DELAYED COMMENCEMENT OF GRANULOCYTE-COLONY-STIMULATING FACTOR FOLLOWING AUTOLOGOUS BONE-MARROW TRANSPLANTATION ACCELERATES NEUTROPHIL RECOVERY AND IS COST-EFFECTIVE

被引:9
作者
CLARK, RE
SHLEBAK, AA
CREAGH, MD
机构
[1] University Department of Haematology, Royal Liverpool University Hospital, Liverpool L7 8XP, Prescot St.
关键词
BONE MARROW TRANSPLANTATION; GROWTH FACTOR THERAPY;
D O I
10.3109/10428199409114151
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is known that Granulocyte colony-stimulating factor (G-CSF) accelerates neutrophil recovery following bone marrow transplantation (BMT), though the optimal timing is not clear. We have undertaken a pilot study in 19 recipients of autologous BMT for non-myeloid malignancy, in which G-CSF was commenced 10 (13 cases) or 7 (6 cases) days after BM infusion. These patients were compared with 18 historical controls, who did not receive G-CSF. The median time to achieve both 0.5 and 1.0 x 10(9) neutrophils/Litre was significantly shorter in the treated group (18 and 21 days respectively) than the control group (20.5 and 29 days; p = 0.03 and 0.02 respectively). No differences between the two groups were seen for the number of febrile days, days on antibiotics or the cost of the antibiotics. G-CSF-treated patients remained in hospital for significantly less time after marrow infusion (21 days compared to 29 days; p = 0.007). The cost of the G-CSF therapy was offset by the decreased bed utilisation, so that the median combined antibiotic, G-CSF and hospitalisation cost was pound 754 less for G-CSF treated patients. It is concluded that delaying the commencement of G-CSF after autologous BMT accelerates neutrophil recovery, and may allow earlier discharge from hospital, whilst not adversely affecting the cost of the procedure.
引用
收藏
页码:141 / 146
页数:6
相关论文
共 17 条
[11]  
Brandwein J.M., Callum J., Sutcliffe S.B., Scott J.G., Keating A., Analysis of factors affecting hematopoietic recovery after autologous bone marrow transplantation for lymphoma, Bone Marrow Transplant., 6, pp. 291-294, (1990)
[12]  
Khwaja A., Mills W., Leveridge K., Goldstone A.H., Linch D.C., Efficacy of delayed granulocyte colony-stimulating factor (G-CSF) after autologous bone marrow transplantation (ABMT), Br. J. Haematol., 84, Suppl. 1, (1993)
[13]  
Demetri G.D., Griffin J.D., Granulocyte colony-stimulating factor and its receptor, Blood, 78, pp. 2791-2808, (1991)
[14]  
Ikebuchi K., Ihle J.N., Hirai Y., Wong G.G., Clark S.C., Ogawa M., Synergistic factors for stem cell proliferation: Further studies of the target stem cells and the mechanism of stimulation by interleukin-1, interleukin-6, and granulocyte colony-stimulating factor, Blood, 72, pp. 2007-2014, (1988)
[15]  
Takaue Y., Kawano Y., Reading C.L., Watanabe T., Abe T., Ninomiya T., Shimuzu E., Ogura T., Kuroda Y., Yokobayashi A., Nakahata T., Asano S., Ventura G., Effects of recombinant human G-CSF, GM-CSF, IL-3 and IL-1 alpha on the growth of purified human peripheral blood progenitors, Blood, 76, pp. 330-335, (1990)
[16]  
Faulds D., Lewis N.J.W., Milne R.J., Recombinant granulocyte colony-stimulating factor (rG-CSF)
[17]  
pharmacoeconomic considerations in chemotherapy-induced neutropenia, Pharmacoeconomics, 1, pp. 231-249, (1992)