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Published:2009
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[1].Outcomes of CAG Regimen for Refractory Biphenotypic Acute Leukemia Patients[J].Chinese Medical Sciences Journal,2009,24(03):178-181.
Guang-sheng He, Xiang Zhang, De-pei Wu, et al. Outcomes of CAG Regimen for Refractory Biphenotypic Acute Leukemia Patients[J]. Chinese medical sciences journal, 2009, 24(3): 178-181.
[1].Outcomes of CAG Regimen for Refractory Biphenotypic Acute Leukemia Patients[J].Chinese Medical Sciences Journal,2009,24(03):178-181. DOI:
Guang-sheng He, Xiang Zhang, De-pei Wu, et al. Outcomes of CAG Regimen for Refractory Biphenotypic Acute Leukemia Patients[J]. Chinese medical sciences journal, 2009, 24(3): 178-181. DOI:
Objective To evaluated the efficiency of low-dose cytosine arabinoside plus aclarubicin with concurrent administration of granulocyte colony-stimulating factor (CAG) regimen for refractory biphenotypic acute leukemia (BAL). Methods We treated 5 refractory BAL patients by CAG regimen (10 mg·m-2 cytosine arabinoside subcutaneously administrated every 12 hours
day 1-14; 5-7 mg·m-2 aclarubicin intravenously administrated daily
day 1-8; and concurrently used 200μg·m-2·d-1 granulocyte colony-stimulating factor subcutaneously) from November 2002 to April 2007. The efficacy of the regimen was evaluated by response rate
and the side effects were also measured. Results The complete remission rate was 80%
median duration of absolute neutrophil count< 5.0×108/L and platelet count<2.0×1010/L was day 13 and day 1
respectively; and the infection rate was low (Ⅲ-Ⅳ infection rate
20.00%). Conclusion CAG regimen as remission induction chemotherapy for BAL patients is effective with a high remission rate and low toxicity.
Objective To evaluated the efficiency of low-dose cytosine arabinoside plus aclarubicin with concurrent administration of granulocyte colony-stimulating factor (CAG) regimen for refractory biphenotypic acute leukemia (BAL). Methods We treated 5 refractory BAL patients by CAG regimen (10 mg·m-2 cytosine arabinoside subcutaneously administrated every 12 hours
day 1-14; 5-7 mg·m-2 aclarubicin intravenously administrated daily
day 1-8; and concurrently used 200μg·m-2·d-1 granulocyte colony-stimulating factor subcutaneously) from November 2002 to April 2007. The efficacy of the regimen was evaluated by response rate
and the side effects were also measured. Results The complete remission rate was 80%
median duration of absolute neutrophil count< 5.0×108/L and platelet count<2.0×1010/L was day 13 and day 1
respectively; and the infection rate was low (Ⅲ-Ⅳ infection rate
20.00%). Conclusion CAG regimen as remission induction chemotherapy for BAL patients is effective with a high remission rate and low toxicity.
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