Cummins M, Cwynarski K, Marktel S, Dazzi F, Cavenagh J, Clark R E, Holyoake T L, Milligan D, Parker A, Russell N H, Marks D I
Adult BMT Unit, Bristol Royal Children's Hospital, Bristol, UK.
Bone Marrow Transplant. 2005 Dec;36(12):1065-9. doi: 10.1038/sj.bmt.1705180.
Donor lymphocyte infusion (DLI) can restore remission in a high percentage of patients with chronic myeloid leukaemia (CML) who relapse after allogeneic stem cell transplant (SCT). Subsequent relapses after a DLI-induced remission do occur and the optimal management of these patients is not defined. A retrospective study of the practice of UK transplant centres was conducted. In all, 13 patients from seven centres were identified: all were treated for relapse post allogeneic SCT with DLI and achieved either a complete cytogenetic (n=5) or molecular (n=8) remission. All patients subsequently had a second relapse, at molecular (n=7), cytogenetic (n=4) and haematological (n=2) levels. Further DLI was used in the treatment of 11 patients, imatinib mesylate in three and chemotherapy in two. The two patients with haematological relapse died of blastic disease. The remaining 11 patients achieved either a complete cytogenetic (n=2) or molecular (n=9) remission. Nine patients remain in molecular remission at a median follow-up of 29 months, seven of whom had received DLI alone as treatment for second relapse, one DLI plus imatinib and one imatinib alone. Toxicity following DLI for second relapse was low. Longer follow-up will be required to see if these second DLI-induced remissions will be durable.
供体淋巴细胞输注(DLI)可使高比例的慢性髓性白血病(CML)患者在异基因干细胞移植(SCT)后复发时恢复缓解状态。DLI诱导缓解后确实会出现后续复发,且这些患者的最佳治疗方案尚未明确。对英国移植中心的实践进行了一项回顾性研究。总共从7个中心确定了13例患者:所有患者均接受了异基因SCT后复发的DLI治疗,并实现了完全细胞遗传学缓解(n = 5)或分子学缓解(n = 8)。所有患者随后均出现了第二次复发,分别为分子学水平(n = 7)、细胞遗传学水平(n = 4)和血液学水平(n = 2)。11例患者采用进一步的DLI治疗,3例采用甲磺酸伊马替尼治疗,2例采用化疗。2例血液学复发患者死于原始细胞疾病。其余11例患者实现了完全细胞遗传学缓解(n = 2)或分子学缓解(n = 9)。9例患者在中位随访29个月时仍处于分子学缓解状态,其中7例仅接受DLI作为第二次复发的治疗,1例接受DLI加伊马替尼治疗,1例仅接受伊马替尼治疗。第二次复发时DLI后的毒性较低。需要更长时间的随访来观察这些第二次DLI诱导的缓解是否持久。