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Rituximab as therapy to induce remission after relapse in ANCA-associated vasculitis

Rituximab as therapy to induce remission after relapse in ANCA-associated vasculitis

Authors :
Smith, Rona M
Jones, Rachel Bronwen
Specks, Ulrich
Bond, Simon
Nodale, Marianna
Aljayyousi, Reem
Andrews, Jacqueline
Bruchfeld, Annette
Camilleri, Brian
Carette, Simon
Cheung, Chee Kay
Derebail, Vimal
Doulton, Tim
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 Ahmed
Makino, Hirofumi
McAlear, Carole
Monach, Paul
Moreland, Larry W
Mynard, Kim
Nachman, Patrick
Pagnoux, Christian
Pearce, Fiona
Peh, Chen Au
Pusey, Charles
Ranganathan, Dwarakanathan
Rhee, Rennie L
Spiera, Robert
Sreih, Antoine G
Tesar, Vladimir
Walters, Giles
Weisman, Michael H
Wroe, Caroline
Merkel, Peter
Jayne, David
RITAZAREM Co-Investigators
Arimura, Y
Clarkson, M
De Zoysa, J
Endo, T
Hamano, Y
Kono, H
Lawman, S
Muso, E
Sada, K
Smith, R
Suzuki, K
Tsukamoto, T
Uchida, S
Vaglio, A
Watts, R
Smith, Rona M [0000-0002-7438-5156]
Jones, Rachel Bronwen [0000-0003-4790-283X]
Nodale, Marianna [0000-0002-0333-8918]
Harper, Lorraine [0000-0003-1343-9234]
Rhee, Rennie L [0000-0002-4907-0304]
Walters, Giles [0000-0003-4854-9353]
Apollo - University of Cambridge Repository
Publication Year :
2020
Publisher :
Apollo - University of Cambridge Repository, 2020.

Abstract

Funder: Research Committee on Intractable Vasculitides; The Ministry of Health, Labour and Welfare of Japan.<br />Objectives: Evaluation of rituximab and glucocorticoids as therapy to induce remission after relapse in ANCA-associated vasculitis (AAV) in a prospective observational cohort of patients enrolled into the induction phase of the RITAZAREM trial. Methods: Patients relapsing with granulomatosis with polyangiitis or microscopic polyangiitis were prospectively enrolled and received remission-induction therapy with rituximab (4×375 mg/m2) and a higher or lower dose glucocorticoid regimen, depending on physician choice: reducing from either 1 mg/kg/day or 0.5 mg/kg/day to 10 mg/day by 4 months. Patients in this cohort achieving remission were subsequently randomised to receive one of two regimens to prevent relapse. Results: 188 patients were studied: 95/188 (51%) men, median age 59 years (range 19–89), prior disease duration 5.0 years (range 0.4–34.5). 149/188 (79%) had previously received cyclophosphamide and 67/188 (36%) rituximab. 119/188 (63%) of relapses had at least one major disease activity item, and 54/188 (29%) received the higher dose glucocorticoid regimen. 171/188 (90%) patients achieved remission by 4 months. Only six patients (3.2% of the study population) did not achieve disease control at month 4. Four patients died in the induction phase due to pneumonia (2), cerebrovascular accident (1), and active vasculitis (1). 41 severe adverse events occurred in 27 patients, including 13 severe infections. Conclusions: This large prospective cohort of patients with relapsing AAV treated with rituximab in conjunction with glucocorticoids demonstrated a high level of efficacy for the reinduction of remission in patients with AAV who have relapsed, with a similar safety profile to previous studies.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....00eb19930c07ed5ca18b8847e880d4f2
Full Text :
https://doi.org/10.17863/cam.54395