Olivieri A, Offidani M, Montanari M, Ciniero L, Cantori I, Ombrosi L, Masia C M, Centurioni R, Mancini S, Brunori M, Leoni P
Department of Hematology, University of Ancona, Italy.
Haematologica. 1998 Apr;83(4):329-37.
While the minimum number of CD34+ cells required for complete and long-lasting engraftment is quite well established, there is not general agreement about the optimal number of CD34+ per kg needed in order to obtain engraftment as rapidly as possible. In the present study we assess factors affecting hemopoietic recovery and the optimal peripheral blood progenitor cell (PBPC) number for rapid engraftment in patients treated with high-dose therapy.
We enrolled 80 consecutive patients affected by hematologic and non-hematologic malignancies treated with a median of 10 chemotherapy courses (range 3-38). PBPC collection was performed after mobilization with high-dose chemotherapy and G-CSF 5 micrograms/kg/day. The circulating and harvested CD34+ cells were recognized in the cytofluorimetric CD45+/CD14- lymphocyte gate. After myeloablative therapy, PBPC infusion was followed by G-CSF 5 micrograms/kg/day from day +5 until WBC > or = 5.0 x 10(9)/L. Univariate and multivariate Cox analyses were performed to investigate factors affecting hemopoietic recovery. The Kaplan-Meier probabilities of hemopoietic reconstitution were compared by log-rank test to assess the optimal CD34+ cell number for rapid engraftment.
We performed a median of two apheresis (range 1-4) per patient and we infused a median of 6.1 x 10(6) CD34+ cells/kg (range 0.5-30.5). Absolute neutrophil count (ANC) > 0.5 x 10(9)/L was reached after 11 days (range 8-15). The only factor affecting granulocyte recovery proved to be the CD34+ cell number; 5.0 to 7.8 x 10(6) CD34+ cells/kg allowed a significantly faster granulocyte recovery than < 2.5 x 10(6) CD34+ cells/kg (p = 0.0312). Platelet transfusion independence (> 20 x 10(9)/L) and 50 x 10(9)/L platelets were reached after 12 (range 8-24) and 15 days (range 9-40), respectively. The CD34+ cell number was also the only factor affecting platelet recovery; the number of 5.0 to 7.8 CD34+ cells/kg allowed a significantly faster platelet recovery than the lower dose, whereas a higher number did not. No late graft failures were observed. Patients receiving 5.0 to 7.8 x 10(9) CD34+ cells/kg had a significantly shorter duration of neutropenia, fewer platelet transfusions and less time spent in hospital than those receiving lower number did, whereas patients transplanted with a higher number had no advantage.
When G-CSF is employed both for PBPC mobilization and after PBPC transplantation, the CD34+ cell number is the only factor that affects hemopoietic recovery. Moreover, > 5.0 x 10(6) CD34+ cells/kg is the optimal number for obtaining rapid platelet recovery and reducing the costs of HDT but there is no advantage exceeding the threshold of 7.8 x 10(6) CD34+ cells/kg.
虽然完全且持久植入所需的CD34+细胞的最低数量已相当明确,但对于为尽快实现植入每千克所需的最佳CD34+细胞数量尚无普遍共识。在本研究中,我们评估了影响造血恢复的因素以及接受大剂量治疗的患者快速植入所需的最佳外周血祖细胞(PBPC)数量。
我们纳入了80例连续的血液系统和非血液系统恶性肿瘤患者,这些患者接受化疗的中位数为10个疗程(范围3 - 38个疗程)。在使用大剂量化疗和5微克/千克/天的粒细胞集落刺激因子(G-CSF)动员后进行PBPC采集。循环中的和采集到的CD34+细胞在细胞荧光分析的CD45+/CD14-淋巴细胞门中识别。在清髓性治疗后,从第5天开始每天给予5微克/千克/天的G-CSF进行PBPC输注,直至白细胞计数≥5.0×10⁹/L。进行单因素和多因素Cox分析以研究影响造血恢复的因素。通过对数秩检验比较造血重建的Kaplan-Meier概率,以评估快速植入所需的最佳CD34+细胞数量。
我们每位患者进行PBPC采集的中位数为2次(范围1 - 4次),输注的CD34+细胞中位数为6.1×10⁶个/千克(范围0.5 - 30.5)。中性粒细胞绝对计数(ANC)>0.5×10⁹/L在11天(范围8 - 15天)后达到。唯一影响粒细胞恢复的因素被证明是CD34+细胞数量;5.0至7.8×10⁶个CD34+细胞/千克比<2.5×10⁶个CD34+细胞/千克能使粒细胞恢复明显更快(p = 0.0312)。血小板输注独立(>20×10⁹/L)和血小板计数达到50×10⁹/L分别在12天(范围8 - 24天)和15天(范围9 - 40天)后实现。CD34+细胞数量也是影响血小板恢复的唯一因素;5.0至7.8个CD34+细胞/千克比低剂量能使血小板恢复明显更快,而更高数量则不然。未观察到晚期移植失败。接受5.0至7.8×10⁹个CD34+细胞/千克的患者与接受较低数量的患者相比,中性粒细胞减少持续时间明显更短,血小板输注次数更少,住院时间更短,而移植数量更高的患者没有优势。
当G-CSF用于PBPC动员和PBPC移植后时,CD34+细胞数量是影响造血恢复的唯一因素。此外,>5.0×10⁶个CD34+细胞/千克是实现快速血小板恢复和降低大剂量治疗成本的最佳数量,但超过7.8×10⁶个CD34+细胞/千克的阈值没有优势。