首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >The addition of daunorubicin to imatinib mesylate in combination with cytarabine improves the response rate and the survival of patients with myeloid blast crisis chronic myelogenous leukemia (AFR01 study)
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The addition of daunorubicin to imatinib mesylate in combination with cytarabine improves the response rate and the survival of patients with myeloid blast crisis chronic myelogenous leukemia (AFR01 study)

机译:甲磺酸伊马替尼与阿糖胞苷合用柔红霉素可改善髓样疾患危机慢性粒细胞性白血病患者的应答率和存活率(AFR01研究)

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Background: The median survival of patients with chronic myelogenous leukemia in myeloid blast crisis (MBC-CML) is poor even for patients treated with tyrosine kinase inhibitors (TKIs). Design and methods: We conducted a dose-escalating study of daunorubicin combined to fixed doses of IM (imatinib mesylate, 600. mg/d) and cytarabine (200. mg/d for 7 days), followed by hematopoietic stem cell transplantation or maintenance therapy with single-agent IM in patients with MBC-CML at onset or after failure of therapy excluding TKIs. Results: Thirty-six patients were evaluated. Median follow-up is 6.1 years. Daunorubicin was escaladed up to 45mg/m 2/d 3 days. Twenty eight patients (77.7%) had hematologic response including 20 patients (55.5%) in complete hematologic response (CHR). Patients who received daunorubicin at 30-45mg/m 2/d had higher CHR rates compared to other patients. Median overall survival was 16 months. Overall survival in patients with hematological response was 35.4 months. Better results were observed in patients diagnosed with MBC-CML at onset. Conclusions: The combination of IM with a standard " 3. +. 7" regiment was well tolerated and provided a high response rate. More than 55% of the patients achieved CHR and hematopoietic stem cell transplantation (SCT) was feasible in half of the cases. This trial was registered at www.clinicaltrials.gov as # NCT00219765.
机译:背景:即使在接受酪氨酸激酶抑制剂(TKIs)治疗的患者中,慢性粒细胞白血病(MBC-CML)患者的中位生存期仍然很差。设计和方法:我们对柔红霉素联合固定剂量的IM(甲磺酸伊马替尼,600. mg / d)和阿糖胞苷(200. mg / d,共7天)进行了剂量递增研究,随后进行了造血干细胞移植或维持MBC-CML患者在开始或治疗失败后(TKI除外)用单药IM治疗。结果:对36例患者进行了评估。中位随访时间为6.1年。柔红霉素逐步升高至45mg / m 2 / d 3天。二十八例(77.7%)有血液学反应,包括二十例(55.5%)完全血液学反应(CHR)。与其他患者相比,以30-45mg / m 2 / d接受柔红霉素的患者具有较高的CHR率。中位总生存期为16个月。血液学反应患者的总生存期为35.4个月。在开始诊断为MBC-CML的患者中观察到更好的结果。结论:IM与标准“ 3 + 7”治疗方案的组合耐受性良好,并具有较高的缓解率。超过55%的患者实现了CHR,在一半的病例中可行造血干细胞移植(SCT)。该试验已在www.clinicaltrials.gov上注册为#NCT00219765。

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