Non-severe eosinophilic granulomatosis with polyangiitis: long-term outcomes after remission-induction trial

Author:

Puéchal Xavier1,Pagnoux Christian12,Baron Gabriel3,Lifermann François4,Geffray Loïk5,Quémeneur Thomas6,Saraux Jean-Luc7,Wislez Marie8,Cottin Vincent9,Ruivard Marc10,Limal Nicolas11,Aouba Achille12,Bonnotte Bernard13,Néel Antoine14,Agard Christian14,Cohen Pascal1,Terrier Benjamin1,Le Jeunne Claire1,Mouthon Luc1,Ravaud Philippe3,Guillevin Loïc1,Holy Benahary,Florence Gény,Pascal Godmer,Cédric Landron,Jean Christophe Lega,Véronique Le Guern,Alfred Mahr,Arsène Mékinian,Denis Mulleman,Jean-Marc Naccache,Louis Olagne,Diallo Alpha Oumar,Sylvain Palat,Vincent Poindron,Alexis Régent,Virginie Rieu,Anne Marie Ruppert,Pascale Soria,

Affiliation:

1. National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, APHP, Université Paris Descartes, Paris, France

2. Vasculitis Clinic, Mount Sinai Hospital, Toronto, Ontario, Canada

3. Université Paris Descartes, Hôtel-Dieu, APHP, Paris, France

4. Centre Hospitalier Côte d’Argent, Dax, France

5. Centre Hospitalier, Lisieux, France

6. Centre Hospitalier, Valenciennes, France

7. Centre Hospitalier Simone-Veil, Eaubonne, France

8. Hôpital Tenon, APHP, Université Pierre et Marie Curie, Paris, France

9. Hôpital Louis-Pradel, Lyon and UMR754, Université Claude Bernard Lyon 1, Lyon, France

10. Centre Hospitalier Universitaire Estaing, Clermont-Ferrand, France

11. Hôpital Henri-Mondor, Université Paris-Est Créteil, APHP, Créteil, France

12. Centre Hospitalier Universitaire Côte de Nacre, Caen, France

13. Centre Hospitalier Universitaire du Bocage, Dijon, France

14. Centre Hospitalier Universitaire Hôtel-Dieu, Nantes, France

Abstract

Abstract Objective In a previous controlled trial, 1-year adjunction of AZA to glucocorticoids (GC) for patients with non-severe, newly diagnosed eosinophilic granulomatosis with polyangiitis (EGPA) failed to lower remission failure, vasculitis relapse and isolated asthma/rhinosinus exacerbation rates, or cumulative GC use at month (M) 24. The aim of this study was to analyse longer-term outcomes to determine whether subsequent vasculitis relapse or isolated asthma/rhinosinus exacerbation (IARE) rates differed. Methods After M24, patients were followed prospectively, being treated based on physicians’ best judgment. Flares and reasons for increased GC dose or immunosuppressant use were recorded, and reviewed according to randomization group to distinguish vasculitis relapses from IAREs according to EGPA Task Force recommendations. Results Fifty EGPA trial participants were followed for a median (interquartile range) of 6.3 (5.4–7.6) years; two (4%) died 11 months post-inclusion. By M24, vasculitis had relapsed in 21/49 (43%) patients and 14/50 (28%) had IAREs. Another patient died 4.8 years post-inclusion (infection). Among nine patients with subsequent vasculitis relapses, three had a major relapse and three had their first relapse after M24; among 25 patients with later IAREs, 17 occurred after M24. At 5 years, respective vasculitis relapse and IARE rates were 48% (95% CI 34.0, 62.6) and 56% (95% CI 41.7, 70.8), with no between-arm differences (P = 0.32 and 0.13). No entry clinical or biological parameter was associated with these outcomes during follow-up. Conclusion These results confirmed that 1-year AZA and GC induction obtained good overall survival but no long-term benefit for non-severe EGPA patients. Vasculitis relapses, occurring mostly during the first 2 years, and IAREs, occurring throughout follow-up, require other preventive treatments. Trial registration ClinicalTrials.gov, https://clinicaltrials.gov, NCT00647166.

Funder

French Ministry of Health

Programme Hospitalier de Recherche Clinique

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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