Efficacy and safety of infliximab-biosimilar compared to other biological drugs in rheumatoid arthritis: a mixed treatment comparison

被引:22
|
作者
Baji, Petra [1 ]
Pentek, Marta [1 ,2 ]
Czirjak, Laszlo [3 ]
Szekanecz, Zoltan [4 ]
Nagy, Gyoergy [5 ,6 ]
Gulacsi, Laszlo [1 ]
Brodszky, Valentin [1 ]
机构
[1] Corvinus Univ Budapest, Dept Hlth Econ, H-1093 Budapest, Hungary
[2] Flor Ferenc Cty Hosp, Dept Rheumatol, H-2143 Kistarcsa, Hungary
[3] Univ Pecs, Dept Rheumatol & Immunol, H-7632 Pecs, Hungary
[4] Univ Debrecen, Med & Hlth Sci Ctr, Inst Med, Dept Rheumatol, H-4032 Debrecen, Hungary
[5] Semmelweis Univ, Dept Genet Cell & Immunobiol, Fac Med, H-1089 Budapest, Hungary
[6] Semmelweis Univ, Sch Med, Dept Rheumatol, H-1023 Budapest, Hungary
来源
关键词
Arthritis; Rheumatoid; Biosimilar pharmaceuticals; Meta-analysis; Mixed treatment comparison; ANTITUMOR NECROSIS FACTOR; MODIFYING ANTIRHEUMATIC DRUGS; ADALIMUMAB PLUS METHOTREXATE; ALPHA MONOCLONAL-ANTIBODY; RECEIVING CONCOMITANT METHOTREXATE; INTERLEUKIN-6 RECEPTOR INHIBITION; EVERY; WEEKS; DOUBLE-BLIND; PHASE-III; INADEQUATE RESPONSE;
D O I
10.1007/s10198-014-0594-4
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objective The aim of this meta-analysis was to compare the efficacy and safety of infliximab-biosimilar and other available biologicals for the treatment of rheumatoid arthritis (RA), namely abatacept, adalimumab, certolizumab pegol, etanercept, golimumab, infliximab, rituximab and tocilizumab. Methods A systematic literature review of MEDLINE database until August 2013 was carried out to identify relevant randomized controlled trials (RCTs). Bayesian mixed treatment comparison method was applied for the pairwise comparison of treatments. Improvement rates by the American College of Rheumatology criteria (ACR20 and ACR50) at week 24 were used as efficacy endpoints, and the occurrence of serious adverse events was considered to assess the safety of the biologicals. Results Thirty-six RCTs were included in themeta-analysis. All the biological agents proved to be superior to placebo. For ACR20 response, certolizumab pegol showed the highest odds ratio (OR) compared to placebo, OR 7.69 [95 % CI 3.69-14.26], followed by abatacept OR 3.7 [95 % CI 2.17-6.06], tocilizumab OR 3.69 [95 % CI 1.87-6.62] and infliximab-biosimilar OR 3.47 [95 % CI 0.85-9.7]. For ACR50 response, certolizumab pegol showed the highest OR compared to placebo OR 8.46 [3.74-16.82], followed by tocilizumab OR 5.57 [95 % CI 2.77-10.09], and infliximab-biosimilar OR 4.06 [95 % CI 1.01-11.54]. Regarding the occurrence of serious adverse events, the results show no statistically significant difference between infliximab-biosimilar and placebo, OR 1.87 [95 % CI 0.74-3.84]. No significant difference regarding efficacy and safety was found between infliximab-biosimilar and the other biological treatments. Conclusion This is thefirst indirectmeta-analysis inRAthat compares the efficacy and safety of biosimilar-infliximab to the other biologicals indicated inRA. We found no significant difference between infliximab-biosimilar and other biological agents in terms of clinical efficacy and safety.
引用
收藏
页码:S53 / S64
页数:12
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