4.7 Article

Significant associations of antidrug antibody levels with serum drug trough levels and therapeutic response of adalimumab and etanercept treatment in rheumatoid arthritis

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 74, Issue 3, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2013-203893

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Objective To evaluate the associations between (1) antidrug antibody (ADAb) and therapeutic response, (2) ADAb and serum drug trough levels and (3) serum drug levels and therapeutic responses in rheumatoid arthritis (RA) patients receiving adalimumab or etanercept. Secondarily, we aim (1) to evaluate the concordance between radioimmunoassay and bridging ELISA for ADAb assessment and to evaluate the correlation between two different ELISA methods for detecting drug levels, and (2) to determine the optimal cut-off drug levels for good European League Against Rheumatism (EULAR) response. Methods ADAb levels were determined by bridging ELISA and radioimmunoassay, and drug levels evaluated using sandwich ELISA among 36 adalimumab-treated patients and 34 etanercept-treated patients at the 6th and 12th month. The optimal cut-off drug levels for EULAR responses were determined by receiver-operating characteristic curve analysis. Results ADAb was detected in 10 (27.8%) and 13 (36.1%) of adalimumab-treated patients after 12-month therapy using bridging ELISA and radioimmunoassay respectively, but not detected in any of etanercept-treated patients. The presence of ADAb was associated with lower EULAR response and lower drug levels compared with those without ADAb (both p<0.001). Drug trough levels were positively associated with DAS28 decrement (Delta DAS28) (all p<0.001). The optimal cut-off trough levels for adalimumab were 1.274 mu g/mL and 1.046 mu g/mL, and those for etanercept were 1.242 mu g/mL and 0.800 mu g/mL for good EULAR response assessed at the 6th and 12th month, respectively. Conclusions ADAb levels were inversely correlated with therapeutic response and drug levels. The positive correlation between drug levels and Delta DAS28 indicates that drug monitoring would be useful to evaluate therapeutic response of TNF-alpha inhibitors.

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