Towards the Lowest Efficacious Dose: Results From a Multicenter Noninferiority Randomized Open‐Label Controlled Trial Assessing Tocilizumab or Abatacept Injection Spacing in Rheumatoid Arthritis in Remission

Author:

Kedra Joanna1ORCID,Dieudé Philippe2,Giboin Caroline1,Marotte Hubert3ORCID,Salliot Carine4ORCID,Schaeverbeke Thierry5,Perdriger Aleth6,Soubrier Martin7,Morel Jacques8ORCID,Constantin Arnaud9,Dernis Emmanuelle10,Royant Valérie11,Salmon Jean‐Hugues12,Pham Thao13,Gottenberg Jacques‐Eric14ORCID,Pertuiset Edouard15,Dougados Maxime16ORCID,Devauchelle‐Pensec Valérie17ORCID,Gaudin Philippe18,Cormier Grégoire19,Goupille Philippe20,Mariette Xavier21ORCID,Berenbaum Francis22,Alcaix Didier23,Rouidi Sid‐Ahmed24,Berthelot Jean‐Marie25ORCID,Monnier Agnès26,Piroth Christine27,Lioté Frédéric28,Goëb Vincent29,Gaujoux‐Viala Cécile30,Chary‐Valckenaere Isabelle31,Hajage David1,Tubach Florence1,Fautrel Bruno1,

Affiliation:

1. Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP‐HP, Hôpital Pitié Salpêtrière Paris France

2. Université de Paris Cité, INSERM UMR 1152 and Hôpital Bichat‐Claude Bernard, AP‐HP Paris France

3. Université Jean Monnet Saint‐Étienne, Centre Hospitalier Universitaire de Saint‐Etienne, Mines Saint‐Etienne, INSERM, SAINBIOSE U1059 Saint‐Étienne France

4. Orleans Regional Hospital Orleans France

5. Bordeaux‐Pellegrin University Hospital Bordeaux France

6. Rennes University Hospital Rennes France

7. Clermont‐Ferrand University Hospital Clermont‐Ferrand France

8. Montpellier University Hospital and University of Montpellier, INSRM, CNRS Montpellier France

9. Pierre‐Paul Riquet University Hospital, Toulouse III ‐ Paul Sabatier University, and INSERM UMR 1291, Purpan University Hospital Toulouse France

10. Le Mans General Hospital Le Mans France

11. Chartres Hospital Chartres France

12. University of Reims Champagne‐Ardenne, Faculty of Medicine, UR 3797 and Maison Blanche Hospital, Reims University Hospitals Reims France

13. Sainte‐Marguerite Hospital, Assistance Publique – Hôpitaux de Marseille Marseille France

14. Hautepierre Hospital, Strasbourg University Hospital Strasbourg France

15. Nord‐Ouest Val‐d'Oise Hospital Pontoise France

16. University of Paris, Hôpital Cochin. AP–HP, INSERM U1153, pôle de recherche et d'enseignement supérieur Sorbonne Paris‐Cité Paris France

17. Brest University Hospital, INSERM U1227 Brest France

18. Grenoble Alpes University Hospital Grenoble France

19. La Roche sur Yon Hospital La Roche sur Yon France

20. University Hospital of Tours and University of Tours Tours France

21. Université Paris‐Saclay, Hôpital Bicêtre, AP‐HP, INSERM UMR1184 Le Kremlin Bicêtre France

22. Sorbonne University–INSERM Centre De Recherche scientifique Saint‐Antoine, AP‐HP Saint‐Antoine Hospital Paris France

23. Le Havre Hospital Le Havre France

24. Châteaudun General Hospital Châteaudun France

25. Nantes University Hospital Nantes France

26. Cote Basque Hospital Bayonne France

27. Dijon University Hospital Dijon France

28. Université de Paris and INSERM UMR1132 Bioscar (Centre Viggo Petersen), Hôpital Lariboisière, AP‐HP Paris France

29. University Hospital of Amiens, Université de Picardie Jules Verne Amiens France

30. Institut Pierre Louis d'Epidémiologie et de Santé Publique University of Montpellier, INSERM, Centre Hospitalier Universitaire de Nîmes Montpellier France

31. Nancy University Hospital Nancy France

Abstract

ObjectiveWe assess the clinical and structural impact at two years of progressively spacing tocilizumab (TCZ) or abatacept (ABA) injections versus maintenance at full dose in patients with rheumatoid arthritis in sustained remission.MethodsThis multicenter open‐label noninferiority (NI) randomized clinical trial included patients with established rheumatoid arthritis in sustained remission receiving ABA or TCZ at a stable dose. Patients were randomized to treatment maintenance (M) at full dose (M‐arm) or progressive injection spacing (S) driven by the Disease Activity Score in 28 joints every 3 months up to biologics discontinuation (S‐arm). The primary end point was the evolution of disease activity according to the Disease Activity Score in 44 joints during the 2‐year follow‐up analyzed per protocol with a linear mixed‐effects model, evaluated by an NI test based on the one‐sided 95% confidence interval (95% CI) of the slope difference (NI margin 0.25). Other end points were flare incidence and structural damage progression.ResultsOverall, 202 of the 233 patients included were considered for per protocol analysis (90 in S‐arm and 112 in M‐arm). At the end of follow‐up, 16.2% of the patients in the S‐arm could discontinue their biologic disease‐modifying antirheumatic drug, 46.9% tapered the dose and 36.9% returned to a full dose. NI was not demonstrated for the primary outcome, with a slope difference of 0.10 (95% CI 0.10–0.31) between the two arms. NI was not demonstrated for flare incidence (difference 42.6%, 95% CI 30.0–55.1) or rate of structural damage progression at two years (difference 13.9%, 95% CI −6.7 to 34.4).ConclusionThe Towards the Lowest Efficacious Dose trial failed to demonstrate NI for the proposed ABA or TCZ tapering strategy.

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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