PMID- 20596502 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20110714 LR - 20220408 IS - 1178-203X (Electronic) IS - 1176-6336 (Print) IS - 1176-6336 (Linking) VI - 6 DP - 2010 Jun 24 TI - Management of ANCA-associated vasculitis: Current trends and future prospects. PG - 253-64 AB - The antineutrophil cytoplasm antibody (ANCA)-associated vasculitides are a spectrum of heterogeneous autoimmune diseases characterized by necrotizing small vessel vasculitis and the presence of ANCA. These chronic multisystem disorders may be life-threatening if there is major organ involvement, such as acute renal failure or pulmonary hemorrhage, and require significant initial immunosuppression and long-term maintenance treatment. Long-established protocols using cyclophosphamide and prednisolone have resulted in dramatically improved outcomes for patients since the 1970s. Subsequently, international collaboration has contributed to a growing evidence base and consensus in the management of these rare disorders. Modifications to traditional treatment protocols by the use of azathioprine or methotrexate rather than cyclophosphamide, and the introduction of newer agents, such as rituximab, has maintained outcomes whilst decreasing toxicity. However, the treatment limitations of incomplete efficacy, infection, and cumulative toxicity persist. These issues have continued to drive the search for safer and more effective modulation of the immune system using targeted immunotherapy. This review will explore the current evidence base for management of ANCA-associated vasculitis and future treatment prospects. FAU - Hamour, Sally AU - Hamour S AD - Imperial College Kidney and Transplant Institute, Imperial College, London, UK. FAU - Salama, Alan D AU - Salama AD FAU - Pusey, Charles D AU - Pusey CD LA - eng PT - Journal Article DEP - 20100624 PL - New Zealand TA - Ther Clin Risk Manag JT - Therapeutics and clinical risk management JID - 101253281 PMC - PMC2893757 OTO - NOTNLM OT - ANCA OT - treatment OT - vasculitis EDAT- 2010/07/03 06:00 MHDA- 2010/07/03 06:01 PMCR- 2010/06/24 CRDT- 2010/07/03 06:00 PHST- 2010/06/10 00:00 [received] PHST- 2010/07/03 06:00 [entrez] PHST- 2010/07/03 06:00 [pubmed] PHST- 2010/07/03 06:01 [medline] PHST- 2010/06/24 00:00 [pmc-release] AID - tcrm-6-253 [pii] AID - 10.2147/tcrm.s6112 [doi] PST - epublish SO - Ther Clin Risk Manag. 2010 Jun 24;6:253-64. doi: 10.2147/tcrm.s6112.