Abstract
The safety and efficacy of a preparation with treosulfan/thiotepa/fludarabine were explored in 20 thalassaemia patients given allogeneic marrow transplantation. Seventeen patients were transplanted from unrelated donors after receiving anti-thymocyte globulin. The regimen was well tolerated. Two patients experienced secondary graft failure; one died of acute graft-versus-host disease. Cumulative incidence (95% confidence interval, CI) of transplantation-related mortality and graft failure was 5% (95% CI, 0-34%) and 11% (95% CI, 3-43%), respectively. Two-year probability of survival and thalassaemia-free survival was 95% (95% CI, 85-100%) and 85% (95% CI, 66-100%), respectively. This regimen might find elective application in patients at high risk of developing life-threatening complications.
Publication types
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Clinical Trial
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Multicenter Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Adult
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Busulfan / adverse effects
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Busulfan / analogs & derivatives*
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Busulfan / therapeutic use
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Child
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Child, Preschool
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Drug Therapy, Combination
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Female
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Graft Rejection
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Graft vs Host Disease
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Hematopoietic Stem Cell Transplantation*
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Humans
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Infant
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Male
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Myeloablative Agonists / adverse effects
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Myeloablative Agonists / therapeutic use
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Thiotepa / adverse effects
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Thiotepa / therapeutic use
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Transplantation Conditioning / adverse effects
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Transplantation Conditioning / methods*
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Treatment Outcome
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Vidarabine / adverse effects
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Vidarabine / analogs & derivatives
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Vidarabine / therapeutic use
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Young Adult
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beta-Thalassemia / drug therapy
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beta-Thalassemia / therapy*
Substances
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Myeloablative Agonists
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Thiotepa
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treosulfan
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Vidarabine
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Busulfan
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fludarabine