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阿扎胞苷用于异基因造血干细胞移植后髓系恶性肿瘤患者的维持治疗。

Maintenance therapy with Azacitidine for patients with myeloid malignancies after allogeneic hematopoietic stem cell transplantation.

作者信息

Lu Linli, Cheng Qian, Yan Yuhan, Chen Xin, Tang Yishu, Li Xin

机构信息

Department of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.

Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China.

出版信息

Sci Rep. 2025 Apr 18;15(1):13402. doi: 10.1038/s41598-025-98059-z.

Abstract

Disease relapse is a major cause of treatment failure after allogeneic haematopoietic stem cell transplantation (allo-HSCT) in patients with acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS). We retrospectively evaluated all patients (n = 145) with high-risk AML and MDS who underwent allo-HSCT between 2016 and 2022. Among them, 53 patients received maintenance therapy with azacitidine (AZA), and 10 of these patients received preemptive therapy. The rest of the 92 patients were in the control arm. The median follow-up time was 1215 days (103-3173 days). The median number of administered AZA cycles was 8. The 2-year relapse-free survival was 86.8% (46/53) in the AZA group compared with 76.1% (70/92) in the control group (P = 0.121). The 2-year overall survival in the AZA and control groups were 88.7% (47/53) and 82.6% (76/92), respectively (P = 0.326). Six patients (11.3%) in the AZA group experienced relapse, all of whom had a minimal residual disease (MRD)-positive status pre-HSCT. A total of 17 (32.1%) patients experienced grade 3-4 adverse events. In the preemptive therapy group, 70% (7/10) of the patients achieved complete remission after AZA treatment. AZA maintenance therapy following allo-HSCT is well tolerated and further follow-up and a larger group of patients will be necessary to confirm the potential to prevent relapse. The pre-transplant MRD status was identified as an important factor affecting the efficacy of AZA maintenance therapy.

摘要

疾病复发是急性髓系白血病(AML)和骨髓增生异常综合征(MDS)患者异基因造血干细胞移植(allo-HSCT)后治疗失败的主要原因。我们回顾性评估了2016年至2022年间接受allo-HSCT的所有高危AML和MDS患者(n = 145)。其中,53例患者接受了阿扎胞苷(AZA)维持治疗,其中10例患者接受了抢先治疗。其余92例患者为对照组。中位随访时间为1215天(103 - 3173天)。AZA给药周期的中位数为8。AZA组的2年无复发生存率为86.8%(46/53),而对照组为76.1%(70/92)(P = 0.121)。AZA组和对照组的2年总生存率分别为88.7%(47/53)和82.6%(76/92)(P = 0.326)。AZA组有6例患者(11.3%)复发,所有这些患者在HSCT前均为微小残留病(MRD)阳性状态。共有17例(32.1%)患者发生3 - 4级不良事件。在抢先治疗组中,70%(7/10)的患者在接受AZA治疗后达到完全缓解。allo-HSCT后AZA维持治疗耐受性良好,需要进一步随访和更大规模的患者群体来确认其预防复发的潜力。移植前MRD状态被确定为影响AZA维持治疗疗效的重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2865/12008360/5505a6b9e8e9/41598_2025_98059_Fig1_HTML.jpg

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