Am. Watson et al., AN EFFECTIVE AGE-UNRESTRICTED M-AMSA-BASED 2ND-LINE REGIMEN FOR POOR-PROGNOSIS ACUTE MYELOID-LEUKEMIA, European journal of haematology, 52(2), 1994, pp. 80-86
The efficacy and toxicity of a regimen consisting of amsacrine (m-AMSA
), cytarabine, and thioguanine for remission-induction therapy in poor
prognosis categories of acute myeloid leukaemia (AML) were determined
in a single arm study of 46 patients. The study group consisted of 17
patients with disease refractory to daunorubicin plus cytarabine-base
d induction regimens, 22 patients with disease which had relapsed duri
ng daunorubicin plus cytarabine maintenance therapy, or following comp
letion of this maintenance programme after receiving greater than or e
qual to 500 mg daunorubicin/m(2) and 7 previously untreated patients w
here cardiac disease contraindicated anthracycline therapy. Complete r
emission (CR) was attained in 46%, and probability of survival was com
parable to published results for first-line treatment with daunorubici
n plus cytarabine regimens. There was no statistically significant dif
ference in CR rate or probability of survival between these three cate
gories of poor prognosis AML, and cardiotoxic complications were uncom
mon despite extensive anthracycline exposure in the majority. In the 4
3% of patients who were 60-76 years of age, there was no statistically
significant difference in CR rate or probability of survival relative
to patients <60 years. This observation fails to support the view tha
t less myelotoxic regimens with lesser efficacy should be the basic ap
proach to treatment of AML in patients greater than or equal to 60 yea
rs of age.