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Homoharringtonine in combination with cytarabine and aclarubicin in the treatment of refractory/relapsed acute myeloid leukemia: a single-center experience

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Abstract

To assess the efficacy and toxicity of HAA regimen (Homoharringtonine 4 mg/m2/day, days 1–3; cytarabine 150 mg/m2/day, days 1–7; aclarubicin 12 mg/m2/day, days 1–7) as a salvage therapy in the treatment of refractory and/or relapsed acute myeloid leukemia (AML), 46 patients with refractory and/or relapsed AML, median age 37 (16–65) years, participated in this clinical study. The median follow-up was 41 (10–86) months. Eighty percent of patients achieved complete remission (CR), and the first single course of re-induction HAA regimen resulted in CR rate of 76.1 %. The study protocol allowed two courses of induction. The CR rates of patients with favorable, intermediate and unfavorable cytogenetics were 90 %, 88.9 %, and 37.5 %, respectively. For all patients, the estimated 3-year overall survival (OS) rate was 42 %, and the estimated relapse free survival (RFS) at 3 years for the 36 CR cases was 49 %. The toxicities associated with HAA regimen were acceptable. HAA is a good choice in cases with refractory/relapsing AML for salvage chemotherapy, preferably with a high-efficacy and low-toxicity profile.

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Acknowledgments

This work was supported by National Natural Science Foundation of China (Grant #30900641), Science Research Fundation of Health Department of Zhejiang Province (Grant #2008B063 and Grant #2009B046) and Research Fund for the Doctoral Program of Higher Education of China (Grant #20090101120112).

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The authors declare that they have no conflict of interest.

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Correspondence to Jie Jin.

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Yu, W., Mao, L., Qian, J. et al. Homoharringtonine in combination with cytarabine and aclarubicin in the treatment of refractory/relapsed acute myeloid leukemia: a single-center experience. Ann Hematol 92, 1091–1100 (2013). https://doi.org/10.1007/s00277-013-1758-5

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