Source:http://linkedlifedata.com/resource/pubmed/id/15931632
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2005-6-2
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pubmed:abstractText |
We prospectively compared outcomes after a fludarabine (Flu) plus oral busulfan (Bu)-containing reduced-intensity conditioning regimen (150 mg/m2 Flu and 10 mg/kg oral Bu), with (n = 32; Flu- T Bu group) or without (n = 30; Flu-Bu group) therapeutic dose monitoring and dose adjustment of Bu. All patients received peripheral blood stem cells from a genoidentical sibling, and study cohorts had similar patient characteristics. Dose adjustments of Bu were required in 20 (63%) patients in the Flu- T Bu group (median final dose, 8.89 mg/kg; range, 6.3-13.34 mg/kg). Donor T-cell and granulocyte engraftments were similar, and early conditioning-related toxicities were mild and similar in both study groups. With a median follow-up of 45 months (51 months in the 37 survivors), posttransplantation outcomes did not differ between cohorts. The strongest predictor of 2-year overall survival and leukemia-free survival was the presence of chronic graft-versus-host disease (77% versus 34% for overall survival and 74% versus 34% for leukemia-free survival; P < .001 for both outcomes). In conclusion, therapeutic dose monitoring of oral Bu in a reduced-intensity conditioning setting does not seem to affect outcome, although further studies may identify very-high-risk patients who benefit from this strategy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1083-8791
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pubmed:author |
pubmed-author:BrionesJavierJ,
pubmed-author:BrunetSalutS,
pubmed-author:CañizoConsueloC,
pubmed-author:CaballeroDoloresD,
pubmed-author:ClopésAnaA,
pubmed-author:MartinoRodrigoR,
pubmed-author:MateosMariviM,
pubmed-author:MorenoEstelaE,
pubmed-author:Pérez-SimónJosé AJA,
pubmed-author:QueraltóJosé MJM,
pubmed-author:San MiguelJesús FJF,
pubmed-author:SierraJorgeJ,
pubmed-author:SuredaAnnaA,
pubmed-author:VazquezLourdesL
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pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
437-47
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15931632-Administration, Oral,
pubmed-meshheading:15931632-Adult,
pubmed-meshheading:15931632-Aged,
pubmed-meshheading:15931632-Busulfan,
pubmed-meshheading:15931632-Disease-Free Survival,
pubmed-meshheading:15931632-Female,
pubmed-meshheading:15931632-Follow-Up Studies,
pubmed-meshheading:15931632-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:15931632-Humans,
pubmed-meshheading:15931632-Immunosuppressive Agents,
pubmed-meshheading:15931632-Leukemia, Myeloid,
pubmed-meshheading:15931632-Male,
pubmed-meshheading:15931632-Middle Aged,
pubmed-meshheading:15931632-Retrospective Studies,
pubmed-meshheading:15931632-Transplantation, Homologous,
pubmed-meshheading:15931632-Transplantation Conditioning,
pubmed-meshheading:15931632-Vidarabine
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pubmed:year |
2005
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pubmed:articleTitle |
Reduced-intensity conditioning allogeneic blood stem cell transplantation with fludarabine and oral busulfan with or without pharmacokinetically targeted busulfan dosing in patients with myeloid leukemia ineligible for conventional conditioning.
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pubmed:affiliation |
Division of Clinical Hematology, Hospital de la Sant Creu i Sant Pau, Universitat Autónoma de Barcelona, Barcelona, Spain. rmartino@hsp.santpau.es
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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