LONG-TERM FOLLOW-UP OF A RANDOMIZED TRIAL COMPARING T-CELL DEPLETION WITH A COMBINATION OF METHOTREXATE AND CYCLOSPORINE IN ADULT LEUKEMIC MARROW TRANSPLANT RECIPIENTS
O. Ringden et al., LONG-TERM FOLLOW-UP OF A RANDOMIZED TRIAL COMPARING T-CELL DEPLETION WITH A COMBINATION OF METHOTREXATE AND CYCLOSPORINE IN ADULT LEUKEMIC MARROW TRANSPLANT RECIPIENTS, Transplantation, 58(8), 1994, pp. 887-891
Forty-eight adult leukemic recipients of HLA-identical sibling marrow
were randomized to T cell depletion using anti-CDS and anti-CD6 antibo
dies plus complement (n=23) or prophylaxis with methotrexate (MTX) and
cyclosporine (CsA) (n=25). Patient characteristics were comparable in
the two groups. The median observation time was 51/2 years. Transfusi
ons, infections, and acute GVHD did not differ between the groups. Chr
onic GVHD occurred in 52% of patients receiving T cell-depleted marrow
and 23% of those receiving MTX+CsA (P=0.06). Overall probability of r
elapse was similar in both groups and actuarial leukemia-free survival
s at 5 years were 39% and 35% in the two groups, respectively. Among p
atients with chronic myeloid leukemia (CML), leukemia-free survival at
5 years was 25% in patients receiving T cell-depleted marrow compared
with 51% in those given MTX+CsA (P=0.09). In patients with acute leuk
emia the probability of relapse was 24% in the group receiving T cell-
depleted marrow compared with 73% in those treated with MTX+CsA (P=0.0
6). Leukemia-free survival was 55% and 21% in the two groups, respecti
vely (NS). CML patients tended to have a poorer prognosis and those wi
th acute-leukemia better outcome with T cell depletion than with combi
ned MTX+CsA. It is concluded that T cell depletion is unsuitable for p
atients with CML, but may be considered in patients with acute leukemi
a.