| Literature DB >> 9136959 |
F Keil1, P Kalhs, O A Haas, G Fritsch, E Reiter, C Mannhalter, K Lechner, G Leitner, H T Greinix.
Abstract
We present a patient who underwent sibling allogeneic BMT because of refractory Ph+ve ALL and remained BCR-ABL-positive after marrow grafting. Haemopoietic precursor cells were predominantly BCR-ABL-negative and of donor origin. In T cells an exclusively donor genotype was demonstrated. Despite donor leucocyte infusion (DLI), 20 weeks after BMT BCR-ABL fusion mRNA increased in semiquantitative polymerase chain reaction and leukaemic infiltration of the patient's bone marrow was seen. After a second course of DLI the patient achieved sustained molecular remission but he developed severe graft-versus-host disease (GvHD) and died from bacterial sepsis 9 months after DLI.Entities:
Mesh:
Year: 1997 PMID: 9136959 DOI: 10.1046/j.1365-2141.1997.262674.x
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998