Rituximab versus azathioprine for maintenance of remission for patients with ANCA-associated vasculitis and relapsing disease: an international randomised controlled trial

Author:

Smith Rona MORCID,Jones Rachel B,Specks Ulrich,Bond Simon,Nodale MariannaORCID,Al-jayyousi Reem,Andrews Jacqueline,Bruchfeld Annette,Camilleri Brian,Carette Simon,Cheung Chee Kay,Derebail Vimal,Doulton Tim,Ferraro Alastair,Forbess Lindsy,Fujimoto ShouichiORCID,Furuta ShunsukeORCID,Gewurz-Singer Ora,Harper LorraineORCID,Ito-Ihara Toshiko,Khalidi NaderORCID,Klocke Rainer,Koening Curry,Komagata Yoshinori,Langford Carol,Lanyon Peter,Luqmani Raashid,McAlear Carol,Moreland Larry W,Mynard Kim,Nachman Patrick,Pagnoux Christian,Peh Chen Au,Pusey Charles,Ranganathan Dwarakanathan,Rhee Rennie LORCID,Spiera RobertORCID,Sreih Antoine G,Tesar Vladamir,Walters GilesORCID,Wroe Caroline,Jayne DavidORCID,Merkel Peter A

Abstract

ObjectiveFollowing induction of remission with rituximab in anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) relapse rates are high, especially in patients with history of relapse. Relapses are associated with increased exposure to immunosuppressive medications, the accrual of damage and increased morbidity and mortality. The RITAZAREM trial compared the efficacy of repeat-dose rituximab to daily oral azathioprine for prevention of relapse in patients with relapsing AAV in whom remission was reinduced with rituximab.MethodsRITAZAREM was an international randomised controlled, open-label, superiority trial that recruited 188 patients at the time of an AAV relapse from 29 centres in seven countries between April 2013 and November 2016. All patients received rituximab and glucocorticoids to reinduce remission. Patients achieving remission by 4 months were randomised to receive rituximab intravenously (1000 mg every 4 months, through month 20) (85 patients) or azathioprine (2 mg/kg/day, tapered after month 24) (85 patients) and followed for a minimum of 36 months. The primary outcome was time to disease relapse (either major or minor relapse).ResultsRituximab was superior to azathioprine in preventing relapse: HR 0.41; 95% CI 0.27 to 0.61, p<0.001. 19/85 (22%) patients in the rituximab group and 31/85 (36%) in the azathioprine group experienced at least one serious adverse event during the treatment period. There were no differences in rates of hypogammaglobulinaemia or infection between groups.ConclusionsFollowing induction of remission with rituximab, fixed-interval, repeat-dose rituximab was superior to azathioprine for preventing disease relapse in patients with AAV with a prior history of relapse.Trial registration numberNCT01697267; ClinicalTrials.gov identifier

Funder

Roche/Genentech

National Center for Research Resources

Versus Arthritis

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Research Committee on Intractable Vasculitides, the Ministry of Health, Labour and Welfare of Japan

Publisher

BMJ

Subject

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

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