| Reference : Accelerated erythroid repopulation with no stem-cell competition effect in children trea... |
| Scientific journals : Article | |||
| Human health sciences : Hematology | |||
| http://hdl.handle.net/2268/6635 | |||
| Accelerated erythroid repopulation with no stem-cell competition effect in children treated with recombinant human erythropoietin after allogeneic bone marrow transplantation. | |
| English | |
| Locatelli, F. [> > > >] | |
| Zecca, M. [> > > >] | |
Beguin, Yves [Centre Hospitalier Universitaire de Liège - CHU > > Hématologie clinique >] | |
| Giorgiani, G. [> > > >] | |
| Ponchio, L. [> > > >] | |
| De Stefano, P. [> > > >] | |
| Cazzola, M. [> > > >] | |
| 1993 | |
| British Journal of Haematology | |
| Blackwell Publishing | |
| 84 | |
| 4 | |
| 752-4 | |
| International | |
| 0007-1048 | |
| 1365-2141 | |
| Oxford | |
| United Kingdom | |
| [en] Adolescent ; Blood Transfusion ; Bone Marrow Transplantation/pathology ; Child ; Child, Preschool ; Erythrocyte Count ; Erythropoiesis/drug effects ; Erythropoietin/therapeutic use ; Female ; Humans ; Infant ; Male ; Pilot Projects ; Postoperative Care/methods ; Postoperative Period ; Receptors, Transferrin/metabolism ; Recombinant Proteins/therapeutic use | |
| [en] We carried out a pilot study on the use of recombinant human erythropoietin (rHuEPO) to accelerate erythropoietic engraftment in paediatric patients undergoing allogeneic BMT. rHuEPO was administered intravenously at a dose of 75 U/kg per day for 30 d after transplant. Erythroid repopulation, evaluated sequentially through the serum transferrin receptor, was faster in 15 patients receiving rHuEPO than in 16 historical controls (P = 0.0003). This faster erythroid engraftment resulted in a reduction in the total number of red blood cell units required to reach transfusion independence (2.7 +/- 1.2 v 4.2 +/- 2.3, P = 0.027). No significant difference in leucocyte or platelet regeneration was observed. These findings indicate that rHuEPO administration can accelerate erythroid recovery after allogeneic BMT and reduce red cell transfusion requirements with no stem-cell competition effect. | |
| http://hdl.handle.net/2268/6635 |
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