Timed sequential salvage chemotherapy for relapsed or refractory acute myeloid leukemia.

Clinical Hematology International Pub Date : 2020-03-01 Epub Date: 2019-12-09 DOI:10.2991/chi.d.191128.001
Bogdan Popescu, Sheenu Sheela, Julie Thompson, Sophia Grasmeder, Therese Intrater, Christin B DeStefano, Christopher S Hourigan, Catherine Lai
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Abstract

Therapy for those with relapsed or refractory acute myeloid leukemia is suboptimal. Studies have suggested that timed sequential salvage combination cytotoxic chemotherapy may have particular utility for that indication. We report here a series of ten such adult patients treated sequentially at a single center with EMA (cytarabine 500 mg/m2/day as continuous infusion on days 1-3 and days 8-10, mitoxantrone 12 mg/m2/day on days 1-3, and etoposide 200 mg/m2/day as continuous infusion on days 8-10). The overall complete remission rate was 40% (including 3 of 4 of those with relapsed disease) but use of this regimen was associated with prolonged cytopenia and a high rate of infectious adverse events. Even with the availability of modern infectious prophylaxis and therapies, the EMA regimen is likely best reserved for those with relapsed disease treated with curative intent prior to an allogeneic hematopoietic cell transplant.

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针对复发或难治性急性髓性白血病的定时序贯挽救性化疗。
对复发或难治性急性髓性白血病患者的治疗效果并不理想。研究表明,定时序贯挽救性联合细胞毒性化疗在该适应症中可能具有特殊疗效。我们在此报告了在一个中心使用 EMA(阿糖胞苷 500 毫克/平方米/天,第 1-3 天和第 8-10 天连续输注;米托蒽醌 12 毫克/平方米/天,第 1-3 天连续输注;依托泊苷 200 毫克/平方米/天,第 8-10 天连续输注)连续治疗的 10 例此类成人患者。总的完全缓解率为 40%(包括 4 例复发患者中的 3 例),但使用该方案会导致细胞减少时间延长,感染性不良反应发生率高。即使现在有了现代的感染预防和治疗方法,EMA 方案也可能只适用于那些在异基因造血细胞移植前接受治愈性治疗的复发患者。
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