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基于算法的普乐沙福在接受化疗的干细胞动员患者中的应用效果。

Effectiveness of an algorithm-based approach to the utilization of plerixafor in patients undergoing chemotherapy-based stem cell mobilization.

作者信息

Chow Eric, Rao Kamakshi V, Wood William A, Covington Deborah, Armistead Paul M, Coghill James, Serody Jonathan S, Gabriel Don A, Jamieson Katarzyna J, Park Yara A, Raval Jay S, Shea Thomas C

机构信息

Department of Pharmacy, University of North Carolina Hospitals and Clinics, Chapel Hill, NC.

Department of Pharmacy, University of North Carolina Hospitals and Clinics, Chapel Hill, NC.

出版信息

Biol Blood Marrow Transplant. 2014 Jul;20(7):1064-8. doi: 10.1016/j.bbmt.2014.03.023. Epub 2014 Apr 3.

DOI:10.1016/j.bbmt.2014.03.023
PMID:24704385
Abstract

Autologous stem cell transplantation remains a mainstay of therapy for diseases such as multiple myeloma and relapsed lymphoma. The use of plerixafor has been shown to augment the ability to collect adequate stem cells, but the optimal use of this agent when used with chemotherapy is not yet clear. We utilized an algorithm-based approach with the addition of plerixafor to 54 patients undergoing chemomobilization with reduced-dose etoposide who had a less than optimal preapheresis CD34(+) cell count. We used a CD34(+) precount of 20 cells/μL as a threshold to initiate stem cell apheresis. Ninety-four percent of patients were successfully collected and proceeded to transplantation. Fourteen of 51 (28%) patients who successfully collected required plerixafor to augment stem cell yield. Of the patients who successfully collected, 94% (89% of the entire population) were able to collect in 2 or fewer days. Compared with previous data from our institution, the rate of patients collecting > 4 × 10(6) CD34(+) cells/kg in a single collection was increased from 39% to 69%. The safety profile of this approach was acceptable. The use of this algorithm-based method to determine when and whether to add plerixafor to chemomobilization was shown to be a successful and cost-effective approach to stem cell collection.

摘要

自体干细胞移植仍然是治疗多发性骨髓瘤和复发性淋巴瘤等疾病的主要方法。已证明使用普乐沙福可增强采集足够干细胞的能力,但与化疗联合使用时该药物的最佳用法尚不清楚。我们采用基于算法的方法,对54例接受低剂量依托泊苷进行化疗动员且单采前CD34(+)细胞计数不理想的患者加用普乐沙福。我们将CD34(+)细胞计数20个/μL作为启动干细胞单采的阈值。94%的患者成功采集并进行了移植。成功采集的51例患者中有14例(28%)需要普乐沙福来提高干细胞产量。在成功采集的患者中,94%(占全部患者的89%)能够在2天或更短时间内完成采集。与我们机构之前的数据相比,单次采集时采集到>4×10(6)个CD34(+)细胞/kg的患者比例从39%提高到了69%。该方法的安全性可接受。使用这种基于算法的方法来确定何时以及是否在化疗动员中添加普乐沙福,被证明是一种成功且具有成本效益的干细胞采集方法。

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1
Effectiveness of an algorithm-based approach to the utilization of plerixafor in patients undergoing chemotherapy-based stem cell mobilization.基于算法的普乐沙福在接受化疗的干细胞动员患者中的应用效果。
Biol Blood Marrow Transplant. 2014 Jul;20(7):1064-8. doi: 10.1016/j.bbmt.2014.03.023. Epub 2014 Apr 3.
2
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引用本文的文献

1
On-demand plerixafor added to high-dose cyclophosphamide and pegylated recombinant human granulocyte colony-stimulating factor in the mobilization of patients with multiple myeloma: a treatment with high effectiveness, convenient, and affordable cost.在多发性骨髓瘤患者动员中,按需添加普乐沙福至高剂量环磷酰胺和聚乙二醇化重组人粒细胞集落刺激因子:一种高效、便捷且成本可承受的治疗方法。
Front Oncol. 2024 Jan 17;13:1306367. doi: 10.3389/fonc.2023.1306367. eCollection 2023.
2
Plerixafor on-demand in association with low-dose cyclophosphamide and G-CSF in the mobilization of patients with multiple myeloma: High effectiveness, low toxicity, and affordable cost.普乐沙福按需联合低剂量环磷酰胺和粒细胞集落刺激因子用于多发性骨髓瘤患者的动员:高效、低毒且成本可承受。
Leuk Res Rep. 2020 Oct 30;14:100227. doi: 10.1016/j.lrr.2020.100227. eCollection 2020.
3
Benefits of Pre-harvest Peripheral Blood CD34 Counts Guided Single Dose Therapy with PLERIXAFOR in Autologous Hematopoietic Stem Cell Transplantation: A Retrospective Study at a Tertiary Care Institute in India.收获前外周血CD34计数指导下普乐沙福单剂量疗法在自体造血干细胞移植中的益处:印度一家三级医疗机构的回顾性研究
Indian J Hematol Blood Transfus. 2019 Jan;35(1):72-76. doi: 10.1007/s12288-018-0979-0. Epub 2018 Jul 2.
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A single center's experience using four different front line mobilization strategies in lymphoma patients planned to undergo autologous hematopoietic cell transplantation.一个中心在计划接受自体造血细胞移植的淋巴瘤患者中使用四种不同一线动员策略的经验。
Bone Marrow Transplant. 2017 Apr;52(4):561-566. doi: 10.1038/bmt.2016.304. Epub 2017 Jan 9.