Popescu Bogdan, Sheela Sheenu, Thompson Julie, Grasmeder Sophia, Intrater Therese, DeStefano Christin B, Hourigan Christopher S, Lai Catherine
Laboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health.
Clin Hematol Int. 2020 Mar;2(1):27-31. doi: 10.2991/chi.d.191128.001. Epub 2019 Dec 9.
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/m/day as continuous infusion on days 1-3 and days 8-10, mitoxantrone 12 mg/m/day on days 1-3, and etoposide 200 mg/m/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.
对于复发或难治性急性髓系白血病患者,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可能对该适应症具有特殊作用。我们在此报告了在单一中心对10例此类成年患者依次进行EMA方案治疗的情况(阿糖胞苷500mg/m²/天,在第1 - 3天和第8 - 10天持续输注;米托蒽醌12mg/m²/天,在第1 - 3天;依托泊苷200mg/m²/天,在第8 - 10天持续输注)。总体完全缓解率为40%(包括4例复发患者中的3例),但使用该方案会导致血细胞减少期延长以及感染性不良事件发生率较高。即使有现代感染预防和治疗手段,EMA方案可能最好仅用于那些在异基因造血细胞移植前接受根治性治疗的复发患者。