Hassan H T, Hinz T, Kroger N, Zeller W, Zander A R
Bone Marrow Transplantation Centre, Hamburg University Hospital Eppendorf, Germany.
Clin Lab Haematol. 1999 Feb;21(1):21-7. doi: 10.1046/j.1365-2257.1999.00179.x.
Delayed platelet recovery following autologous PBPCs transplantation after myeloablative therapy remains an unresolved problem in lymphoma patients heavily pretreated with several chemotherapy cycles and/or radiotherapy. In the present study of 50 lymphoma patients, the factors influencing platelet recovery after myeloablative therapy followed by autologous PBPCs transplantation were analysed retrospectively. The median age was 42 years (range, 15-58). Fourteen patients had HD and 36 had NHL (13 high-grade and 23 low-grade); most (80%) had stage III or IV. Twenty-two patients had received radiotherapy to various extents before mobilization. The mean number of previous chemotherapy cycles was seven (range 3-24) of different regimens (range 1-4). A median of three leukapheresis procedures (range 1-5) was performed after G-CSF mobilization. Single leukapheresis was sufficient in only one patient. A significant correlation was found between the BFU-E content of autografts and platelet recovery after transplantation. Neither the patient's age and sex nor the stage and grade of lymphoma had any effect on platelet recovery after transplantation. Neither the type of myeloablative therapy used or the dose of G-CSF administered after transplantation had any effect on platelet recovery after transplantation. The type of previous chemotherapy cycles was a major adverse factor affecting the progenitor cell yield in the autografts. Lymphoma patients previously treated with ASHAP and/or Dexa-BEAM cycles had less progenitor cell yield. The chemotherapeutic agents used in previous cycles also had a clear adverse effect on the progenitor cell yield in the autografts. Lymphoma patients previously treated with cycles including cytarabine and/or cisplatin showed significantly less progenitor cell yield and slower platelet recovery after transplantation. All seven patients with delayed platelet recovery had received cytarabine and/or cisplatin in several previous ASHAP and/or Dexa-BEAM cycles. All seven patients had a BFU-E count of less than 1 x 10(5)/kg yield in the autografts.
在接受过多个化疗周期和/或放疗的淋巴瘤患者中,清髓性治疗后自体外周血祖细胞移植后血小板延迟恢复仍是一个未解决的问题。在本项针对50例淋巴瘤患者的研究中,对清髓性治疗后行自体外周血祖细胞移植后影响血小板恢复的因素进行了回顾性分析。中位年龄为42岁(范围15 - 58岁)。14例患者为霍奇金淋巴瘤(HD),36例为非霍奇金淋巴瘤(NHL)(13例高级别和23例低级别);大多数(80%)为Ⅲ期或Ⅳ期。22例患者在动员前接受了不同程度的放疗。既往化疗周期的平均次数为7次(范围3 - 24次),采用不同的化疗方案(范围1 - 4种)。在粒细胞集落刺激因子(G - CSF)动员后,中位进行了3次白细胞单采程序(范围1 - 5次)。仅1例患者单次白细胞单采就足够了。发现自体移植物中爆式红系集落形成单位(BFU - E)含量与移植后血小板恢复之间存在显著相关性。患者的年龄和性别、淋巴瘤的分期和分级对移植后血小板恢复均无影响。所用清髓性治疗的类型或移植后给予G - CSF的剂量对移植后血小板恢复均无影响。既往化疗周期的类型是影响自体移植物中祖细胞产量的主要不利因素。既往接受过阿糖胞苷、顺铂、阿霉素、泼尼松、环磷酰胺、阿霉素、地塞米松、阿霉素、美法仑(ASHAP)和/或地塞米松、卡莫司汀、依托泊苷、阿霉素、美法仑(Dexa - BEAM)周期治疗的淋巴瘤患者,其祖细胞产量较低。既往周期中使用的化疗药物对自体移植物中祖细胞产量也有明显的不利影响。既往接受过包括阿糖胞苷和/或顺铂的周期治疗的淋巴瘤患者,其祖细胞产量明显较低,移植后血小板恢复较慢。所有7例血小板恢复延迟的患者在既往的几个ASHAP和/或Dexa - BEAM周期中均接受过阿糖胞苷和/或顺铂治疗。所有7例患者自体移植物中的BFU - E计数均低于1×10⁵/kg产量。