Effect of tapered versus stable treatment with tumour necrosis factor inhibitors on disease flares in patients with rheumatoid arthritis in remission: a randomised, open label, non-inferiority trial

Author:

Lillegraven SiriORCID,Paulshus Sundlisæter NinaORCID,Aga Anna-BirgitteORCID,Sexton Joseph,Olsen Inge Christoffer,Lexberg Åse Stavland,Madland Tor Magne,Fremstad Hallvard,Høili Christian A.,Bakland Gunnstein,Spada Cristina,Haukeland Hilde,Hansen Inger Myrnes,Moholt Ellen,Uhlig TillORCID,Solomon Daniel H,van der Heijde DésiréeORCID,Kvien Tore KORCID,Haavardsholm Espen A

Abstract

ObjectivesMany patients with rheumatoid arthritis (RA) require treatment with tumour necrosis factor inhibitor (TNFi) to reach remission. It is debated whether tapering of TNFi to discontinuation should be considered in sustained remission. The aim of ARCTIC REWIND TNFi was to assess the effect of tapering TNFi to withdrawal compared with stable treatment on the risk of disease activity flares in patients with RA in remission ≥1 year.MethodsThis randomised, open-label, non-inferiority trial was undertaken at nine Norwegian rheumatology departments. Patients with RA in remission ≥12 months on stable TNFi therapy were allocated by computer-based block-randomisation to tapering to discontinuation of TNFi or stable TNFi. Conventional synthetic disease-modifying antirheumatic co-medication was unchanged. The primary endpoint was disease flare during the 12-month study period (non-inferiority margin 20%), assessed in the per-protocol population.ResultsBetween June 2013 and January 2019, 99 patients were enrolled and 92 received the allocated treatment strategy. Eighty-four patients were included in the per-protocol population. In the tapering TNFi group, 27/43 (63%) experienced a flare during 12 months, compared with 2/41 (5%) in the stable TNFi group; risk difference (95% CI) 58% (42% to 74%). The tapering strategy was not non-inferior to continued stable treatment. The number of total/serious adverse events was 49/3 in the tapering group, 57/2 in the stable group.ConclusionIn patients with RA in remission for more than 1 year while using TNFi, an increase in flare rate was reported in those who tapered TNFi to discontinuation. However, most regained remission after reinstatement of full-dose treatment.Trial registration numbersEudraCT: 2012-005275-14 and clinicaltrials.gov:NCT01881308.

Funder

Helse Sør-Øst RHF

Norges Forskningsråd

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

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