Association of previous treatment with anti-tumour necrosis factor inhibitors with the effectiveness of secukinumab in the treatment of psoriatic arthritis: systematic review and meta-analysis

被引:1
|
作者
Xu, Yantao [1 ]
Li, Yuting [1 ]
Dong, Mengyuan [1 ]
Gao, Zi'ang [1 ]
Chen, Xiang [1 ,2 ,3 ]
Liu, Hong [1 ,2 ,3 ]
Shen, Minxue [1 ,2 ,3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Dermatol, Changsha, Peoples R China
[2] Cent South Univ, Hunan Engn Res Ctr Skin Hlth & Dis, Changsha, Peoples R China
[3] Cent South Univ, Hunan Key Lab Skin Canc & Psoriasis, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Sch Publ Hlth, Dept Social Med & Hlth Management, 110 Xiangya Rd, Changsha 410008, Peoples R China
基金
中国国家自然科学基金;
关键词
PsA; tumour necrosis factors inhibitor; interleukin-17; inhibitor; secukinumab; switching; PHASE-III; DOUBLE-BLIND; EFFICACY; ADALIMUMAB; THERAPY; MODERATE; SAFETY; PLACEBO; INTERLEUKIN-17A; ETANERCEPT;
D O I
10.1093/rheumatology/keaa449
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. We sought to systematically investigate the effectiveness of secukinumab in psoriatic arthritis (PsA) patients who previously received TNFs inhibitor (TNFi) treatment and those who were TNFi naive. Methods. Databases (PubMed, EMBase and Cochrane library) and ClinicalTrials.gov were searched from inception to 22 May 2020 for randomized control trails and observational studies of secukinumab, with or without a history of previous anti-TNFi treatment, in PsA. Effectiveness data were extracted and combined using a random-effects meta-analysis. The ACR20 and ACR50 (20% and 50% improvement in American College of Rheumatology response criteria) responses were the endpoints. Results. Six randomized controlled trials that reported the effectiveness of secukinumab by previous anti-TNFi treatment were included. Among patients exposed to a prior anti-TNFi treatment (n = 7 38) , 33.7% (249/738) of patients achieved an ACR20 response. In contrast, in the anti-TNFi-ndive group (n = 1 7 54) , 49.8% (873/1754) of patients achieved an ACR20 response. Prior treatment with anti-TNFi was significantly associated with a poorer response to secukinumab compared with the anti-TNFi-naive group with an effect size of 2.09 (95% CI: 1.69, 2.58). Conclusion. Some patients benefit from switching from TNFi to secukinumab, but previous anti-TNFi treatment is associated with poorer effectiveness of secukinumab.
引用
收藏
页码:3657 / 3665
页数:9
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