Bratislava Medical Journal | |
The use of granulocyte colony stimulating factor after autologous hematopoietic stem cell transplantation | |
article | |
F. Farkas1  M. Mistrik1  A. Batorova1  | |
[1] Department of Hematology and Transfusion Medicine, LF UK, SZU and UNB, University Hospital;Comenius University | |
关键词: autologous HSCT; G-CSF; lymphoid malignancies; engraftment; febrile neutropenia; | |
DOI : 10.4149/BLL_2019_111 | |
学科分类:医学(综合) | |
来源: AEPress, s.r.o. | |
【 摘 要 】
Restrospective study to evaluate the efficacy of early vs. delayed initiation of G-CSF after autologous hematopoietic stem cell transplantation (AHSCT) in patients with lymphoid malignancies. BACKGROUND: Granulocyte colony stimulating factor (G-CSF) is commonly used after AHSCT to accelerate stem cell engraftment to minimize the morbidity and mortality associated with prolonged neutropenia. However, there is no consensus on the optimal timing of G-CSF after HSCT. METHODS: A total of 117 patients with lymphoid malignancies who underwent AHSCT were included. All patients received G-CSF (filgrastim 5 μg/kg s.c.) daily after AHSCT (43 patients on day 6–8 and 74 patients on day 3 or 4). All patients received standard conditioning regimen for the underlying disease, and standard supportive treatment, including treatment of febrile neutropenia. RESULTS: The incidence of severe neutropenia was 81 % vs 17 %, and very severe neutropenia 61 % vs 4 % in the delayed and early G-CSF groups, respectively (p < 0.0001). The rate of fungal infection was higher in the group of patients who received delayed G-CSF (p < 0.005). CONCLUSION: An early administration of G-CSF after AHSCT (on day 3 or 4) accelerates neutophil engraftment; decreases the incidence of severe neutropenia and the risk of infectious complications (especially fungal infections) (Tab. 1, Fig. 3, Ref. 22).
【 授权许可】
CC BY
【 预 览 】
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RO202302200000936ZK.pdf | 262KB | download |