Suppr超能文献

在干细胞移植前根据微小残留病水平对高危儿科急性淋巴细胞白血病患者进行抢先性同种免疫干预。

Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantation.

机构信息

Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Leukemia. 2010 Aug;24(8):1462-9. doi: 10.1038/leu.2010.133. Epub 2010 Jun 10.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验