Ra. Mandanas et al., G-CSF-MOBILIZED DONOR LEUKOCYTE INFUSIONS AS IMMUNOTHERAPY IN ACUTE-LEUKEMIA RELAPSING AFTER ALLOGENEIC MARROW TRANSPLANTATION, Journal of hematotherapy, 7(5), 1998, pp. 449-456
Citations number
28
Categorie Soggetti
Transplantation,Hematology,"Medicine, Research & Experimental
Eight patients who relapsed with acute leukemia within a year after al
logeneic BMT were treated with G-CSF-mobilized donor leukocyte infusio
ns (mDLI) to induce GVHD as a form of immunotherapy. Prior to mDLI, 7
who had systemic relapse received one (2 AML, 1 ALL, 1 CML myeloid bla
st crisis) or two (2 AML, 1 ALL) rounds of conventional dose induction
chemotherapy, and 1 patient with isolated central nervous system (CNS
) lymphoid blast crisis CML received intrathecal chemotherapy followed
by craniospinal irradiation. G-CSF (10 mu g/kg/day) was given to orig
inal HLA-matched sibling donors for 4-5 days before leukapheresis of a
t least 6.0 x 10(8) mononuclear cells per kilogram of recipient weight
, No GVHD prophylaxis was used when mDLI was given in 6 patients at th
e nadir of hematologic counts and in 2 who were in hematologic remissi
on, There was no regimen-related mortality, as pancytopenic patients h
ad rapid recovery of neutrophil counts (6-18 days after mDLI), All pat
ients developed moderate to severe GVHD (5 grade III/IV, 3 grade II) a
t a median of 30 days (range 22-59) after mDLI, Two patients Pied of c
omplications from refractory GVHD while in remission. The other 6 had
short remissions lasting 2.2-9.4 months until leukemic relapse as thei
r GVHD was reversed by corticosteroids with or without cyclosporine. P
atients who relapse with acute leukemia within a year after BMT still
have a poor prognosis. The success of GVHD as a form of immunotherapy
in these patients may depend on the ability to control it to a state t
hat is both safe and continually exerting an antileukemia effect.