Laughlin M J, Kirkpatrick G, Sabiston N, Peters W, Kurtzberg J
Duke University Bone Marrow Transplant Program, Duke University Medical Center, Durham, NC.
Ann Hematol. 1993 Dec;67(6):267-76. doi: 10.1007/BF01696346.
Hematopoietic recovery in 115 patients with metastatic breast cancer or metastatic melanoma, enrolled in phase-I studies of recombinant growth factors while undergoing treatment with high-dose chemotherapy with autologous bone marrow support, was examined with assays of bone marrow progenitor cells and peripheral blood progenitor cells, and by evaluation of peripheral blood counts. Groups of patients receiving hematopoietic cytokine support [with interleukin-1 (IL-1), interleukin-2 (IL-2), granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage CSF (GM-CSF), or monocyte CSF (M-CSF)] post marrow infusion were compared with contemporaneous control patients not receiving growth factor support. Patients receiving GM-CSF demonstrated statistically significant increases in the growth of granulocyte/macrophage colony-forming units (CFU-GM) in the bone marrow and peripheral blood compared with control patients. The effect of GM-CSF was dose dependent in the early period post marrow infusion (day +6) with bone marrow CFU-GM colonies at doses 8-16 micrograms/kg/day 34 times those measured in controls. Significant increases in bone marrow multipotential progenitor cells (CFU-GEMM) were seen in patients receiving GM-CSF day +21 post marrow infusion. Patients receiving IL-1 demonstrated significant increases in bone marrow CFU-GM at day +21, maximal at dosages of 24-32 ng/kg/day. There were no significant increases in burst forming unit-erythroid (BFU-E) among any study group. Patients receiving G-CSF had significantly increased absolute neutrophil counts (ANC) and total white blood cell counts (WBC) by day +11 post transplant compared with control patients. Patients receiving GM-CSF demonstrated significantly increased WBC (greater than 2000/mm3) at day +11 and ANC greater than 500/mm3 at day +16. Optimal dose of G-CSF and GM-CSF to stimulate neutrophil recovery post transplant was 4-8 micrograms/kg/day and 8-16 micrograms/kg/day, respectively. Platelet recovery did not differ among the six study groups. These data demonstrate accelerated myeloid recovery after high-dose chemotherapy and autologous bone marrow support in patients receiving either G-CSF or GM-CSF. Moreover, GM-CSF and IL-1 stimulate myelopoiesis at the level of bone marrow CFU-GM, while G-CSF causes earlier neutrophil recovery peripherally.
115例转移性乳腺癌或转移性黑色素瘤患者参加了重组生长因子的I期研究,在接受高剂量化疗并自体骨髓支持治疗期间,通过骨髓祖细胞和外周血祖细胞检测以及外周血细胞计数评估造血恢复情况。将骨髓输注后接受造血细胞因子支持[使用白细胞介素-1(IL-1)、白细胞介素-2(IL-2)、粒细胞集落刺激因子(G-CSF)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)或单核细胞集落刺激因子(M-CSF)]的患者组与同期未接受生长因子支持的对照患者进行比较。与对照患者相比,接受GM-CSF的患者骨髓和外周血中粒细胞/巨噬细胞集落形成单位(CFU-GM)的生长有统计学意义的增加。GM-CSF的作用在骨髓输注后的早期(第+6天)呈剂量依赖性,剂量为8-16微克/千克/天的骨髓CFU-GM集落是对照组的34倍。在骨髓输注后第+21天接受GM-CSF的患者中,骨髓多能祖细胞(CFU-GEMM)有显著增加。接受IL-1的患者在第+21天骨髓CFU-GM显著增加,在剂量为24-32纳克/千克/天时达到最大值。任何研究组中红系爆式集落形成单位(BFU-E)均无显著增加。与对照患者相比,接受G-CSF的患者在移植后第+11天绝对中性粒细胞计数(ANC)和总白细胞计数(WBC)显著增加。接受GM-CSF的患者在第+11天WBC显著增加(大于2000/mm³),在第+16天ANC大于500/mm³。刺激移植后中性粒细胞恢复的G-CSF和GM-CSF的最佳剂量分别为4-8微克/千克/天和8-16微克/千克/天。六个研究组之间血小板恢复情况无差异。这些数据表明,接受G-CSF或GM-CSF的患者在高剂量化疗和自体骨髓支持后骨髓恢复加速。此外,GM-CSF和IL-1在骨髓CFU-GM水平刺激骨髓生成,而G-CSF使外周血中性粒细胞恢复更早。