Risk of serious infection in biological treatment of patients with rheumatoid arthritis: a systematic review and meta-analysis

被引:445
作者
Singh, Jasvinder A. [1 ,2 ,3 ]
Cameron, Chris [4 ]
Noorbaloochi, Shahrzad [5 ]
Cullis, Tyler
Tucker, Matthew [2 ]
Christensen, Robin [6 ,7 ]
Ghogomu, Elizabeth Tanjong [4 ]
Coyle, Doug [4 ]
Clifford, Tammy [4 ]
Tugwell, Peter [4 ]
Wells, George A. [4 ]
机构
[1] Birmingham Vet Aff airs Med Ctr, Birmingham, AL USA
[2] Univ Alabama Birmingham, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[3] Mayo Clin, Coll Med, Dept Orthoped Surg, Rochester, MN USA
[4] Univ Ottawa, Sch Epidemiol Publ Hlth & Prevent Med, Ottawa, ON K1N 6N5, Canada
[5] Amer Univ, Washington, DC 20016 USA
[6] Copenhagen Univ Hosp, Dept Rheumatol, Musculoskeletal Stat Unit, Parker Inst, Bispebjerg, Denmark
[7] Copenhagen Univ Hosp, Dept Rheumatol, Parker Inst, Musculoskeletal Stat Unit, Frederiksberg, Denmark
关键词
MODIFYING ANTIRHEUMATIC DRUGS; ANTITUMOR-NECROSIS-FACTOR; ISPOR TASK-FORCE; EULAR RECOMMENDATIONS; THERAPY; HOSPITALIZATION; INHIBITION; MANAGEMENT; UPDATE; AGENTS;
D O I
10.1016/S0140-6736(14)61704-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Serious infections are a major concern for patients considering treatments for rheumatoid arthritis. Evidence is inconsistent as to whether biological drugs are associated with an increased risk of serious infection compared with traditional disease-modifying antirheumatic drugs (DMARDs). We did a systematic review and meta-analysis of serious infections in patients treated with biological drugs compared with those treated with traditional DMARDs. Methods We did a systematic literature search with Medline, Embase, Cochrane Central Register of Controlled Trials, and ClinicalTrials.gov from their inception to Feb 11, 2014. Search terms included "biologics", "rheumatoid arthritis" and their synonyms. Trials were eligible for inclusion if they included any of the approved biological drugs and reported serious infections. We assessed the risk of bias with the Cochrane Risk of Bias Tool. We did a Bayesian network meta-analysis of published trials using a binomial likelihood model to assess the risk of serious infections in patients with rheumatoid arthritis who were treated with biological drugs, compared with those treated with traditional DMARDs. The odds ratio (OR) of serious infection was the primary measure of treatment effect and calculated 95% credible intervals using Markov Chain Monte Carlo methods. Findings The systematic review identified 106 trials that reported serious infections and included patients with rheumatoid arthritis who received biological drugs. Compared with traditional DMARDs, standard-dose biological drugs (OR 1.31, 95% credible interval [CrI] 1.09-1.58) and high-dose biological drugs (1.90, 1.50-2.39) were associated with an increased risk of serious infections, although low-dose biological drugs (0.93, 0.65-1.33) were not. The risk was lower in patients who were methotrexate naive compared with traditional DMARD-experienced or anti-tumour necrosis factor biological drug-experienced patients. The absolute increase in the number of serious infections per 1000 patients treated each year ranged from six for standard-dose biological drugs to 55 for combination biological therapy, compared with traditional DMARDs. Interpretation Standard-dose and high-dose biological drugs (with or without traditional DMARDs) are associated with an increase in serious infections in rheumatoid arthritis compared with traditional DMARDs, although low-dose biological drugs are not. Clinicians should discuss the balance between benefit and harm with the individual patient before starting biological treatment for rheumatoid arthritis.
引用
收藏
页码:258 / 265
页数:8
相关论文
共 30 条
[1]  
[Anonymous], 2010, COCHRANE DATABASE SY
[2]   Time-dependent increase in risk of hospitalisation with infection among Swedish RA patients treated with TNF antagonists [J].
Askling, Johan ;
Fored, C. Michael ;
Brandt, Lena ;
Baecklund, Eva ;
Bertilsson, Lennart ;
Feltelius, Nils ;
Coster, Lars ;
Geborek, Pierre ;
Jacobsson, Lennart T. ;
Lindblad, Staffan ;
Lysholm, Jorgen ;
Rantapaa-Dahlqvist, Solbritt ;
Saxne, Tore ;
van Vollenhoven, Ronald F. ;
Klareskog, Lars .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (10) :1339-1344
[3]   Observational Studies of Infections in Rheumatoid Arthritis: A Metaanalysis of Tumor Necrosis Factor Antagonists [J].
Bernatsky, Sasha ;
Habel, Youssef ;
Rahme, Elham .
JOURNAL OF RHEUMATOLOGY, 2010, 37 (05) :928-931
[4]   Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies - Systematic review and meta-analysis of rare harmful effects in randomized controlled trials [J].
Bongartz, T ;
Sutton, AJ ;
Sweeting, MJ ;
Buchan, I ;
Matteson, EL ;
Montori, V .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (19) :2275-2285
[5]   Much ado about nothing: a comparison of the performance of meta-analytical methods with rare events [J].
Bradburn, Michael J. ;
Deeks, Jonathan J. ;
Berlin, Jesse A. ;
Localio, A. Russell .
STATISTICS IN MEDICINE, 2007, 26 (01) :53-77
[6]   Evidence Synthesis for Decision Making 2: A Generalized Linear Modeling Framework for Pairwise and Network Meta-analysis of Randomized Controlled Trials [J].
Dias, Sofia ;
Sutton, Alex J. ;
Ades, A. E. ;
Welton, Nicky J. .
MEDICAL DECISION MAKING, 2013, 33 (05) :607-617
[7]   Serious infection following anti-tumor necrosis factor α therapy in patients with rheumatoid arthritis -: Lessons from interpreting data from observational studies [J].
Dixon, W. G. ;
Symmons, D. P. M. ;
Lunt, M. ;
Watson, K. D. ;
Hyrich, K. L. ;
Silman, A. J. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (09) :2896-2904
[8]   Anti-TNF therapy is associated with an increased risk of serious infections in patients with rheumatoid arthritis especially in the first 6 months of treatment: updated results from the British Society for Rheumatology Biologics Register with special emphasis on risks in the elderly [J].
Galloway, James B. ;
Hyrich, Kimme L. ;
Mercer, Louise K. ;
Dixon, William G. ;
Fu, Bo ;
Ustianowski, Andrew P. ;
Watson, Kath D. ;
Lunt, Mark ;
Symmons, Deborah P. M. .
RHEUMATOLOGY, 2011, 50 (01) :124-131
[9]   Efficacy of conventional synthetic disease-modifying antirheumatic drugs, glucocorticoids and tofacitinib: a systematic literature review informing the 2013 update of the EULAR recommendations for management of rheumatoid arthritis [J].
Gaujoux-Viala, Cecile ;
Nam, Jackie ;
Ramiro, Sofia ;
Landewe, Robert ;
Buch, Maya H. ;
Smolen, Josef S. ;
Gossec, Laure .
ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 (03) :510-515
[10]   Initiation of Tumor Necrosis Factor-α Antagonists and the Risk of Hospitalization for Infection in Patients With Autoimmune Diseases [J].
Grijalva, Carlos G. ;
Chen, Lang ;
Delzell, Elizabeth ;
Baddley, John W. ;
Beukelman, Timothy ;
Winthrop, Kevin L. ;
Griffin, Marie R. ;
Herrinton, Lisa J. ;
Liu, Liyan ;
Ouellet-Hellstrom, Rita ;
Patkar, Nivedita M. ;
Solomon, Daniel H. ;
Lewis, James D. ;
Xie, Fenglong ;
Saag, Kenneth G. ;
Curtis, Jeffrey R. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2011, 306 (21) :2331-2339