Source:http://linkedlifedata.com/resource/pubmed/id/11128811
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-12-20
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pubmed:abstractText |
Chronic graft-versus-host disease (GVHD) is the principal cause of transplantation-related morbidity and nonrelapse mortality late after allogeneic hematopoietic stem cell transplantation. The safety and potential efficacy of tacrolimus for the salvage treatment of chronic GVHD was evaluated in a single-arm, open-label phase 2 study. A total of 39 evaluable patients with chronic GVHD who failed previous immunosuppressive therapy with cyclosporine and prednisone were treated with tacrolimus starting at a median of 20 months (range, 3-68 months) after transplantation. At 3 years after the start of treatment, 5 patients (13%) had discontinued tacrolimus and were in complete remission, and 3 were considered clinically stable but not able to discontinue tacrolimus. A total of 31 patients (79%) experienced treatment failure; 22 (56%) who failed therapy had a change in immunosuppressive regimen because of progression (n = 18) or toxicity (n = 4). Nine patients (23%) died during continued treatment with tacrolimus. Two patients were lost to follow-up, at 11 and 19 months. The median duration of treatment with tacrolimus was 9 months (range, 1-29 months). Infections (144 episodes) were the most frequent adverse event. Nephrotoxicity occurred in 16 patients (41%); tacrolimus was discontinued in only 2 patients because of progressive deterioration in renal function. The Kaplan-Meier estimate of survival was 64% (95% confidence interval, 49%-79%) at 3 years posttransplantation. Seven patients had discontinued all immunosuppression at last contact, leading to an estimated 29% probability of stopping all immunosuppression by 3 years posttransplantation. Four patients died after relapse of malignancy. The response rate is consistent with previous reports of salvage treatment for chronic GVHD, indicating that a small group of patients failing cyclosporine may respond or stabilize with tacrolimus.
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pubmed:grant | |
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:issn |
1083-8791
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
613-20
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11128811-Adolescent,
pubmed-meshheading:11128811-Adult,
pubmed-meshheading:11128811-Child,
pubmed-meshheading:11128811-Child, Preschool,
pubmed-meshheading:11128811-Chronic Disease,
pubmed-meshheading:11128811-Cyclosporine,
pubmed-meshheading:11128811-Female,
pubmed-meshheading:11128811-Graft vs Host Disease,
pubmed-meshheading:11128811-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:11128811-Humans,
pubmed-meshheading:11128811-Immunosuppressive Agents,
pubmed-meshheading:11128811-Male,
pubmed-meshheading:11128811-Salvage Therapy,
pubmed-meshheading:11128811-Tacrolimus,
pubmed-meshheading:11128811-Transplantation, Homologous,
pubmed-meshheading:11128811-Treatment Outcome
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pubmed:year |
2000
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pubmed:articleTitle |
Changing from cyclosporine to tacrolimus as salvage therapy for chronic graft-versus-host disease.
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pubmed:affiliation |
Clinical Research Division, Fred Hutchinson Cancer Research Center, University of Washington Schools of -Medicine, Seattle, 98109-1024, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase II
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