Solá C., Maroto P., Salazar R., Mesía R., Mendoza L., Brunet J., López-Pousa A., Tabernero J. M., Montesinos J., Pericay C., Martínez C., Cancelas J. A., López-López J. J.
Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Hematology. 1999;4(3):195-209. doi: 10.1080/10245332.1999.11746443.
To prospectively analyze factors that influence peripheral blood stem cell (PBSC) collection and hematopoietic recovery after high-dose chemotherapy (HDC), 39 patients received cyclophosphamide 4 g/m(2) and rHuG-CSF (Filgrastim) 5 &mgr;g/kg/day. Leukapheresis was started when CD34(+) cells/mL were > 5 x 10(3). A minimum of 2 x 10(6) CD34(+) cells/kg was collected. Median steady-state bone marrow CD34(+) cell percentage was 0.8% (range, 0.1 to 6). Thirty-two patients received HDC with autologous PBSC transplantation plus Filgrastim. A median of 2 (range, 0 to 6) leukapheresis per patient were performed and a median of 6.3 x 10(6) CD34(+) cells/kg (range, 0 to 44.4) collected; four patients failed to mobilize CD34(+) cells. The number of cycles of prior chemotherapy had an inverse correlation with the number CD34(+) cells/kg collected (r = -0.38; p < 0.005). Patients with <7 cycles had a higher predictability for onset of leukapheresis than patients with (3) 7 (93% versus 50%; p < 0.005). The four patients who failed to mobilize had received >/=7 cycles. The number of CD34(+) cells/kg infused after HDC had an inverse correlation with days to recovery to 0.5 x 10(9) neutrophils/L and 20 x 10(9) platelets/L (r = -0.68 and -0.56; p < 0.005). The effect of these factors on mobilization and hematopoietic recovery were confirmed by multivariate analysis. Requirements for supportive measures were significantly lower in patients given a higher dose of CD34(+) cells/kg. Therefore, PBSC collection should be planned early in the course of chemotherapy. Larger number of CD34(+) cells/kg determined a more rapid hematopoietic recovery and a decrease of required supportive measures.
为前瞻性分析影响大剂量化疗(HDC)后外周血干细胞(PBSC)采集及造血恢复的因素,39例患者接受了4 g/m²的环磷酰胺及5 μg/kg/天的重组人粒细胞集落刺激因子(非格司亭)治疗。当CD34⁺细胞/毫升>5×10³时开始进行白细胞单采。至少采集2×10⁶ CD34⁺细胞/千克。骨髓CD34⁺细胞稳态百分比中位数为0.8%(范围0.1%至6%)。32例患者接受了HDC及自体PBSC移植加非格司亭治疗。每位患者白细胞单采次数中位数为2次(范围0至6次),采集的CD34⁺细胞中位数为6.3×10⁶细胞/千克(范围0至44.4);4例患者未能动员出CD34⁺细胞。既往化疗周期数与采集的CD34⁺细胞/千克数量呈负相关(r = -0.38;p<0.005)。化疗周期<7个的患者白细胞单采开始的可预测性高于化疗周期≥7个的患者(93%对50%;p<0.005)。未能动员出细胞的4例患者接受的化疗周期≥7个。HDC后输注的CD34⁺细胞/千克数量与恢复至0.5×10⁹中性粒细胞/升及20×10⁹血小板/升所需天数呈负相关(r = -0.68及-0.56;p<0.005)。多因素分析证实了这些因素对动员及造血恢复的影响。给予较高剂量CD34⁺细胞/千克的患者对支持措施的需求显著更低。因此,应在化疗过程中尽早规划PBSC采集。较高数量的CD34⁺细胞/千克可确定更快的造血恢复及所需支持措施的减少。