Azacitidine combined with interferon-α for pre-emptive treatment of AML/MDS after allogeneic peripheral blood stem cell transplantation: A prospective phase II study

IF 5.1 2区 医学 Q1 HEMATOLOGY
Chongmei Huang, Yannan Jia, Jun Yang, Yu Cai, Yin Tong, Huiying Qiu, Kun Zhou, Xinxin Xia, Ying Zhang, Chang Shen, Liping Wan, Xianmin Song
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Abstract

This prospective clinical study aimed to evaluate the efficacy and safety of the pre-emptive treatment modality of azacitidine in combination with interferon-α (IFN-α) in AML/MDS patients post-transplantation. Forty-seven patients aged 17–62 were enrolled with 14 patients having completed the planned 12 cycles. Following initiation, 72.3% responded positively after the first cycle, peaking at 77.2% by the fifth cycle. Notably, 24 patients maintained sustained responses throughout a median follow-up of 1050 days (range, 866–1234). Overall survival, leukaemia-free survival and event-free survival probabilities at 3 years were 69.5%, 60.4% and 35.7% respectively. Cumulative incidences of relapse and non-relapse mortality were 36.5% and 4.3% respectively. Multivariate analysis identified that receiving pre-emptive treatment for fewer than six cycles and the absence of chronic graft-versus-host disease after intervention was significantly associated with poorer clinical outcomes. The combination of azacitidine with IFN-α was well-tolerated with no observed severe myelotoxicity, and the majority of adverse events were reversible and manageable. In conclusion, the use of azacitidine in conjunction with IFN-α as pre-emptive therapy is a safe and effective treatment to prevent disease progression in AML/MDS patients with MRD positivity post-allo-HSCT.

Abstract Image

阿扎胞苷联合干扰素α用于异体外周血干细胞移植后急性髓细胞白血病/骨髓增生异常综合征的先期治疗:前瞻性 II 期研究。
这项前瞻性临床研究旨在评估阿扎胞苷联合干扰素-α(IFN-α)对移植后急性髓细胞白血病/骨髓增生异常综合征患者进行先期治疗的有效性和安全性。47名年龄在17-62岁之间的患者接受了治疗,其中14名患者完成了计划的12个周期。开始治疗后,72.3%的患者在第一个周期后产生了积极反应,到第五个周期时达到77.2%的峰值。值得注意的是,24 名患者在中位 1050 天(866-1234 天)的随访过程中保持了持续反应。3年的总生存率、无白血病生存率和无事件生存率分别为69.5%、60.4%和35.7%。复发和非复发死亡率的累积发生率分别为36.5%和4.3%。多变量分析表明,接受少于6个周期的先期治疗以及干预后未出现慢性移植物抗宿主病与较差的临床预后显著相关。阿扎胞苷与 IFN-α 的联合治疗耐受性良好,未观察到严重的骨髓毒性,大多数不良反应是可逆和可控的。总之,阿扎胞苷与IFN-α联用作为先期治疗是一种安全有效的治疗方法,可预防骨髓造血干细胞移植后MRD阳性的AML/MDS患者的疾病进展。
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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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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