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首页> 外文期刊>Leukemia and lymphoma >CHAG priming regimen containing of cytarabine, aclacinomycin homoharringtonine and G-CSF for relapsed refractory acute myelogenous Leukemia: A modified combination chemotherapeutic combination
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CHAG priming regimen containing of cytarabine, aclacinomycin homoharringtonine and G-CSF for relapsed refractory acute myelogenous Leukemia: A modified combination chemotherapeutic combination

机译:CHAG引发方案,包含阿糖胞苷,阿克拉霉素高灵敏素和G-CSF用于复发性难治性急性粒细胞性白血病:一种改良的化疗组合

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摘要

With the emergence of novel drugs, ameliorated chemotherapy, molecular targeted therapy and hematopoietic stem cell transplant, complete remission (CR) rates for acute myelog-enous leukemia (AML) have markedly improved recently. In 1986, Griffin and Lowenberg reported that granulocyte colony-stimulating factor (G-CSF) played a role in the proliferation of leukemic progenitors in AML [1]. The application of G-CSF in AML treatment thus became a core concern. Yamada et al. [2] first applied a CAG regimen (cytarabine, aclacinomycin and G-CSF) to treat patients with AML in 1995, and they obtained dramatic results. Since then, priming regimens (including CAG, CHG [3] and HAG [4]; see Appendix for definitions) have been widely employed in AML and similar outcomes have been reported. However, their curative effects in refractory and relapsed AML (RR-AML) are still unsatisfactory.
机译:随着新药,改良化学疗法,分子靶向疗法和造血干细胞移植的出现,急性骨髓性白血病(AML)的完全缓解(CR)率最近已显着提高。 1986年,Griffin和Lowenberg报道了粒细胞集落刺激因子(G-CSF)在AML中白血病祖细胞的增殖中发挥了作用[1]。因此,G-CSF在AML治疗中的应用成为一个核心问题。山田等。 [2] 1995年首次应用CAG方案(阿糖胞苷,阿克拉霉素和G-CSF)治疗AML患者,并获得了可喜的结果。从那时起,启动疗法(包括CAG,CHG [3]和HAG [4];定义见附录)已广泛应用于AML中,并且已报道了类似的结果。但是,它们在难治性和复发性AML(RR-AML)中的疗效仍不令人满意。

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