Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.
Leukemia. 2010 Aug;24(8):1462-9. doi: 10.1038/leu.2010.133. Epub 2010 Jun 10.
Relapse of pediatric acute lymphoblastic leukemia (ALL) remains the main cause of treatment failure after allogeneic stem cell transplantation (alloSCT). A high level of minimal residual disease (MRD) before alloSCT has been shown to predict these relapses. Patients at risk might benefit from a preemptive alloimmune intervention. In this first prospective, MRD-guided intervention study, 48 patients were stratified according to pre-SCT MRD level. Eighteen children with MRD level >or=1 x 10(-4) were eligible for intervention, consisting of early cyclosporine A tapering followed by consecutive, incremental donor lymphocyte infusions (n=1-4). The intervention was associated with graft versus host disease >or=grade II in only 23% of patients. Event-free survival in the intervention group was 19%. However, in contrast with the usual early recurrence of leukemia, relapses were delayed up to 3 years after SCT. In addition, several relapses presented at unusual extramedullary sites suggesting that the immune intervention may have altered the pattern of leukemia recurrence. In 8 out of 11 evaluable patients, relapse was preceded by MRD recurrence (median 9 weeks, range 0-30). We conclude that in children with high-risk ALL, immunotherapy-based regimens after SCT are feasible and may need to be further intensified to achieve total eradication of residual leukemic cells.
异基因造血干细胞移植(alloSCT)后小儿急性淋巴细胞白血病(ALL)的复发仍然是治疗失败的主要原因。alloSCT 前微小残留病(MRD)水平高已被证明可预测这些复发。高危患者可能受益于抢先异体免疫干预。在这项首次前瞻性、基于 MRD 的干预研究中,48 名患者根据 pre-SCT MRD 水平进行分层。18 名 MRD 水平 >或=1 x 10(-4) 的患儿有资格进行干预,包括早期环孢素 A 逐渐减量,然后连续、递增供者淋巴细胞输注(n=1-4)。该干预仅在 23%的患者中引起 >或=2 级移植物抗宿主病。干预组无事件生存时间为 19%。然而,与通常的白血病早期复发不同,复发延迟至 SCT 后 3 年。此外,一些复发出现在非骨髓外部位,表明免疫干预可能改变了白血病复发的模式。在 11 名可评估患者中的 8 名中,复发前出现 MRD 复发(中位数 9 周,范围 0-30)。我们得出结论,对于高危 ALL 患儿,alloSCT 后基于免疫疗法的方案是可行的,可能需要进一步强化以实现残留白血病细胞的完全消除。