O. Kloke et al., Interferon alfa as primary treatment of chronic myeloid leukemia: long-term followup of 71 patients observed in a single center, LEUKEMIA, 14(3), 2000, pp. 389-392
The purpose of this study was to evaluate the long-term outcome of interfer
on (IFN) alfa treatment in patients with Philadelphia chromosome-positive c
hronic myeloid leukemia (CML). Between 1984 and 1990, a total of 71 patient
s with newly diagnosed CML had been enrolled into two consecutive IFN trial
s at our institution. Follow-up extended to December 1998, resulting in a m
edian observation period for surviving patients of 11.4 years. The median s
urvival time from diagnosis was 5.9 years. A plateau in the actuarial survi
val curve was found from 8.2 to 12.3 years following diagnosis with a proje
cted 10-year survival rate of 32%. 'Landmark' studies showed a significant
survival advantage for patients with karyotype responses. Of 68 patients ac
cessible to calculation of the Hasford score, three were in the high risk g
roup, 24 belonged to the medium risk group, and 41 had low risk features, T
he majority of cytogenetic responders including all eight assessable patien
ts in complete cytogenetic remission were in the low risk group. Achieving
a cytogenetic remission was found to provide a survival advantage also for
patients with low risk disease. Of the seven patients surviving more than 1
1 years, six were in continuous complete cytogenetic remission. Their favor
able outcome appears to translate into an out-flattening of the survival cu
rve for the 71 single center patients presented. It will be of interest to
see whether prolonged follow-ups of the large multicentric randomized trial
s will similarly show a subset of long-term surviving patients with ongoing
IFN-induced remission.