Rituximab for treatment of severe renal disease in ANCA associated vasculitis
Language English Country Italy Media print-electronic
Document type Comparative Study, Journal Article, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
UL1 TR 001079
NCATS NIH HHS - United States
PubMed
25986390
DOI
10.1007/s40620-015-0208-y
PII: 10.1007/s40620-015-0208-y
Knihovny.cz E-resources
- Keywords
- ANCA vasculitis, Renal disease, Rituximab,
- MeSH
- Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis diagnosis drug therapy immunology mortality MeSH
- Time Factors MeSH
- Kidney Failure, Chronic immunology prevention & control MeSH
- Cyclophosphamide therapeutic use MeSH
- Renal Dialysis MeSH
- Glomerulonephritis diagnosis drug therapy immunology mortality MeSH
- Glucocorticoids therapeutic use MeSH
- Glomerular Filtration Rate drug effects MeSH
- Immunosuppressive Agents adverse effects therapeutic use MeSH
- Remission Induction MeSH
- Drug Therapy, Combination MeSH
- Combined Modality Therapy MeSH
- Kidney drug effects physiopathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Recovery of Function MeSH
- Disease Progression MeSH
- Retrospective Studies MeSH
- Rituximab adverse effects therapeutic use MeSH
- Aged MeSH
- Severity of Illness Index MeSH
- Plasma Exchange MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Comparative Study MeSH
- Geographicals
- Europe MeSH
- United States MeSH
- Names of Substances
- Cyclophosphamide MeSH
- Glucocorticoids MeSH
- Immunosuppressive Agents MeSH
- Rituximab MeSH
BACKGROUND: Rituximab (RTX) is approved for remission induction in ANCA associated vasculitis (AAV). However, data on use of RTX in patients with severe renal disease is lacking. METHODS: We conducted a retrospective multi-center study to evaluate the efficacy and safety of RTX with glucocorticoids (GC) with and without use of concomitant cyclophosphamide (CYC) for remission induction in patients presenting with e GFR less than 20 ml/min/1.73 m(2). We evaluated outcomes of remission at 6 months (6 M), renal recovery after acute dialysis at diagnosis, e-GFR rise at 6 M, patient and renal survival and adverse events. RESULTS: A total 37 patients met the inclusion criteria. The median age was 61 years. (55-73), 62 % were males, 78 % had new diagnosis and 59 % were MPO ANCA positive. The median (IQR) e-GFR at diagnosis was 13 ml/min/1.73 m(2) (7-16) and 15 required acute dialysis. Eleven (30 %) had alveolar hemorrhage. Twelve (32 %) received RTX with GC, 25 (68 %) received RTX with GC and CYC and seventeen (46 %) received plasma exchange. The median (IQR) follow up was 973 (200-1656) days. Thirty two of 33 patients (97 %) achieved remission at 6 M and 10 of 15 patients (67 %) requiring dialysis recovered renal function. The median prednisone dose at 6 M was 6 mg/day. The mean (SD) increase in e-GFR at 6 months was 14.5 (22) ml/min/m(2). Twelve patients developed ESRD during follow up. There were 3 deaths in the first 6 months. When stratified by use of concomitant CYC, there were no differences in baseline e GFR, use of plasmapheresis, RTX dosing regimen or median follow up days between the groups. No differences in remission, renal recovery ESRD or death were observed. CONCLUSIONS: This study of AAV patients with severe renal disease demonstrates that the outcomes appear equivalent when treated with RTX and GC with or without concomitant CYC.
Addenbrooke's Hospital Cambridge UK
Department of Clinical and Experimental Medicine Linköping University Linköping Sweden
Department of Medicine Hospital of the University of Pennsylvania Philadelphia USA
Department of Medicine Johns Hopkins University Baltimore MD USA
Department of Medicine Linkoping University Linkoping Sweden
Department of Nephrology Charles University Prague Czech Republic
Department of Rheumatology Linköping University Linköping Sweden
Hospital 12 de Octubre in Madrid Madrid Spain
Johns Hopkins Bayview Medical Center Johns Hopkins University Baltimore MD 21224 USA
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