Disease activity guided stepwise tapering or discontinuation of rhTNFR:Fc, an etanercept biosimilar, in patients with ankylosing spondylitis: a prospective, randomized, open-label, multicentric study

Ting Zhang, Jianing Zhu, Dongyi He, Xiaowei Chen, Hongzhi Wang, Ying Zhang, Qin Xue, Weili Liu, Guangbo Xiang, Yasong Li, Zhongming Yu, Huaxiang Wu, Ting Zhang, Jianing Zhu, Dongyi He, Xiaowei Chen, Hongzhi Wang, Ying Zhang, Qin Xue, Weili Liu, Guangbo Xiang, Yasong Li, Zhongming Yu, Huaxiang Wu

Abstract

Background: The aim of this study was to evaluate disease-activity-guided stepwise tapering or discontinuation of rhTNFR:Fc, an etanercept biosimilar, in patients with ankylosing spondylitis (AS) in a prospective, randomized, open-label, multicentric study.

Methods: Active AS patients with AS disease activity score (ASDAS) ⩾2.1 recruited from 10 hospitals were treated with rhTNFR:Fc 50 mg weekly for 12 weeks, and further randomized into different tapering or discontinuation groups according to ASDAS at week 12. Patients who achieved clinical remission (ASDAS < 1.3) were assigned randomly to stepwise tapering group or discontinuation group. Patients who achieved low disease activity (LDA, 1.3⩽ASDAS < 2.1) were assigned randomly to stepwise tapering, delayed tapering, or discontinuation group. All patients were evaluated every 12 weeks until week 48. The primary endpoint was cumulative flare rates in different groups at week 48.

Results: A total of 311 patients were enrolled with an average ASDAS of 3.6 ± 1.0, and 259 completed 12 weeks of rhTNFR:Fc induction therapy, with 148 patients (57.1%) achieved clinical remission, 100 (38.6%) achieved LDA, and 11 (4.3%) remained as high disease activity (ASDAS⩾2.1). In patients who achieved clinical remission at week 12, stepwise tapering of rhTNFR:Fc demonstrated significantly lower flare rates at each evaluation compared with discontinuation. In patients who achieved LDA, there was no significant difference of flare rates between stepwise tapering, delayed tapering, and discontinuation. With stepwise tapering of rhTNFR:Fc, flare rates were comparable in AS patients, irrespective of initial ASDAS before tapering.

Conclusion: Stepwise tapering of rhTNFR:Fc when patients achieved clinical remission was able to maintain favorable low flare rates in 48 weeks. LDA was an alternative therapeutic target, as well as an viable timing for initiation of rhTNFR:Fc tapering. rhTNFR:Fc 25 mg monthly maintained flare-free status in a considerable number of patients. However, abrupt discontinuation of rhTNFR:Fc even if patients achieved clinical remission should be avoided.

Trial registration: ClinicalTrials.gov: NCT03880968,URL: https://ichgcp.net/clinical-trials-registry/NCT03880968.

Keywords: ankylosing spondylitis; disease activity; etanercept biosimilar; tapering.

Conflict of interest statement

Conflict of interest statement: The authors declare that there is no conflict of interest.

© The Author(s), 2020.

Figures

Figure 1.
Figure 1.
Study design. Patients with AS enrolled were treated with rhTNFR:Fc 50 mg subcutaneously each week for 12 weeks, and then randomized into subgroups with different tapering or discontinuation strategies according to the ASDAS at the end of week 12. AS, ankylosing spondylitis; ASDAS, ankylosing spondylitis disease activity score; cDMARDs, conventional disease modifying anti-rheumatic drugs; NSAIDs, non-steroidal anti-inflammatory drugs; Q2w, each two weeks; Qm, each month; Qw, each week.
Figure 2.
Figure 2.
Study profile. Patients were randomized to different tapering or discontinuation groups according to the disease activity at week 12. AS, ankylosing spondylitis; ASDAS, ankylosing spondylitis disease activity score; cDMARDs, conventional disease modifying anti-rheumatic drugs; NSAIDs, nonsteroidal anti-inflammatory drugs.
Figure 3.
Figure 3.
Average time to flare with different tapering or discontinuation strategies. The average flare time in patients with different tapering or discontinuation strategies, including patients with remission who initiated stepwise tapering, or discontinuation of rhTNFR:Fc, and patients with LDA who initiated stepwise tapering, delayed tapering, or discontinuation. The error bars represent standard deviation. LDA, low disease activity.
Figure 4.
Figure 4.
Flare-free survival rates. Flare-free survival rates in patients with different tapering or discontinuation strategies: (A) patients with clinical remission (ASDAS 

References

    1. Taurog JD, Chhabra A, Colbert RA. Ankylosing spondylitis and axial spondyloarthritis. N Engl J Med 2016; 374: 2563–2574.
    1. van der Heijde D, Ramiro S, Landewe R, et al. 2016 update of the ASAS-EULAR management recommendations for axial spondyloarthritis. Ann Rheum Dis 2017; 76: 978–991.
    1. Cinar M, Dinc A, Simsek I, et al. Evaluation of the short-term efficacy of NSAIDs on patients with active ankylosing spondylitis in daily practice: a 3-month, longitudinal, observational study. Rheumatol Int 2010; 30: 331–340.
    1. Ward MM, Deodhar A, Akl EA, et al. American college of rheumatology/spondylitis association of America/spondyloarthritis research and treatment network 2015 recommendations for the treatment of ankylosing spondylitis and nonradiographic axial spondyloarthritis. Arthritis Rheumatol 2016; 68: 282–298.
    1. Ward MM, Deodhar A, Gensler LS, et al. 2019 update of the American college of rheumatology/spondylitis association of America/spondyloarthritis research and treatment network recommendations for the treatment of ankylosing spondylitis and nonradiographic axial spondyloarthritis. Arthritis Rheumatol 2019; 71: 1599–1613.
    1. Liu YF, Dong H, Tu SH, et al. Etanercept in the treatment of ankylosing spondylitis: a systematic review and meta-analysis. Exp Ther Med 2014; 8: 1585–1592.
    1. Li ZH, Zhang Y, Wang J, et al. Etanercept in the treatment of ankylosing spondylitis: a meta-analysis of randomized, double-blind, placebo-controlled clinical trials, and the comparison of the Caucasian and Chinese population. Eur J Orthop Surg Traumatol 2013; 23: 497–506.
    1. Lee SH, Lee YA, Hong SJ, et al. Etanercept 25 mg/week is effective enough to maintain remission for ankylosing spondylitis among Korean patients. Clin Rheumatol 2008; 27: 179–181.
    1. Lee J, Noh JW, Hwang JW, et al. Extended dosing of Etanercept 25 mg can be effective in patients with ankylosing spondylitis: a retrospective analysis. Clin Rheumatol 2010; 29: 1149–1154.
    1. Navarro-Compán V, Moreira V, Ariza-Ariza R, et al. Low doses of etanercept can be effective in ankylosing spondylitis patients who achieve remission of the disease. Clin Rheumatol 2011; 30: 993–996.
    1. Cantini F, Niccoli L, Cassara E, et al. Duration of remission after halving of the etanercept dose in patients with ankylosing spondylitis: a randomized, prospective, long-term, follow-up study. Biologics 2013; 7: 1–6.
    1. De Stefano R, Frati E, De Quattro D, et al. Low doses of etanercept can be effective to maintain remission in ankylosing spondylitis patients. Clin Rheumatol 2014; 33: 707–711.
    1. Almirall M, Salman-Monte TC, Lisbona MP, et al. Dose reduction of biological treatment in patients with axial spondyloarthritis in clinical remission: are there any differences between patients who relapsed and to those who remained in low disease activity? Rheumatol Int 2015; 35: 1565–1568.
    1. Plasencia C, Kneepkens EL, Wolbink G, et al. Comparing tapering strategy to standard dosing regimen of tumor necrosis factor inhibitors in patients with spondyloarthritis in low disease activity. J Rheumatol 2015; 42: 1638–1646.
    1. Arends S, van der Veer E, Kamps FB, et al. Patient-tailored dose reduction of TNF-α blocking agents in ankylosing spondylitis patients with stable low disease activity in daily clinical practice. Clin Exp Rheumatol 2015; 33: 174–180.
    1. Yates M, Hamilton LE, Elender F, et al. Is Etanercept 25 mg once weekly as effective as 50 mg at maintaining response in patients with ankylosing spondylitis? A randomized control trial. J Rheumatol 2015; 42: 1177–1185.
    1. Li J, Wang X, Han Z, et al. Dose reduction of recombinant human tumor necrosis factor inhibitors (etanercept) can be effective in ankylosing spondylitis patients with synovitis of the hip in a Chinese population. Int J Immunopathol Pharmacol 2016; 29: 510–505.
    1. Park JW, Yoon YI, Lee JH, et al. Low dose etanercept treatment for maintenance of clinical remission in ankylosing spondylitis. Clin Exp Rheumatol 2016; 34: 592–599.
    1. Zavada J, Uher M, Sisol K, et al. A tailored approach to reduce dose of anti-TNF drugs may be equally effective, but substantially less costly than standard dosing in patients with ankylosing spondylitis over 1 year: a propensity score-matched cohort study. Ann Rheum Dis 2016; 75: 96–102.
    1. Zhao M, Zhang P, Fang L, et al. Possible predictors for relapse from etanercept discontinuation in ankylosing spondylitis patients in remission: a three years’ following-up study. Clin Rheumatol 2018; 37: 87–92.
    1. van der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. A proposal for modification of the New York criteria. Arthritis Rheum 1984; 27: 361–368.
    1. Machado P, Landewe R, Lie E, et al. Ankylosing spondylitis disease activity score (ASDAS): defining cut-off values for disease activity states and improvement scores. Ann Rheum Dis 2011; 70: 47–53.
    1. Machado PM, Landewe R, Heijde DV; Assessment of SpondyloArthritis International Society (ASAS). Ankylosing Spondylitis Disease Activity Score (ASDAS): 2018 update of the nomenclature for disease activity states. Ann Rheum Dis 2018; 77: 1539–1540.
    1. Gossec L, Portier A, Landewe R, et al. Preliminary definitions of ‘flare’ in axial spondyloarthritis, based on pain, BASDAI and ASDAS-CRP: an ASAS initiative. Ann Rheum Dis 2016; 75: 991–996.
    1. Edwards CJ, Fautrel B, Schulze-Koops H, et al. Dosing down with biologic therapies: a systematic review and clinicians’ perspective. Rheumatology (Oxford) 2017; 56: 1847–1856.
    1. Lee H, Jung Y, Song S, et al. Dosage and duration of etanercept therapy for ankylosing spondylitis: a meta-analysis. Int J Technol Assess Health Care 2017; 33: 69–75.
    1. Wendling D, Lukas C, Prati C, et al. 2018 update of French society for rheumatology (SFR) recommendations about the everyday management of patients with spondyloarthritis. Joint Bone Spine 2018; 85: 275–284.
    1. Smolen JS, Schols M, Braun J, et al. Treating axial spondyloarthritis and peripheral spondyloarthritis, especially psoriatic arthritis, to target: 2017 update of recommendations by an international task force. Ann Rheum Dis 2018; 77: 3–17.
    1. van der Heijde D, Braun J, Dougados M, et al. Sensitivity and discriminatory ability of the ankylosing spondylitis disease activity score in patients treated with etanercept or sulphasalazine in the ASCEND trial. Rheumatology (Oxford) 2012; 51: 1894–1905.
    1. Molto A, Gossec L, Meghnathi B, et al. An assessment in spondyloarthritis international society (ASAS)-endorsed definition of clinically important worsening in axial spondyloarthritis based on ASDAS. Ann Rheum Dis 2018; 77: 124–127.

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