前期氟达拉滨损害多发性骨髓瘤的干细胞收获:来自NMSG 13/03随机安慰剂对照II期试验的中期分析报告

H. Johnsen, L. Knudsen, A. Mylin, P. Gimsing, H. Gregersen, N. Abildgaard, N. F. Andersen, T. Plesner, A. Vangsted, T. Mourits‐Andersen
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引用次数: 1

摘要

化疗耐药B细胞对多发性骨髓瘤(MM)的影响需要通过体内靶向治疗来评估。在此,我们报告了一项II期随机安慰剂对照试验的结论,该试验将氟达拉滨加入环磷酰胺-地塞米松诱导。根据中期毒性和安全性分析,在计划纳入80例患者中的34例后,由于实验组实际收获的患者数量(4/17)少于对照组(11/17;p < 0.05)。综上所述,2个周期的氟达拉滨剂量联合烷基化治疗会损害年轻MM患者的干细胞动员和标准治疗,不应预先给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Up-front fludarabine impairs stem cell harvest in multiple myeloma: report from an interim analysis of the NMSG 13/03 randomized placebo controlled phase II trial
The impact of chemotherapy resistant B cells in multiple myeloma (MM) needs to be evaluated by in vivo targeted therapy. Here we report the conclusions from a phase II randomized, placebo controlled trial adding fludarabine to the induction with cyclophosphamide-dexamethasone. Based on an interim toxicity and safety analysis, the trial was stopped following inclusion of 34 of a planned 80 patients due to a reduced number of patients (4/17) actually harvested in the experimental arm compared to the control arm (11/17; p<0.05). In conclusion, the scheduled fludarabine dosage in 2 cycles combined with alkylating therapy impairs stem cell mobilization and standard therapy in young MM patients and should not be administrated up-front.
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