Cao Junjie, Li Aizhen, Pei Renzhi, Lu Ying, Chen Dong, Du Xiaohong, Liu Xuhui, Li Shuangyue, Ye Peipei
Department of Hematology, The Affiliated People's Hospital of Ningbo University, Ningbo, China.
Institute of Hematology, Ningbo University, Ningbo, China.
Ann Hematol. 2023 Dec;102(12):3567-3573. doi: 10.1007/s00277-023-05469-y. Epub 2023 Sep 29.
A single injection of 12 mg pegfilgrastim was used to mobilize peripheral blood progenitor cells (PBPCs) from healthy donors in some studies. The purpose of this study was to determine if 6 mg of pegfilgrastim was effective and safe for mobilizing CD34+ cells in donors for allogeneic hematopoietic stem cell transplantation. We conducted a retrospective case-matched design. A single dosage of 6 mg pegfilgrastim was used to mobilize PBPCs from 60 healthy donors. Granulocyte colony-stimulating factor (G-CSF, 10 μg/kg) was administered daily to the matched donors. Leukapheresis was scheduled to commence on day 4 of the mobilization regimen. The median yielded CD34+ cell in the pegfilgrastim group was higher than those in the G-CSF group, at 5.06 × 10/kg recipient weight. The 73.3% of donors mobilized with pegfilgrastim yielded >4 × 10 cells/kg CD34+ cells in a single apheresis procedure when compared to the 33.3% of donors mobilized with G-CSF (P < 0.001). The myeloid-derived suppressor cells (MDSC) proportion in the pegfilgrastim group was significantly higher than that in the G-CSF group (P < 0.001). The cumulative incidence of grade II-IV acute graft-versus-host disease (aGVHD) was higher in the G-CSF group than that in the pegfilgrastim group (26.7% vs. 11.7%), without statistical difference. In comparison to the G-CSF group, the pegfilgrastim group had a reduced median pain intensity numerical rating scale score (1 vs. 2). A single 6 mg dosage of pegfilgrastim is effective and safe for allogeneic PBPCs collection from healthy donors. Pegfilgrastim may decrease the incidence of aGVHD by boosting MDSCs, which need further investigation.
在一些研究中,单次注射12毫克聚乙二醇化重组人粒细胞刺激因子用于动员健康供者的外周血祖细胞(PBPC)。本研究的目的是确定6毫克聚乙二醇化重组人粒细胞刺激因子对动员异基因造血干细胞移植供者的CD34+细胞是否有效且安全。我们进行了一项回顾性病例匹配设计。使用单次剂量6毫克聚乙二醇化重组人粒细胞刺激因子动员60名健康供者的PBPC。对匹配的供者每日给予粒细胞集落刺激因子(G-CSF,10μg/kg)。白细胞分离术计划在动员方案的第4天开始。聚乙二醇化重组人粒细胞刺激因子组获得的CD34+细胞中位数高于G-CSF组,为5.06×10/kg受者体重。与33.3%使用G-CSF动员的供者相比,73.3%使用聚乙二醇化重组人粒细胞刺激因子动员的供者在单次采集过程中获得的CD34+细胞>4×10细胞/kg(P<0.001)。聚乙二醇化重组人粒细胞刺激因子组髓源性抑制细胞(MDSC)比例显著高于G-CSF组(P<0.001)。G-CSF组II-IV级急性移植物抗宿主病(aGVHD)的累积发生率高于聚乙二醇化重组人粒细胞刺激因子组(26.7%对11.7%),但无统计学差异。与G-CSF组相比,聚乙二醇化重组人粒细胞刺激因子组的疼痛强度数字评分量表中位数得分降低(1对2)。单次6毫克剂量的聚乙二醇化重组人粒细胞刺激因子用于从健康供者采集异基因PBPC是有效且安全的。聚乙二醇化重组人粒细胞刺激因子可能通过增强MDSC降低aGVHD的发生率,这需要进一步研究。