TY - JOUR
T1 - Effects of macrophage colony-stimulating factor (M-CSF) on the mobilization of peripheral blood stem cells
AU - Eto, T.
AU - Takamatsu, Y.
AU - Harada, M.
AU - Harada, N.
AU - Akashi, K.
AU - Teshima, T.
AU - Inaba, S.
AU - Okamura, T.
AU - Niho, Y.
N1 - Copyright:
Copyright 2004 Elsevier B.V., All rights reserved.
PY - 1994
Y1 - 1994
N2 - We studied the effects of human urinary macrophage colony-stimulating factor (huM-CSF) on the mobilization of peripheral blood stem cells (PBSC) following cytotoxic chemotherapy in 6 patients with acute leukemia. After complete remission (CR) was achieved, two courses of consolidation chemotherapy consisting of an intermediate dose of cytosine arabinoside were administered to the patients. During a recovery phase after each course of consolidation chemotherapy, two successive cycles of leukapheresis were performed every other day. M-CSF was administered intravenously at a dose of 8 x 106 U/day during a recovery phase after the second course of consolidation chemotherapy (cytotoxic plus M-CSF mobilization). There was no significant difference in white blood cell (WBC) or platelet recovery between the first and second cycles, regardless of the administration of M-CSF. Furthermore, between cytotoxic and cytotoxic/M-CSF mobilization, significant differences were not observed in the harvest of mononuclear cells (average 1.43 x 108/kg vs 1.62 x 108/kg), granulocyte/macrophage progenitor cells (CFU-GM) (1.82 x 104/kg vs 3.07 x 104/kg) or erythroid progenitor cells (BFU-E) (2.86 x 104/kg vs 2.66 x 104/kg). Thus M-CSF is not effective for expanding a pool of circulating hematopoietic stem cells when administered at a conventional dose during hematologic recovery following chemotherapy.
AB - We studied the effects of human urinary macrophage colony-stimulating factor (huM-CSF) on the mobilization of peripheral blood stem cells (PBSC) following cytotoxic chemotherapy in 6 patients with acute leukemia. After complete remission (CR) was achieved, two courses of consolidation chemotherapy consisting of an intermediate dose of cytosine arabinoside were administered to the patients. During a recovery phase after each course of consolidation chemotherapy, two successive cycles of leukapheresis were performed every other day. M-CSF was administered intravenously at a dose of 8 x 106 U/day during a recovery phase after the second course of consolidation chemotherapy (cytotoxic plus M-CSF mobilization). There was no significant difference in white blood cell (WBC) or platelet recovery between the first and second cycles, regardless of the administration of M-CSF. Furthermore, between cytotoxic and cytotoxic/M-CSF mobilization, significant differences were not observed in the harvest of mononuclear cells (average 1.43 x 108/kg vs 1.62 x 108/kg), granulocyte/macrophage progenitor cells (CFU-GM) (1.82 x 104/kg vs 3.07 x 104/kg) or erythroid progenitor cells (BFU-E) (2.86 x 104/kg vs 2.66 x 104/kg). Thus M-CSF is not effective for expanding a pool of circulating hematopoietic stem cells when administered at a conventional dose during hematologic recovery following chemotherapy.
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M3 - Article
C2 - 8205080
AN - SCOPUS:0028012802
SN - 0268-3369
VL - 13
SP - 125
EP - 129
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 2
ER -