BioMed Research International · 2014 · 41 citations · 46 references
Life SciencesImmunologyPharmacotherapyAutoimmunityImmunotherapyRheumatologyAutoimmune Rheumatic DiseasesImmunogenicity Of Therapeutic AntibodiesPharmacokinetics Of ImmunotherapiesPharmacokinetics Of Monoclonal AntibodiesResponse AssessmentRheumatoid ArthritisImmunogenicity Of Biologic AgentsInadequate TreatmentMonitoring Treatment ResponseRheumatoid Arthritis TherapySerum Drug Concentration MeasurementSerum Drug Level InterpretationSerum Level MonitoringSerum Therapeutic Drug Monitoring
Clinical response in patients with rheumatoid arthritis (RA) treated with biologic agents can be influenced by their pharmacokinetics and immunogenicity. The present study evaluated the concordance between serum drug and antidrug levels as well as the clinical response in RA patients treated with biological agents who experience their first disease exacerbation while being on a stable biologic treatment. 154 RA patients treated with rituximab (RTX), infliximab (IFX), adalimumab (ADL), or etanercept (ETN) were included. DAS28, SDAI, and EULAR response were assessed at baseline and reevaluated at precise time intervals. At the time of their first sign of inadequate response, patients were tested for both serum drug level and antidrug antibodies level. At the next reevaluation, patients retreated with RTX that had detectable drug level had a better EULAR response (P = 0.038) with lower DAS28 and SDAI scores (P = 0.01 and P = 0.03). The same tendency was observed in patients treated with IFX and ETN regarding EULAR response (P = 0.002 and P = 0.023), DAS28 score (P = 0.002 and P = 0.003), and SDAI score (P = 0.001 and P = 0.026). Detectable biologic drug levels correlated with a better clinical response in patients experiencing their first RA inadequate response while being on a stable biologic treatment with RTX, IFX, and ETN.
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