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类风湿关节炎病情得到控制的患者能否从靶向治疗中逐渐减少甲氨蝶呤用量并维持病情缓解?一项系统评价和荟萃分析。

Can Patients With Controlled Rheumatoid Arthritis Taper Methotrexate From Targeted Therapy and Sustain Remission? A Systematic Review and Metaanalysis.

作者信息

Meng Charis F, Rajesh Diviya A, Jannat-Khah Deanna P, Jivanelli Bridget, Bykerk Vivian P

机构信息

C.F. Meng MD, V.P. Bykerk, MD, Division of Rheumatology, Hospital for Special Surgery, and Department of Medicine, Weill Cornell Medical College.

D.A. Rajesh, BA, Division of Rheumatology, Hospital for Special Surgery.

出版信息

J Rheumatol. 2023 Jan;50(1):36-47. doi: 10.3899/jrheum.220152. Epub 2022 Aug 15.

Abstract

OBJECTIVE

To determine the risk of not being able to sustain remission after tapering methotrexate (MTX) from targeted therapy in patients with controlled rheumatoid arthritis (RA).

METHODS

A systematic literature search was conducted in MEDLINE, Embase, and the Cochrane Library for studies reporting remission outcomes after tapering MTX from targeted therapies in RA. Full-text articles and abstracts reported in English were included. Metaanalyses were conducted using random-effects models. Forest and funnel plots were created.

RESULTS

A total of 10 articles were included. Studies evaluated MTX being tapered from combination treatment with tumor necrosis factor inhibitors, tocilizumab, abatacept, and tofacitinib. A total of 9 studies used a randomized design and 1 was observational. Out of 10 studies, 3 focused on early RA (ie, < 1 yr). The MTX-tapering strategy was gradual in 2 studies and rapid in 8 studies. Follow-up ranged from 3 to 18 months in randomized trials and up to 3 years in the observational study. Our metaanalysis, which included 2000 participants with RA from 10 studies, showed that patients who tapered MTX from targeted therapy had a 10% reduction in the ability to sustain remission and an overall pooled risk ratio of 0.90 (95% CI 0.84-0.97). There was no heterogeneity ( = 0%, = 0.94). Our funnel plot indicated minimal publication bias.

CONCLUSION

Patients with controlled RA may taper MTX from targeted therapy with a 10% reduction in the ability to sustain remission for up to 18 months. Longer follow-up studies with attention to radiographic, functional, and patient-reported outcomes are needed. The risk of disease worsening should be discussed with the patient with careful follow-up and prompt retreatment of disease worsening.

摘要

目的

确定类风湿关节炎(RA)病情得到控制的患者在从靶向治疗中逐渐减少甲氨蝶呤(MTX)用量后无法维持病情缓解的风险。

方法

在MEDLINE、Embase和Cochrane图书馆进行系统文献检索,查找关于RA患者从靶向治疗中逐渐减少MTX用量后缓解结局的研究。纳入以英文报道的全文文章和摘要。采用随机效应模型进行荟萃分析。绘制森林图和漏斗图。

结果

共纳入10篇文章。研究评估了MTX从与肿瘤坏死因子抑制剂、托珠单抗、阿巴西普和托法替布联合治疗中逐渐减量的情况。共有9项研究采用随机设计,1项为观察性研究。在10项研究中,3项关注早期RA(即<1年)。2项研究中MTX逐渐减量策略为逐渐减量,8项研究为快速减量。随机试验的随访时间为3至18个月,观察性研究的随访时间长达3年。我们的荟萃分析纳入了10项研究中的2000例RA患者,结果显示从靶向治疗中逐渐减少MTX用量的患者维持缓解的能力降低了10%,总体合并风险比为0.90(95%CI 0.84 - 0.97)。无异质性(I² = 0%,P = 0.94)。我们的漏斗图显示发表偏倚最小。

结论

病情得到控制的RA患者从靶向治疗中逐渐减少MTX用量时,维持缓解的能力可能降低10%,长达18个月。需要进行更长时间的随访研究,并关注影像学、功能和患者报告的结局。应与患者讨论疾病恶化的风险,并进行仔细随访,一旦疾病恶化应及时重新治疗。

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