TY - JOUR
T1 - Folinic acid does not mobilize hemopoietic progenitors following repeated consolidation chemotherapy for acute leukemia
AU - Teshima, Takanori
AU - Harada, Mine
AU - Takamatsu, Yasushi
AU - Inaba, Shoichi
AU - Kondo, Seiji
AU - Akashi, Koichi
AU - Okamura, Takashi
AU - Niho, Yoshiyuki
PY - 1992
Y1 - 1992
N2 - Folinic acid (FA) has been reported to expand the pool of peripheral blood stem cells (PBSC) after chemotherapy. We evaluated the efficacy of FA for harvesting PBSC following cytotoxic chemotherapy in 4 patients with acute leukemia. After achieving a complete remission (CR), 3 courses of chemotherapy for a consolidation of the CR were administered to the patients. Two successive cycles of leukapheresis were performed during the recovery phase from consolidation chemotherapy, which consisted of an intermediate dose of cytosine arabinoside. For the second cycle of leukapheresis. FA was administered intravenously at a dose of 50 mg/day following consolidation. The yields of either mononuclear cells or burst‐forming units‐erythroid (BFU‐E) were not affected by FA administration. In contrast, the yields of colony‐forming units‐granulocyte/macrophage (CFU‐GM) were significantly decreased in all patients compared to the CFU‐GM yields after the first cycle of leukapheresis (P = 0.032). Thus FA is considered not to be effective in expanding the peripheral blood progenitor pool when given in a fashion different from the original report. © 1992 Wiley‐Liss, Inc.
AB - Folinic acid (FA) has been reported to expand the pool of peripheral blood stem cells (PBSC) after chemotherapy. We evaluated the efficacy of FA for harvesting PBSC following cytotoxic chemotherapy in 4 patients with acute leukemia. After achieving a complete remission (CR), 3 courses of chemotherapy for a consolidation of the CR were administered to the patients. Two successive cycles of leukapheresis were performed during the recovery phase from consolidation chemotherapy, which consisted of an intermediate dose of cytosine arabinoside. For the second cycle of leukapheresis. FA was administered intravenously at a dose of 50 mg/day following consolidation. The yields of either mononuclear cells or burst‐forming units‐erythroid (BFU‐E) were not affected by FA administration. In contrast, the yields of colony‐forming units‐granulocyte/macrophage (CFU‐GM) were significantly decreased in all patients compared to the CFU‐GM yields after the first cycle of leukapheresis (P = 0.032). Thus FA is considered not to be effective in expanding the peripheral blood progenitor pool when given in a fashion different from the original report. © 1992 Wiley‐Liss, Inc.
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U2 - 10.1002/jca.2920070410
DO - 10.1002/jca.2920070410
M3 - Article
C2 - 1299660
AN - SCOPUS:0027096716
SN - 0733-2459
VL - 7
SP - 213
EP - 216
JO - Journal of Clinical Apheresis
JF - Journal of Clinical Apheresis
IS - 4
ER -