Department of Bone Marrow Transplantation, Karmanos Cancer Institute, 4100 John R, 4 HWCRC, Rm: 4257, Detroit, MI 48201, USA.
Support Care Cancer. 2013 Sep;21(9):2437-42. doi: 10.1007/s00520-013-1808-5. Epub 2013 Apr 17.
Lenalidomide (LEN) is a relatively new and very effective therapy for multiple myeloma (MM). Prior LEN therapy is associated with an increased risk of peripheral blood stem cell collection (PBSC) failure, particularly with filgrastim (G-CSF) alone. We performed a retrospective chart review of 319 consecutive MM patients who underwent apheresis to collect PBSCs for the first autologous stem cell transplant (ASCT).
The median number of PBSCs collected in the LEN (+) group was significantly less than the LEN (-) group (6.34 vs. 7.52 × 10(6) CD34(+) cells/kg; p = 0.0004). In addition, the median number of apheresis sessions required for adequate PBSCs collection were significantly more in the LEN (+) group as compared to LEN (-) group (2 vs. 1 sessions; p = 0.002). In the LEN (+) group, there was a negative correlation between PBSCs collected and prior number of cycles of LEN (p = 0.0001). Rate of PBSC collection failure was 9% in the LEN (+) group and 5% in the LEN (-) group (p = 0.16). Only six patients who failed PBSC collection with G-CSF were able to collect adequate PBSCs with G-CSF + plerixafor. LEN exposure had no effect on neutrophil or platelet recovery post-ASCT.
Up to four cycles of LEN exposure have minimal negative impact on PBSC collection. Despite prolong exposure of LEN, PBSC collection was adequate for two ASCTs in the majority of patients and post-ASCT engraftment was not longer than expected; however, clinical relevance (complication rate, quality of life, cost) of prolonged LEN exposure on both PBSC and ASCT, should be evaluated in prospective clinical trials.
来那度胺(LEN)是多发性骨髓瘤(MM)的一种相对较新且非常有效的治疗方法。先前的 LEN 治疗与外周血干细胞采集(PBSC)失败的风险增加有关,特别是单独使用粒细胞集落刺激因子(G-CSF)时。我们对 319 例连续接受采集 PBSC 以进行首次自体干细胞移植(ASCT)的 MM 患者进行了回顾性图表审查。
LEN(+)组采集的 PBSC 中位数明显少于 LEN(-)组(6.34 与 7.52×10(6)CD34(+)细胞/kg;p=0.0004)。此外,与 LEN(-)组相比,LEN(+)组需要足够的 PBSC 采集的平均单采次数明显更多(2 与 1 次;p=0.002)。在 LEN(+)组中,采集的 PBSC 与先前 LEN 周期数之间存在负相关(p=0.0001)。LEN(+)组的 PBSC 采集失败率为 9%,LEN(-)组为 5%(p=0.16)。仅 6 例因 G-CSF 导致 PBSC 采集失败的患者能够使用 G-CSF+plerixafor 采集足够的 PBSC。LEN 暴露对 ASCT 后中性粒细胞或血小板恢复没有影响。
多达四个周期的 LEN 暴露对 PBSC 采集的负面影响最小。尽管 LEN 暴露时间延长,但大多数患者仍能采集足够的 PBSC 进行两次 ASCT,并且 ASCT 后植入时间不超过预期;然而,应在前瞻性临床试验中评估 LEN 暴露对 PBSC 和 ASCT 的长期影响(并发症发生率、生活质量、成本)的临床意义。