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1
The immunogenicity, safety, and efficacy of etanercept liquid administered once weekly in patients with rheumatoid arthritis.类风湿关节炎患者每周一次注射用依那西普溶液的免疫原性、安全性及疗效。
Clin Exp Rheumatol. 2007 Jan-Feb;25(1):40-6.
2
The incidence of new onset congestive heart failure and heart failure exacerbation in Veteran's Affairs patients receiving tumor necrosis factor alpha antagonists.在接受肿瘤坏死因子α拮抗剂治疗的退伍军人事务部患者中,新发充血性心力衰竭和心力衰竭加重的发生率。
Rheumatol Int. 2007 Feb;27(4):369-73. doi: 10.1007/s00296-006-0215-3. Epub 2006 Oct 7.
3
Increased unrecognized coronary heart disease and sudden deaths in rheumatoid arthritis: a population-based cohort study.类风湿关节炎患者中未被识别的冠心病和猝死增加:一项基于人群的队列研究。
Arthritis Rheum. 2005 Feb;52(2):402-11. doi: 10.1002/art.20853.
4
Demyelination and inhibition of tumor necrosis factor (TNF).脱髓鞘与肿瘤坏死因子(TNF)的抑制
Clin Exp Rheumatol. 2004 Sep-Oct;22(5 Suppl 35):S134-40.
5
Benefit/risk of therapies for rheumatoid arthritis: underestimation of the "side effects" or risks of RA leads to underestimation of the benefit/risk of therapies.类风湿关节炎治疗的获益/风险:对类风湿关节炎“副作用”或风险的低估导致对治疗获益/风险的低估。
Clin Exp Rheumatol. 2004 Sep-Oct;22(5 Suppl 35):S2-11.
6
Considerations with the use of biological therapy in the treatment of rheumatoid arthritis.类风湿关节炎治疗中使用生物疗法的注意事项。
Expert Opin Drug Saf. 2004 Sep;3(5):391-403. doi: 10.1517/14740338.3.5.391.
7
Etanercept treatment of psoriatic arthritis: safety, efficacy, and effect on disease progression.依那西普治疗银屑病关节炎:安全性、疗效及对疾病进展的影响。
Arthritis Rheum. 2004 Jul;50(7):2264-72. doi: 10.1002/art.20335.
8
Lymphoma in rheumatoid arthritis: the effect of methotrexate and anti-tumor necrosis factor therapy in 18,572 patients.类风湿关节炎中的淋巴瘤:甲氨蝶呤和抗肿瘤坏死因子治疗对18572例患者的影响。
Arthritis Rheum. 2004 Jun;50(6):1740-51. doi: 10.1002/art.20311.
9
Drugs that block tumour necrosis factor: experience in patients with rheumatoid arthritis.阻断肿瘤坏死因子的药物:类风湿关节炎患者的用药经验
Pharmacoeconomics. 2004;22(2 Suppl 1):39-53. doi: 10.2165/00019053-200422001-00005.
10
Epidemiology and burden of illness of rheumatoid arthritis.类风湿关节炎的流行病学与疾病负担
Pharmacoeconomics. 2004;22(2 Suppl 1):1-12. doi: 10.2165/00019053-200422001-00002.

依那西普在老年风湿性疾病患者中的长期安全性。

Long term safety of etanercept in elderly subjects with rheumatic diseases.

作者信息

Fleischmann R, Baumgartner S W, Weisman M H, Liu T, White B, Peloso P

机构信息

University of Texas Southwestern Medical Center at Dallas, 5939 Harry Hines Boulevard, Dallas, Texas 75235, USA.

出版信息

Ann Rheum Dis. 2006 Mar;65(3):379-84. doi: 10.1136/ard.2005.035287. Epub 2005 Sep 8.

DOI:10.1136/ard.2005.035287
PMID:16150792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1798057/
Abstract

OBJECTIVES

To determine the long term safety profile of the tumour necrosis factor (TNF) antagonist etanercept in subjects with rheumatoid arthritis (RA), psoriatic arthritis (PsA), or ankylosing spondylitis (AS) aged > or =65 years in comparison with subjects aged <65 years.

METHODS

Safety data from an integrated database of 4322 subjects enrolled in 18 RA trials, 2 PsA trials, and 2 AS trials were analysed. Safety end points included subject incidence of all adverse events (AE), serious adverse events (SAE), infectious events (IE), medically important infections (MII), and deaths. Events of particular interest in subjects treated with TNF modulating biological treatments, including demyelinating diseases, tuberculosis, lymphomas, and cardiovascular diseases, were also evaluated.

RESULTS

The incidence of AE, SAE, IE, MII, and malignancies was not significantly raised in elderly subjects in comparison with subjects aged <65 years. No cases of tuberculosis were reported in the trials. Demyelinating diseases were seen only in subjects aged <65 years. The incidence and types of death in the elderly subjects were consistent with the expected rates for subjects of comparable age.

CONCLUSIONS

Etanercept is a generally safe and well tolerated biological agent for treatment of rheumatological diseases in the elderly, and the risk of AE in these studies was no greater in subjects aged > or =65 years than in younger subjects.

摘要

目的

比较年龄≥65岁的类风湿关节炎(RA)、银屑病关节炎(PsA)或强直性脊柱炎(AS)患者与年龄<65岁的患者使用肿瘤坏死因子(TNF)拮抗剂依那西普的长期安全性。

方法

分析了来自18项RA试验、2项PsA试验和2项AS试验的4322名受试者综合数据库的安全性数据。安全性终点包括所有不良事件(AE)、严重不良事件(SAE)、感染事件(IE)、具有重要医学意义的感染(MII)和死亡的受试者发生率。还评估了接受TNF调节生物治疗的受试者特别关注的事件,包括脱髓鞘疾病、结核病、淋巴瘤和心血管疾病。

结果

与年龄<65岁的受试者相比,老年受试者中AE、SAE、IE、MII和恶性肿瘤的发生率没有显著升高。试验中未报告结核病病例。脱髓鞘疾病仅在年龄<65岁的受试者中出现。老年受试者的死亡率和死亡类型与同龄受试者的预期发生率一致。

结论

依那西普是一种用于治疗老年风湿性疾病的总体安全且耐受性良好的生物制剂,在这些研究中,年龄≥65岁的受试者发生AE的风险并不高于年轻受试者。