Long-term outcome of adult acute leukemia patients who are alive and well two years after allogeneic bone marrow transplantation from an HLA-identical sibling
S. Singhal et al., Long-term outcome of adult acute leukemia patients who are alive and well two years after allogeneic bone marrow transplantation from an HLA-identical sibling, LEUK LYMPH, 34(3-4), 1999, pp. 287-294
We studied the long-term outcome of 136 adults with acute leukemia (age 15-
48 years at transplant, median 28; 112 myeloid, 22 lymphoblastic, 2 undiffe
rentiated) who were alive in continuous remission two years after allograft
ing from HLA-identical sibling donors. Six relapsed 25-46 months (median 30
) after BMT. Fourteen (10%) died of non-relapse causes (12 transplant-relat
ed and 2 unrelated) 24-140 months (median 73) after BMT; mainly due to comp
lications of chronic GVHD (8 infections, 3 secondary malignancies). One hun
dred and seventeen (86%) patients are alive in remission 25-226 months (med
ian 103) after BMT; 116 (85%) in continuous remission. Eight survivors have
symptomatic chronic GVHD requiring therapy (Karnofsky scores 60-90%, media
n 80%). The majority of those without chronic GVHD have Karnofsky scores of
100%. The 10-year probabilities of survival, toxic death, and relapse (fro
m the 2-year mark) are 81%, 13%, and 5%. Twenty-two (19%) survivors had cre
atinine levels of > 110 mu mol/L tone more than double), and 11 (9%) had bi
lirubin levels of > 17 mmol/L tone more than double) at the last follow-up.
The absence of chronic GVHD at the 2-year mark OCR 3.5, P=.004), and femal
e sex (RR 2.9, P=.04) influenced overall survival favorably, and the absenc
e of chronic GVHD at the 2-year mark (RR 8.1, P=.001) influenced toxic deat
h favorably. We conclude that patients with acute leukemia who are alive an
d well without chronic GVHD two years following an allograft have a high pr
obability of being cured, whereas patients with active chronic GVHD requiri
ng immunosuppression continue to be at risk of non-relapse death. The incid
ence of long-term liver and kidney dysfunction measured by serum bilirubin
and creatinine is low.