首页> 外文期刊>Acta Haematologica >Clinical Efficacy of Mitoxantrone and Ara-C with or without Etoposide Salvage Chemotherapy in Adult Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia: Retrospective Multicenter Study of the Korean Adult ALL Working Party
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Clinical Efficacy of Mitoxantrone and Ara-C with or without Etoposide Salvage Chemotherapy in Adult Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia: Retrospective Multicenter Study of the Korean Adult ALL Working Party

机译:米托蒽醌和Ara-C联合或不联合依托泊苷抢救化疗在成人复发或难治性急性淋巴细胞白血病中的临床疗效:韩国成人ALL工作组的回顾性多中心研究

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Mitoxantrone is a conventional agent for relapsed or refractory acute lymphoblastic leukemia (ALL). However, an effective combination with other drugs and a feasible dosage has not been identified. A retrospective study of 46 patients with relapsed or refractory ALL was conducted to determine the efficacy of mitoxantrone and Ara-C treatment with (MEC) and or without etoposide (MC). Twenty-seven and 19 patients received MC and MEC chemotherapy, respectively. Twenty-two (48%) patients showed overall response [complete response (CR), 33%; CR with incomplete platelet recovery (CRp), 15%], and 10 of 22 responders received allogeneic stem cell transplantation (SCT). Median overall survival (OS) was 6.2 months (95% confidence interval, 3.41-9.0). Thirteen (48%) patients in the MC group and 9 (47%) in the MEC group achieved CR/CRp (p = 0.96). Treatment-related mortalities in the MC and MEC groups were 3 (11%) and 4 (21%), respectively (p = 0.36). However, the MEC group frequently presented with grade 3 or higher bacteremia/candidemia (p = 0.013). No difference in OS was observed between the two groups (p = 0.769). In conclusion, salvage therapy consisting of mitoxantrone and Ara-C without etoposide appeared to be an effective bridge therapy to allogeneic SCT for patients with refractory or relapsed ALL. (C) 2014 S. Karger AG, Basel
机译:米托蒽醌是复发或难治性急性淋巴细胞白血病(ALL)的常规药物。然而,尚未确定与其他药物的有效组合和可行的剂量。对46例复发或难治性ALL患者进行了回顾性研究,以确定米托蒽醌和Ara-C联合(MEC)和不联合依托泊苷(MC)的疗效。二十七和十九例患者分别接受了MC和MEC化疗。 22名(48%)患者显示出总体缓解[完全缓解(CR),33%;血小板恢复不完全(CRp)的CR(15%),22名应答者中有10名接受了异体干细胞移植(SCT)。中位总生存期(OS)为6.2个月(95%置信区间为3.41-9.0)。 MC组有13名(48%)患者,MEC组有9名(47%)患者达到CR / CRp(p = 0.96)。 MC组和MEC组的治疗相关死亡率分别为3(11%)和4(21%)(p = 0.36)。但是,MEC组经常出现3级或更高的菌血症/念珠菌血症(p = 0.013)。两组之间的OS无差异(p = 0.769)。总之,对于难治性或复发性ALL患者,由米托蒽醌和Ara-C组成但不含依托泊苷的抢救疗法似乎是通向异基因SCT的有效桥梁疗法。 (C)2014 S.Karger AG,巴塞尔

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