Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes

R. Peffault De Latour, C. Peters, B. Gibson, B. Strahm, A. Lankester, C. D. De Heredia, D. Longoni, F. Fioredda, Franco Locatelli, I. Yaniv, J. Wachowiak, J. Donadieu, A. Lawitschka, M. Bierings, M. Wlodarski, S. Corbacioglu, S. Bonanomi, S. Samarasinghe, T. Leblanc, C. DufourJ. H. Dalle

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) offers the potential to cure patients with an inherited bone marrow failure syndrome (IBMFS). However, the procedure involves the risk of treatment-related mortality and may be associated with significant early and late morbidity. For these reasons, the benefits should be carefully weighed against the risks. IBMFS are rare, whereas case reports and small series in the literature illustrate highly heterogeneous practices in terms of indications for HSCT, timing, stem cell source and conditioning regimens. A consensus meeting was therefore held in Vienna in September 2012 on behalf of the European Group for Blood and Marrow Transplantation to discuss HSCT in the setting of IBMFS. This report summarizes the recommendations from this expert panel, including indications for HSCT, timing, stem cell source and conditioning regimen.
Lingua originaleEnglish
pagine (da-a)1168-1172
Numero di pagine5
RivistaBone Marrow Transplantation
Volume50
DOI
Stato di pubblicazionePubblicato - 2015

Keywords

  • HSCT

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