| Literature DB >> 20456363 |
Philip S Rosenberg1, Cornelia Zeidler, Audrey A Bolyard, Blanche P Alter, Mary A Bonilla, Laurence A Boxer, Yigal Dror, Sally Kinsey, Daniel C Link, Peter E Newburger, Akiko Shimamura, Karl Welte, David C Dale.
Abstract
In severe congenital neutropenia (SCN), long-term therapy with granulocyte colony-stimulating factor (G-CSF) has reduced mortality from sepsis, revealing an underlying predisposition to myelodysplastic syndrome and acute myeloid leukaemia (MDS/AML). We have reported the early pattern of evolution to MDS/AML, but the long-term risk remains uncertain. We updated a prospective study of 374 SCN patients on long-term G-CSF enrolled in the Severe Chronic Neutropenia International Registry. Long-term, the annual risk of MDS/AML attained a plateau (2.3%/year after 10 years). This risk now appears similar to, rather than higher than, the risk of AML in Fanconi anaemia and dyskeratosis congenita.Entities:
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Year: 2010 PMID: 20456363 PMCID: PMC2906693 DOI: 10.1111/j.1365-2141.2010.08216.x
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998