risk. Patients can be risk-stratified based on both modifiable and non-modifiable patient characteristics such as age, co-morbidity, glucocorticoid use, functional status and recent previous SI. (c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:290 / 305
页数:16
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