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首页> 外文期刊>Haematologica >Lenalidomide combined with intensive chemotherapy in acute myeloid leukemia and higher-risk myelodysplastic syndrome with 5q deletion. Results of a phase II study by the Groupe Francophone Des Myélodysplasies
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Lenalidomide combined with intensive chemotherapy in acute myeloid leukemia and higher-risk myelodysplastic syndrome with 5q deletion. Results of a phase II study by the Groupe Francophone Des Myélodysplasies

机译:来那度胺联合强化化疗可治疗5q缺失的急性髓细胞白血病和高危骨髓增生异常综合征。法语国家集团的二期研究的结果

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摘要

Patients with acute myeloblastic leukemia or higher risk myelodysplastic syndromes with 5q deletion (generally within a complex karyotype) respond poorly to intensive chemotherapy and have very poor survival. In this population, we evaluated escalating doses of lenalidomide combined with intensive chemotherapy in a phase II study. Treatment consisted of daunorubicin (45 mg/m~(2)/day, days 1–3 in cohort 1, escalated to 60 mg/m~(2)/day, days 1–3 in cohorts 2 and 3) combined with cytosine arabinoside (200 mg/m~(2)/day, days 1–7) and lenalidomide (10 mg/day, days 1–21 in cohorts 1 and 2, escalated to 25 mg/day, days 1–21 in cohort 3). Eighty-two patients with 5q deletion were enrolled, including 62 with acute myeloblastic leukemia, 62/79 (78%) of whom had a complex karyotype (median 7 cytogenetic abnormalities, all but 2 of them monosomal) and three had unknown karyotypes. Thirty-eight patients (46%) achieved complete remission and the overall response rate was 58.5%. Among the 62 patients with a complex karyotype, 27 achieved complete remission (44%) and 21 had cytogenetic responses. A lower response rate was observed in patients with acute myeloblastic leukemia but other pretreatment factors, including cytogenetic complexity and treatment cohort, did not significantly influence response. Fifteen patients underwent allogeneic stem cell transplantation, including 11 patients in first remission. The 1-year cumulative incidence of relapse was 64.6% and the median overall survival was 8.2 months. By comparison with conventional intensive chemotherapy, the treatment protocol we used appeared to produce higher hematologic and cytogenetic complete remission rates in patients with very poor cytogenetics, but response duration was short in this very poor risk population, highlighting the need for better post-induction strategies. Clinical trial registry number. {"type"."clinical-trial","attrs".{"text"."NCT00885508","term_id"."NCT00885508"}}NCT00885508 .
机译:患有5q缺失的急性粒细胞白血病或高危骨髓增生异常综合征患者(通常在复杂的核型中)对强化化疗的反应较差,生存期非常差。在该人群中,我们在II期研究中评估了来那度胺与强化化疗相结合的逐步增加的剂量。治疗由柔红霉素(45 mg / m〜(2)/天,第1组的第1-3天,升级为60 mg / m〜(2)/天,第2和3组的第1-3天)联合胞嘧啶第1组和第2组中的阿拉伯糖苷(200 mg / m〜(2)/天,第1–7天)和来那度胺(10 mg /天,第1–21天,在第3组中增加至25 mg /天,第1–21天)。入选了82例5q缺失的患者,包括62例急性粒细胞性白血病,其中62/79例(78%)具有复杂的核型(中位为7个细胞遗传学异常,除2例均为染色体外),另外3例具有未知的核型。 38例患者(46%)完全缓解,总缓解率为58.5%。在62例复杂核型患者中,有27例完全缓解(44%),其中21例具有细胞遗传学应答。在急性粒细胞性白血病患者中观察到较低的反应率,但其他预处理因素,包括细胞遗传学复杂性和治疗队列,并未显着影响反应。 15例患者接受了异基因干细胞移植,其中11例首次缓解。 1年累积复发率是64.6%,中位总生存期是8.2个月。与传统的强化化疗相比,我们使用的治疗方案似乎在细胞遗传学非常差的患者中产生更高的血液学和细胞遗传学完全缓解率,但是在这一极度危险的人群中,反应持续时间较短,这表明需要更好的诱导后策略。临床试验注册号。 {“类型”。“临床试验”,“属性”。{“文本”。“ NCT00885508”,“ term_id”。“ NCT00885508”}} NCT00885508。

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