TY - JOUR
T1 - Biological agents in polyarticular juvenile idiopathic arthritis
T2 - A meta-analysis of randomized withdrawal trials
AU - Amarilyo, Gil
AU - Tarp, Simon
AU - Foeldvari, Ivan
AU - Cohen, Neta
AU - Pope, Tracy D.
AU - Woo, Jennifer M.P.
AU - Christensen, Robin
AU - Furst, Daniel E.
N1 - Publisher Copyright:
© 2016
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background and objective Although various biological agents are in use for polyarticular juvenile idiopathic arthritis (pJIA), head-to-head trials comparing the efficacy and safety among them are lacking. We aimed to compare the efficacy and safety of biological agents in pJIA using all currently available randomized withdrawal trials (wRCTs). Methods A systematic search of MEDLINE, EMBASE, CENTRAL, and clinicaltrials.gov was performed. Eligible wRCTs: patients with pJIA where a biological agent was compared with another biological agent or placebo. Efficacy was evaluated using disease flare as a measure. Adverse events (AEs) and serious AEs were evaluated. Network meta-analysis compared biological agents based on a (empirical Bayes) mixed-effects logistic regression model that combines statistical inference from both direct and indirect comparisons of the treatment effects between biological agents. Results Of 496 references identified, five wRCTs were included—abatacept, adalimumab, anakinra, etanercept, and tocilizumab, one trial each, all vs. placebo. There were no differences in efficacy among biological agents and most showed statistically significant efficacy compared with placebo (nearly all exceptions were in agreement with the original study data). Serious AEs occurred very infrequently (0–8%) and an analysis was not possible. There were no differences for AEs when compared among biological agents or to placebo. Conclusion There were no statistical differences among biological agents for efficacy or safety. Overall, biological agents were effective and safe when compared to placebo. Based on these data, other considerations such as price and availability may need to be used to decide among biological agents when treating pJIA patients.
AB - Background and objective Although various biological agents are in use for polyarticular juvenile idiopathic arthritis (pJIA), head-to-head trials comparing the efficacy and safety among them are lacking. We aimed to compare the efficacy and safety of biological agents in pJIA using all currently available randomized withdrawal trials (wRCTs). Methods A systematic search of MEDLINE, EMBASE, CENTRAL, and clinicaltrials.gov was performed. Eligible wRCTs: patients with pJIA where a biological agent was compared with another biological agent or placebo. Efficacy was evaluated using disease flare as a measure. Adverse events (AEs) and serious AEs were evaluated. Network meta-analysis compared biological agents based on a (empirical Bayes) mixed-effects logistic regression model that combines statistical inference from both direct and indirect comparisons of the treatment effects between biological agents. Results Of 496 references identified, five wRCTs were included—abatacept, adalimumab, anakinra, etanercept, and tocilizumab, one trial each, all vs. placebo. There were no differences in efficacy among biological agents and most showed statistically significant efficacy compared with placebo (nearly all exceptions were in agreement with the original study data). Serious AEs occurred very infrequently (0–8%) and an analysis was not possible. There were no differences for AEs when compared among biological agents or to placebo. Conclusion There were no statistical differences among biological agents for efficacy or safety. Overall, biological agents were effective and safe when compared to placebo. Based on these data, other considerations such as price and availability may need to be used to decide among biological agents when treating pJIA patients.
KW - juvenile idiopathic arthritis
KW - meta-analysis
KW - randomized withdrawal trials
UR - http://www.scopus.com/inward/record.url?scp=85006317866&partnerID=8YFLogxK
U2 - 10.1016/j.semarthrit.2016.07.001
DO - 10.1016/j.semarthrit.2016.07.001
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 27989499
AN - SCOPUS:85006317866
SN - 0049-0172
VL - 46
SP - 312
EP - 318
JO - Seminars in Arthritis and Rheumatism
JF - Seminars in Arthritis and Rheumatism
IS - 3
ER -