HLA-matched related hematopoietic cell transplantation for chronic-phase CML using a targeted busulfan and cyclophosphamide preparative regimen

被引:128
作者
Radich, JP
Gooley, T
Bensinger, W
Chauncey, T
Clift, R
Flowers, M
Martin, P
Slattery, J
Sultan, D
Appelbaum, FR
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[2] Univ Washington, Sch Med, Seattle, WA USA
[3] Seattle Vet Affairs Med Ctr, Seattle, WA USA
关键词
D O I
10.1182/blood-2002-08-2619
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic blood or marrow transplantation (BMT) is a curative therapy for chronic myeloid leukemia (CML). We have previously reported that the pharmacologic targeting of busulfan combined with cyclophosphamide ((BU)-B-T/CY) can minimize regimen-related toxicity while preserving antileukemic effects. We report here on 131 consecutive chronic-phase CML patients treated with allogeneic related BMT using a TBU/CY preparative regimen, where the busulfan dose was targeted to achieve a steady-state plasma concentration of at least 900 ng/mL. The median age of the patients was 43 years (range, 14-66 years). Estimates of the probabilities of nonrelapse mortality, relapse, survival, and disease-free survival 3 years after transplantation were 14%, 8%, 86%, and 78%, respectively. Age had no statistically significant effect on survival. Although approximately 60% of the patients developed clinically extensive chronic graft-versus-host disease, the median Karnofsky score at last contact date among survivors was 95%. Of surviving patients, 11% were molecularly positive for the bcr-abl mRNA at last contact, with a median level of bcr-abl transcripts of 4.6 copies/mug RNA. These data suggest that (BU)-B-T/CY is a very effective preparative regimen for CML in chronic phase, associated with an expected survival at 3 years of approximately 85%, with most patients being in molecular remission. (C) 2003 by The American Society of Hematology.
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收藏
页码:31 / 35
页数:5
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