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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11 Suppl
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pubmed:dateCreated |
1993-12-27
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pubmed:abstractText |
Colony stimulating factors (CSF) are now widely used in marrow transplantation. Randomized trials have shown that granulocyte macrophage-CSF accelerates marrow recovery after autologous marrow transplantation, resulting in fewer infections, shorter hospitalization, and lower costs. Similar results have been seen with granulocyte-CSF. Both factors also can accelerate engraftment after allogenic marrow transplantation, but there is, so far, less evidence for clinical benefit in this setting. Both granulocyte macrophage-CSF and granulocyte-CSF benefit some patients with graft failure. The recent demonstration that both granulocyte-CSF and granulocyte macrophage-CSF can mobilize large numbers of hematopoietic stem cells into peripheral blood has resulted in the widespread use of this technique as an alternative to autologous marrow transplantation. A number of colony stimulating factors, including IL-1, IL-3, and steel factor, which act on early hematopoietic progenitors, have recently been entered into clinical trials, with the hope that the progress already made with G-CSF and GM-CSF can be continued.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0008-543X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3387-92
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8242572-Bone Marrow Transplantation,
pubmed-meshheading:8242572-Colony-Stimulating Factors,
pubmed-meshheading:8242572-Graft Rejection,
pubmed-meshheading:8242572-Humans,
pubmed-meshheading:8242572-Transplantation, Autologous,
pubmed-meshheading:8242572-Transplantation, Homologous
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pubmed:year |
1993
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pubmed:articleTitle |
The use of colony stimulating factors in marrow transplantation.
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pubmed:affiliation |
Fred Hutchinson Cancer Research Center, Seattle, WA 98104-2092.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review
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