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FRI0120 Serum calprotectin is not predictive for successful dose reduction or discontinuation of tnf inhibitors in ra patients with low disease activity
  1. N Den Broeder1,
  2. L Tweehuysen1,
  3. T Vogl2,
  4. N van Herwaarden1,
  5. FHJ van den Hoogen1,3,
  6. RM Thurlings3,
  7. AA den Broeder1
  1. 1Rheumatology, Sint Maartenskliniek, Nijmegen, Netherlands
  2. 2University of Münster, Münster, Germany
  3. 3Rheumatology, Radboudumc, Nijmegen, Netherlands

Abstract

Background Dose reduction and discontinuation of TNF inhibitors (TNFi) have been shown feasible in a large proportion of RA patients with low disease activity.1 However, to date, no predictors for successful dose reduction or discontinuation have been identified.2 Calprotectin (a heterodimer of S100A8/S100A9) might be a promising biomarker in this context, as preliminary data showed this pro-inflammatory marker to be associated with disease activity and radiographic progression in RA and to be predictive for response in RA patients starting treatment with a TNFi.3,4

Objectives To investigate the predictive value of baseline serum calprotectin for successful TNFi dose reduction or discontinuation in RA patients with low disease activity.

Methods Data was derived from the intervention arm of the DRESS (Dose REduction Strategies of Subcutaneous TNFi) study, which showed non-inferiority of a dose reduction strategy of adalimumab or etanercept compared to usual care.1 TNFi dose interval was reduced stepwise every 3 months until flare (DAS28-CRP increase >1.2 or >0.6 if current DAS28-CRP ≥3.2) or discontinuation. Patients were classified at 18 months as being successfully dose reduced, discontinued or not able to reduce the TNFi dose. At baseline, quantification of calprotectin was carried out on serum samples using ELISA. To assess the predictive value, calprotectin levels were compared between each group and receiver-operator-characteristic (ROC) curves were created. In addition, calprotectin was correlated cross-sectionally with several clinical markers for disease activity.

Results Calprotectin levels were available for 102 of 121 patients randomised to the intervention group; 61% were women, 63% received etanercept and 37% received adalimumab. Overall, 46% of patients successfully reduced their TNFi dose, 19% of patients successfully discontinued their TNFi and 35% of patients could not reduce their TNFi dose. In these groups, median calprotectin levels were 599 ng/ml (p25-p75: 473–965), 629 ng/mL (p25-p75: 453–896) and 624 ng/mL (p25-p75: 514–931) (p=0.801) (Figure 1). The area under the ROC-curve was 0.52 (95% CI: 0.40–0.63) for predicting successful TNFi dose reduction, 0.53 (95% CI: 0.38–0.67) for successful TNFi discontinuation and 0.54 (95% CI: 0.42–0.66) for no dose reduction possible. Calprotectin levels were significantly but weakly correlated with C-reactive protein (CRP) levels with a Spearman ρ of 0.21 (p=0.03). No significant correlation was found between calprotectin and age, gender, DAS28-CRP, rheumatoid factor or ACPA positivity.

Conclusions Serum calprotectin is not predictive for successful TNFi dose reduction or discontinuation in the context of RA patients with low disease activity, and calprotectin was only weakly correlated to CRP levels. These results might be caused by the lack of variability in calprotectin levels at baseline as all patients were in low disease activity state.

References

  1. van Herwaarden et al. BMJ 2015;350:h1389.

  2. Tweehuysen et al. Arthritis Rheumatol 2016.

  3. Berner Hammer et al. Ann Rheum Dis 2010;69(1):150–4.

  4. Choi et al. Ann Rheum Dis 2015;74(3):499–505.

References

Disclosure of Interest N. Den Broeder: None declared, L. Tweehuysen: None declared, T. Vogl: None declared, N. van Herwaarden: None declared, F. van den Hoogen Consultant for: Biogen, Celltrion, Janssen, Mundipharma and Sandoz, R. Thurlings: None declared, A. den Broeder Consultant for: AMGEN

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