首页> 美国卫生研究院文献>Haematologica >Intensive induction is effective in selected octogenarian acute myeloid leukemia patients: prognostic significance of karyotype and selected molecular markers used in the European LeukemiaNet classification
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Intensive induction is effective in selected octogenarian acute myeloid leukemia patients: prognostic significance of karyotype and selected molecular markers used in the European LeukemiaNet classification

机译:强化诱导对某些八岁以上的急性髓细胞性白血病患者有效:核型和欧洲白血病网分类中使用的所选分子标记物的预后意义

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摘要

We investigated whether octogenarian patients with acute myeloid leukemia enrolled onto Cooperative Group clinical trials and treated with intensive induction therapy could be cured, and whether karyotype and selected molecular markers had any prognostic significance in these patients. Among 138 patients with cytogenetic information, normal karyotype was the most common (47.1%) followed by complex karyotype (14.5%) and sole +8 (9.4%). Among these patients, the relapse-free survival rate at 1 year was 37% and 13% at 3 years, and the respective overall survival rates were 24% and 8%. Whereas the 90 patients who survived beyond 30 days had the same relapse-free survival rates, their 1-year and 3-year overall survival rates were 36% and 11%, respectively. Of the 66 patients surviving beyond 30 days who could be classified into European LeukemiaNet genetic groups, those in the intermediate-I group had better overall survival than patients in the adverse group (P=0.01). Among patients with cytogenetically normal acute myeloid leukemia who were tested for the European LeukemiaNet-associated molecular alterations, FLT3-internal tandem duplication and NPM1 mutations, it was found that FLT3-internal tandem duplication (detected in 29% of patients) did not associate with overall survival (P=0.31), whereas NPM1 mutations (30%) were associated with a significantly longer overall survival (P=0.002). We conclude that intensive induction is effective and indicated in selected octogenarians with acute myeloid leukemia, that their overall survival varies among the European LeukemiaNet genetic groups and that NPM1 mutations may be of prognostic significance among octogenarian patients with cytogenetically normal acute myeloid leukemia.
机译:我们调查了参加合作组临床试验并接受强化诱导疗法治疗的八十岁以上急性髓性白血病患者是否可以治愈,并且核型和所选分子标记物对这些患者是否具有预后意义。在138位具有细胞遗传学信息的患者中,正常核型最为常见(47.1%),其次是复杂核型(14.5%)和唯一+8型(9.4%)。在这些患者中,1年无复发生存率分别为37%和3%13年,总的总生存率分别为24%和8%。 90例存活超过30天的患者具有相同的无复发生存率,但其1年和3年总生存率分别为36%和11%。可以分类为欧洲LeukemiaNet基因组的66例存活超过30天的患者中,中I组的总体生存率高于不良组(P = 0.01)。在细胞遗传学上正常的急性髓性白血病患者中进行了欧洲白血病网相关分子改变,FLT3内部串联重复和NPM1突变的检测,发现FLT3内部串联重复(检出率29%)与总生存期(P = 0.31),而NPM1突变(30%)与更长的总生存期相关(P = 0.002)。我们得出的结论是,强诱导是有效的,并在某些患有急性髓性白血病的八岁患者中有效,表明其总体存活率在欧洲LeukemiaNet基因组之间有所不同,并且NPM1突变在具有细胞遗传学上正常的急性髓性白血病的八十岁患者中可能具有预后意义。

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