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The Risk of Cytomegalovirus Infection in Non-myeloablative Peripheral Stem Cell Transplantation Compared with Conventional Bone Marrow Transplantation
Non-myeloablative allogeneic peripheral stem cell transplantation (NST) is a novel therapeutic strategy for patients with hematologic malignancies. Whether non-mye-loablative transplants are associated with increased risk of cytomegalovirus (CMV) infections is unknown. To clarify this issue, we comp...
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Published in: | Journal of Korean medical science 2004, 19(2), , pp.172-176 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | Korean |
Subjects: | |
Online Access: | Get full text |
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Summary: | Non-myeloablative allogeneic peripheral stem cell transplantation (NST) is a novel
therapeutic strategy for patients with hematologic malignancies. Whether non-mye-loablative transplants are associated with increased risk of cytomegalovirus (CMV)
infections is unknown. To clarify this issue, we compared the outcome of CMV infec-tion
following 24 allogeneic non-myeloablative peripheral blood stem cell transplants
and 40 conventional bone marrow transplants (CBT). The NST regimen consisted of busulfan (4 mg/kg/day), fludarabine (30 mg/m2) and anti-thymocyte globulin (10mg/kg). Twelve patients (50%) in the NST group and 17 (43%) in the CBT group developed positive antigenemia before day 100 (p=0.60). The time to the first appear-ance of positive antigenemia was not different between these two groups (p=0.40),
and two groups showed similar initial and maximal antigenemia values (p=0.56 and
p=0.68, respectively). Only one case of CMV colitis developed in the CBT group
whereas CMV disease did not develop in the NST group. Although statistically in-significant, the treatment response against CMV antigenemia using ganciclovir was
in favor of NST group. In conclusion, there was no difference in the risk of CMV in-fection between NST group and CBT group. Further prospective and controlled study is needed to clarify the impact of non-myeloablative procedure on the outcome of CMV infection. KCI Citation Count: 4 |
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ISSN: | 1011-8934 1598-6357 |