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Rituximab versus azathioprine for maintenance of remission for patients with ANCA-associated vasculitis and relapsing disease: an international randomised controlled trial.
Smith, Rona M; Jones, Rachel B; Specks, Ulrich; Bond, Simon; Nodale, Marianna; Al-Jayyousi, Reem; Andrews, Jacqueline; Bruchfeld, Annette; Camilleri, Brian; Carette, Simon; Cheung, Chee Kay; Derebail, Vimal; Doulton, Tim; Ferraro, Alastair; Forbess, Lindsy; Fujimoto, Shouichi; Furuta, Shunsuke; Gewurz-Singer, Ora; Harper, Lorraine; Ito-Ihara, Toshiko; Khalidi, Nader; 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 L; Spiera, Robert; Sreih, Antoine G; Tesar, Vladamir; Walters, Giles; Wroe, Caroline; Jayne, David; Merkel, Peter A.
Affiliation
  • Smith RM; Medicine, University of Cambridge, Cambridge, UK rms50@cam.ac.uk.
  • Jones RB; Renal Medicine, Addenbrooke's Hospital, Cambridge, UK.
  • Specks U; Pulmonary Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Bond S; Cambridge Clinical Trials Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Nodale M; Cambridge Clinical Trials Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Al-Jayyousi R; Nephrology, University Hospitals of Leicester NHS Trust, Leicester, UK.
  • Andrews J; NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals Trust, Leeds, UK.
  • Bruchfeld A; Nephrology, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden.
  • Camilleri B; Nephrology, Ipswich Hospital NHS Trust, Ipswich, UK.
  • Carette S; Rheumatology, University of Toronto, Toronto, Ontario, Canada.
  • Cheung CK; Nephrology, University of Leicester, Leicester, UK.
  • Derebail V; Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Doulton T; Nephrology, East Kent Hospitals University NHS Foundation Trust, Canterbury, UK.
  • Ferraro A; Nephrology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Forbess L; Rheumatology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Fujimoto S; Hemovascular Medicine and Artificial Organs, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Furuta S; Allergy and Clinical Immunology, Chiba University, Chiba, Japan.
  • Gewurz-Singer O; Rheumatology, University of Michigan, Ann Arbor, Michigan, USA.
  • Harper L; Nephrology, University of Birmingham, Birmingham, UK.
  • Ito-Ihara T; The Clinical and Translational Research Center, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Khalidi N; Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Klocke R; Rheumatology, Dudley Group of Hospitals NHS Trust, Dudley, UK.
  • Koening C; Rheumatology, The University of Utah, Salt Lake City, Utah, USA.
  • Komagata Y; First Department of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan.
  • Langford C; Rheumatic and Immunologic Diseases, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
  • Lanyon P; Rheumatology, Nottingham University Hospital, Nottingham, UK.
  • Luqmani R; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science (NDORMs), University of Oxford, Oxford, UK.
  • McAlear C; Rheumatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Moreland LW; Medicine/Rheumatology, University of Pittsburg, Pittsburg, Pennsylvania, USA.
  • Mynard K; Vasculitis and lupus clinic, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Nachman P; UNC Kidney Center, Division of Nephrology and Hypertension, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Pagnoux C; Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Peh CA; Nephrology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Pusey C; Medicine, Imperial College London, London, UK.
  • Ranganathan D; Medicine, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.
  • Rhee RL; Rheumatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Spiera R; Rheumatology, Hospital for Special Surgery, New York, New York, USA.
  • Sreih AG; Rheumatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Tesar V; Medicine, Charles University, Praha, Czech Republic.
  • Walters G; Nephrology, Australian National University Medical School, Canberra, Australian Capital Territory, Australia.
  • Wroe C; Nephrology, South Tees Hospitals NHS Foundation Trust, Middlesbrough, UK.
  • Jayne D; Medicine, Addenbrooke's Hospital, Cambridge, UK.
  • Merkel PA; Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Ann Rheum Dis ; 82(7): 937-944, 2023 07.
Article in En | MEDLINE | ID: mdl-36958796
ABSTRACT

OBJECTIVE:

Following 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.

METHODS:

RITAZAREM 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).

RESULTS:

Rituximab 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.

CONCLUSIONS:

Following 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 NUMBER NCT01697267; ClinicalTrials.gov identifier.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Azathioprine / Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Ann Rheum Dis Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Azathioprine / Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Ann Rheum Dis Year: 2023 Document type: Article Affiliation country:
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