V. Mattijssen et al., OUTCOME OF ALLOGENEIC BONE-MARROW TRANSPLANTATION WITH LYMPHOCYTE-DEPLETED MARROW GRAFTS IN ADULT PATIENTS WITH MYELODYSPLASTIC SYNDROMES, Bone marrow transplantation, 19(8), 1997, pp. 791-794
Thirty-five patients with myelodysplastic syndromes (MDS) were treated
with BMT between 1986 and 1994. Their median age was 41 years (range
23-60), Thirteen patients had transfusion-dependent refractory anaemia
(RA), Twenty-two patients suffered from more advanced stages of MDS,
15 being in complete remission (CR) after chemotherapy, In 31 recipien
ts, pretransplant conditioning consisted of cyclophosphamide and TBI w
ith or without the addition of idarubucin; four patients were conditio
ned with other schedules, Donors were genotypically HLA-identical and
MLC-negative siblings in 32, and others in three cases, All patients r
eceived a graft depleted of 98% of T lymphocytes using counterflow cen
trifugation, Fourteen patients are alive and in continuous remission w
ith a median follow-up of 20 months (range 15-113) after BMT, Seven pa
tients relapsed between 3 and 18 months after BMT and subsequently die
d, Fourteen transplantation-related deaths occurred, Outcome in patien
ts under and over 40 years old was comparable, The probability of dise
ase-free survival (DFS) at 2 years after BMT was 39% (95% confidence i
nterval (CI), 22-56%), Considering patients with HLA-identical and MLC
-negative sibling donors transplanted for RA (it = 11) or more advance
d stages of MDS in CR (it = 14), the probabilities of DFS were 73% (95
% CI, 47-99%) and 42% (95% CI, 15-69%), respectively, This indicates t
hat BMT with lymphocyte-depleted grafts can cure a substantial number
of relatively old patients with MDS, especially when grafts from HLA-i
dentical and MLC-negative siblings are used and patients are suffering
from RA.