Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial

Author:

Hartman Linda12,Rasch Linda A1ORCID,Turk Samina A3,ter Wee Marieke M2,Kerstens Pit J S M4,van der Laken Conny J1,Nurmohamed Michael T13,van Schaardenburg Dirkjan35,van Tuyl Lilian H D16,Voskuyl Alexandre E1,Boers Maarten2,Lems Willem F1

Affiliation:

1. Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit , Amsterdam, The Netherlands

2. Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Vrije Universiteit , Amsterdam, The Netherlands

3. Amsterdam Rheumatology and Immunology Center , Reade, Amsterdam, The Netherlands

4. Department of Rheumatology, Dijklander Ziekenhuis , Hoorn, The Netherlands

5. Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Universiteit van Amsterdam , Amsterdam, The Netherlands

6. Netherlands Institute for Health Services Research , Utrecht, The Netherlands

Abstract

Abstract Objective The aim of this study was to investigate the effect of treat-to-target combination therapy with intensification at 13 weeks in early RA. Methods Early RA patients were classified as being at high or low risk of worsening RA based on disease activity and prognostic factors. High-risk patients received COBRA-light (prednisolone 30 mg/day tapered to 7.5 mg/day, MTX increasing to 25 mg/week), and low-risk patients received MTX monotherapy increasing to 25 mg/week. The primary outcome (target) was DAS44 < 1.6 or EULAR good response at 26 weeks. At 13 weeks, non-responders were randomized to (open-label) intensification [high-risk patients: prednisolone 60 mg/day tapered to 7.5 mg/day, addition of SSZ (2 g/day) and HCQ (400 mg/day); low-risk patients: prednisolone 30 mg/day tapered to 7.5 mg/day] or continuation. Results In the high-risk group (n = 150), 110 patients (73%) reached the target at 13 weeks, and 9 dropped out. Non-responders were randomized to intensification (n = 15) or continuation (n = 16), and after 26 weeks, 12 (80%) vs 7 (44%) of these, respectively, reached the target [difference: 36%, (95% CI 2%, 71%); P = 0.04]. In the low-risk group (n = 40), 17 (43%) reached the target. Non-responders were randomized to intensification (n = 8) or continuation (n = 7); 4 vs 3, respectively, reached the target. Adverse event rates were higher in the high-risk group, and higher in the intensification subgroup of that group. Serious adverse events were rare. Protocol violations were frequent and mostly led to mitigation of actual treatment intensification. Conclusion Initial combination therapy was very successful in high-risk RA, and early intensification was beneficial in patients not reaching the strict target. The low-risk group was too small for drawing conclusions. In routine practice, adherence to early intensification based on strict targets is difficult. Trial registration Netherlands Trial Register (NTR), NL4393, https://www.trialregister.nl/.

Funder

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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