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首页> 外文期刊>AMERICAN JOURNAL OF HEMATOLOGY >Second-line mitoxantrone, etoposide, and cytarabine for acute myeloid leukemia: A single-center experience†
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Second-line mitoxantrone, etoposide, and cytarabine for acute myeloid leukemia: A single-center experience†

机译:二线米托蒽醌,依托泊苷和阿糖胞苷治疗急性髓性白血病:单中心经验†

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摘要

The majority of patients with acute myeloid leukemia (AML) will require second-line chemotherapy for either relapsed or refractory disease. Currently, only allogeneic hematopoietic cell transplantation (HCT) offers a curative option in this setting and no preferred regimen has been established. The reported efficacy of second-line regimens is widely disparate, thus limiting informed clinical decision making. A retrospective review of 77 patients receiving therapy between 2001 and 2008 with relapsed, 42, and refractory, 35, AML was performed to determine overall response rate and survival following mitoxantrone (8 mg/m2/day), etoposide (100 mg/m2/day), and cytarabine (1,000 mg/m2/day) chemotherapy administered over 5 days. Among 77 patients (median age of 54 years and 64% intermediate risk karyotype) with median follow-up of 153 days, 18% achieved a complete response and 8% a morphologic leukemia-free state. Fifty-seven (74%) experienced treatment failure, 10 of whom achieved a remission after additional therapy. Median overall survival (OS) was 6.8 months. Among patients achieving a response, 50% received consolidation with allogeneic HCT, autologous HCT (5%), or consolidation chemotherapy alone (45%). A nonsignificant trend in overall response (50%, 27%, and 23.8%) and median OS (8.3, 6.8, and 4.7 months) was observed by cytogenetic stratification into favorable, intermediate, and unfavorable risk. Patients with refractory versus relapsed disease had similar overall responses (20% and 31%, P = 0.41) and median OS (5.3 and 7.6 months, P = 0.36). Despite risk stratification by the European Prognostic Index, our series demonstrates inferior rates of response and survival, illustrating the limited activity of this regimen in our cohort. Am. J. Hematol., 2010. © 2010 Wiley-Liss, Inc.
机译:对于复发性或难治性疾病,大多数急性髓细胞性白血病(AML)患者将需要二线化疗。目前,在这种情况下,只有同种异体造血细胞移植(HCT)提供了治疗选择,并且尚未建立首选方案。报道的二线治疗方案的疗效差异很大,因此限制了知情的临床决策。回顾性分析了2001年至2008年间77例复发,42例和35例难治性AML患者的治疗情况,以确定米托蒽醌(8 mg / m 2 /天)的总体缓解率和生存率,依托泊苷(100 mg / m 2 /天)和阿糖胞苷(1,000 mg / m 2 /天)的化疗在5天内进行。在中位随访时间为153天的77例患者(中位年龄为54岁,中度危险性核型为64%)中,有18%达到完全缓解,有8%为无形态性白血病。五十七(74%)位患者经历了治疗失败,其中10位在接受其他疗法后获得了缓解。中位总生存期(OS)为6.8个月。在获得缓解的患者中,50%接受了同种异体HCT,自体HCT(5%)或单独进行巩固化疗(45%)的巩固治疗。通过细胞遗传分层分为有利,中度和不利风险,观察到总体缓解(50%,27%和23.8%)和中位OS(8.3、6.8和4.7个月)无明显趋势。难治性与复发性疾病患者的总体缓解率相似(20%和31%,P = 0.41)和中位OS(5.3和7.6个月,P = 0.36)。尽管根据欧洲预后指数对风险进行了分层,但我们的系列病例显示出较低的反应率和生存率,说明了该方案在我们队列中的活动有限。上午。 J. Hematol。,2010年。©2010 Wiley-Liss,Inc.。

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  • 来源
    《AMERICAN JOURNAL OF HEMATOLOGY》 |2010年第11期|p.877-881|共5页
  • 作者单位

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Pharmacology, Stanford University, Stanford, California 94305;

    Department of Pharmacology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

    Department of Medicine, Division of Hematology, Stanford University, Stanford, California 94305;

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