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白消安/环磷酰胺预处理及异基因干细胞移植后急性髓系白血病髓外复发的高发生率。

High incidence of extramedullary relapse of AML after busulfan/cyclophosphamide conditioning and allogeneic stem cell transplantation.

作者信息

Simpson D R, Nevill T J, Shepherd J D, Fung H C, Horsman D E, Nantel S H, Vickars L M, Sutherland H J, Toze C L, Hogge D E, Klingemann H G, Naiman S C, Barnett M J

机构信息

Division of Hematology, British Columbia Cancer Agency, Vancouver Hospital and Health Sciences Centre, Canada.

出版信息

Bone Marrow Transplant. 1998 Aug;22(3):259-64. doi: 10.1038/sj.bmt.1701319.

DOI:10.1038/sj.bmt.1701319
PMID:9720739
Abstract

While allogeneic stem cell transplantation (SCT) is curative for a significant number of patients with AML, relapse of disease within the bone marrow and/or extramedullary (EM) sites following high-dose therapy continues to limit the success of this treatment. Between October 1985 and December 1996, 81 adults underwent allogeneic SCT for de novo AML at our centre. Forty-two patients remain alive and free of leukaemia with a median follow-up of 50 months. The 5-year actuarial event-free survivals (EFS) for all patients and for those undergoing SCT in CR1 or with advanced disease were 46% (95% confidence interval (CI) 34-58%), 63% (CI 46-76%), and 19% (CI 7-36%), respectively. Twenty-two patients relapsed at a median of 8 (range 1.6-54.5) months with the actuarial risk of relapse for all, CR1 and advanced disease patients being 38%, (CI 27-52%), 23% (CI 13-40%) and 68% (CI 46-88%), respectively. Ten patients relapsed at EM sites; six of these (27% of relapses) had an isolated EM relapse at a median of 31 (range 8.5-54) months. Three of the patients with isolated EM relapse survived > or =24 months following relapse and two patients remain disease-free at 29+ and 33+ months. BuCy conditioning followed by allogeneic SCT in AML results in satisfactory EFS although there is a significant risk of late isolated EM relapse.

摘要

虽然异基因干细胞移植(SCT)可治愈大量急性髓系白血病(AML)患者,但大剂量治疗后骨髓和/或髓外(EM)部位的疾病复发仍然限制了这种治疗方法的成功率。1985年10月至1996年12月期间,81名成人在我们中心接受了异基因SCT治疗初发AML。42例患者仍然存活且无白血病,中位随访时间为50个月。所有患者以及在完全缓解(CR1)期或疾病进展期接受SCT患者的5年无事件生存率(EFS)分别为46%(95%置信区间(CI)34 - 58%)、63%(CI 46 - 76%)和19%(CI 7 - 36%)。22例患者复发,中位复发时间为8(范围1.6 - 54.5)个月,所有患者、CR1期患者和疾病进展期患者的复发精算风险分别为38%(CI 27 - 52%)、23%(CI 13 - 40%)和68%(CI 46 - 88%)。10例患者在髓外部位复发;其中6例(占复发患者的27%)为孤立性髓外复发,中位复发时间为31(范围8.5 - 54)个月。3例孤立性髓外复发患者在复发后存活≥24个月,2例患者在29 +和33 +个月时仍无疾病。AML患者采用环磷酰胺联合白消安预处理后进行异基因SCT可获得满意的EFS,尽管存在晚期孤立性髓外复发的显著风险。

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