Jr. Schofield et al., LOW-DOSES OF INTERFERON-ALPHA ARE AS EFFECTIVE AS HIGHER DOSES IN INDUCING REMISSIONS AND PROLONGING SURVIVAL IN CHRONIC MYELOID-LEUKEMIA, Annals of internal medicine, 121(10), 1994, pp. 736-744
Objective: To determine the toxicity and efficacy of low-dose interfer
on-alpha therapy in inducing remissions and prolonging survival in pat
ients with chronic myeloid leukemia. Design: Phase II evaluation and c
omparison with historical control patients and other series in which t
he investigators used higher interferon-alpha doses. Setting: Tertiary
care leukemia research clinic. Patients: 41 patients with newly diagn
osed or previously treated chronic-phase, Philadelphia chromosome-posi
tive chronic myeloid leukemia received interferon-alpha at a dose of 2
x 10(6) U/m(2) body surface area daily for 28 days and then three tim
es weekly. Measurements: Complete blood counts and physical examinatio
ns were done monthly to determine hematologic remission and toxicity.
To determine karyotypic response, bone marrow cytogenetic analyses wer
e done at 6 monthly intervals in patients who achieved a complete hema
tologic remission. In addition, Kaplan-Meier survival curves and media
n survival values were generated from diagnosis and the start of thera
py with interferon-alpha. Results: 70% of patients treated with low-do
se interferon-alpha within 1 year of diagnosis achieved a complete hem
atologic remission, and 22% of these patients had a major or complete
karyotypic response. Investigators who used higher interferon-alpha do
ses in similar patient populations have reported complete hematologic
remission rates of 59% to 70% and major and complete cytogenetic respo
nse rates of 16% to 29%. The Kaplan-Meier estimated 5-year survival ra
te of minimally pretreated patients in our study is 73% (95% Cl, 51% t
o 95%), which compares favorably with survivals reported by investigat
ors who used higher doses. The estimated yearly cost of the interferon
-alpha used in our study is $5953 compared with a median of $24 375 fo
r the higher doses used by other investigators. Less toxicity was also
observed. Conclusion: Low-dose interferon-alpha is as effective as hi
gher-dose interferon-alpha in inducing remissions and prolonging survi
val in patients with chronic myeloid leukemia but is considerably less
expensive and toxic.