Blood and Marrow Transplantation, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO.
Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Blood Adv. 2019 Apr 9;3(7):1118-1128. doi: 10.1182/bloodadvances.2018025908.
When hematopoietic stem cell transplant (HSCT) is necessary for children with acute myeloid leukemia (AML), there remains debate about the best stem cell source. Post-HSCT relapse is a common cause of mortality, and complications such as chronic graft versus host disease (cGVHD) are debilitating and life-threatening. To compare post-HSCT outcomes of different donor sources, we retrospectively analyzed consecutive transplants performed in several international centers from 2005 to 2015. A total of 317 patients were studied: 19% matched sibling donor (MSD), 23% matched unrelated donor (MUD), 39% umbilical cord blood (UCB), and 19% double UCB (dUCB) recipients. The median age at transplant was 10 years (range, 0.42-21 years), and median follow-up was 4.74 years (range, 4.02-5.39 years). Comparisons were made while controlling for patient, transplant, and disease characteristics. There were no differences in relapse, leukemia-free survival, or nonrelapse mortality. dUCB recipients had inferior survival compared with matched sibling recipients, but all other comparisons showed similar overall survival. Despite the majority of UCB transplants being HLA mismatched, the rates of cGVHD were low, especially compared with the well-matched MUD recipients (hazard ratio, 0.3; 95% confidence interval, 0.14-0.67; = .02). The composite measure of cGVHD and leukemia-free survival (cGVHD-LFS), which represents both the quality of life and risk for mortality, was significantly better in the UCB compared with the MUD recipients (HR, 0.56; 95% confidence interval, 0.34-1; = .03). In summary, the use of UCB is an excellent donor choice for pediatric patients with AML when a matched sibling cannot be identified.
当儿童急性髓系白血病(AML)需要进行造血干细胞移植(HSCT)时,对于最佳干细胞来源仍存在争议。HSCT 后复发是导致死亡的常见原因,慢性移植物抗宿主病(cGVHD)等并发症会使人衰弱并危及生命。为了比较不同供体来源 HSCT 后的结果,我们回顾性分析了 2005 年至 2015 年在多个国际中心进行的连续移植。共研究了 317 例患者:19%为匹配同胞供体(MSD),23%为匹配无关供体(MUD),39%为脐带血(UCB),19%为双份 UCB(dUCB)受者。移植时的中位年龄为 10 岁(范围,0.42-21 岁),中位随访时间为 4.74 年(范围,4.02-5.39 年)。在控制患者、移植和疾病特征的情况下进行了比较。在复发、无白血病生存和非复发死亡率方面无差异。dUCB 受者的生存率低于匹配的同胞受者,但所有其他比较的总生存率相似。尽管大多数 UCB 移植存在 HLA 不匹配,但 cGVHD 的发生率较低,与高度匹配的 MUD 受者相比(风险比,0.3;95%置信区间,0.14-0.67; =.02)。UCB 与 MUD 相比,cGVHD 和无白血病生存(cGVHD-LFS)的复合指标(代表生活质量和死亡率风险)显著更好(HR,0.56;95%置信区间,0.34-1; =.03)。总之,当无法找到匹配的同胞供体时,UCB 是 AML 儿科患者的极好供体选择。