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Consensus of German Transplant Centers on Hematopoietic Stem Cell Transplantation in Fanconi Anemia
Author(s) -
Mwe Mwe Chao,
Wolfram Ebell,
Peter Bader,
Rita Beier,
Birgit Burkhardt,
Tobias Feuchtinger,
Rupert Handgretinger,
Helmut Hanenberg,
Ulrike Koehl,
Christian P. Kratz,
Bernhard Kremens,
Peter Lang,
Roland Meisel,
Ingo Mueller,
C. Roessig,
Martin G. Sauer,
Paul G. Schlegel,
Ansgar Schulz,
Brigitte Strahm,
Felicitas Thol,
Karl W. Sykora
Publication year - 2015
Publication title -
klinische pädiatrie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.228
H-Index - 44
eISSN - 1439-3824
pISSN - 0300-8630
DOI - 10.1055/s-0035-1548841
Subject(s) - fanconi anemia , hematopoietic stem cell transplantation , medicine , transplantation , savior sibling , graft versus host disease , stem cell , anemia , oncology , disease , aplastic anemia , pediatrics , surgery , intensive care medicine , dna repair , bone marrow , biology , biochemistry , genetics , gene
Allogeneic hematopoietic stem cell transplantation (HSCT) is currently the only curative therapy for the severe hematopoietic complications associated with Fanconi anemia (FA). In Germany, it is estimated that 10-15 transplants are performed annually for FA. However, because FA is a DNA repair disorder, standard conditioning regimens confer a high risk of excessive regimen-related toxicities and mortality, and reduced intensity regimens are linked with graft failure in some FA patients. Moreover, development of graft-versus-host disease is a major contributing factor for secondary solid tumors. The relative rarity of the disorder limits HSCT experience at any single center. Consensus meetings were convened to develop a national approach for HSCT in FA. This manuscript outlines current experience and knowledge about HSCT in FA and, based on this analysis, general recommendations reached at these meetings.

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