Multicenter prospective study of interferon-alpha versus bone marrow transplantation for newly diagnosed patients with chronic myelogenous leukemia: a preliminary analysis
K. Ohnishi et al., Multicenter prospective study of interferon-alpha versus bone marrow transplantation for newly diagnosed patients with chronic myelogenous leukemia: a preliminary analysis, CANC CHEMOT, 48, 2001, pp. S59-S64
Interferon-alpha (IFN-alpha) therapy was compared with bone marrow transpla
ntation (BMT) in patients with chronic myelogenous leukemia (CML) in a mult
icenter, prospective study. Of 254 evaluable patients, 175 received IFN-alp
ha and 79 received allogeneic BMT, 50 of whom received transplants from hum
an leukocyte antigen (HLA)-identical related donors and 29 from HLA-matched
unrelated donors. Complete hematologic response was achieved by 148 patien
ts (89%) in the IFN-alpha group and 53 (78%) in the BMT group. In the IFN-a
lpha group, a complete cytogenetic response was induced in 25 patients (15%
), a partial cytogenetic response in 37 (23%), and a minor cytogenetic resp
onse in 41 (25%). At a median follow-up of 38 months, in the IFN-alpha grou
p the predicted 5-year survival rate was 79%, and the predicted 5-year rate
of remaining in chronic phase was 66%. In the BMT group the predicted 5-ye
ar survival rate was 72% for related-donor BMT and 67% for unrelated-donor
BMT. Among low Sokal-risk patients, 5-year survival did not differ between
IFN-alpha therapy and BMT, irrespective of age. In higher Sokal-risk patien
ts, survival for related-donor BMT and unrelated-donor BMT tended to be bet
ter than that with IFN-alpha, therapy in younger patients. On the other han
d, in older patients, survival in the BMT group, especially for those recei
ving unrelated-donor BMT, appeared to be inferior to that in the IFN-alpha
group. Unrelated-donor BMT can be recommended for high-risk younger patient
s. However, for older patients, it should be performed after careful consid
eration of prognostic factors such as age, Sokal score, and response to IFN
-alpha.