Tapering of TNF inhibitors in axial spondyloarthritis in routine care — 2-year clinical and MRI outcomes and predictors of successful tapering

Author:

Wetterslev Marie12ORCID,Georgiadis Stylianos1,Sørensen Inge Juul3,Pedersen Susanne Juhl1,Christiansen Sara Nysom1ORCID,Hetland Merete Lund124ORCID,Brahe Cecilie Heegaard1ORCID,Bakkegaard Mads1,Duer Anne5,Boesen Mikael6,Gosvig Kasper Kjærulf7,Møller Jakob Møllenbach7ORCID,Krogh Niels Steen8,Jensen Bente3,Madsen Ole Rintek3,Christensen Jan3,Hansen Annette3,Nørregaard Jesper3,Røgind Henrik3,Østergaard Mikkel12ORCID

Affiliation:

1. Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Copenhagen, Denmark

2. Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark

3. Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Copenhagen, Denmark

4. The DANBIO Registry, Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Copenhagen, Denmark

5. Department of Radiology, Rigshospitalet Glostrup, Copenhagen, Denmark

6. Department of Radiology, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark

7. Department of Radiology, Herlev and Gentofte Hospital, Copenhagen, Denmark

8. Zitelap Aps, Copenhagen, Denmark

Abstract

Abstract Objectives In a 2-year follow-up study of patients with axial spondyloarthritis (axSpA) in clinical remission who tapered TNF inhibitor (TNFi) treatment according to a clinical guideline, we aimed to investigate the proportion who successfully tapered/discontinued therapy and baseline predictors thereof. The proportion regaining clinical remission after flare and the progression on MRI/radiography were also assessed. Methods One-hundred-and-nine patients (78 [72%]/31 [28%] receiving standard and reduced dose, respectively) in clinical remission (BASDAI < 40, physician global score < 40) and no signs of disease activity the previous year tapered TNFi as follows: to two-thirds of standard dose at baseline, half at week 16, one-third at week 32 and discontinuation at week 48. Patients experiencing clinical, BASDAI or MRI flare (predefined criteria) stopped tapering and escalated to previous dose. Prediction analyses were performed by multivariable regression. Results One hundred and six patients (97%) completed 2 years’ follow-up; 55 patients (52%) had successfully tapered: 23 (22%) receiving two-thirds, 15 (14%) half, 16 (15%) one-third dose and 1 (1%) discontinued. In patients at standard dose at baseline (n = 78), lower physician global score was the only independent predictor of successful tapering (odds ratio [OR] = 0.79 [95% CI: 0.64, 0.93]; P = 0.003). In the entire patient group lower physician global score (OR = 0.86 [0.75, 0.98]; P = 0.017), lower Spondyloarthritis Research Consortium of Canada (SPARCC) Sacroiliac Joint Erosion score (OR = 0.78 [0.57, 0.98]; P = 0.029) and current smoker (OR = 3.28 [1.15, 10.57]; P = 0.026) were independent predictors of successful tapering. At 2 years, 97% of patients were in clinical remission. Minimal changes in imaging findings were observed. Conclusion After 2 years following a clinical guideline, 52% of patients with axSpA in clinical remission had successfully tapered TNFi, only 1% discontinued. Baseline physician global score was an independent predictor of successful tapering.

Funder

Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet

The Danish Rheumatism Association

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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