Abstract
Most of the primary conditions with eosinophilia have now been characterized by clonality in 2008 by the WHO classification, which thereby provide a basis for separation of patients who may benefit a targeted therapy, i.e. by tyrosine kinase inhibition--and who may not. Treatment with interferon-a was introduced some 20 years ago and still has a role in subsets of patients, which is evident from this review of casuistic reports of treatment. However, controlled, randomized, prospective, clinical trials in multi-center studies are needed to clarify dosages, monitoring, prognosis and perhaps combination therapies with interferon-a, i.e. antibodies or other immune suppressants, in the rare patients with primary eosinophilia.
Originalsprog | Engelsk |
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Tidsskrift | Current Drug Targets |
Vol/bind | 12 |
Udgave nummer | 3 |
Sider (fra-til) | 429-32 |
Antal sider | 4 |
ISSN | 1389-4501 |
Status | Udgivet - 2011 |