Klinikum Augsburg, University of Munich, Munich, Germany.
Blood. 2012 Feb 9;119(6):1599-606. doi: 10.1182/blood-2011-08-375840. Epub 2011 Dec 13.
Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants performed for AML in complete remission (CR) between 1999 and 2008, cumulative incidence of relapse was 32% ± 1%. Relapsed patients (263) were included into a detailed analysis of risk factors for overall survival (OS) and building of a prognostic score. CR was reinduced in 32%; remission duration after transplantation was the only prognostic factor for response (P = .003). Estimated 2-year OS from relapse was 14%, thereby resembling results of AML relapse after standard conditioning. Among variables available at the time of relapse, remission after HSCT > 5 months (hazard ratio [HR] = 0.50, 95% confidence interval [CI], 0.37-0.67, P < .001), bone marrow blasts less than 27% (HR = 0.53, 95% CI, 0.40-0.72, P < .001), and absence of acute GVHD after HSCT (HR = 0.67, 95% CI, 0.49-0.93, P = .017) were associated with better OS. Based on these factors, 3 prognostic groups could be discriminated, showing OS of 32% ± 7%, 19% ± 4%, and 4% ± 2% at 2 years (P < .0001). Long-term survival was achieved almost exclusively after successful induction of CR by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidation.
由于关于异基因造血干细胞移植(HSCT)后采用减低强度预处理(RIC)治疗的 AML 复发的管理和结果的信息有限,因此 EBMT 的急性白血病工作组进行了一项回顾性登记研究。在 1999 年至 2008 年间,有 2815 例处于完全缓解(CR)的 AML 患者接受了 RIC 移植,复发的累积发生率为 32%±1%。在复发的 263 例患者中,我们对其进行了总体生存(OS)和预后评分的危险因素详细分析。32%的患者重新诱导 CR;移植后缓解时间是反应的唯一预后因素(P=0.003)。从复发开始估计的 2 年 OS 为 14%,与标准预处理后 AML 复发的结果相似。在复发时可用的变量中,HSCT 后缓解时间>5 个月(危险比[HR] = 0.50,95%置信区间[CI],0.37-0.67,P<0.001)、骨髓原始细胞<27%(HR = 0.53,95% CI,0.40-0.72,P<0.001)和 HSCT 后无急性移植物抗宿主病(HR = 0.67,95% CI,0.49-0.93,P=0.017)与更好的 OS 相关。基于这些因素,可以区分 3 个预后组,2 年时的 OS 分别为 32%±7%、19%±4%和 4%±2%(P<0.0001)。几乎仅在通过细胞减少性治疗成功诱导 CR 后,通过供者淋巴细胞输注或进行第二次 HSCT 巩固治疗,才能实现长期生存。