早期的总白细胞恢复是低单采数和良好的CD34+细胞产量的预测因子

J.F.C Marques , A.C Vigorito , F.J.P Aranha , I Lorand-Metze , E.C.M Miranda , E.C Lima Filho , M Valbonesi , G Santini , C.A De Souza
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引用次数: 19

摘要

目标。我们分析了外周血祖细胞(PBPC)的动员和收集,以评估血液学恶性肿瘤患者中与CD34+细胞产量相关的主要因素。患者和方法。研究了恶性血液病患者自体骨髓移植后CD34+细胞动员的特点。动员化疗主要是环磷酰胺(CY) 4或7 g/m2,其次是生长因子。白细胞计数达到1.0 × 109/l时开始采白细胞,目的是每公斤体重收集至少5 × 106个CD34+细胞。在连续流式血细胞分离器上进行分离。分析的变量为:年龄、诊断、CT动员方案、生长因子类型、既往CT线数、既往放疗、白细胞恢复天数和达到CD34+细胞目标的细胞学操作次数。41例患者(26例M/15例F): 21例非霍奇金淋巴瘤(NHL), 15例霍奇金病(HD), 2例慢性髓性白血病(CML)和3例多发性骨髓瘤(MM)。11例患者无法收集到CD34+细胞的阈值。cy4动员患者WBC计数在较短时间内恢复(P=0.03)。通过方差分析,到白细胞恢复的天数与预测因子“血小板数量”和“活动CT类型”呈线性关系(系数分别为0.86和0.95)。CT动员后白细胞恢复与血小板数量的相关系数为0.36 (P=0.02)。这项研究表明,在之前接受过CT治疗或不接受rt治疗的患者中,动员和收集PBPC是可行的。白细胞恢复的天数与收集CD34+细胞目标数量所需的细胞质数量呈线性相关。该研究表明,主要使用cy4动员化疗的早期WBC恢复是实现良好CD34+产率的低数量细胞质的重要预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early total white blood cell recovery is a predictor of low number of apheresis and good CD34+ cell yield

Objective. We analysed peripheral blood progenitor cell (PBPC) mobilisation and collection in order to assess the main factors related to CD34+ cell yields in patients affected by haematological malignancies.

Patients and Methods. The features of CD34+ cell mobilisation of patients with haematological malignancies that underwent autologous bone marrow transplantation were examined. Mobilisation chemotherapy consisted mainly of cyclophosphamide (CY) 4 or 7 g/m2 followed by growth factors. Leukapheresis was started when the WBC counts reached 1.0 × 109/l with the aim to collect at least 5 × 106 CD34+ cells/kg body weight. The aphereses were performed on continuous-flow blood cell separators. The analysed variables were: age, diagnosis, CT mobilisation regimen, type of growth factor, number of previous CT lines, prior radiotherapy, days for WBC recovery and number of aphereses procedures to achieve the target of CD34+ cells.

Results. There were 41 consecutive patients (26 M/15 F): 21 non-Hodgkin’s lymphoma (NHL), 15 Hodgkin’s disease (HD), two chronic myeloid leukaemia (CML) and three multiple myeloma (MM). Eleven patients could not collect the proposed threshold of CD34+ cells. CY 4 mobilised patients recovered WBC counts in less days (P=0.03). By ANOVA, the days to WBC recovery had a linear function of the predictors “number of aphereses” and “type of mobilisation CT” (coefficients: 0.86 and 0.95, respectively). For the number of aphereses and WBC recovery after CT mobilisation, we obtained a correlation coefficient of 0.36 (P=0.02).

Conclusion. This study shows that it is feasible to mobilise and collect PBPC in patients previously treated with CT with or without RT. There was a linear correlation between the days for WBC recovery and the number of aphereses needed to collect the target number of CD34+ cells. The study suggests that early WBC recovery, using mainly CY 4 mobilisation chemotherapy, is an important predictor of a low number of aphereses to achieve a good CD34+ yield.

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