Ogawa H, Tsuboi A, Oji Y, Tamaki H, Soma T, Inoue K, Sugiyama H
Department of Medicine III, Osaka University Medical School, Suita City, Japan.
Bone Marrow Transplant. 1998 Mar;21(5):525-7. doi: 10.1038/sj.bmt.1701123.
We report here that a patient with relapsed AML after allogeneic bone marrow transplantation achieved and maintained complete remission (CR) after effective donor leukocyte transfusion (DLT), without the occurrence of GVHD and marrow aplasia, for more than 21 months. This continuous CR maintenance is mainly due to the application of DLT at molecular relapse that was diagnosed by monitoring minimal residual disease (MRD) by the quantitation of WT1 (Wilms tumor gene) expression levels (WT1 assay). The present case demonstrates that early application of DLT at molecular relapse is essential for the improvement of the efficacy of DLT for relapsed AML after BMT.
我们在此报告,一名异基因骨髓移植后复发的急性髓系白血病(AML)患者,在接受有效的供体白细胞输注(DLT)后实现并维持了完全缓解(CR),超过21个月未发生移植物抗宿主病(GVHD)和骨髓再生障碍。这种持续的CR维持主要归因于在分子复发时应用DLT,分子复发是通过定量WT1(威尔姆斯肿瘤基因)表达水平(WT1检测)监测微小残留病(MRD)而诊断出来的。本病例表明,在分子复发时早期应用DLT对于提高DLT治疗BMT后复发AML的疗效至关重要。