| Literature DB >> 26810455 |
Paolo Ricchi1, Silvia Costantini2, Anna Spasiano2, Gianfranco De Dominicis3, Tiziana Di Matola4, Patrizia Cinque2, Massimiliano Ammirabile2, Maria Marsella2, Aldo Filosa2.
Abstract
Patients with Non-Transfusion-Dependent Thalassemia may require regular transfusion therapy. However, these patients are at risk of developing irregular antibodies, making them untransfusable. Second line treatment usually includes hydroxyurea, which however is not effective in all patients. Other treatment options include thalidomide, which has been reported to be safe and effective in selected patients. We report the case of a patient who experienced improvement of hemoglobin levels and of a part of NTDT related complications, following 36months of continuous therapy with low doses of thalidomide.Entities:
Keywords: Bone marrow; Macrophages; NTDT; Thalidomide
Mesh:
Substances:
Year: 2016 PMID: 26810455 DOI: 10.1016/j.bcmd.2016.01.003
Source DB: PubMed Journal: Blood Cells Mol Dis ISSN: 1079-9796 Impact factor: 3.039