Yt. Lin et al., ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR PHILADELPHIA-CHROMOSOME-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA IN CHILDHOOD, Journal of the Formosan Medical Association, 96(5), 1997, pp. 320-324
Allogeneic bone marrow transplantation (BMT) offers the only potential
for long-term control of chronic myelogenous leukemia. From November
1992 to August 1994, we prospectively studied five pediatric patients
with Philadelphia chromosome-positive chronic myelogenous leukemia, a
unique finding in Taiwan, who were treated with allogeneic BMT at diff
erent stages of the disease. Their ages at diagnosis ranged from 2 to
10 years. Four donors were HLA-matched siblings and the other was an H
LA-matched unrelated donor. All patients received busulfan (4 mg/kg/da
y for 4 days) followed by cyclophosphamide (60 mg/kg/day for 2 success
ive days) as the conditioning regimen. Engraftment was documented with
in 22 days after transplantation in all five patients. Two our of the
four patients in the sibling donor group, both of whom had BRIT in the
first chronic phase, achieved event-free survival after follow-up for
41 months and 17 months. The other two patients, Mho had BMT in the s
econd lymphoblastic crisis and the second chronic phase, died within 6
months after transplantation due to lymphoid blastic crisis and compl
ication of cytomegaloviral pneumonitis, respectively. The patient who
received marrow from the unrelated donor underwent BRIT in the acceler
ated phase and died within 6 months after transplantation due to myelo
id blastic crisis. In conclusion, allogeneic BRIT performed in the fir
st chronic phase of childhood Philadelphia chromosome-positive chronic
myelogenous leukemia seems to have better results than BMT after the
first chronic phase.