Preliminary experience of allogeneic stem cell transplantation for lymphoproliferative disorders using BEAM-CAMPATH conditioning: an effective regimen with low procedure-related toxicity
Gm. Cull et al., Preliminary experience of allogeneic stem cell transplantation for lymphoproliferative disorders using BEAM-CAMPATH conditioning: an effective regimen with low procedure-related toxicity, BR J HAEM, 108(4), 2000, pp. 754-760
Autologous transplantation has an established role in the treatment of lymp
hoproliferative disorders, but allogeneic transplantation remains controver
sial. In an attempt to reduce the high procedure-related mortality reported
with allografting in lymphoma, we have used BEAM (BCNU, etoposide, cytarab
ine and melphalan), a standard conditioning regimen for autologous transpla
ntation. As BEAM may be insufficiently immunosuppressive to permit durable
engraftment in the allogeneic setting, patients received additional pretran
splant immunosuppression with the anti-CD52 antibody CAMPATH-1G from day -5
to day -1.
Twelve patients (median age 46 years) underwent allogeneic transplantation
for lymphoma (n = 11) or chronic lymphocytic leukaemia (n = 1) from HLA-ide
ntical (n = 9) or mismatched (n = 3) sibling donors. Cyclosporin A and meth
otrexate were used as graft-versus-host disease (GVHD) prophylaxis. One pat
ient died of progressive lymphoma at day +12, the remaining 11 patients eng
rafted rapidly, with eight demonstrating full donor chimerism, One patient
had an episode of rejection and received a further stern cell infusion with
sustained recovery Only one patient developed GVHD (grade I). The low inci
dence of acute GVHD may be in part related to persisting levels of in vivo
CAMPATH-1G at the time of transplantation. Of 11 evaluable patients, nine a
chieved complete remission (CR), and a further patient achieved CR after do
nor lymphocyte infusion at 5 months.
Our preliminary experience is that this regimen was well tolerated with a l
ow risk of GVHD and appears no more toxic than a BEAM autograft. Further fo
llow-up is required to see whether the low incidence of GVHD impacts upon r
elapse risk.