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Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
被引:18
|作者:
Kanda, J.
[1
]
Horwitz, M. E.
[1
]
Long, G. D.
[1
]
Gasparetto, C.
[1
]
Sullivan, K. M.
[1
]
Chute, J. P.
[1
]
Morris, A.
[1
]
Hennig, T.
[1
]
Li, Z.
[2
]
Chao, N. J.
[1
]
Rizzieri, D. A.
[1
]
机构:
[1] Duke Univ, Med Ctr, Div Cellular Therapy, Dept Med, Durham, NC 27705 USA
[2] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC 27705 USA
关键词:
allogeneic hematopoietic cell transplantation;
primary graft failure;
re-transplantation;
UMBILICAL-CORD BLOOD;
ANTI-HLA ANTIBODIES;
BONE-MARROW;
ADOPTIVE IMMUNOTHERAPY;
UNRELATED DONORS;
HIGH-RISK;
DEPLETION;
LEUKEMIA;
THERAPY;
ADULTS;
D O I:
10.1038/bmt.2011.158
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
Primary graft failure after allogeneic hematopoietic cell transplantation is a life-threatening complication. A shortened conditioning regimen may reduce the risk of infection and increase the chance of survival. Here, we report the outcome of 11 patients with hematologic diseases (median age, 44; range, 25-67 years, seven males) who received a 1-day reduced-intensity preparative regimen given as a re-transplantation for primary graft failure. The salvage regimen consisted of fludarabine, cyclophosphamide, alemtuzumab and TBI, all administered 1 day before re-transplantation. All patients received T-cell replete PBSCs from the same or a different haploidentical donor (n = 10) or from the same matched sibling donor (n = 1). Neutrophil counts promptly increased to >500/mu L for 10 of the 11 patients at a median of 13 days. Of these, none developed grade III/IV acute GVHD. At present, 8 of the 11 patients are alive with a median follow-up of 11.2 months from re-transplantation and 5 of the 8 are in remission. In conclusion, this series suggests that our 1-day preparative regimen is feasible, leads to successful engraftment in a high proportion of patients, and is appropriate for patients requiring immediate re-transplantation after primary graft failure following reduced-intensity transplantation. Bone Marrow Transplantation (2012) 47, 700-705; doi:10.1038/bmt.2011.158; published online 1 August 2011
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页码:700 / 705
页数:6
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