Infliximab is a chimeric monoclonal antibody that binds to human
tumor necrosis factor alpha and is approved for refractory
rheumatoid arthritis. We studied the association between
infliximab concentration and long-term control of disease activity in patients with
rheumatoid arthritis treated on a routine basis both in cross-sectional analysis and over the long term. Trough serum
infliximab concentrations were measured in patients with
rheumatoid arthritis receiving
infliximab infusions during the period August to October 2006. Disease activity was assessed by the Disease Activity Score for 28 Joints (DAS28) and usual
biologic markers. During a 42-week follow-up period, patients were classified into two groups: those continuing with the same or lower doses of
infliximab (Group A = treatment success) and those who switched to another biopharmaceutical or required an increase in
infliximab dose (Group B = treatment failure). Treatment maintenance for Group A was analyzed by categories of
infliximab concentration at baseline and compared by the log rank test. In 28 patients,
C-reactive protein and
infliximab concentrations were inversely related.
Infliximab concentration in patients with low disease activity (DAS28 3.2 or less) was higher than in those with persistent active disease (DAS28 greater than 3.2); median values were 3.26 and 0.16 mg/L, respectively (P < 0.01). Analysis after 42 weeks showed that patients in Group A had higher
infliximab concentrations at baseline than those with treatment failure (P < 0.01). In
rheumatoid arthritis,
infliximab concentration is predictive of sustained efficacy with the same
infliximab regimen and should be considered on a routine basis.