Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, NC, United States; UNC Eshelman School of Pharmacy, Chapel Hill, NC, United States.
University of Washington Medical Center, Seattle, WA, United States.
Transfus Apher Sci. 2022 Apr;61(2):103303. doi: 10.1016/j.transci.2021.103303. Epub 2021 Oct 30.
Addition of plerixafor (P) to granulocyte colony stimulating factor (G-CSF) during peripheral blood mobilization of hematopoietic stem cells (HSC) increases the number of patients meeting collection goals prior to autologous stem cell transplant (aSCT). However, use of P is not universal among transplant centers due to cost. This study aims to compare clinical and financial impacts of using an algorithm-based P mobilization strategy versus use in all patients. This was a single center, retrospective analysis of adult patients with myeloma or amyloidosis receiving aSCT who received apheresis of their HSC between 3/1/2017 and 3/1/2019. Patients prior to 3/1/2018 were classified as receiving P "per algorithm" and those after this date were classified as "up-front" P. For the per-algorithm group, P was given for a pre-apheresis CD34+ cell count of <20 cells/μL on mobilization day 5 and patients returned on day 6 for apheresis. Of the 129 patients included, 55 received P per-algorithm and 74 received up-front P. There was a reduction in median number of apheresis days (1.5 vs 1 day, p < 0.001) and an increase in median number of CD34+ cells collected (6.6 vs 8.5 × 10 cells/kg, p < 0.001) with up-front P. Up-front P increased drug cost but reduced apheresis costs, which resulted in a net savings of $121 per patient in total mobilization costs. These findings suggest that use of up-front P for mobilization significantly reduces apheresis days and increases HSC collection yield without increasing overall cost per patient.
在造血干细胞(HSC)外周血动员期间添加普乐沙福(P)到粒细胞集落刺激因子(G-CSF)可以增加在自体干细胞移植(aSCT)前符合采集目标的患者数量。然而,由于成本原因,并非所有移植中心都普遍使用 P。本研究旨在比较基于算法的 P 动员策略与所有患者使用 P 的临床和财务影响。这是一项单中心、回顾性分析,纳入了在 2017 年 3 月 1 日至 2019 年 3 月 1 日期间接受 aSCT 的多发性骨髓瘤或淀粉样变性的成年患者,他们接受了 HSC 采集。2018 年 3 月 1 日前的患者被归类为接受 P“按算法”,此后的患者被归类为“ upfront” P。对于按算法的 P 组,在动员第 5 天的 CD34+细胞计数<20 个/μL 时给予 P,患者在第 6 天返回进行采集。在 129 名纳入患者中,55 名患者接受按算法的 P,74 名患者接受 upfront P。 upfront P 减少了中位采集天数(1.5 天对 1 天,p < 0.001),增加了中位 CD34+细胞采集量(6.6 对 8.5×10 个细胞/kg,p < 0.001)。 upfront P 增加了药物成本,但降低了采集成本,总动员成本每人节省 121 美元。这些发现表明, upfront P 动员可显著减少采集天数,增加 HSC 采集量,而不增加每位患者的总体成本。