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[在混合嵌合体增加的关键阶段,通过供体淋巴细胞输注可预防儿童急性淋巴细胞白血病、急性髓系白血病和骨髓增生异常综合征异基因造血干细胞移植后的复发]

[Relapse of childhood ALL, AML and MDS after allogeneic stem cell transplantation can be prevented by donor lymphocyte infusion in a critical stage of increasing mixed chimerism].

作者信息

Beck J F, Klingebiel T, Kreyenberg H, Schaudt A, Wölle W, Niethammer D, Bader P

机构信息

Abteilung für Pädiatrische Hämatologie und Onkologie, Universitäts-Kinderklinik Greifswald, Germany.

出版信息

Klin Padiatr. 2002 Jul-Aug;214(4):201-5. doi: 10.1055/s-2002-33176.

DOI:10.1055/s-2002-33176
PMID:12165902
Abstract

BACKGROUND

Mortality in children with acute leukemias or MDS after allogeneic stem cell transplantation (allo-SCT) is mostly determined by relapses. It was recently shown by us that patients who develop increasing quantities of autologous hematopoietic cells in peripheral blood (increasing mixed chimerism, in-MC) after allo-SCT do significantly more often relapse (P < 0.0001) than patients with a complete chimerism (CC). In a small series of patients with in-MC, the relapse rate could be significantly reduced by administration of donor lymphocytes (DLI).

METHODOLOGY

A prospective multicenter study was initiated under the question whether number of relapses can be significantly reduced either by withdrawal of post-transplant immunosuppression and/or by DLI in the critical stage of in-MC.

RESULTS

Highly repetitive determination of the genetic status of 114 children with acute leukemias or MDS (ALL: n = 41, AML: n = 39, MDS: n = 34) revealed 55 cases with CC and 43 with in-MC. Relapses occurred significantly (P < 0.0001) more often in patients with in-MC (25/43) than in patients with CC (12/55). In-MC-patients showed a significantly (P < 0.01) enhanced event free survival rate (11/24) when DLI was given and/or post-transplant immunosuppression was stopped compared to patients which did not receive such an interventional regimen (1/19). Two in-MC-patients developed fatal GVHD after immunological intervention.

CONCLUSION

These data substantiate that prophylactic immunotherapy on the basis of in-MC is a powerful treatment approach to suppress relapses of acute leukemias and MDS after allo-SCT.

摘要

背景

异基因造血干细胞移植(allo-SCT)后急性白血病或骨髓增生异常综合征(MDS)患儿的死亡率大多由复发决定。我们最近发现,allo-SCT后外周血中自体造血细胞数量增加(混合嵌合率增加,in-MC)的患者比完全嵌合(CC)患者更容易复发(P < 0.0001)。在一小部分in-MC患者中,给予供体淋巴细胞(DLI)可显著降低复发率。

方法

启动了一项前瞻性多中心研究,探讨在in-MC的关键阶段,通过停用移植后免疫抑制和/或给予DLI是否能显著降低复发率。

结果

对114例急性白血病或MDS患儿(急性淋巴细胞白血病:n = 41,急性髓系白血病:n = 39,MDS:n = 34)的基因状态进行高度重复性检测,发现55例为CC,43例为in-MC。in-MC患者(25/43)的复发率显著高于CC患者(12/55)(P < 0.0001)。与未接受此类干预方案的患者(1/19)相比,给予DLI和/或停用移植后免疫抑制的in-MC患者的无事件生存率显著提高(P < 0.01)(11/24)。两名in-MC患者在免疫干预后发生了致命的移植物抗宿主病(GVHD)。

结论

这些数据证实,基于in-MC的预防性免疫治疗是抑制allo-SCT后急性白血病和MDS复发的有效治疗方法。

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1
[Relapse of childhood ALL, AML and MDS after allogeneic stem cell transplantation can be prevented by donor lymphocyte infusion in a critical stage of increasing mixed chimerism].[在混合嵌合体增加的关键阶段,通过供体淋巴细胞输注可预防儿童急性淋巴细胞白血病、急性髓系白血病和骨髓增生异常综合征异基因造血干细胞移植后的复发]
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Increasing mixed chimerism is an important prognostic factor for unfavorable outcome in children with acute lymphoblastic leukemia after allogeneic stem-cell transplantation: possible role for pre-emptive immunotherapy?混合嵌合体增加是急性淋巴细胞白血病儿童异基因干细胞移植后不良预后的重要预后因素:抢先免疫疗法的可能作用?
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引用本文的文献

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Quantitative chimerism: an independent acute leukemia prognosis indicator following allogeneic hematopoietic SCT.定量嵌合率:异基因造血干细胞移植后独立的急性白血病预后指标。
Bone Marrow Transplant. 2014 Oct;49(10):1269-77. doi: 10.1038/bmt.2014.158. Epub 2014 Aug 4.