Filgrastim support in allogeneic HSCT for myeloid malignancies: a review of the role of G-CSF and the implications for current practice

被引:26
作者
Battiwalla, M. [1 ]
McCarthy, P. L. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14202 USA
关键词
G-CSF; BMT; monosomy; 7; leukemogenesis; filgrastim; COLONY-STIMULATING-FACTOR; VERSUS-HOST-DISEASE; BLOOD STEM-CELLS; BONE-MARROW TRANSPLANT; SEVERE APLASTIC-ANEMIA; UMBILICAL-CORD BLOOD; MYELODYSPLASTIC SYNDROME; CYTOGENETIC ABNORMALITIES; EUROPEAN-GROUP; GROWTH-FACTORS;
D O I
10.1038/bmt.2008.443
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The cytokine G-CSF stimulates myeloid progenitors and is routinely used to accelerate neutrophil recovery in the treatment of hematological malignancy and blood or marrow transplantation. Despite significant reductions in the frequency and duration of febrile neutropenia episodes, infections and the length of hospitalization, filgrastim has never been conclusively proven to produce a survival benefit in allogeneic HSCT and is considered a supportive measure. In this review, we analyze the conflicting evidence and appraise the utility of G-CSF in allogeneic HSCT. G-CSF administration after allogeneic HSCT needs to take into consideration the impact on immune reconstitution, risk of leukemic progression in patients with chromosome 7 abnormalities and the absence of proven benefit in patients receiving marrow or peripheral blood progenitors as the stem cell source.
引用
收藏
页码:351 / 356
页数:6
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