Certolizumab pegol in rheumatoid arthritis: current update

被引:11
|
作者
Fechtenbaum, Marie [1 ,2 ]
Yusof, Md Yuzaiful Md [1 ,2 ]
Emery, Paul [1 ,2 ]
机构
[1] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Chapel Allerton Hosp, Leeds LS7 4SA, W Yorkshire, England
[2] Leeds Teaching Hosp NHS Trust, NIHR Leeds Musculoskeletal Biomed Res Unit, Leeds, W Yorkshire, England
关键词
anti-TNF; biological therapy; certolizumab; PEGylation; rheumatoid arthritis; ANTITUMOR-NECROSIS-FACTOR; PATIENT-REPORTED OUTCOMES; POST-HOC ANALYSIS; LONG-TERM SAFETY; PLUS METHOTREXATE; PHASE IIIB; TNF RECEPTORS; DOUBLE-BLIND; EFFICACY; ADALIMUMAB;
D O I
10.1517/14712598.2014.900043
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: The development of TNF-alpha inhibitors (TNF-is) represents a major advancement in the treatment of rheumatoid arthritis (RA). Currently, there are five agents licensed for moderate--to-severely active RA. Certolizumab pegol (CZP) is a novel PEGylated, constant fragment-free TNF-i therapy, which is the focus of this review. Areas covered: Data from Phase III randomised controlled trials in terms of clinical efficacy, radiographic progression, patient-reported outcomes and safety profile are reviewed. These include long-term data from open-label extension studies. Expert opinion: The advantages of CZP include rapid reduction of disease activity, low rates of injection-site reaction and may be safe for use in pregnancy. The long-term data strengthen the position of CZP for use either as monotherapy or preferably in combination with disease modifying anti-rheumatic drugs (DMARDs), in moderate-to-severely active RA, comparable to other TNF-is. Notably, prolonged CZP exposure is not associated with increased risk of severe infection compared to general population, contrasting with preliminary analysis of short-term data. Over the next few years, evidence will be available on the use of CZP in combination with methotrexate for remission induction in DMARD-nayve patients, biomarkers and the development and licensing of TNF-i biosimilars.
引用
收藏
页码:841 / 850
页数:10
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