[Safety and efficacy of mitoxantrone liposome combined chemotherapy in the treatment of mixed phenotype acute leukemia].

Q3 Medicine
H W Jiang, C Lu, J He, Q Z Wei, M F Su, Y H Wu, J B Hu
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引用次数: 0

Abstract

Objective: To evaluate the safety and efficacy of mitoxantrone liposome (MIT-LIP) combined chemotherapy in treating mixed phenotype acute leukemia (MPAL) . Methods: December 2021 to November 2024, MPAL patients who underwent the MAED (MIT-LIP + cytarabine + etoposide + dexamethasone) regimen were retrospectively analyzed. Data on clinical characteristics, adverse reactions, therapeutic outcomes, and long-term prognoses were collected. Results: A total of 7 MPAL patients who received MAED regimen were admitted. Among them, two patients were initially diagnosed with T-ALL or B-ALL, respectively, and transformed into AML after treatment. Three patients were initially diagnosed as MPAL (B/myeloid), one as MPAL (T/myeloid), and one with MPAL (myeloid/plasmacytoid dendritic cell). Among the 7 patients, there were 3 males and 4 females, 1 chromosome abnormalities and 6 gene abnormalities, including 1 case with BCR∷ABL fusion gene. The median age was 38 years (range: 16-58 years). There was no clear related drug allergy and organ toxicity during MAED regimen, and the main adverse effect was hematological toxicity. After induced chemotherapy, all patients achieved complete remission (CR), 2 maintained MRD-negative CR and 1 maintained MRD-positive CR. The other 4 patients underwent allogeneic hematopoietic stem cell transplantation, 2 maintained MRD-negative CR, and 2 relapsed. The current median follow-up time was 12 months, the overall survival (OS) rate was 100%, the relapse-free survival (RFS) rate was 60%, and the median OS time and median RFS time were not reached. Conclusion: The MAED regimen demonstrates high safety and a favorable CR rate in MPAL treatment.

[米托蒽醌脂质体联合化疗治疗混合表型急性白血病的安全性和有效性]。
目的:评价米托蒽醌脂质体(MIT-LIP)联合化疗治疗混合表型急性白血病(MPAL)的安全性和有效性。方法:回顾性分析2021年12月至2024年11月接受MAED (MIT-LIP +阿糖胞苷+依托泊苷+地塞米松)方案治疗的MPAL患者。收集临床特征、不良反应、治疗结果和长期预后的数据。结果:共有7例MPAL患者接受了MAED方案。其中2例患者最初分别诊断为T-ALL或B-ALL,经治疗后转化为AML。3例患者最初诊断为MPAL (B/髓),1例为MPAL (T/髓),1例为MPAL(髓/浆细胞样树突状细胞)。7例患者中男性3例,女性4例,染色体异常1例,基因异常6例,其中BCR∷ABL融合基因1例。中位年龄为38岁(范围16-58岁)。在MAED治疗方案中,药物过敏和器官毒性无明显相关性,主要不良反应为血液毒性。诱导化疗后,所有患者均达到完全缓解(CR), 2例维持mrd阴性CR, 1例维持mrd阳性CR,其余4例接受同种异体造血干细胞移植,2例维持mrd阴性CR, 2例复发。目前中位随访时间为12个月,总生存率(OS)为100%,无复发生存率(RFS)为60%,中位OS时间和中位RFS时间均未达到。结论:MAED方案治疗MPAL安全性高,CR率好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
自引率
0.00%
发文量
100
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