Low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor (CAG regimen) for previously treated patients with relapsed or primary resistant acute myelogenous leukemia (AML) and previously untreated elderly patients with AML, secondary AML, and refractory anemia with excess blasts in transformation
K. Saito et al., Low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor (CAG regimen) for previously treated patients with relapsed or primary resistant acute myelogenous leukemia (AML) and previously untreated elderly patients with AML, secondary AML, and refractory anemia with excess blasts in transformation, INT J HEMAT, 71(3), 2000, pp. 238-244
We used the CAG regimen (low-dose cytarabine [10 mg/m(2) per 12 hours, days
1-14], aclarubicin [14 mg/m(2) per day, days 1-4], and granulocyte colony-
stimulating factor [200 mu g/m(2) per day, days 1-14]) for the treatment of
patients with primary resistant acute myelogenous leukemia (AML) and previ
ously untreated elderly patients with AML, secondary AML, and refractory an
emia with excess blasts in transformation (RAEB-T) in addition to relapsed
AML. Forty-three of 69 (62%) patients achieved complete remission (CR), inc
luding 29 of 35 (83%) patients with relapsed AML, 1 of 8 patients with prim
ary resistant AML, 5 of 8 elderly patients with previously untreated AML, a
nd 8 of 18 patients with previously untreated secondary AML or RAEB-T. Ten
of 22 (45%) patients greater than or equal to 65 years old achieved CR. The
patients who achieved CR received at least 1 course of modified CAG therap
y as the first consolidation therapy, followed by various second consolidat
ion and intensification therapies. The median disease-free survival and ove
rall survival were 8 and 15 months, respectively, for relapsed AML; 11 and
8 months for the elderly patients; and 8 and 17 months for secondary AML an
d RAEB-T; Myelosuppression was mild to moderate, and other than fever, seve
re nonhematologic toxicity was rare. CAG as the induction therapy seems pro
mising for the treatment of various categories of poor-prognosis AML. Int J
Hematol. 2000;71:238-244 (C) 2000 The Japanese Society of Hematology.