Millot F, Esperou H, Bordigoni P, Dalle J-H, Michallet M, Michel G, Bourhis J L, Kuenz M, Blaise D, Garban F, Plouvier E, Rome A, Guilhot J, Guilhot F
Service d'oncologie hématologique et de thérapie cellulaire, Centre Hospitalier Universitaire, Hôpital Jean Bernard, Poitiers 86000, France.
Bone Marrow Transplant. 2003 Nov;32(10):993-9. doi: 10.1038/sj.bmt.1704255.
To determine the results of allogeneic hematopoietic stem cell (HSC) transplantation for chronic myelogenous leukemia (CML) at various stages of the disease in children, a retrospective analysis was carried out on the outcome of transplants performed on 76 children and teenagers with CML between 1982 and 1998. In all, 60 patients were transplanted from a matched sibling donor (MSD) and 16 from a matched unrelated donor (MUD). There was a higher incidence of acute graft-versus-host disease after MUD transplantation (P<10(-3)). The main cause of death was transplant-related toxicity in both groups. In MSD recipients, the probability of relapse at 5 years for patients transplanted in the first chronic phase was lower than in patients transplanted in the advanced phase (relative risk (rr)=5.90; 95% confidence interval (CI), 1.85-18.82, P<0.01). The estimated 5-year event-free survival (EFS) rate was higher after MSD vs MUD transplantation (61% (95% CI, 48-73%) vs 27% (95% CI, 4-49%), rr=0.25, P<10(-3)). In children transplanted from MSD, the 5-year EFS was higher when transplantation was performed in the first chronic phase vs the advanced phases (73% (95% CI, 59-87%) vs 32% (95% CI, 10-54%), P<10(-3)). Disease status at transplantation was the unique factor influencing survival in patients undergoing transplantation from MSD with a better outcome for those transplanted in the first chronic phase. Allogeneic HSC offers a possibility of curing childhood CML with a significant advantage for patients transplanted in chronic phase using a human leukocyte antigen-identical sibling donor.
为确定异基因造血干细胞(HSC)移植治疗儿童慢性粒细胞白血病(CML)各疾病阶段的效果,对1982年至1998年间76例儿童和青少年CML患者的移植结局进行了回顾性分析。其中,60例患者接受了同胞匹配供体(MSD)移植,16例接受了无关匹配供体(MUD)移植。MUD移植后急性移植物抗宿主病的发生率更高(P<10(-3))。两组的主要死亡原因均为移植相关毒性。在MSD受者中,处于慢性期早期移植的患者5年复发概率低于晚期移植患者(相对风险(rr)=5.90;95%置信区间(CI),1.85 - 18.82,P<0.01)。MSD移植后的估计5年无事件生存率(EFS)高于MUD移植(61%(95%CI,48 - 73%)对27%(95%CI,4 - 49%),rr = 0.25,P<10(-3))。在接受MSD移植的儿童中,慢性期早期移植的5年EFS高于晚期(73%(95%CI,59 - 87%)对32%(95%CI,10 - 54%),P<10(-3))。移植时的疾病状态是影响接受MSD移植患者生存的唯一因素,慢性期早期移植患者的结局更好。异基因HSC移植为治愈儿童CML提供了可能,对于使用人类白细胞抗原相同的同胞供体在慢性期移植的患者具有显著优势。