Limitations of standard immunosuppressive treatment in ANCA-associated vasculitis and lupus nephritis
Language English Country Switzerland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
25412878
DOI
10.1159/000368569
PII: 000368569
Knihovny.cz E-resources
- MeSH
- Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis drug therapy MeSH
- Immunosuppressive Agents adverse effects therapeutic use MeSH
- Drug Therapy, Combination MeSH
- Humans MeSH
- Lupus Nephritis drug therapy MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Immunosuppressive Agents MeSH
Introduction of the standard immunosuppressive treatment has dramatically changed the outcome of patients with both ANCA-associated vasculitis and lupus nephritis, transforming them from incurable diseases with very high short-term mortality to chronic debilitating diseases with much lower short-term, but still relatively high long-term, morbidity/mortality. Long-term morbidity with damage accumulating partly due to the adverse events of the available treatment (namely gonadal toxicity, malignancy, bone disease, cataracts, diabetes, and thromboembolic and cardiovascular disease) has become a major concern. Although cyclophosphamide-based regimens have been partly replaced by newer agents in both ANCA-associated vasculitis and lupus nephritis (namely rituximab or mycophenolate, respectively) their short-term and medium-term adverse events may not be significantly less frequent and we can only hope that new treatments will translate into better long-term outcomes including better long-term safety.
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