首页> 外文期刊>Leukemia and lymphoma >Mitoxantrone and etoposide in patients with newly diagnosed acute myeloid leukemia with persistent leukemia after a course of therapy with cytarabine and idarubicin.
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Mitoxantrone and etoposide in patients with newly diagnosed acute myeloid leukemia with persistent leukemia after a course of therapy with cytarabine and idarubicin.

机译:阿糖胞苷和依托泊苷在阿糖胞苷和伊达比星治疗疗程后新诊断为急性髓性白血病并伴有持续性白血病的患者中。

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摘要

The most effective regimen for patients with acute myeloid leukemia (AML) who do not achieve complete remission (CR) after one course of cytarabine and an anthracycline has not been extensively studied. We evaluated retrospectively the efficacy, toxicity, and prognostic factors for the achievement of CR following mitoxantrone and etoposide in 74 patients with newly diagnosed AML who did not respond to one course of therapy with cytarabine and idarubicin. CR was achieved in 39% of patients; 14% died of infectious complications; no grade 3 or 4 hepatic toxicities were observed. Median duration of overall survival was 9.0 months (95% CI 5.8-14.9 months). The median duration of relapse-free survival was 11.0 months (95% CI: 9.0-19.3 months). A lower CR rate was associated with unfavorable risk status at diagnosis and higher percent blasts. Our data suggest that the combination of etoposide and mitoxantrone is an effective second-course therapy in patients with newly diagnosed AML.
机译:对于经过一个疗程的阿糖胞苷和蒽环类药物治疗后未达到完全缓解(CR)的急性髓细胞性白血病(AML)患者,最有效的方案尚未得到广泛研究。我们回顾性评估了74例新诊断为AML,对阿糖胞苷和伊达比星治疗没有反应的AML患者中,米托蒽醌和依托泊苷后CR达到CR的疗效,毒性和预后因素。 39%的患者达到CR; 14%死于传染性并发​​症;没有观察到3级或4级肝毒性。中位总生存期为9.0个月(95%CI 5.8-14.9个月)。无复发生存的中位时间为11.0个月(95%CI:9.0-19.3个月)。较低的CR率与诊断时不良的风险状态和较高的爆炸率相关。我们的数据表明,依托泊苷和米托蒽醌的组合在新诊断为AML的患者中是一种有效的第二疗程疗法。

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