Department of Internal Medicine, University of Maryland Medical Center, Baltimore, MD, USA.
Department of Medicine, University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
Clin Lymphoma Myeloma Leuk. 2022 Aug;22(8):e716-e729. doi: 10.1016/j.clml.2022.03.013. Epub 2022 Mar 28.
Induction therapy for multiple myeloma is traditionally capped at 6 cycles of lenalidomide due to concerns that longer treatment compromises the ability to collect sufficient stem cells for autologous stem cell transplantation (ASCT). However, during the COVID-19 pandemic, many of our patients received prolonged lenalidomide induction due to concerns about proceeding to ASCT. We investigated whether prolonged induction with lenalidomide affects the efficacy of stem cell collection among patients mobilized with cyclophosphamide and/or plerixafor.
This single center, retrospective study included patients who were treated with lenalidomide induction regimens, received mobilization with cyclophosphamide or plerixafor, and underwent apheresis in preparation for ASCT. 94 patients were included, 40 of whom received prolonged induction with >6 cycles of lenalidomide containing regimen.
Patients who received prolonged induction were more likely to require >1 day of apheresis (38% vs. 15%; OR 3.45; P = .0154), and there was a significant correlation between the duration of lenalidomide treatment and the apheresis time required to collect sufficient cells for transplant (R = 0.06423, P = .0148). However, there was no significant difference between patients who received prolonged induction and those who did not with respect to CD34 stem cell yields at completion of apheresis (9.99 vs. 10.46 cells/Kg, P = .5513) or on the first day of collection (8.29 vs. 9.59 cells/Kg, P = .1788).
Among patients treated with >6 cycles of lenalidomide, mobilization augmented with cyclophosphamide and/or plerixafor will likely facilitate sufficient stem cell harvest to permit ASCT.
由于担心延长治疗会影响自体干细胞移植 (ASCT) 的干细胞采集能力,多发性骨髓瘤的诱导治疗传统上限制在 6 个周期的来那度胺。然而,在 COVID-19 大流行期间,由于对进行 ASCT 的担忧,我们的许多患者接受了延长的来那度胺诱导治疗。我们研究了延长来那度胺诱导是否会影响用环磷酰胺和/或培非格司亭动员的患者的干细胞采集效果。
这项单中心回顾性研究纳入了接受来那度胺诱导方案治疗、接受环磷酰胺或培非格司亭动员以及接受为 ASCT 准备的单采术的患者。共纳入 94 例患者,其中 40 例接受了>6 个周期含来那度胺方案的延长诱导。
接受延长诱导的患者更有可能需要>1 天的单采术(38%比 15%;OR 3.45;P=0.0154),来那度胺治疗时间与采集足够细胞进行移植所需的单采时间之间存在显著相关性(R=0.06423,P=0.0148)。然而,在完成单采时的 CD34 干细胞产量(9.99 比 10.46 细胞/Kg,P=0.5513)或采集首日(8.29 比 9.59 细胞/Kg,P=0.1788)方面,接受延长诱导和未接受延长诱导的患者之间没有显著差异。
在接受>6 个周期来那度胺治疗的患者中,用环磷酰胺和/或培非格司亭增强动员可能会促进足够的干细胞采集,以允许进行 ASCT。