Defining and characterizing sustained remission in patients with rheumatoid arthritis

被引:0
作者
Jeffrey R. Curtis
Mona Trivedi
Boulos Haraoui
Paul Emery
Grace S. Park
David H. Collier
Girish A. Aras
James Chung
机构
[1] University of Alabama at Birmingham,Leeds Institute of Rheumatic and Musculoskeletal Medicine
[2] Amgen Inc.,undefined
[3] Centre Hospitalier de l’Université de Montréal,undefined
[4] University of Leeds,undefined
[5] Chapel Allerton Hospital,undefined
[6] NIHR Leeds Biomedical Research Centre,undefined
[7] Leeds Teaching Hospitals NHS Trust,undefined
来源
Clinical Rheumatology | 2018年 / 37卷
关键词
Etanercept; Methotrexate; Remission; Rheumatoid arthritis;
D O I
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学科分类号
摘要
The objective of this study is to characterize stability and clinical features of patients with rheumatoid arthritis (RA) in sustained remission. Combination therapy with methotrexate and tumor necrosis factor inhibitors (TNFi) has increased remission rates in RA but optimal regimens to maintain remission are unknown. We describe Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subjects with Rheumatoid Arthritis (SEAM-RA) and data from a run-in period of longitudinal observation. Patients in Simplified Disease Activity Index (SDAI) remission (score ≤ 3.3) receiving etanercept and methotrexate were screened and had to maintain remission over 3 run-in visits/24 weeks before randomization to combination therapy or withdrawal of etanercept or methotrexate. Baseline characteristics were examined for predictive factors for maintaining remission. As of November 2016, 141 patients have enrolled; of these, 64 have been randomized, 34 were ineligible after run-in, and 43 are in run-in period; 70% have completed run-in. Enrolled and randomized patients, respectively, had mean (standard deviation [SD]) disease duration 11.0 (8.6) and 12.6 (9.7) years; mean (SD) duration of etanercept use 4.2 (3.8) and 4.9 (4.2) years; mean (SD) methotrexate dose 15.9 (4.8) and 15.5 (4.9) mg/week; and mean (SD) SDAI scores 1.5 (0.9) and 1.4 (0.8). At enrollment, 73% and 63% were in Boolean remission based on 28 joints and 66/68 joints, respectively. No enrollment characteristic predicted successful completion of run-in. Two-thirds of patients considered to be in remission at enrollment sustained remission through 24 weeks. Baseline characteristics of enrolled patients and those who completed run-in were comparable.
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页码:885 / 893
页数:8
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  • [1] Smolen JS(2014)EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update Ann Rheum Dis 73 492-509
  • [2] Landewe R(2011)American College of Rheumatology/European League Against Rheumatism provisional definition of remission in rheumatoid arthritis for clinical trials Ann Rheum Dis 70 404-413
  • [3] Breedveld FC(2016)Impact of sustained remission on risk for infection in patients with rheumatoid arthritis enrolled in a US registry [abstract OP0259] Ann Rheum Dis 75 156-1249
  • [4] Buch M(2014)Remission in rheumatoid arthritis: benefit over low disease activity in patient-reported outcomes and costs Arthritis Res Ther 16 R56-2035
  • [5] Burmester G(2009)Rheumatoid arthritis joint progression in sustained remission is determined by disease activity levels preceding the period of radiographic assessment Arthritis Rheum 60 1242-2139
  • [6] Dougados M(2013)Is it possible to withdraw biologics from therapy in rheumatoid arthritis? Clin Ther 35 2028-2022
  • [7] Emery P(2013)Systematic review of tumor necrosis factor inhibitor discontinuation studies in rheumatoid arthritis Clin Ther 35 2129-565
  • [8] Gaujoux-Viala C(2014)Intensive intervention can lead to a treatment holiday from biological DMARDs in patients with rheumatoid arthritis Drugs 74 2012-929
  • [9] Gossec L(2016)Induction maintenance with tumour necrosis factor-inhibitor combination therapy with discontinuation versus methotrexate monotherapy in early rheumatoid arthritis: a systematic review and meta-analysis of efficacy in randomised controlled trials RMD Open 2 550-A435
  • [10] Nam J(2015)Flare rate in patients with rheumatoid arthritis in low disease activity or remission when tapering or stopping synthetic or biologic DMARD: a systematic review J Rheumatol 42 S1077-2151