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Defining the optimal biological monotherapy in rheumatoid arthritis: A systematic review and meta-analysis of randomised trials
被引:20
作者:
Tarp, Simon
[1
]
Furst, Daniel E.
[2
]
Dossing, Anna
[1
]
Ostergaard, Mikkel
[3
,4
]
Lorenzen, Tove
[5
]
Hansen, Michael S.
[6
,7
]
Singh, Jasvinder A.
[8
,9
,10
,11
]
Choy, Ernest H.
[12
,13
]
Boers, Maarten
[14
,15
]
Suarez-Almazor, Maria E.
[16
]
Kristensen, Lars E.
[1
]
Bliddal, Henning
[1
]
Christensen, Robin
[1
]
机构:
[1] Bispebjerg & Frederiksberg Hosp, Parker Inst, Musculoskeletal Stat Unit, Copenhagen, Denmark
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[3] Glostrup Cty Hosp, Ctr Rheumatol & Spine Dis, Copenhagen Ctr Arthrit Res, Copenhagen, Denmark
[4] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[5] Silkeborg Reg Hosp, Ctr Diagnost, Dept Rheumatol, Copenhagen, Denmark
[6] ReumaKlin Roskilde, Roskilde, Denmark
[7] Gildhoj Privathosp, Brondby, Denmark
[8] VA Med Ctr, Med Serv, Birmingham, AL USA
[9] VA Med Ctr, Ctr Surg Med Acute Care Res & Transit, Birmingham, AL USA
[10] Univ Alabama Birmingham, Sch Publ Hlth, Div Epidemiol, Dept Med,Sch Med, Birmingham, AL 35294 USA
[11] Mayo Clin, Coll Med, Dept Orthoped Surg, Rochester, MN USA
[12] Arthrit Res UK, Rheumatol Sect, Cardiff, S Glam, Wales
[13] Cardiff Univ, Sch Med, Hlth & Care Res Wales CREATE Ctr, Cardiff, S Glam, Wales
[14] Vrije Univ Amsterdam, Med Ctr, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[15] Vrije Univ Amsterdam, Med Ctr, Amsterdam Rheumatol & Immunol Ctr, Amsterdam, Netherlands
[16] Univ Texas MD Anderson Canc Ctr, Sect Rheumatol & Clin Immunol, Houston, TX 77030 USA
关键词:
Rheumatoid arthritis;
Meta-analysis;
Biological agents;
Systematic review;
MODIFYING ANTIRHEUMATIC DRUGS;
DOUBLE-BLIND;
TOCILIZUMAB MONOTHERAPY;
ADALIMUMAB MONOTHERAPY;
INADEQUATE RESPONSE;
DISEASE-ACTIVITY;
JAK INHIBITOR;
METHOTREXATE;
AGENTS;
RECOMMENDATIONS;
D O I:
10.1016/j.semarthrit.2016.09.003
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives: To summarize and compare the benefits and harms of biological agents used as monotherapy for rheumatoid arthritis (RA) in order to inform decisions for patients who are intolerant to conventional DMARD therapy. Methods: We searched MEDLINE, EMBASE, CENTRAL, and other sources for randomised trials that compared biological monotherapy with methotrexate, placebo, or other biological monotherapies. Primary outcomes were ACR50 and the number of patients who discontinued due to adverse events. Our network meta-analysis was based on mixed-effects logistic regression, including both direct and indirect comparisons of the treatment effects, while preserving the randomised comparisons within each trial. PROSPERO identifier: CRD42012002800. Results: The analysis comprises 28 trials (8602 patients), including all nine biological agents approved for RA. Eight trials included "DMARD-naive", and 20 "DMARD-Inadequate responder" (DMARD-IR) patients. All agents except anakinra and infliximab were superior (p < 0.05) to placebo (i.e., no DMARD treatment) with regard to ACR50. Etanercept and rituximab were superior to anakinra (p = 0.018 and p = 0.049, respectively). Tocilizumab was superior to adalimumab (p = 0.0082), anakinra (p = 0.0083), certolizumab (p = 0.037), and golimumab (p = 0.049). No differences among etanercept, tocilizumab, and rituximab were found (p > 0.52). However, because rituximab was evaluated in just 40 patients, our confidence in the estimates is limited. When including only DMARD-IR trials, the same statistical pattern emerged; in addition etanercept and tocilizumab were superior to abatacept. At recommended doses, both etanercept and tocilizumab were superior to adalimumab and certolizumab. No statistically significant differences among biological agents were found with respect to discontinuation due to adverse events (p > 0.068). Conclusions: Evidence from randomised trials suggests that most biological agents are effective as mono therapy. Although our confidence in the estimates is limited, etanercept or tocilizumab may be the optimal choice for most patients who need treatment with biological monotherapy. However, given our limited confidence in the estimates including possibility of bias, it is appropriate to strongly weight patients' preferences and values in the final treatment choice. (C) 2017 Elsevier Inc. All rights reserved.
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页码:699 / 708
页数:10
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