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Cancer ; 48(10): 2136-42, 1981 Nov 15.
Article in English | MEDLINE | ID: mdl-6170414

ABSTRACT

Fifty-one adult patients with acute nonlymphocytic leukemia (excluding acute promyelocytic leukemia) were treated on the L-12 protocol. The L-12 differed from the preceding L-6 in that 2,2-anhydro-1-B-D-arabinofuranosyl-5-fluorocytosine (AAFC), replaced arabinosylcytosine (ara-C) together with 6-thioguanine (TG) for remission induction. Achievement of remission was followed by an extended 14-week multi-drug consolidation program. With this more intense regimen, an overall complete remission rate of 49% and a median remission duration of 23.7 months were achieved; these results were not significantly better than the 57% complete remission rate and 8.6 months median remission duration obtained with the L-6 regimen. Four year disease-free survival was 22% on the L-12 compared with 16% on the L-6 protocol. No relationship between prognosis and FAB classification was found on either the L-6 or the L-12 protocol.


Subject(s)
Ancitabine/analogs & derivatives , Antineoplastic Agents/administration & dosage , Cytarabine/analogs & derivatives , Leukemia, Myeloid, Acute/drug therapy , Leukemia/drug therapy , Thioguanine/administration & dosage , Adolescent , Adult , Aged , Ancitabine/administration & dosage , Ancitabine/adverse effects , Antineoplastic Agents/adverse effects , Bacterial Vaccines/administration & dosage , Drug Therapy, Combination , Female , Humans , Leukemia/pathology , Leukemia/therapy , Male , Middle Aged , Prognosis , Pseudomonas aeruginosa , Random Allocation , Thioguanine/adverse effects
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