Dl. Porter et al., Treatment of relapsed leukemia after unrelated donor marrow transplantation with unrelated donor leukocyte infusions, BLOOD, 95(4), 2000, pp. 1214-1221
The efficacy and toxicity of donor leukocyte infusions (DLI) after unrelate
d donor bone marrow transplantation (BMT) is largely unknown. We identified
58 recipients of unrelated DLI (UDLI) for the treatment of relapsed diseas
e from the National Marrow Donor Program database. A retrospective analysis
was performed to determine response, toxicity, and survival after UDLI and
to identify factors associated with successful therapy. UDLI was administe
red for relapsed chronic myelogenous leukemia (CML) (n = 25), acute myeloge
nous leukemia (AML) (n = 23), acute lymphoblastic leukemia (ALL) (n = I), a
nd other diseases (n = 3). Eight patients were in complete remission (CR) b
efore UDLI, and 50 were evaluable for response. Forty-two percent (95% conf
idence interval [CI], 28%-56%) achieved CR, including 11 of 24 (46%; 95% CI
, 26%-66%) with CML, 8 of 19(42%; 95% CI, 20%-64%) with AML, and 2 of 4 (50
%; 95% CI, 1%-99%) with ALL. The estimated probability of disease-free surv
ival (DFS) at 1 year after CR was 65% (95% CI, 50%-79%) for CML, 23% (95% C
I, 9%-38%) for AML, and 30% (95% CI, 6%-54%) for ALL. Acute graft-versus-ho
st disease (GVHD) complicated UDLI in 37% of patients (grade II-IV, 25%). A
total of 13 of 32 evaluable patients (41%) developed chronic GVHD. There w
as no association between cell dose administered and either response or tox
icity. In a multivariable analysis, only a longer interval from BMT to rela
pse and BMT to UDLI was associated with improved survival and DFS, respecti
vely. UDLI is an acceptable alternative to other treatment options for rela
pse after unrelated donor BMT. (Blood. 2000;95:1214-1221) (C) 2000 by The A
merican Society of Hematology.