Bolwell B, Vredenburgh J, Overmoyer B, Gilbert C, Chap L, Menchaca D M, Cruickshank S, Glaspy J
The Cleveland Clinic Foundation, OH 44195, USA.
Bone Marrow Transplant. 2000 Jul;26(2):141-5. doi: 10.1038/sj.bmt.1702465.
Forty-seven patients with stage II, III, or IV breast cancer undergoing autologous peripheral blood progenitor cell (PBPC) transplantation were randomized to placebo (n = 13) or to one of five sequential dose cohorts of pegylated (PEG) recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF) (1.0, 2.5, 5.0, 7.5, or 10.0 microg/kg/day) (n= 34). Blinded study drug was started on the day of transplantation and was continued until the platelet count was > or =100 x 109/l or a maximum of 21 days. PBPCs were mobilized with filgrastim (r-metHuG-CSF) and all patients received filgrastim starting on day +2 after transplantation. The nadir platelet count was not affected by treatment. The median time to platelet recovery was 11 and 12 days for the placebo and combined PEG-rHuMGDF groups, respectively. No trends in adverse events suggested dose- or treatment-related toxicity. Two patients withdrew from the study because of an adverse event (allergic reaction in the 7.5 microg/kg group) probably related to study drug, and veno-occlusive disease (VOD) (in the 5 microg/kg group) which was felt not to be related to study drug by the investigator. No patients developed neutralizing antibodies to MGDF. Day +21 and day +28 platelet counts were higher in the group receiving PEG-rHuMGDF (246 vs 148 x 109/l and 299 vs 145 x 109/l, respectively; both P < 0. 05). PEG-rHuMGDF up to 10 microg/kg/day was well tolerated. In this study, there was no effect of study drug on initial platelet engraftment at the doses studied. However, the efficacy of other doses is unknown.
47例接受自体外周血祖细胞(PBPC)移植的II、III或IV期乳腺癌患者被随机分为安慰剂组(n = 13)或聚乙二醇化(PEG)重组人巨核细胞生长与发育因子(PEG-rHuMGDF)五个连续剂量组之一(1.0、2.5、5.0、7.5或10.0μg/kg/天)(n = 34)。在移植当天开始使用盲法研究药物,并持续使用至血小板计数≥100×10⁹/L或最长21天。用非格司亭(r-metHuG-CSF)动员PBPC,所有患者在移植后第2天开始接受非格司亭治疗。最低血小板计数不受治疗影响。安慰剂组和PEG-rHuMGDF联合组血小板恢复的中位时间分别为11天和12天。不良事件无趋势表明存在剂量或治疗相关毒性。两名患者因不良事件退出研究,一名可能与研究药物有关(7.5μg/kg组的过敏反应),另一名是静脉闭塞性疾病(VOD)(5μg/kg组),研究者认为与研究药物无关。没有患者产生针对MGDF的中和抗体。接受PEG-rHuMGDF组在第21天和第28天的血小板计数较高(分别为246对148×10⁹/L和299对145×10⁹/L;P均<0.05)。高达10μg/kg/天的PEG-rHuMGDF耐受性良好。在本研究中,在所研究的剂量下,研究药物对初始血小板植入无影响。然而,其他剂量的疗效未知。