依托泊苷、米托蒽醌和卡他滨(EMA)强化序贯化疗对异基因干细胞移植后急性髓系白血病复发患者的疗效:回顾性分析

LLM Dergi Pub Date : 2019-12-10 DOI:10.5578/llm.68966
Ayla Gökmen, E. Soydan, Zafer Gökgöz, Ozan Özkumur, Ş. Şen, Ö. Arslan, M. Özcan
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引用次数: 0

摘要

alınama-ABSTRACT目的:异基因干细胞移植后的疾病复发,取决于疾病类型和手术时的状态,仍然是急性髓性白血病(AML)患者治疗失败的主要原因。干细胞移植后AML复发患者的最佳治疗策略仍存在争议,预后普遍较差。我们回顾性分析了我们血液科同种异体干细胞移植后急性髓系白血病复发患者采用依托糖苷、米托蒽醌和阿糖胞苷(EMA)强化序次化疗的疗效。患者与方法:回顾性分析2015-2018年16例同种异体干细胞移植后复发的急性髓系白血病患者的EMA化疗。结果:16例患者中有7例(43.7%)达到完全缓解。所有患者均出现4级中性粒细胞减少症、血小板减少症和中性粒细胞减少热。5例(31.3%)患者在治疗期间因感染死亡。7名患者在EMA后获得完全缓解,接受了基于供体细胞的进一步治疗。有效患者的一年生存率为%57。结论:干细胞移植后AML复发患者采用供体细胞为基础的治疗策略可实现长期生存。通过细胞减少疗法诱导完全缓解可以影响适合强化治疗的患者的生存。在这些患者中,强化序贯EMA化疗是诱导缓解的有效选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intensive Sequential Chemotherapy with Etoposide, Mitoxantrone and Ctarabine (EMA) as Salvage in Patients with Acute Myeloid Leukemia Relapsing After Allogeneic Stem Cell Transplantation a Retrospective Analysis
alınama-ABSTRACT Objective: Disease relapse following allogeneic stem cell transplantation which depends on the type of the disease and the status at the time of procedure, remains the major cause of treatment failure in patients with acute myeloid leukemia (AML). The optimal treatment strategy for patients with AML relapsing after stem cell transplantation remains contraversial and the prognosis is generally poor. We retrospectively analysed the efficacy of intensive sequential chemoterapy with etoside, mitoxantrone and cytarabine (EMA) to achieve remission in patients with AML relapsing after allogeneic stem cell transplantation in our hematology department. Patients and Methods: Sixteen AML patients relapsing after allogeneic stem cell transplantation who were treated with EMA chemoterapy between 2015-2018 were analysed retrospectively. Results: Complete remission was achieved in 7 (43.7%) of 16 patients. All patients suffered grade 4 neutropenia, thrombocytopenia and neutropenic fever. Five (31.3%) patients were died during treatment due to infection. Further treatment with donor cell based therapies was given in seven patients who achieved complete remission after EMA. One-year survival rates in responding patients was %57. Conclusion: Long term survival can be achieved with donor cell based treatment strategy in patients with AML relapsing after stem cell transplantation. Induction of complete remission with cytoreductive therapy can influence the survival of patients who are suitable for intensive therapy. Intensive sequential EMA chemoterapy is an efficacious option to induce remission in theese patients.
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