The Application of Personalized Conditioning Regimens in Relapsed/Refractory Acute Myeloid Leukemia Receiving Allogeneic Hematopoietic Stem Cell Transplantation.

IF 0.8
Shuangzhu Liu, Biqi Zhou, Chongsheng Qian, Zheng Li, Yanjun Wu, Zhen Yao, Mingzhu Xu, Sheng-Li Xue
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Abstract

Objective: To evaluate the efficacy and safety of personalized conditioning regimens in allogeneic hematopoietic stem cell transplantation (allo-HSCT) for the treatment of relapsed/ refractory acute myeloid leukemia (R/R AML).

Methods: A retrospective analysis of the clinical data of 14 R/R AML patients who underwent allo-HSCT with a personalized conditioning regimen was conducted.

Results: Among the 14 patients, there were 8 males and 6 females with a median age of 34.5 years (range 14-56). One patient received a transplant from a fully matched related donor, 2 from unrelated donors, and 12 from haploidentical donors. Prior to transplantation, all patients had a myeloblast percentage greater than 5% before transplantation, with a median myeloblast of 8.5 (6-88)%. Thirteen patients (92.86%) achieved morphologic leukemia-free state (MLFS) after conditioning. All patients achieved successful engraftment and hematopoietic recovery. The median time to neutrophil engraftment was 12 days (range 10-14), and the median time to platelet engraftment was 21.5 days (range 17-29). There was no obvious hepatorenal toxicity during the conditioning, and no mucositis more than grade 2 according to CTCAE 5.0 [1]. Bone marrow biopsies at +30 days post-transplant indicated remission in all cases. Two patients relapsed at 2 and 3 months post-transplant, with 2 dying after relapse. Additionally, 2 patients had CMV infections; 1 became negative after treatment, while the other remained positive and later died due to severe infection. As of the last follow-up, 11 out of 14 patients were alive (with marrow morphology and MRD Continuously negative).

Conclusion: Allo-HSCT with a personalized conditioning regimen can be considered a treatment option for patients with R/R AML.

个性化调理方案在复发/难治性急性髓系白血病异基因造血干细胞移植中的应用
目的:评价同种异体造血干细胞移植(alloo - hsct)治疗复发/难治性急性髓系白血病(R/R AML)个体化调理方案的有效性和安全性。方法:回顾性分析14例接受同种异体造血干细胞移植和个性化治疗方案的急性髓系白血病患者的临床资料。结果:14例患者中,男性8例,女性6例,年龄14 ~ 56岁,中位年龄34.5岁。1名患者接受了完全匹配的亲属供者的移植,2名患者接受了非亲属供者的移植,12名患者接受了单倍体相同的供者的移植。移植前,所有患者的成髓细胞百分比均大于5%,中位成髓细胞百分比为8.5%(6-88)%。13例(92.86%)患者经调理后达到形态无白血病状态(MLFS)。所有患者移植成功,造血功能恢复。中性粒细胞移植的中位时间为12天(范围10-14),血小板移植的中位时间为21.5天(范围17-29)。调理期间无明显肝肾毒性,CTCAE 5.0[1]无黏膜炎2级以上。移植后+30天的骨髓活检显示所有病例缓解。2例患者移植后2个月和3个月复发,2例复发后死亡。此外,2例患者有巨细胞病毒感染;1例经治疗后呈阴性,1例仍呈阳性,后因严重感染死亡。截至最后一次随访,14例患者中有11例存活(骨髓形态和MRD持续阴性)。结论:Allo-HSCT配合个性化的治疗方案可以被认为是R/R AML患者的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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