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

被引:14
作者
Emamikia, Sharzad [1 ]
Arkema, Elizabeth V. [2 ]
Gyori, Noemi [1 ]
Detert, Jacqueline [3 ]
Chatzidionysiou, Katerina [1 ]
Dougados, Maxime [4 ]
Burmester, Gerd Ruediger [3 ]
van Vollenhoven, Ronald [1 ,5 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp, CIinTRID, Dept Med, Solna, Sweden
[2] Karolinska Inst, Clin Epidemiol Unit, Stockholm, Sweden
[3] Charite, Inst Clin Immunol & Rheumatol, Berlin, Germany
[4] Paris Descartes Univ, Hop Cochin, AP HP,Dept Rheumatol,PRES Sorbonne Paris Cite, INSERM,U1153,Clin Epidemiol & Biostat, Paris, France
[5] Acad Med Ctr, Dept Clin Immunol & Rheumatol, Amsterdam, Netherlands
关键词
D O I
10.1136/rmdopen-2016-000323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine whether an inductionmaintenance strategy of combined therapy (methotrexate (MTX)+tumour necrosis factor (TNF) inhibitor (TNFi)) followed by withdrawal of TNFi could yield better long-term results than a strategy with MTX monotherapy, since it is unclear if the benefits from an induction phase with combined therapy are sustained if TNFi is withdrawn. Methods: We performed a meta-analysis of trials using the initial combination of MTX+TNFi in conventional synthetic disease-modifying antirheumatic drug-naive patients with early rheumatoid arthritis (RA). A systematic literature search was performed for induction-maintenance randomised controlled trials (RCTs) where initial combination therapy was compared with MTX monotherapy in patients with clinically active early RA. Our primary outcome was the proportion of patients who achieved low disease activity (LDA; Disease Activity Score (DAS) 28<3.2) and/or remission (DAS28<2.6) at 12-76 weeks of follow-up. A random-effects model was used to pool the risk ratio (RR) for LDA and remission and heterogeneity was explored by subgroup analyses. Results: We identified 6 published RCTs, 4 of them where MTX+adalimumab was given as initial therapy and where adalimumab was withdrawn in a subset of patients after LDA/remission had been achieved. 2 additional trials used MTX+infliximab as combination therapy. The pooled RRs for achieving LDA and clinical remission at follow-up after withdrawal of TNFi were 1.41 (95% CI 1.05 to 1.89) and 1.34 (95% CI 0.95 to 1.89), respectively. There was significant heterogeneity between trials due to different treatment strategies, which was a limitation to this study. Conclusions: Initial therapy with MTX+TNFi is associated with a higher chance of retaining LDA and/or remission even after discontinuation of TNFi.
引用
收藏
页数:10
相关论文
共 40 条
[1]  
Allaart CF, 2013, CLIN EXP RHEUMATOL, V31, pS14
[2]  
Anderson JJ, 2000, ARTHRITIS RHEUM, V43, P22, DOI 10.1002/1529-0131(200001)43:1<22::AID-ANR4>3.0.CO
[3]  
2-9
[4]   Methotrexate and Rheumatoid Arthritis: Current Evidence Regarding Subcutaneous Versus Oral Routes of Administration [J].
Bianchi, Gerolamo ;
Caporali, Roberto ;
Todoerti, Monica ;
Mattana, Paolo .
ADVANCES IN THERAPY, 2016, 33 (03) :369-378
[5]   The PREMIER study - A multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment [J].
Breedveld, FC ;
Weisman, MH ;
Kavanaugh, AF ;
Cohen, SB ;
Pavelka, K ;
van Vollenhoven, R ;
Sharp, J ;
Perez, JL ;
Spencer-Green, GT .
ARTHRITIS AND RHEUMATISM, 2006, 54 (01) :26-37
[6]   When to initiate and discontinue biologic treatments for rheumatoid arthritis? [J].
Chatzidionysiou, K. ;
van Vollenhoven, R. F. .
JOURNAL OF INTERNAL MEDICINE, 2011, 269 (06) :614-625
[7]   Combination of infliximab and methotrexate therapy for early rheumatoid arthritis - A randomized, controlled trial [J].
Clair, EWS ;
van der Heijde, DMFM ;
Smolen, JS ;
Maini, RN ;
Bathon, JM ;
Emery, P ;
Keystone, E ;
Schiff, M ;
Kalden, JR ;
Wang, B ;
DeWoody, K ;
Weiss, R ;
Baker, D .
ARTHRITIS AND RHEUMATISM, 2004, 50 (11) :3432-3443
[8]   Treatment Strategies in Early Rheumatoid Arthritis and Prevention of Rheumatoid Arthritis [J].
Demoruelle, M. Kristen ;
Deane, Kevin D. .
CURRENT RHEUMATOLOGY REPORTS, 2012, 14 (05) :472-480
[9]   Induction therapy with adalimumab plus methotrexate for 24 weeks followed by methotrexate monotherapy up to week 48 versus methotrexate therapy alone for DMARD-naive patients with early rheumatoid arthritis: HIT HARD, an investigator-initiated study [J].
Detert, Jacqueline ;
Bastian, Hans ;
Listing, Joachim ;
Weiss, Anja ;
Wassenberg, Siegfried ;
Liebhaber, Anke ;
Rockwitz, Karin ;
Alten, Rieke ;
Krueger, Klaus ;
Rau, Rolf ;
Simon, Christina ;
Gremmelsbacher, Eva ;
Braun, Tanja ;
Marsmann, Bettina ;
Hoehne-Zimmer, Vera ;
Egerer, Karl ;
Buttgereit, Frank ;
Burmester, Gerd-R .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (06) :844-850
[10]   Methotrexate dosage as a source of bias in biological trials in rheumatoid arthritis: a systematic review [J].
Duran, Josefina ;
Bockorny, Margarita ;
Dalal, Deepan ;
LaValley, Michael ;
Felson, David T. .
ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 (09) :1595-1598