Department of Medicine V, University of Heidelberg, Heidelberg, Germany.
Blood. 2010 Oct 7;116(14):2438-47. doi: 10.1182/blood-2010-03-275420. Epub 2010 Jul 1.
The purpose of this prospective multicenter phase 2 trial was to investigate the long-term outcome of reduced-intensity conditioning allogeneic stem cell transplantation (alloSCT) in patients with poor-risk chronic lymphocytic leukemia. Conditioning was fludarabine/ cyclophosphamide-based. Longitudinal quantitative monitoring of minimal residual disease (MRD) was performed centrally by MRD-flow or real-time quantitative polymerase chain reaction. One hundred eligible patients were enrolled, and 90 patients proceeded to alloSCT. With a median follow-up of 46 months (7-102 months), 4-year nonrelapse mortality, event-free survival (EFS) and overall survival (OS) were 23%, 42%, and 65%, respectively. Of 52 patients with MRD monitoring available, 27 (52%) were alive and MRD negative at 12 months after transplant. Four-year EFS of this subset was 89% with all event-free patients except for 2 being MRD negative at the most recent assessment. EFS was similar for all genetic subsets, including 17p deletion (17p-). In multivariate analyses, uncontrolled disease at alloSCT and in vivo T-cell depletion with alemtuzumab, but not 17p-, previous purine analogue refractoriness, or donor source (human leukocyte antigen-identical siblings or unrelated donors) had an adverse impact on EFS and OS. In conclusion, alloSCT for poor-risk chronic lymphocytic leukemia can result in long-term MRD-negative survival in up to one-half of the patients independent of the underlying genomic risk profile. This trial is registered at http://clinicaltrials.gov as NCT00281983.
这项前瞻性、多中心 2 期临床试验的目的是研究在低危慢性淋巴细胞白血病患者中,采用降低强度的预处理条件异基因造血干细胞移植(alloSCT)的长期结果。预处理方案基于氟达拉滨/环磷酰胺。通过 MRD-flow 或实时定量聚合酶链反应对微小残留病(MRD)进行纵向定量监测。共纳入 100 例符合条件的患者,其中 90 例进行 alloSCT。中位随访 46 个月(7-102 个月),4 年无复发生存率(EFS)和总生存率(OS)分别为 23%、42%和 65%。在有 MRD 监测的 52 例患者中,有 27 例(52%)在移植后 12 个月时仍存活且 MRD 阴性。该亚组的 4 年 EFS 为 89%,除 2 例患者在最近的评估中 MRD 阴性外,所有无事件患者均存活。所有遗传学亚组的 EFS 相似,包括 17p 缺失(17p-)。在多变量分析中,alloSCT 时疾病未得到控制以及使用阿仑单抗进行体内 T 细胞耗竭,而不是 17p-、先前嘌呤类似物耐药或供者来源(HLA 相同的同胞或无关供者)对 EFS 和 OS 有不利影响。总之,alloSCT 治疗低危慢性淋巴细胞白血病,在多达一半的患者中可获得长期的 MRD 阴性生存,与潜在的基因组风险谱无关。该试验在 ClinicalTrials.gov 上注册,编号为 NCT00281983。