Bogden A E, Moreau J P, Gamba-Vitalo C, Deschamps de Paillette E, Tubiana M, Frindel E, Carde P
Biomeasure Inc., Milford, MA 01757, USA.
Int J Cancer. 1998 Mar 30;76(1):38-46. doi: 10.1002/(sici)1097-0215(19980330)76:1<38::aid-ijc8>3.0.co;2-z.
The aim of our study was to investigate the protection afforded to the bone marrow by Goralatide (AcSDKP), an inhibitor of hemopoietic stem cell proliferation, when administered alone or in combination with a growth factor (granulocyte/macrophage colony-stimulating factor [GM-CSF]) during iterative cycles of Ara-C (cytarabine) treatment. In control mice receiving the inhibitor alone without Ara-C, the number of granulocytes was reduced during treatment, and a surge in number of peripheral blood cells was observed after its completion. Peripheral hematological responses were monitored during 3 consecutive cycles of Ara-C chemotherapy and the resultant nadir and recoveries. Analysis of variance of the treatment effects pooled over the 3 cycles showed that a treatment regimen in which the inhibitor was administered during the myelotoxic periods of chemotherapy confirmed the existence of a surge after completion of administration of the inhibitor and showed a significant protective effect. When the cycles of chemotherapy plus Goralatide were followed by GM-CSF, the recovery from leukopenic nadirs was accelerated and the white blood cells and granulocyte levels were markedly increased over those observed in control mice and in mice treated either with Goralatide alone or with GM-CSF alone. The differences were highly significant. A consistent and significant increase (p < 0.001) in platelet count was also noted in animals given Goralatide in conjunction with Ara-C or Ara-C + GM-CSF. After three treatment cycles, this response to the CSF was far better in mice treated by the inhibitor than when CSF was given alone, suggesting a protection of the stem cell pool.
我们研究的目的是调查造血干细胞增殖抑制剂戈拉替德(AcSDKP)在阿糖胞苷(Ara-C)反复治疗周期中单独给药或与生长因子(粒细胞/巨噬细胞集落刺激因子[GM-CSF])联合给药时对骨髓的保护作用。在未接受Ara-C仅接受抑制剂的对照小鼠中,治疗期间粒细胞数量减少,治疗结束后外周血细胞数量出现激增。在Ara-C化疗的3个连续周期以及由此产生的最低点和恢复过程中监测外周血液学反应。对3个周期汇总的治疗效果进行方差分析表明,在化疗的骨髓毒性期给予抑制剂的治疗方案证实了抑制剂给药后存在激增现象,并显示出显著的保护作用。当化疗加戈拉替德的周期之后给予GM-CSF时,白细胞减少最低点的恢复加速,白细胞和粒细胞水平比对照小鼠以及单独用戈拉替德或单独用GM-CSF治疗的小鼠显著升高。差异非常显著。在给予戈拉替德联合Ara-C或Ara-C + GM-CSF的动物中,血小板计数也持续且显著增加(p < 0.001)。三个治疗周期后,抑制剂治疗的小鼠对CSF的反应比单独给予CSF时要好得多,表明对干细胞池有保护作用。