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Multicenter Study
. 2010 Jan;25(1):9-15.
doi: 10.3346/jkms.2010.25.1.9. Epub 2009 Dec 26.

Idarubicin plus behenoyl cytarabine and 6-thioguanine compares favorably with idarubicin plus cytarabine-based regimen for children with previously untreated acute myeloid leukemia: 10-year retrospective, multicenter study in Korea

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Multicenter Study

Idarubicin plus behenoyl cytarabine and 6-thioguanine compares favorably with idarubicin plus cytarabine-based regimen for children with previously untreated acute myeloid leukemia: 10-year retrospective, multicenter study in Korea

Dae Hyoung Lee et al. J Korean Med Sci. 2010 Jan.

Abstract

We investigated the outcome of idarubicin plus N(4)-behenoyl-1-beta-D-arabinofuranosyl cytosine (BHAC)-based chemotherapy (BHAC group, n=149) compared to idarubicin plus cytarabine-based chemotherapy (cytarabine group, n=191) for childhood acute myeloid leukemia (AML). Between January 1996 and December 2005, 340 children with AML from 5 university hospitals in Korea received the BHAC-based or cytarabine-based chemotherapy, with or without hematopoietic stem cell transplantation. After induction therapy, 264 (77.6%) of 340 children achieved a complete remission (CR) and 43 (12%) achieved a partial remission (PR). The CR rate in the BHAC group was higher than in the cytarabine group (85.2% vs. 71.7%, P=0.004). However, the overall response rate (CR+PR) was not different between the two groups (93.3% vs. 87.9%, P=0.139). The 5-yr estimates of overall survival (OS) of children in the two groups were similar (54.9% for the BHAC group vs. 52.4% for the cytarabine group, P=0.281). Although the results were analyzed according to the treatment type and cytogenetic risk, the OS showed no significant difference between the BHAC group and the cytarabine group. In the present study, the clinical outcomes of the BHAC-based chemotherapy, consisting of BHAC, idarubicin, and 6-TG, are comparable to that of the cytarabine-based chemotherapy for childhood AML.

Keywords: Childhood; Enocitabine; Leukemia, Myeloid, Acute.

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Figures

Fig. 1
Fig. 1
Kaplan-Meier estimates of OS at 5 yr for the 340 children.
Fig. 2
Fig. 2
Kaplan-Meier estimates of OS of children without HSCT (A) and with HSCT (B) at 5 yr.
Fig. 3
Fig. 3
Kaplan-Meier estimates of EFS of children without HSCT (A) and with HSCT (B) at 5 yr.

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