Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, Sichuan, China.
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ann Med. 2024 Dec;56(1):2329140. doi: 10.1080/07853890.2024.2329140. Epub 2024 Mar 12.
The combination of granulocyte-colony stimulating factor (G-CSF) and plerixafor is one of the approaches for hematopoietic stem cell mobilization in patients with multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), and Hodgkin's lymphoma (HL). This systematic review and meta-analysis aimed to determine the ability of G-CSF + plerixafor to mobilize peripheral blood (PB) CD34+ cells and examine its safety profile.
We performed a database search using the terms 'granulocyte colony stimulating factor', 'G-CSF', 'AMD3100', and 'plerixafor', published up to May 1, 2023. The methodology is described in further detail in the PROSPERO database (CRD42023425760).
Twenty-three studies were included in this systematic review and meta-analysis. G-CSF + plerixafor resulted in more patients achieving the predetermined apheresis yield of CD34+ cells than G-CSF alone (OR, 5.33; 95%, 4.34-6.55). It was further discovered that G-CSF + plerixafor could mobilize more CD34+ cells into PB, which was beneficial for the next transplantation in both randomized controlled (MD, 18.30; 95%, 8.74-27.85) and single-arm (MD, 20.67; 95%, 14.34-27.00) trials. Furthermore, G-CSF + plerixafor did not cause more treatment emergent adverse events than G-CSF alone (OR, 1.25; 95%, 0.87-1.80).
This study suggests that the combination of G-CSF and plerixafor, resulted in more patients with MM, NHL, and HL, achieving the predetermined apheresis yield of CD34+ cells, which is related to the more effective mobilization of CD34+ cells into PB.
粒细胞集落刺激因子(G-CSF)与plerixafor 的联合应用是多发性骨髓瘤(MM)、非霍奇金淋巴瘤(NHL)和霍奇金淋巴瘤(HL)患者造血干细胞动员的方法之一。本系统评价和荟萃分析旨在确定 G-CSF+plerixafor 动员外周血(PB)CD34+细胞的能力,并检查其安全性概况。
我们使用术语“粒细胞集落刺激因子”、“G-CSF”、“AMD3100”和“plerixafor”,对截至 2023 年 5 月 1 日发表的数据库进行了搜索。该方法在 PROSPERO 数据库(CRD42023425760)中有更详细的描述。
本系统评价和荟萃分析共纳入 23 项研究。与 G-CSF 单药治疗相比,G-CSF+plerixafor 使更多患者达到了预定的 CD34+细胞采集量(OR,5.33;95%,4.34-6.55)。进一步发现,G-CSF+plerixafor 可以动员更多的 CD34+细胞进入 PB,这对随机对照(MD,18.30;95%,8.74-27.85)和单臂试验(MD,20.67;95%,14.34-27.00)中下一阶段的移植均有益。此外,G-CSF+plerixafor 并未导致比 G-CSF 单药治疗更多的治疗后新发不良事件(OR,1.25;95%,0.87-1.80)。
本研究表明,G-CSF 与 plerixafor 的联合应用使更多的 MM、NHL 和 HL 患者达到了预定的 CD34+细胞采集量,这与 CD34+细胞更有效地动员进入 PB 有关。