Long-term remission of APL with a second allogeneic BMT after CNS relapse following HLA-identical allogeneic BMT

Bone Marrow Transplant. 2003 Oct;32(8):843-6. doi: 10.1038/sj.bmt.1704225.

Abstract

Second allogeneic bone marrow transplantation (BMT) for AML relapsing after an initial BMT has a poor prognosis, with a probability of a 2-y disease-free survival below 30 per cent, caused both by treatment-related mortality (TRM) and high relapse rate. While TRM is most likely due to heavy pretreatment, AML relapse after BMT may be due to resistant disease or to a poor graft-versus-leukaemia (GvL) effect of the transplant. The degree of GvL may depend on individual donor/recipient immunoreactivity. In most published cases of second allogeneic BMT, both transplants were performed from the same donor. Here, we describe a patient who was first transplanted for acute promyelocytic leukaemia (APL) (AML FAB M3v) from his HLA-identical brother and received intensive immunotherapy including donor lymphocytes and IL2. He remained free from GvHD >I degrees, but developed CNS relapse. After a second BMT from another HLA-identical brother, he spontaneously developed GvHD III degrees, and has now been disease free for nearly 3 years. In this patient, long-term remission of AML relapsing after BMT was achieved by combining remission induction using an individual chemotherapy protocol with a second BMT from an alternative matched related donor and transient GvHD III degrees, which probably conferred a GVL effect.

Publication types

  • Case Reports

MeSH terms

  • Bone Marrow Transplantation*
  • Central Nervous System
  • Child, Preschool
  • Graft vs Leukemia Effect
  • Histocompatibility Testing
  • Humans
  • Infant
  • Leukemia, Promyelocytic, Acute / immunology
  • Leukemia, Promyelocytic, Acute / therapy*
  • Recurrence
  • Remission Induction
  • Transplantation, Homologous