Reduction of biologics in rheumatoid arthritis: a systematic review and meta-analysis

被引:11
作者
Vasconcelos, Leticia B. [1 ]
Silva, Marcus T. [2 ]
Galvao, Tais F. [1 ]
机构
[1] Univ Estadual Campinas, Sch Pharmaceut Sci, R Candido Portinari 200,Cidade Univ Zeferino Vaz, BR-13083871 Campinas, SP, Brazil
[2] Univ Sorocaba, Rod Raposo Tavares,Km 92-5, BR-18023000 Sorocaba, SP, Brazil
关键词
Rheumatoid arthritis; Antirheumatic agents; Biological products; Remission induction; Systematic review; Meta-analysis; LOW DISEASE-ACTIVITY; EMPIRICAL-EVIDENCE; NON-INFERIORITY; DOSE REDUCTION; OPEN-LABEL; REMISSION; DISCONTINUATION; WITHDRAWAL; OUTCOMES; THERAPY;
D O I
10.1007/s00296-020-04651-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effects of dose reduction or spacing of all types of biologics in rheumatoid arthritis has not been consistently assessed in systematic reviews. We aimed to assess the effects of biologics reduction compared with dose maintenance in patients with rheumatoid arthritis in low disease activity or remission. We performed a systematic review with meta-analysis according to a previously registered protocol (PROSPERO registration: CRD42017069080); and searched MEDLINE, Embase, Scopus, Cochrane Library and trial registers up to July, 2020. Two researchers selected, extracted and assessed the risk of bias of controlled trials that randomized patients to reduction/spacing or dose maintenance of biologics. Low disease activity, disability and other clinically important outcomes were summarized in random effect meta-analyses. We rated the certainty of evidence according to the Grading of Recommendations Assessment, Development, and Evaluation approach. We included ten studies (n = 1331 patients), which assessed reduction or spacing of abatacept, adalimumab, certolizumab pegol, etanercept, or tocilizumab. Risk of bias was high in over half of trials, mainly due to lack of blinding. No statistically significant difference was found in low disease activity (RR = 0.90; 95% CI 0.78-1.04;I-2 = 60%, very low certainty), and other outcomes. Subgroup analysis of blinded studies led to homogeneous results, which remained heterogeneous in open-label studies. Reduction or spacing biologics did not affect disease activity and other important outcome. Changes in the doses regimen should consider patient preferences, considering the low certainty of evidence.
引用
收藏
页码:1949 / 1959
页数:11
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