E. Carreras et al., Unrelated donor bone marrow transplantation as treatment for chronic myeloid leukemia: the Spanish experience, HAEMATOLOG, 85(5), 2000, pp. 530-538
Background and Objectives. To analyze the results of unrelated bone marrow
transplantation (UDBMT) as treatment for chronic myeloid leukemia (CML) In,
Spain,
Designs and Methods. Eighty-seven consecutive UDBMT performed in 9 centers
between October 1989 and February 1998 were evaluated. This represents more
than 95% of UDBMT for CML performed formed in adult transplant centers in
Spain during this period. The patients' median age was 31.5 years (range 12
-49), The median Interval from CML. diagnosis to UDBMT was 30 months (range
, 3-160). Seventy-nine percent of transplants were per formed during the fi
rst chronic phase (1CP),
Results, Actuarial probability of survival and disease;free survival at 4 y
ears for the whole series was 24% (95% confidence interval [CI]: 14%-34%) a
nd 20% (CI: 10%-30%) respectively. The cumulative Incidence of relapse and
transplant-related mortality (TRM) was 7% (CI: 4%-10%) and 71% (CI: 60%-82%
), respectively. The main causes of death were graft failure (n=7), infecti
on (n=23), and graft-versus-host disease (GVHD) (n=25), The actuarial proba
bility of acute GVHD grade Ii-IV and grade III-IV was 56% (CI:46%-66%) and
36% (CI: 26%-36%), respectively. The cumulative Incidence of extensive chro
nic GvHD was 18% (CI: 9%-27%), Univariate analyses showed that the pre-tran
splant factor with the highest influence on survival was disease status at
transplant (30% in 1CP vs. 0% in advanced phases; p=0.0001). ether pre-tran
splant factors influencing survival among patients in 1CP were: patient's a
ge (older than 30 years 11% vs. 48%), interval diagnosis-transplantation (l
onger than 2 17% vs. 55%), donor type (HLA, a, DRB1 identical vs, 25%), CMV
serologic status (donor recipient negative 63% vs. 24%), year of trans(bef
ore plantation (before 1995 19% vs. 40%), and conditioning regimen (cycloph
osphamide plus total body radiation 40% vs, 16%), The main risk factors had
a cumulative effect on survival. Thus, probability of survival ranged from
66% (CI: 39%-93%) In patients in 1CP, under 40 years of age, transplanted
from an HLA, A, B, DRB1 identical donor during the first two years after di
agnosis, to 0% in those with three or mom risk factors.
Interpretation and Conclusions. This experience shows that UDBMT used to ha
ve a high TRM that has progressively decreased along the years. At the pres
ent time, the results are encouraging, particularly when UDBMT Is performed
under favorable conditions
(C) 2000 Ferrata Stortl Foundation.