Tanimoto Kazuki, Sakamoto Keiji, Kawano Ichiro, Yamanaka Ikumi, Henzan Hideho
Department of Hematology and Oncology, Japanese Red Cross Fukuoka Hospital, Fukuoka, Japan.
Blood Cell Ther. 2020 Oct 9;3(4):78-83. doi: 10.31547/bct-2020-006. eCollection 2020 Nov 25.
Adequate hematopoietic progenitor cell collection is critical for autologous peripheral blood stem cell transplantation. Conventionally, patients with multiple myeloma are treated with high-dose cyclophosphamide and granulocyte colony-stimulating factor (G-CSF) or G-CSF alone to mobilize their peripheral blood stem cells. However, some patients exhibit insufficient stem cell recruitment in response to these regimens. Recently, plerixafor has been approved for coverage by insurance in Japan. Combination treatment with plerixafor and G-CSF is now a standard procedure. In addition, treatment with bortezomib and G-CSF results in efficient stem cell recruitment. On the basis of the results from mouse studies, we hypothesized that combination treatment with bortezomib ensures efficient mobilization and mediates purging of malignant cells. Therefore, we administered a regimen of bortezomib, G-CSF, and preemptive plerixafor to 10 patients with multiple myeloma, and analyzed its efficacy and safety. The median patient age was 68 years. We collected CD34-positive cells (median: 4.9×10/kg) in a single session of apheresis from all patients. We observed no obvious myeloma cell contamination in the collected product or serious toxicity during treatment and collection. After collection, we performed autologous peripheral blood stem cell transplantation and confirmed engraftment in all patients (median: day 10). We found that the regimen is safe and reliably facilitated the collection of sufficient autologous peripheral blood stem cells by apheresis from all patients in a single day. Despite the small patient group size, we conclude that the regimen is promising for safe and efficient collection of peripheral blood stem cells for autologous transplantation in patients with multiple myeloma.
充足的造血祖细胞采集对于自体外周血干细胞移植至关重要。传统上,多发性骨髓瘤患者采用大剂量环磷酰胺和粒细胞集落刺激因子(G-CSF)或仅用G-CSF治疗,以动员其外周血干细胞。然而,一些患者对这些方案的干细胞募集反应不足。最近,普乐沙福在日本已被批准纳入医保范围。普乐沙福与G-CSF联合治疗现已成为标准程序。此外,硼替佐米与G-CSF联合治疗可有效募集干细胞。基于小鼠研究结果,我们推测硼替佐米联合治疗可确保有效动员并介导清除恶性细胞。因此,我们对10例多发性骨髓瘤患者采用硼替佐米、G-CSF和抢先使用普乐沙福的方案进行治疗,并分析其疗效和安全性。患者中位年龄为68岁。我们在单次采集术中从所有患者采集到了CD34阳性细胞(中位数:4.9×10/kg)。我们在采集产物中未观察到明显的骨髓瘤细胞污染,在治疗和采集过程中也未出现严重毒性反应。采集后,我们进行了自体外周血干细胞移植,并确认所有患者均实现植入(中位数:第10天)。我们发现该方案安全可靠,可在一天内通过单次采集术从所有患者中顺利采集到足够的自体外周血干细胞。尽管患者组规模较小,但我们得出结论,该方案对于安全有效地采集多发性骨髓瘤患者自体移植所需的外周血干细胞很有前景。