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-α 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-α, i.e. antibodies or other immune suppressants, in the rare patients with primary eosinophilia.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Current Drug Targets |
| Vol/bind | 12 |
| Udgave nummer | 3 |
| Sider (fra-til) | 429-32 |
| Antal sider | 4 |
| ISSN | 1389-4501 |
| Status | Udgivet - 2011 |
Fingeraftryk
Dyk ned i forskningsemnerne om 'Interferon treatment in patients with hypereosinophilia'. Sammen danner de et unikt fingeraftryk.Citationsformater
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