美法仑和阿糖胞苷治疗复发或难治性急性白血病

C. Malaval, M. Queudeville, Michaela D ring, U. Hartmann, P. Lang, R. Handgretinger, M. Ebinger
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摘要

背景:儿童白血病预后良好,急性淋巴细胞白血病患儿总治愈率为85%,急性髓细胞白血病患儿总治愈率为50-60%。然而,对于难治性或复发性白血病患者,预后有限,只能通过补救性化疗来治愈,在大多数情况下,随后进行异体造血干细胞移植。方法:在这项回顾性病例队列分析中,我们研究了8例复发或难治性急性髓系(n=2)、淋巴母细胞(n=4)、双表型(n=1)白血病或t淋巴母细胞淋巴瘤(n=1)患者的预后,这些患者对标准挽救方案无效。他们在2015年至2019年期间在我们机构接受了美法兰和阿糖胞苷的补救性治疗。结果:经美法兰和阿糖胞苷补救性化疗后,63%的患者病情缓解,符合后续异基因造血干细胞移植的条件。1年总生存率50%,3年总生存率29%。25%的患者经历了短暂的发烧和SIRS。结论:我们报道的病例队列分析结果表明,美法兰和阿糖胞苷对复发或难治性白血病的补救性治疗可能是一种治疗方法,有可能实现缓解和随后的异基因造血干细胞移植。需要未来的多中心研究来验证本文提出的结果。
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Melphalan and cytarabine as a salvage therapy in children with relapsed or refractory acute leukemia
Background: Leukemia in children has a good prognosis with an overall cure rate of 85% in pediatric patients with acute lymphoblastic leukemia and 50-60% in pediatric patients with acute myeloid leukemia. Nevertheless in patients with refractory or relapsed leukemia the prognosis is limited and can only be cured by a salvage chemotherapy, in most cases followed by an allogeneic hematopoietic stem cell transplantation. Methods: In this retrospective case cohort ananlysis we investigated the outcome of eight patients with relapsed or refractory acute myeloid (n=2), lymphoblastic (n=4), biphenotypic (n=1) leukemia or T-lymphoblastic lymphoma (n=1) who failed to respond to standard salvage regimens. They received a salvage therapy with melphalan and cytarabine at our institution between 2015 and 2019. Results: After salvage chemotherapy with melphalan and cytarabine 63% of the patients achieved a remission of the disease and qualified for subsequent allogeneic hematopoietic stem cell transplantation. The one year overall survival rate was 50%, the three year overall survival rate was 29%. 25% of patients experienced a temporary period of fever and SIRS. Conclusions: The reported results of our case cohort analysis indicate that a salvage therapy with melphalan and cytarabine in relapsed or refractory leukemia could represent a curative approach with the possibility of achieving remission and subsequent allogeneic hematopoietic stem cell transplantation. Future multicentre studies are needed to verify the here presented results.
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