Rheumatoid arthritis

Non-trough adalimumab and certolizumab drug levels associated with a therapeutic EULAR response in adherent patients with rheumatoid arthritis

Rheumatology (Oxford)Published Prospective observational study

Authors' conclusion

In fully adherent patients, higher SDLs are detected in good responders, suggesting that interventions to improve SDLs, such as encouraging adherence, could improve treatment response.

Study context

Population
Patients with RA treated with adalimumab or certolizumab; fully adherent patients analysed as a subgroup
Participants
475 patients
Exposure
Serum drug levels in EULAR good vs non-/moderate responders, adalimumab and certolizumab
  • Adalimumabn = 283
  • Certolizumabn = 192
Outcome
Relationship between adalimumab/certolizumab serum drug levels (SDLs) and EULAR good vs non-/moderate response; SDL cut-offs associated with good response in fully adherent patients
Methodological detailsROC analysis, fully adherent subgroup
  • ROC analysis
  • Fully adherent subgroup

Main finding

As reported in the abstract

Median SDLs, good vs non-/moderate responders (fully adherent); 3-month non-trough SDL ROC discrimination · 3 months (ROC)
GroupAUCCut-offSpecificitySensitivity
Adalimumab0.63 (95% CI 0.52, 0.75)7.5 mg/l39.1%80.9%
Certolizumab0.65 (95% CI 0.51, 0.78)26.0 mg/l43.9%77.8%

AUC

Adalimumab0.63 (95% CI 0.52, 0.75)
Certolizumab0.65 (95% CI 0.51, 0.78)

Cut-off

Adalimumab7.5 mg/l
Certolizumab26.0 mg/l

Specificity

Adalimumab39.1%
Certolizumab43.9%

Sensitivity

Adalimumab80.9%
Certolizumab77.8%
  • Good responders vs Non-/moderate responders: P = 0.04 — significantly higher in fully adherent good responders
  • Good responders vs Non-/moderate responders: P = 0.0005 — significantly higher in fully adherent good responders

Observational data: associations, not effects.

Original publication

Non-trough adalimumab and certolizumab drug levels associated with a therapeutic EULAR response in adherent patients with rheumatoid arthritis. Rheumatology (Oxford). Published 3 October 2022. doi:10.1093/rheumatology/keac564

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