Abstract | OBJECTIVE: METHODS: Clinical and safety data of patients with AAV treated with RTX were retrospectively assessed from the data of a German national registry. RESULTS: In total, 58 patients were included in this analysis (50/58 with granulomatosis with polyangiitis; 8/58 with microscopic polyangiitis who received at least 1 cycle, 17 patients who received 2 cycles, and 3 patients who received 3 cycles of RTX). Response was classified as complete and partial in 22 (40%) and in 29 cases (52.7%), respectively. Four patients (7.3%) were classified as nonresponders. CONCLUSION: RTX was well tolerated with good clinical efficacy in patients with refractory AAV.
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Authors | Petra Roll, Eva Ostermeier, Marion Haubitz, Svjetlana Lovric, Leonore Unger, Julia Holle, Ina Kötter, Jörg C Henes, Raoul Bergner, Andrea Rubbert-Roth, Christof Specker, Hendrik Schulze-Koops, Ulf Müller-Ladner, Martin Fleck, Gerd-Rüdiger Burmester, Falk Hiepe, Stefan Heitmann, Martin Aringer, Rebecca Fischer-Betz, Thomas Dörner, Hans-Peter Tony |
Journal | The Journal of rheumatology
(J Rheumatol)
Vol. 39
Issue 11
Pg. 2153-6
(Nov 2012)
ISSN: 0315-162X [Print] Canada |
PMID | 22984269
(Publication Type: Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal, Murine-Derived
- Antirheumatic Agents
- Rituximab
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Topics |
- Adult
- Aged
- Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
(drug therapy, epidemiology)
- Antibodies, Monoclonal, Murine-Derived
(adverse effects, therapeutic use)
- Antirheumatic Agents
(adverse effects, therapeutic use)
- Cohort Studies
- Dose-Response Relationship, Drug
- Female
- Germany
(epidemiology)
- Humans
- Male
- Middle Aged
- Registries
- Retrospective Studies
- Rituximab
- Time Factors
- Treatment Outcome
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