Incidence of mixed chimerism using busulfan/cyclophosphamide containing regimens in allogeneic bone marrow transplantation

Bone Marrow Transplant. 1992 Apr;9(4):293-7.

Abstract

The incidence of mixed chimerism (MC) following allogeneic bone marrow transplantation (allo-BMT) is in part a measure of the marrow ablative effect of preparative regimens. Although the incidence of MC has been reported for many patients treated with total body irradiation (TBI), limited data for busulfan/cyclophosphamide (BU/CY) recipients have been examined. We performed restriction fragment length polymorphism (RFLP) analysis on 68 peripheral blood samples from 26 patients treated with BU/CY prior to allo-BMT for chronic myelogenous leukemia or acute myeloid leukemia. MC was detected in four of 26 patients for an overall incidence of 15.4%. Three of four MC patients are alive with no evidence of disease at 263 to 795 days post-transplantation. A fourth patient is alive at day 501 but developed CNS relapse at day 274. The level of recipient origin cells was less than 10% in all samples and detectable MC was transitory with an RFLP pattern that reverted to full chimerism. These results are comparable to those reported for TBI-containing regimens in patients receiving non-T cell-depleted bone marrow. The efficacy of BU/CY in conjunction with a T cell depletion still requires exploration.

MeSH terms

  • Adult
  • Bone Marrow Transplantation / methods*
  • Busulfan / therapeutic use*
  • Chimera / genetics*
  • Cyclophosphamide / therapeutic use*
  • DNA Probes
  • Female
  • Humans
  • Leukemia, Myeloid / genetics
  • Leukemia, Myeloid / surgery
  • Male
  • Middle Aged
  • Oncogenes
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA Probes
  • Cyclophosphamide
  • Busulfan