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Long‐Term Outcomes Among Participants in the WEGENT Trial of Remission‐Maintenance Therapy for Granulomatosis With Polyangiitis (Wegener's) or Microscopic Polyangiitis

医学 显微镜下多血管炎 肉芽肿伴多发性血管炎 中止 内科学 硫唑嘌呤 不利影响 置信区间 随机对照试验 维持疗法 血管炎 外科 胃肠病学 化疗 疾病
作者
Xavier Puéchal,Christian Pagnoux,Élodie Perrodeau,M. Hamidou,Jean‐Jacques Boffa,X. Kyndt,François Lifermann,Thomas Papo,Dominique Merrien,Amar Smaïl,Philippe Delaval,Catherine Hanrotel‐Saliou,B. Imbert,C. Khouatra,M. Lambert,Charles Leské,K.H. Ly,Édouard Pertuiset,P. Roblot,M. Ruivard,Jean‐François Subra,Jean‐François Viallard,Benjamin Terrier,Pascal Cohen,Luc Mouthon,Claire Le Jeunne,Philippe Ravaud,Loı̈c Guillevin
出处
期刊:Arthritis & rheumatology [Wiley]
卷期号:68 (3): 690-701 被引量:123
标识
DOI:10.1002/art.39450
摘要

Findings from the WEGENT trial and other short-term studies have suggested that azathioprine (AZA) or methotrexate (MTX) could effectively maintain remission of granulomatosis with polyangiitis (Wegener's) (GPA) or microscopic polyangiitis (MPA). This study was undertaken to examine whether differences in rates of relapse or adverse events would appear after discontinuation of these 2 maintenance regimens, when assessed over a longer followup period.Long-term outcomes in patients enrolled in the WEGENT trial were analyzed according to their randomized treatment group (AZA or MTX). Parameters at trial entry were evaluated as potential prognostic factors for death, relapse, or damage in multivariate models.Data from 10 years of followup were available for 112 (88.8%) of the 126 original trial participants. The median followup time was 11.9 years (95% confidence interval [95% CI] 11.3-12.5 years). In patients receiving AZA and those receiving MTX, the 10-year overall survival rates were 75.1% (95% CI 64.8-86.9%) and 79.9% (95% CI 70.3-90.8%) (P = 0.56), respectively, and relapse-free survival rates were 26.3% (95% CI 17.3-40.1%) and 33.5% (95% CI 23.5-47.7%) (P = 0.29), respectively. No between-treatment differences were observed with regard to rates of relapse, adverse events, damage, survival without severe side effects, and survival without relapse and severe side effects. In analyses limited to the 97 patients with GPA, no between-treatment differences in survival rates were observed. The 10-year relapse-free survival rate was lower in patients with GPA than in patients with MPA. However, in the multivariate analysis, anti-proteinase 3 antineutrophil cytoplasmic antibody (ANCA) positivity, and not GPA, was retained as being independently associated with the relapse rate.The results of this long-term analysis confirm that AZA and MTX are comparable treatment options for maintaining remission of GPA or MPA. Despite achieving good overall survival with these treatments, relapse rates, adverse events, and damage remain matters of concern and further studies are needed to reduce their frequency in these ANCA-associated vasculitides.
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