Knechtli C J, Goulden N J, Hancock J P, Harris E L, Garland R J, Jones C G, Grandage V L, Rowbottom A W, Green A F, Clarke E, Lankester A W, Potter M N, Cornish J M, Pamphilon D H, Steward C G, Oakhill A
Department of Pathology and Microbiology, School of Medical Sciences, University of Bristol.
Br J Haematol. 1998 Aug;102(3):860-71. doi: 10.1046/j.1365-2141.1998.00873.x.
We have analysed the behaviour of minimal residual disease (MRD) after allogeneic bone marrow transplantation (allo-BMT) in 71 children with acute lymphoblastic leukaemia (ALL). The method relied on PCR of IgH, TCRdelta and/or TCRgamma gene rearrangements followed by electrophoretic size resolution and allele-specific oligoprobing. Patients were similarly conditioned; 55 received marrow from unrelated donors and 16 from related donors. MRD was assessed at various time-points up to 24 months after BMT. Three children were not evaluable due to transplant-related mortality. MRD was detected in 28/32 patients (88%) who relapsed post-BMT; 16 were positive at all times and 12 were initially negative but became positive at a median of 3 months (range 1.5-11) prior to relapse. In contrast, only eight of 36 (22%) patients who remained in continuing complete remission (CCR) (median follow-up 43 months, range 20-94) showed MRD at any time after BMT (P<0.0001). In these eight patients MRD was found up to 9 months after transplant and at low levels (0.01-0.001%). All eight (median follow-up 39 months, range 24-87) had at least two MRD-negative samples tested subsequently and five of the eight had evidence of grade I-II acute graft-versus-host disease (GvHD), raising the possibility of a graft-versus-leukaemia effect. In general, any evidence of MRD after allo-BMT is a poor prognostic sign. However, if immunotherapy were to be targeted towards patients with evidence of persisting MRD after BMT, the method described would expose only a small proportion of patients to unnecessary additional toxicity.
我们分析了71例急性淋巴细胞白血病(ALL)患儿接受异基因骨髓移植(allo-BMT)后微小残留病(MRD)的情况。该方法依赖于对IgH、TCRδ和/或TCRγ基因重排进行聚合酶链反应(PCR),随后进行电泳大小分辨率分析和等位基因特异性寡核苷酸探针检测。患者接受了相似的预处理;55例接受了无关供者的骨髓,16例接受了相关供者的骨髓。在BMT后长达24个月的不同时间点评估MRD。3例患儿因移植相关死亡率而无法评估。在32例BMT后复发的患者中有28例(88%)检测到MRD;16例始终为阳性,12例最初为阴性,但在复发前中位3个月(范围1.5 - 11个月)时转为阳性。相比之下,在36例持续完全缓解(CCR)(中位随访43个月,范围20 - 94个月)的患者中,只有8例(22%)在BMT后的任何时间显示有MRD(P<0.0001)。在这8例患者中,移植后长达9个月检测到MRD,且水平较低(0.01 - 0.001%)。所有8例(中位随访39个月,范围24 - 87个月)随后至少有两个MRD阴性样本进行检测,其中8例中有5例有Ⅰ - Ⅱ级急性移植物抗宿主病(GvHD)的证据,这增加了移植物抗白血病效应的可能性。一般来说,allo-BMT后任何MRD证据都是不良预后标志。然而,如果免疫治疗针对BMT后有持续MRD证据的患者,所述方法只会使一小部分患者暴露于不必要的额外毒性中。