Beck J F, Klingebiel T, Kreyenberg H, Schaudt A, Wölle W, Niethammer D, Bader P
Abteilung für Pädiatrische Hämatologie und Onkologie, Universitäts-Kinderklinik Greifswald, Germany.
Klin Padiatr. 2002 Jul-Aug;214(4):201-5. doi: 10.1055/s-2002-33176.
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).
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.
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.
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.
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。
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。
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)。
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。