首页> 美国卫生研究院文献>British Journal of Cancer >ESHAP and G-CSF is a superior blood stem cell mobilizing regimen compared to cyclophosphamide 1.5 g m−2 and G-CSF for pre-treated lymphoma patients: a matched pairs analysis of 78 patients
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ESHAP and G-CSF is a superior blood stem cell mobilizing regimen compared to cyclophosphamide 1.5 g m−2 and G-CSF for pre-treated lymphoma patients: a matched pairs analysis of 78 patients

机译:与治疗前的淋巴瘤患者相比ESHAP和G-CSF是优于1.5 g m-2和环磷酰胺的G-CSF的血液干细胞动员方案:78对患者的配对分析

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摘要

Cyclophosphamide 1.5 g m−2followed by granulocyte colony-stimulating factor (G-CSF) is an effective peripheral blood stem cell (PBSC) mobilizing regimen, but has limited anti-lymphoma activity. We therefore assessed the mobilizing potential of ESHAP (etoposide, ara-C, methylprednisolone and cisplatin), a potent second-line lymphoma regimen followed by G-CSF. The results were compared in 78 patients with relapsed or resistant lymphomas with the use of cyclophosphamide 1.5 g m−2followed by G-CSF in a matched pairs analysis, matching the ESHAP recipients (for predetermined prognostic factors) from a cohort of 178 lymphoma patients mobilized with cyclophosphamide and G-CSF. The total numbers of mononuclear cells collected at apheresis was similar with both regimens but ESHAP plus G-CSF resulted in a significantly higher percentage of CD34+ cells, absolute number of CD34+ cells and GM-CFC (all with P -values < 0.001). The number of patients requiring only one apheresis harvest to achieve a CD34+ cell yield of > 2.0 × 106kg−1was greatly increased in the ESHAP recipients (56/78 vs 17/78, P< 0.001). The total number of progenitor cells collected was not significantly different with the two mobilization regimens because of this higher number of apheresis in the cyclophosphamide group. The proportion of patients who failed to achieve a minimum CD34+ cell target of 1 × 106kg−1with the pooled harvests was less in the ESHAP arm (four patients vs nine patients) despite an increased number of aphereses in the cyclophosphamide recipients. ESHAP plus G-CSF is well tolerated and is an excellent mobilization regimen in patients with pre treated lymphoma. © 2000 Cancer Research Campaign
机译:1.5 g m −2 的环磷酰胺,粒细胞集落刺激因子(G-CSF)是一种有效的外周血干细胞(PBSC)动员方案,但抗淋巴瘤活性有限。因此,我们评估了ESHAP(依托泊苷,ara-C,甲基泼尼松龙和顺铂)的动员潜力,这是一种有效的二线淋巴瘤治疗方案,其后是G-CSF。在匹配对分析中,对78例复发或耐药淋巴瘤患者(使用1.5 gm −2 环磷酰胺和G-CSF进行配对结果分析)进行了比较,结果与符合条件的ESHAP接受者(针对预定的预后因素) 178名淋巴瘤患者联合环磷酰胺和G-CSF动员。两种方案在采血时收集的单核细胞总数相似,但是ESHAP加G-CSF导致CD34 +细胞,CD34 +细胞和GM-CFC的绝对数量显着更高(所有P值<0.001)。在ESHAP接受者中,仅需进行一次采血术即可实现CD34 +细胞产量> 2.0×10 6 kg -1 的患者数量大大增加(56/78 vs 17/78,P <0.001)。两种动员方案收集的祖细胞总数没有显着差异,因为环磷酰胺组的单采血液数目较高。在ESHAP组中,未达到收集的最低CD34 +细胞靶标的1×10 6 kg −1 的患者比例较低(4例患者与9例患者患者),尽管环磷酰胺接受者中的球蛋白数量增加。 ESHAP加G-CSF具有良好的耐受性,并且对于已治疗的淋巴瘤患者是一种很好的动员方案。 ©2000癌症研究运动

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