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地昔帕明通过刺激肾上腺素能活性增强多发性骨髓瘤患者造血干细胞和祖细胞动员作用及其与 G-CSF 的协同作用:一项初步研究。

Stimulation of adrenergic activity by desipramine enhances hematopoietic stem and progenitor cell mobilization along with G-CSF in multiple myeloma: A pilot study.

机构信息

Department of Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, New York.

Department of Oncology, Fox Chase Cancer Center, Pennsylvania.

出版信息

Am J Hematol. 2017 Oct;92(10):1047-1051. doi: 10.1002/ajh.24843. Epub 2017 Jul 29.

DOI:10.1002/ajh.24843
PMID:28675459
Abstract

Hematopoietic stem cell (HSC) release is positively regulated by the sympathetic nervous system through the β3 adrenergic receptor. Preclinical studies have demonstrated that the combination of desipramine and G-CSF resulted in improved HSC mobilization. Here, we present the results of an open-label single-arm pilot study in patients with multiple myeloma undergoing autologous stem cell transplantation (ASCT) to assess the safety and efficacy of desipramine combined with G-SCF to induce HSC mobilization. The primary endpoint was safety of the combination including engraftment kinetics. The secondary endpoint was the proportion of patients who collected ≥5 × 10 CD34 cells/kg. Outcomes were compared with historical matched controls during the same time period with multiple myeloma mobilized with G-CSF. All study patients received desipramine 100 mg daily for 7 days, starting 4 days prior to G-CSF administration (D-3) and continued taking it along with G-CSF for a total of 7 days. Six of ten patients enrolled completed the protocol with minimal side effects. All of them achieved the target collection of 5 × 10 CD34 cells/kg in a median of 1.5 apheresis session with two patients needing additional plerixafor (16%), while 11 out of 13 patients (85%) achieved the target of 5 × 10 CD34 cells/kg in the historical control group in a median of 2 apheresis procedures and seven patients needed plerixafor (54%). The combination of desipramine and G-CSF is safe and signals improved mobilization over G-CSF alone, providing a possible alternative means of mobilization that needs further investigation.

摘要

造血干细胞(HSC)的释放受到交感神经系统的正向调节,这种调节是通过β3 肾上腺素能受体实现的。临床前研究表明,去甲丙咪嗪与 G-CSF 的联合使用可导致 HSC 动员的改善。在此,我们介绍了一项在接受自体干细胞移植(ASCT)的多发性骨髓瘤患者中进行的开放性、单臂试验研究的结果,以评估去甲丙咪嗪联合 G-CSF 诱导 HSC 动员的安全性和有效性。主要终点是包括植入动力学在内的联合用药的安全性。次要终点是收集≥5×10 CD34 细胞/kg 的患者比例。将结果与同一时期接受 G-CSF 动员的多发性骨髓瘤患者的历史匹配对照进行比较。所有研究患者均在 G-CSF 给药前 4 天(D-3)开始接受每天 100mg 的去甲丙咪嗪治疗,持续 7 天,同时服用去甲丙咪嗪和 G-CSF。10 名入组患者中的 6 名完成了方案,副作用最小。他们所有人都在中位数为 1.5 次的 1 次采集过程中达到了 5×10 CD34 细胞/kg 的目标采集量,其中 2 名患者需要额外使用plerixafor(16%),而在历史对照组中,13 名患者中的 11 名(85%)在中位数为 2 次采集过程中达到了 5×10 CD34 细胞/kg 的目标采集量,其中 7 名患者需要使用 plerixafor(54%)。去甲丙咪嗪与 G-CSF 的联合使用是安全的,并且与单独使用 G-CSF 相比,提示动员效果改善,为动员提供了一种可能的替代方法,需要进一步研究。

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