Endo T, Sato N, Mogi Y, Koizumi K, Nishio M, Fujimoto K, Sakai T, Kumano K, Obara M, Ikeda H, Koike T
Department of Internal Medicine II, Hokkaido University School of Medicine, Sapporo, Japan.
Bone Marrow Transplant. 2004 Apr;33(7):703-7. doi: 10.1038/sj.bmt.1704413.
We mobilized peripheral blood stem cells (PBSC) following CHOP plus rituximab (CHOP-R) therapy, and compared with the findings following CHOP therapy without rituximab. All patients were given G-CSF starting from day 11 after CHOP therapy. Patients in the CHOP-R group (n=8) were given rituximab on day 12. Target CD34(+) cells number was collected in a single leukapheresis on day 14, from all the eight patients in the CHOP-R group. PBSC mobilization kinetics, CD34(+) cells yield and colony-forming ability in the graft collection, toxicity during mobilization, and engraftment after transplantation of CHOP-R group were not significantly different from those in the CHOP group (n=8). In all patients given CHOP-R therapy, CD20(+) cells and immunoglobulin heavy chain (IgH) rearrangement in the graft collection were undetectable by flow-cytometric analysis and Southern blot analysis, respectively, but with PCR analysis two of eight grafts were positive for IgH rearrangement. While further studies are needed to evaluate the efficacy of purging and the outcome of patients undergoing autologous transplantation, CHOP-R therapy can be safely and effectively used in the mobilization phase of PBSC collection, without excess clinical toxicity or deleterious effect on PBSC mobilization kinetics or engraftment time.
我们在CHOP加利妥昔单抗(CHOP-R)治疗后动员外周血干细胞(PBSC),并与未使用利妥昔单抗的CHOP治疗后的结果进行比较。所有患者在CHOP治疗后第11天开始给予粒细胞集落刺激因子(G-CSF)。CHOP-R组(n = 8)的患者在第12天给予利妥昔单抗。在第14天,对CHOP-R组的所有8名患者进行单次白细胞分离术,收集目标CD34(+)细胞数量。CHOP-R组的PBSC动员动力学、移植物采集中CD34(+)细胞产量和集落形成能力、动员期间的毒性以及移植后的植入情况与CHOP组(n = 8)相比无显著差异。在所有接受CHOP-R治疗的患者中,通过流式细胞术分析和Southern印迹分析分别检测不到移植物采集中的CD20(+)细胞和免疫球蛋白重链(IgH)重排,但通过PCR分析,8个移植物中有2个IgH重排呈阳性。虽然需要进一步研究来评估清除的疗效和接受自体移植患者的结局,但CHOP-R疗法可安全有效地用于PBSC采集的动员阶段,不会产生过度临床毒性或对PBSC动员动力学或植入时间产生有害影响。